Wong Et Al. (2007)

Reviews in Medical Virology
REVIEW
Rev. Med. Virol. 2007; 17: 6791.

Published online 16 October 2006 in Wiley InterScience
(www.interscience.wiley.com)
DOI: 10.1002/rmv.520
Bats as a continuing source of emerging

infections in humans
Samson Wong, Susanna Lau, Patrick Woo and Kwok-Yung Yuen*
Department of Microbiology, Research Centre of Infection and Immunology, The University of Hong Kong,
4/F University Pathology Building, Queen Mary Hospital, 102 Pokfulam Road, Hong Kong
SUMMARY
Amongst the 60 viral species reported to be associated with bats, 59 are RNA viruses, which are potentially important
in the generation of emerging and re-emerging infections in humans. The prime examples of these are the lyssaviruses
and Henipavirus. The transmission of Nipah, Hendra and perhaps SARS coronavirus and Ebola virus to humans may
involve intermediate amplication hosts such as pigs, horses, civets and primates, respectively. Understanding of the
natural reservoir or introductory host, the amplifying host, the epidemic centre and at-risk human populations are
crucial in the control of emerging zoonosis. The association between the bat coronaviruses and certain lyssaviruses
with particular bat species implies co-evolution between specic viruses and bat hosts. Cross-infection between the
huge number of bat species may generate new viruses which are able to jump the trans-mammalian species barrier
more efciently. The currently known viruses that have been found in bats are reviewed and the risks of transmission
to humans are highlighted. Certain families of bats including the Pteropodidae, Molossidae, Phyllostomidae, and Vespertilionidae are most frequently associated with known human pathogens. A systematic survey of bats is warranted to
better understand the ecology of these viruses. Copyright # 2006 John Wiley & Sons, Ltd.
Supplementary electronic material for this paper is available in Wiley Interscience at http://www.interscience.wiley.
com/jpages/10529276/suppmat
Received: 24 May 2006; Revised: 8 August 2006; Accepted: 29 August 2006
INTRODUCTION
Zoonoses are diseases and infections which are
naturally transmitted between vertebrate animals
and man [1]. Zoonotic pathogens are currently
considered to be the major sources of emerging
and re-emerging infections in humans and RNA
viruses account for the overwhelming majority of
emerging pathogens [2]. At the time of writing, the
most important non-mammalian vertebrates associated with emerging infections in humans are the
birds. The avian species have an enormous population: the estimated world poultry population in
agriculture (chickens, ducks, geese and turkeys)
in 2005 was over 18 billion [3]. Poultry birds often
*Corresponding author: Kwok-Yung Yuen, Department of Microbiology, The University of Hong Kong, 4/F University Pathology
Building, Queen Mary Hospital, 102 Pokfulam Road, Hong Kong.
E-mail: [email protected]
Abbreviations used
SARS, severe acute respiratory syndrome.
Copyright # 2006 John Wiley & Sons, Ltd.
have large populations reared in relatively

restricted environments. Wild birds have a tendency to gather in ocks and many species y or
migrate over long distances. All these are important attributes which allow them to harbour and
disseminate infectious agents over vast geographical areas. Their impacts on public health and economy are best exemplied by the West Nile virus
encephalitis in North America and the global
inuenza A H5N1 outbreaks. The latter carries
major economic losses in agriculture and the
potential to cause a pandemic associated with signicant morbidity and mortality in humans.
Infectious agents exist in commensal, mutual or
parasitic relationships with their harbouring animal hosts. The relationship is often restricted to a
limited number of host species owing to genetic
adaptations that developed during co-evolution.
This gives rise to the concept of species barrier in
infectious diseases. However, spillage of infectious
agents between different animal species does
68
occur sporadically. This may result from accidental or deliberate intrusion by one animal species
into the ecological niche of another, resulting in
the direct exposure to the infectious agents from
the original harbouring species or acquisition
from the environment. Severe diseases often occur
in the new animal hosts in the absence of genetic
adaptations of the infectious agent to these new
hosts. These new animals may become dead
end hosts when the infectious agent fails to
cause further transmission under natural conditions (e.g. Japanese encephalitis in humans), or
they may contribute to further transmissions
resulting in an epidemic (e.g. SARS). The transmission dynamics of some important bat-associated
viruses are summarised in Table 1. Understanding
the amplifying host, the routes of transmission, the
type of susceptible human hosts, and the epicentres for zoonotic and human transmissions in crucial in the control of these infections.
The relative probability of an infectious agent
jumping from one animal species to another is
often assumed to be related to the phylogenetic
relatedness of the host species. However, experience from zoonoses acquired from birds shows
that we should focus not just on those animals
which are phylogenetically close to humans
(such as the primates and rodents), but also on
those which are more distantly related but have
attributes that enable them to harbour and spread
novel microbes. Hunting of non-human primates
for bushmeat has been practised in tropical Africa
for aeons. Such exposures have resulted in transmission of pathogens like Ebola virus, simian
foamy viruses, simian immunodeciency virus,
and human immunodeciency viruses to humans
[46]. Rodents are not only the largest order of all
mammals but also often exist in large numbers in
urban and rural habitats. They are important
sources of zoonotic pathogens including Sin Nombre and other hantaviruses. Bats are the only mammals possessing true ying ability. In recent years
bats have increasingly been recognised to be
potential reservoirs for various emerging infections. The bats and their associated viral pathogens will be discussed in this article.
BAT BIOLOGY, ECOLOGY AND HUMAN
INFECTIOUS DISEASES
The bats represent the second largest order within
the mammals. There are currently over 4600
S. Wong et al.
known species of mammals (Class Mammalia)
[7]. The largest order within Mammalia consists
of the rodents (Order Rodentia) with over 2000
species, and there are over 930 species of bats
(Order Chiroptera), or about 20% of all mammalian species. There are two suborders within
Chiroptera, the Megachiroptera and Microchiroptera. Pteropodidae (ying foxes) is the only family
within Megachiroptera (166 species) and they
mainly feed on plant materials. There are 16
families within Microchiroptera (over 760 species)
with diverse biology and ecology (Table 2) [7,8].
Bats are found in all continents except the polar
regions and a few oceanic islands. The nature of
their diet is equally diverse, varying from plants,
insects, animals and, unique among mammals,
blood. The diversity of bat species and some of
their unique biological and ecological features
allow them to become the hosts for a large number
of medically important infectious agents. Most
bats are nocturnal animals and seek shelter in
roosts during the day. A few species are diurnal.
The roosting environment ranges from natural to
man-made structures and they can be temporary
or permanent (Figure 1). Natural roosts can be
found in caves, rock crevices, nests of birds or
ants and termites, cavities in trees, or exposed on
tree branches and trunks [9]. Man-made habitats
include mines, tombs, buildings, bridges and so
on. The occupation of man-made habitats could
bring the bats into closer association with humans
and their companion animals or livestock. The signicance of this is seen in the transmission of some
pathogens, such as bat rabies viruses, from peridomestic bats to humans and livestocks. The number
of bats in each colony varies greatly from less than
10 to over 200 000 individuals [9]. The large number of individuals, together with the social habits
of the bats, such as mutual grooming and biting
during courtship and mating, facilitates the
transmission of infectious agents between them
through direct contact, aerosols or arthropod
vectors.
The dietary habits of bats can broadly be divided
into insectivorous, frugivorous, carnivorous, omnivorous and sanguivorous [10]. Predatory bats
could potentially acquire infectious agents from
other animal species, such as birds and insects.
Sanguinivory in bats is limited to only three species
of vampire bats, Desmodus rotundus, Diphylla ecaudara, and Diaemus youngi, all belonging to the
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv

Bats
Bats,
carnivores
Bats
Nipah virus
Rabies viruses
European and
Australian bat
lyssaviruses
Nil (direct bat-tohuman transmission)
Nil (direct bat-tohuman transmission);

occasionally spillover
to terrestrial mammals;
rarely through organ
transplantation
Pigs
Pigs
Biologist and other

personnel
handling bats
Biologist and other

personnel handling
bats; residents in
endemic areas
(e.g. Latin America)
Pig farmers,
abbatoir workers
Pig farmers
Close contacts with

horses
Sporadic cases only
Rural residents;
occasionally in urban
environment
Pig farm,
abbatoirs
Pig farms
Horse farms
Transmission from bats to human has been postulated for these viruses but has not been proven.
Bats
Menangle virus
Horses
Bats
Hendra virus
Forests
Non-human primates
Batsa
Ebola virus
Biologists handling
primates, bushmeat
hunters
Palm civets and

Restaurant or market
Wet markets
possibly other animals workers handling wild (SARS-CoV)
in wet markets
animals (SARS-CoV)
Batsa
Epicentre for
animal-to-human
transmission
Coronaviruses
related to
SARS-CoV
Populations at-risk
of zoonotic
infection
Amplication
host(s)
Natural
reservoir
host
Virus
Table 1. Transmission dynamics of selected bat-associated viruses
Nil
Nil; rarely through

organ transplantation
Health care facilities

(possible), families
(possible)
Nil
Nil
Health care facilities,

families
Health care facilities

(SARS-CoV)
Epicentre for
human-to-human
transmission
Bats and emerging infection

69
Rev. Med. Virol. 2007; 17: 6791.

DOI: 10.1002/rmv
S. Wong et al.
70
Table 2. Summary of bat families (7,8)

Familya
Common
names
Major feeding
habits
Main geographical
distribution
Pteropodidae*
Flying foxes
Craseonycteridae
Emballonuridae*
Furipteridae
Megadermatidae
Bumblebee bats
Sheath-tailed bats
Smoky bats
False vampires
Molossidae*
Free-tailed bats
Fruit, nectar,
pollen, insects
Insects
Insects
Insects
Arthropods,
small vertebrates
Insects
Mormoopidae
Mystacinidae
Mustached bats
Short-tailed bats
Tropical Asia, Australia,

Africa
Thailand
Worldwide, tropical
New World, tropical
Tropical Asia, Australia,
Africa
Worldwide, tropical and
subtropical
New World, tropical
New Zealand
Myzpodidae
Natalidae
Noctilionidae
Sucker-footed bats
Funnel-eared bats
Bulldog bats, sherman
bats
Slit-faced bats
New World leaf-nosed
bats
Nycteridae
Phyllostomidae*
Rhinolophidae*
Rhinopomatidae
Thyropteridae
Vespertilionidae*
Horseshoe bats and Old

World leaf-nosed bats
Mouse-tailed bats
Disc-winged bats
Evening bats
Insects
Fruit, pollen, nectar,
small vertebrates, carrion
Insects
Insects
Arthropods, sh
Arthropods
Insects, fruit, pollen,
nectar, small vertebrates,
blood (only Desmodus
rotundus, Diaemus youngi,
and Diphylla ecaudata)
Insects
Insects
Insects
Insects
Madagascar
New World, tropical
New World, tropical
Africa, Southeast Asia
New World, tropical
Old World, tropical and

temperate
North Africa, India
New World, tropical
Worldwide
Families for which bat species carry known human pathogens are marked with an asterisk.
family Phyllostomidae and found only in Latin

America. The vampire bats prey on birds and
mammals and may also supplement their diet
with insects. The diet of bats may not have direct
relationships with the nature of pathogens they
carry, as the same group of infectious agents could
be carried by diverse bat species with different
dietary habits. However, the search for foods may
bring certain bats into close contacts with humans
and other animals, thereby facilitating interspecies
transmission of infectious agents. Such aberrant
interactions often occur as a result of natural or
man-made environmental perturbations and have
been implicated in the transmission of the Nipah
and bat rabies viruses to humans and Ebola virus

to primates.
Bats y over a relatively large distance from
their roosting sites in search for food. Microchiropterans commonly have a foraging distance of 10
15 km while some may y over 80 km a night.
Megachiropterans can travel up to 50 km [10].
Some species may utilise night roosts near feeding
sites and distant from their day roosts. Despite
their small sizes, bats have a relatively long life
span and develop slowly. Many species live for
over 1020 years with some species living for
over 30 years in the wild [10,11]. Host longevity
facilitates the persistence of infectious agents in
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv
71
bats and thereby increases the chance of spread
through natural or accidental dispersal of the
bats into new geographical areas.
When faced with winter and shortage of food
supply, bats may either hibernate or migrate. The
megachiropterans do not hiberbnate. Hibernation
in microchiropterans involves substantial physiological changes during torpor, including an accumulation of brown adipose tissue. Hibernating
bats can remain torpid continuously for up to
75 days, though many will have periodic arousal
alternating with torpor periods lasting from 2 to
15 days [12]. Seasonal migration has been
observed for bats living in both temperate and tropical environments, which demonstrate substantial seasonal changes in food supply and/or
temperature. The maximal distance of migration
of the studied bat species ranges from 200
300 km to almost 2000 km [13].
Of all the vertebrate hosts, bats are considered to
be less important than ungulates, carnivores,
rodents, non-mammals and primates in terms of
the prevalence of zoonotic pathogens [2]. Nevertheless, bats do harbour a relatively large number
of known or potential pathogens. Some of these
appear to have co-evolved with specic bat hosts
(e.g. lyssaviruses). Transmission of viruses carried
by bats to humans can occur in a variety of ways,
with direct contact through bites and scratches the
most obvious example. Bats do not normally prey
on humans. However, Desmodus rotundus has been
known to feed on humans in Latin America when
alternative animal hosts are scarce [14,15]. Bites
sustained from other bat species are usually the
result of accidental encounters rather than deliberate attack on humans. Lyssaviruses are typical
examples of direct bat-to-human transmission of
pathogens.
Another possible route of transmission involves
inhalation of infectious particles by humans. These
infective aerosols could arise from the secretions
(e.g. saliva) or guano of the bats. This route of
transmission may possibly occur in lyssavirus
3
Figure 1. (A) Typical roosts of Rhinolophus sinicus, a cavedwelling bat that can be found in Hong Kong. (B) Rhinolophus
sinicus, bats that carry SARS-like coronaviruses in Hong Kong.
(C) Miniopterus magnater, bats that carry group 1 coronaviruses.
(D) Bats are often consumed as delicacies in some parts of the
world including China. A Cynopterus sphinx bat being served
in a restaurant in southern China
Rev. Med. Virol. 2007; 17: 6791.

DOI: 10.1002/rmv
72
infections. Arthropod vectors could serve as
another mode of transmission of pathogens
between bats and humans. Important categories
of arthropods in this regard include mosquitoes,
sand ies, and ectoparasites infesting bats such
as bat ticks, bugs and bat ies. Insects, such as
mosquitoes and sand ies may feed on both bats
and humans as shown in entomological and virological studies [16,17]. There is currently no evidence to implicate an active role of these vectors
in disease transmission, presumably because of
the lack of efcient vector-pathogen combinations
or host specicity of the vectors. Vectorborne
transmission is therefore a route that requires
further study.
The consumption of bat meat is practised in
some parts of the world including China, Guam,
and some parts of Asia where it is considered
to have therapeutic effects against asthma
(Figure 1). Adequately cooked bat meat is unlikely
to pose any risk for transmission of infections.
However, capture and slaughtering of bats could
expose the handler to the bats blood and body
uids or bites and scratches. In situations where
live bats are kept in captivity in game markets,
they may come into close contact with other
animals, which are susceptible to viruses carried
by bats. This is one of the postulated mechanisms
linking the nding of SARS-coronavirus (SARSCoV) in bats and palm civets in southern China.
The bats may have transmitted a SARS-CoV-like
virus to the civets, which in turn act as amplifying
hosts before transmitting the virus to humans.
In some situations, transmission of bat pathogens to humans occurs via a secondary vertebrate
host serving as an amplifying host. The outbreak
of Nipah virus in Southeast Asia involved pigs
as an efcient secondary host for multiplication
of the virus and horses were involved in the transmission of Hendra virus to humans, while the
palm civet is postulated to be the intermediate
host for SARS-CoV. In an extreme example,
another human host could be involved before
such transmissions are clinically evident. This is
exemplied by the transmission of the rabies virus
to four organ transplant recipients from a donor
who died of encephalitis of unknown aetiology
who, in retrospect, was found to have been bitten
by a bat [18].
The factors that promote the transmission of
pathogens from bats to humans are incompletely
S. Wong et al.
understood. One aspect is environmental changes,
either as a result of natural or climatic alterations
or conditions related to human activities. Examples include a change of feeding hosts of the vampire bat Desmodus rotundus from livestock to
humans due to a decline in the livestock population [14]. Another example is the Nipah outbreak
in Malaysia in which the loss of the normal forest
habitats of the bats forced them to reside in areas
close to livestock and human inhabitation [19,20].
The spread of the infectious disease within human
communities was further augmented by trade
in domestic animals, such as the transport of
infected pigs in the spread of Nipah virus infection. Movement of bats over large geographical
distances either as a result of natural migration,
accidental or deliberate transport via articial
vehicles can occur and these may further
facilitate the long-distance spread of potential
pathogens [21].
SYSTEMATIC REVIEW OF VIRUSES
ASSOCIATED WITH BATS
The following section summarises the important
viruses that have been found to be associated
with bats. Emphasis is put on viruses that have
clinical or veterinary signicance and those that
are better characterised. Supplementary Table
summarises the viruses together with their
main geographical distribution and natural hosts.
Table 3 summarises their potential to be
transmitted to humans based on current clinical,
virological and epidemiological information.
The detection of viruses in bats or other animals
is problematic. Unequivocal evidence for natural
infection can be obtained with a positive viral culture obtained from the animals. Another acceptable detection method is the use of direct
immunouorescent staining of bat tissues, most
commonly used in the detection of lyssaviruses
in the brains of bats. Nucleic acid amplication
may offer similar condence if the tests are
performed competently without contamination.
Unfortunately, many viruses are not readily
cultivable in vitro. Consequently, a number of eld
studies employed serological tests to look for
evidence of infection. While serology can offer
valuable information, cross-reactivity between
different members of the same family of viruses
may be observed for some test formats (e.g. haemagglutination inhibition, complement xation).
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv
73
Tacaribe virus
Kaeng Khoi virus
Moju dos Campos virus
Bimiti virus, Catu virus,
Guama virus, Manzanilla
virus, Nepuyo virus,
Oriboca virus
Toscana virus
Coronaviruses
Ebola virus
Dengue virus
Ilheus virus
Japanese encephalitis
virus
Kyasanur Forest
disease virus
Montana Myotis
leukoencephalitis
Rio Bravo virus
St Louis encephalitis
virus
Tamana bat virus
West Nile virus
Yellow fever virus
Yokose virus
Inuenza viruses
Hendra virus
Menangle virus
Nipah virus
Bat parainuenza virus
Mapuera virus
Tioman virus
Nelson Bay virus
Pulau virus
Betaretrovirus
Mount Elgon bat virus
Rabies virus
Lagos bat virus
Duvenhage virus
Vespertilionidae
Thyropteridae
Rhinopomatidae
Rhinolophidae
Phyllostomidae
Nycteridae
Noctilionidae
Natalidae
Myzpodidae
Mystacinidae
Mormoopidae
Molossidae
Megadermatidae
Furipteridae
Emballonuridae
Craseonycteridae
Viruses
Pteropodidae
Bat families
Not specified
Table 3. Risk ranking of bat-associated viruses in causing human infectionsa
D
B
D
D D
C
B
C
C
C
C
C
C
D
B
C C
C
C C
C
A
A
A
D
C
D
C
D
D
D
D
D
D
A
D
A
A
(Continues)
Rev. Med. Virol. 2007; 17: 6791.

DOI: 10.1002/rmv
S. Wong et al.
74
European bat lyssavirus 1

European bat lyssavirus 2
Australian bat lyssavirus
Aravan virus
Irkut virus
Khujand virus
West Caucasian virus
Other lyssaviruses
in Southeast Asia
Mount Elgon virus
Chikungunya virus
Eastern equine
encephalitis virus
Mucambo virus
Venezuelan equine
encephalitis virus
Western equine
encephalitis virus
B
A
Vespertilionidae
Thyropteridae
Rhinopomatidae
Rhinolophidae
Phyllostomidae
Nycteridae
Noctilionidae
Natalidae
Myzpodidae
Mystacinidae
Mormoopidae
Molossidae
Megadermatidae
Furipteridae
Emballonuridae
Craseonycteridae
Viruses
Pteropodidae
Bat families
Not specified
Table 3. (Continued)
A
A
D
D
D
D
C
D
C
C
C
D
D
C
C
Risk of bat-to-human transmission of the respective pathogens: A, documented direct bat-to-human transmission or
through secondary hosts or denite epidemiological linkage; B, potential risk of transmission directly from bats
or through secondary hosts or vectors because presence of known human pathogens documented and microbes
present in relatively high frequency in bats; C, low risk of transmission directly from bats or through vectors
because of low prevalence of pathogens in bats, inefcient vectorial capacity of bats or arthropod vectors, or
insufcient epidemiological data to support a link; D, little risk of transmission because viruses not known to infect
humans.
This is especially common in families such as

Flaviviridae. Neutralising antibodies are generally
considered to be the most specic for individual
viruses. Newer studies frequently utilise RT-PCR
and sequencing information to discriminate
between viral orders, families and genera,
irrespective of whether the viruses are cultivable
or not.
Arenaviridae
An arenavirus, Tacaribe virus, was found in a
number of bat species in Trinidad by culture and
serology [22,23]. It has not been found to infect

humans.
Bunyaviridae
Bunyaviridae includes ve genera, Bunyavirus,
Hantavirus, Nairovirus, Phlebovirus, and Tospovirus.
They constitute a huge family of viruses with a
number of prominent human pathogens such as
the hantaviruses (e.g. Hantaan, Seoul, and Sin
Nombre viruses), Crimean-Congo haemorrhagic
fever virus, and Rift Valley fever virus. The bunyaviruses have a global occurrence and many of
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv

them are arthropod-borne and have reservoirs in
vertebrates.
The Kaeng Khoi virus was initially isolated
in 1969 from the wrinkle-lipped free-tailed bat
(Chaerephon plicata) and Theobalds tomb bat
(Taphozous theobaldi) in a cave in Thailand. Subsequent studies also found virological and
serological evidence of infection in these two bats
in Thailand [24]. The virus was recently isolated
from Chaerephon plicata in Cambodia [25]. Interestingly, the virus was also isolated from bedbugs
(Stricticimex parvus and Cimex insuetus) collected
in the same bat caves, and these insects have
been postulated to play a role in transmission of
the virus between bats [24]. There is some serological evidence showing that Kaeng Khoi virus
can infect humans entering bat caves to collect
guano, and a seroprevalence of 29% among these
workers has been described. Bedbug bites were
incriminated to cause an inuenza-like illness in
the workers, which might be related to this viral
infection.
The Toscana virus is endemic in Mediterranean
countries where it is a major cause of viral meningitis and encephalitis [26]. It has been isolated
from the brain of a bat (Pipistrellus kuhli) once
but the sandiesrather than vertebratesare
considered to be its natural reservoir host [27].
Other bunyaviruses that have been detected in
bats but with uncertain clinical signicance are
listed in Supplementary Table.
Coronaviridae
The coronaviruses have become the focus of
research since the 2003 global epidemic of SARS
caused by the SARS-CoV. Coronaviruses are
known to have diverse animal hosts ranging
from mammalian to avian species. Human coronavirus infections prior to the SARS outbreak were
caused by human coronaviruses 229E and OC43
which commonly result in the common cold.
The rst cases of SARS occurred in late 2002 in
the southern Chinese province of Guangdong. The
rst conrmed case of SARS was a chef working in
a local restaurant and he had had contacts with
wild game animals prior to the onset of disease
[28]. The emergence of a novel viral infection,
together with the occupational history of contact
with wild animals among four index patients in
the Guangdong outbreak, prompted the search
for an animal reservoir of SARS-CoV. The live
75
animal retail markets in the city of Shenzhen,
Guangdong, was investigated and evidence of
infection was found in the Himalayan palm civet
(Paguma larvata) and to a lesser extent, Chinese ferret badgers (Melogale moschata) and raccoon dogs
(Nyctereutes procyonoides) [29]. Further evidence
for zoonotic transmission of SARS-CoV came
from studies which showed that wild animal
traders and slaughterers had a signicantly higher
seroprevalence (20 to 45%) against SARS-CoV
than vegetable traders and control populations (0
to 5%) [30]. Review of seroprevalence studies
showed that persons with an occupational history
of contact with wild animals had a substantially
higher prevalence of antibodies as compared to
healthy blood donors, household contact or health
care workers caring for SARS patients (12.99 to
16.69% vs. 0 to 2.92%, respectively) [31]. A recent
study showed that contact with game animals
could result in asymptomatic infection with the
SARS-CoV but that the individual could still
have detectable coronavirus antigenaemia and
seroconversion [32]. Restrictions on the sale and
consumption of game animals therefore became
important control measures during the SARS
epidemic in China. In contrast to other zoonotic
pathogens that crossed the species barrier to
humans, the SARS-CoV is notable in that it
spreads readily from person-to-person and therefore outbreaks within health care facilities was a
prominent feature during the SARS epidemic
with a fth of all global cases being health care
workers [33]. It is also unique amongst coronaviruses in that a wide host range is observed,
with the virus being able to infect (with or without
the development of illness) humans, Chinese
ferret badgers (Melogale moschata) and raccoon
dogs (Nyctereutes procyonoides), cynomolgus macaques (Macaca fascicularis), African green monkeys
(Cercopithecus atheiops, Chlorocebus sabeus), rhesus
monkeys (Macaca mulata), ferrets (Mustela furo),
domestic cats (Felis domesticus), mice, golden
Syrian hamsters (Mesocricetus auratus), common
marmosets (Callithrix jacchus), pigs, and chickens
[34,35,36,37,38].
The sudden emergence of the SARS-CoV was
initially linked to the palm civet and related animals which were found to carry the SARS-CoV
asymptomatically. The palm civet was consumed
as a game animal in southern China and sold in
the wet markets. Subsequent studies however
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv
S. Wong et al.
76
did not show a signicant amount of SARS-CoV in
wild or farmed palm civets. This suggested that
the caged palm civets in the markets may not be
a primary reservoir host of SARS-CoV in nature,
but merely a secondary amplifying host that
increases the viral burden and provides ample
contact with humans, thereby facilitating animal
to human transmission, a situation that is similar
to the Henipavirus discussed below. The search
for the primary reservoir host of SARS-CoV led
to the nding of novel coronaviruses among bats
in Hong Kong. One of these was detected in
Chinese horseshoe bats (Rhinolophus sinicus (R.
rouxii)) in Hong Kong which is currently named
bat SARS-CoV (bat-SARS-CoV) [39]. The batSARS-CoV was initially found by RT-PCR in 39%
of R. sinicus tested but seropositivity of bats ranged
from 67 to 84% when the sera were tested by western blot and enzyme immunoassay respectively.
It is postulated that the bats might serve as the natural reservoir of the SARS-CoV (or a related virus)
and the palm civets acquired the virus from the
bats before passing it on to humans.
Another new coronavirus was detected in the
lesser bent-winged bats (Miniopterus pusillus),
large bent-winged bats (Miniopterus magnater),
and Japanese long-winged bats (Miniopterus
schreibersii) [40]. This virus belongs to group 1
coronaviruses, which also includes the human
pathogens human coronaviruses 229E and NL63.
The virus was detected in 3 of 25 (12%) Miniopterus
pusillus bats in a subsequent survey in Hong
Kong which also revealed a great diversity of
coronaviruses among the bat population [41].
Coronaviruses were detected by RT-PCR of the
anal swabs in 37 of 309 bats (12%) with the batSARS-CoV being detected in 21 of 118 (17.8%) R.
sinicus. Six other coronaviruses were also discovered in different bat species: bat-CoV-HKU2 from
2 of 118 R. sinicus; bat-CoV-HKU4 from 4 of 21
(19%) lesser bamboo bats (Tylonycteris pachypus);
bat-CoV-HKU5 from 4 of 14 (28.6%) Japanese
pipistrelle bats (Pipistrellus abramus); bat-CoVHKU6 from 1 of 23 (4.3%) Ricketts big-footed
bat (Myotis ricketti); bat-CoV-HKU7 from 1 of 51
(1.9%) Miniopterus magnater, and bat-CoV-HKU8
from 1 of 25 (4%) Miniopterus pusillus. Bat-CoVHKU2, HKU6, HKU7, and HKU8 all belong to
group 1 coronaviruses, while bat-CoV-HKU4,
HKU5 belong to group 2 coronaviruses, the latter
also includes human coronaviruses OC43, HKU1
and the SARS-CoV. The association of coronaviruses with bats is also conrmed in another
study by Li et al. who documented the presence
of SARS-like coronavirus infection of bats in
Guangxi and Hubei, two provinces in southern
and central China respectively [42]. Notably,
with the exception of two positive samples which
came from Rousettus leschenaulti (Family Pteropodidae), the majority of bats carrying SARS-like
coronaviruses in China were Rhinolophus spp.,
members of which were also found to be infected
with SARS coronavirus-like virus in Hong Kong.
Figure 2 shows the phylogenetic relationship
between the known human and bat-associated coronaviruses. These ndings suggest that bats could
represent a hitherto undiscovered reservoir of the
coronaviruses, many of which might have important clinical or veterinary signicance.
Filoviridae
Filoviruses known to cause human infection
belong of two genera: Marburgvirus and Ebolavirus,
the latter containing four species, viz Sudan, Zaire,
Reston and Ivory Coast. Both Marburg and Ebola
viruses are endemic in Africa, except the Ebola
Reston virus which was acquired from primates
imported from the Philippines. Human infections
due to loviruses typically occur in outbreaks
due to interpersonal and nosocomial transmission,
and mortality rates in outbreaks reach a staggering
5080%. The most recent outbreak of Marburg
virus occurred in Angola in 2005, involving 374
cases and 329 deaths (88% case-fatality rate) [43];
the Ebola virus outbreak which occurred in 2005
in the Republic of Congo involved 12 cases and
9 deaths (75% case-fatality rate) [44].
Primary human infections in most cases resulted
from contact with non-human primates which are
generally sick or dead as a result of lovirus infection. The primates, however, are not believed to be
important reservoirs of loviruses in nature since
they regularly die from the infections. Epidemiological and virological studies suggested that the
regular outbreaks of lovirus infection in primates
probably did not occur as a result of interspecies
transmission between primates, but due to introduction to a hitherto unknown animal or environmental source [45]. The nature of such natural
reservoirs remains elusive despite extensive
surveys until a recent study which discovered
the presence of Ebola virus (by serology and
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv
77
Figure 2. Phylogenetic tree of RNA-dependent RNA polymerase showing the relationship of the bat coronaviruses to other
coronaviruses. The trees were inferred from amino acid sequence data (949 amino acid positions) by the neighbour-joining
method. Numbers at nodes indicated levels of bootstrap support calculated from 1000 trees. The scale bar indicates the estimated number
of substitutions per 50 amino acids. Coronaviruses found in bats are in bold and species of bats in which the corresponding
coronaviruses are found are in brackets. HCoV-229E, human coronavirus 229E; PEDV, porcine epidemic diarrhoea virus; TGEV, porcine
transmissible gastroenteritis virus; FCoV, feline coronavirus; HCoV-NL63, human coronavirus NL63; HCoV-OC43, human coronavirus
OC43; MHV, murine hepatitis virus; BCoV, bovine coronavirus; PHEV, porcine haemagglutinating encephalomyelitis virus; CoV-HKU1,
coronavirus HKU1; SARS-CoV, SARS coronavirus; bat-SARS-CoV, SARS coronavirus-like virus found in bats; IBV, infectious
bronchitis virus
RT-PCR) in three species of bats captured in

Gabon and the Republic of Congo. These include
Hypsignathus monstrousus (4 of 17 animals,
23.5%), Epomops fraqueti (8 of 117 animals, 6.8%),
and Myonycteris torquata (4 of 58 animals, 6.9%),
all belonging to the Pteropodidae family of
ying foxes [46]. If the bats are indeed the natural
reservoir of the Ebola virus, two factors have been
suggested to facilitate their transmission to primates [46]. The scarcity of food during the dry season is thought to affect the immune system of bats,
thereby facilitating viral replication. At the same
time, primates and bats could come into closer
contact in search for food so cross species transmission of the virus from bats to primates could
become easier. These ndings have important

implications in future studies of the ecology
and epidemiology of Ebola virus. The natural
reservoir hosts of Marburg virus have not been
identied, though bats would now be an obvious
and important group of animals to investigate.
Direct transmission of either of the loviruses
from bats to humans has not been conrmed.
However, it is interesting to note that in some of
the previous outbreaks of loviruses in Africa
not involving contact with primates, bats were
sighted in caves or buildings which the index cases
had visited or worked in [45]. With the present
knowledge in the epidemiology of the loviruses,
it appears that direct bat-to-human transmission of
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv
78
the viruses might occur, though it is a relatively
inefcient route. The more important and efcient
route of transmission could involve primates
which develop illness and/or fatal infections,
thereby serving as an amplifying host before transmission to humans, a theme which is shared by the
ecology of Nipah virus and SARS-CoV.
Flaviviridae
The aviviruses encompass a diverse group of
viruses with global distribution, important public
health and clinical signicance, and distinctive
clinical syndromes. Many of the clinically important viruses are transmitted via arthropod vectors
and have reservoirs in either arthropods or vertebrates. The most important clinical syndromes
caused by aviviruses include central nervous
system infection (e.g. St. Louis encephalitis virus,
Japanese encephalitis virus, West Nile virus,
Murray Valley encephalitis virus, and tick-borne
encephalitis virus), fever and rash (e.g. dengue
viruses), and haemorrhagic fever (e.g. yellow
fever virus, dengue viruses, Omsk haemorrhagic
fever virus, and Kyasanur Forest disease virus).
Bats are not generally considered to be important
reservoirs of aviviruses though a number of bats
have been shown to be susceptible to viral infection either in experimental or natural settings.
The ardeid birds are the major reservoir of Japanese encephalitis virus while the domestic pig is
the most important amplifying host responsible
for human infections and outbreaks. Birds are likewise the key reservoirs of St. Louis encephalitis
and West Nile viruses. However, West Nile virus
was isolated from bats more than 30 years ago in
India [47]. Recent surveillance studies in the USA
also showed occasional infection of bats by the
West Nile virus [48,49,50]. In a series of experiments by Sulkin et al., bats (Tadarida brasiliensis
mexicana, Myotis lucifugus lucifugus, Eptescius fuscus
fuscus) were shown to be susceptible to infection
by Japanese encephalitis and St. Louis encephalitis
viruses by either the subcutaneous and intracerebral route [51]. The susceptibility of bats to infection
and the level of viral replication varied with different viral strains and the species of bats tested.
Of particular interest is that bats developed relatively long periods of viraemia (upto 30 days) after
infection and developed no clinicopathological
sequelae following inoculation, even though there
was signicant viral multiplication in the brain folCopyright # 2006 John Wiley & Sons, Ltd.
S. Wong et al.
lowing intracerebral inoculation. Importantly,
infections due to these neurotropic viruses produced signicant viral loads not only in the blood
but also in the interscapular brown fat, in contrast
to brains and kidneys which were less frequently
found positive for viruses. Sulkin et al. also
demonstrated that infection at low temperatures
(from 8 C to 24 C) was associated with prolonged
viraemia of over 100 days and persistence of
viruses in the brown fat [52]. Transplacental infection of Japanese encephalitis virus also occurred
readily in Tadarida brasiliensis mexicana, again without any clinicopathological sequelae to the fetuses
[53]. Similar experiments also showed that the big
brown bat (Eptesicus fuscus) can maintain St.
Louis encephalitis during hibernation [54]. Isolation of Japanese encephalitis virus in naturally
infected bats in Japan and Taiwan, and serological
evidence of St. Louis encephalitis infection in Ohio
and Trinidad have been reported [16,23,54,55].
These data suggested that bats could easily
serve as a suitable host for the persistence of these
viruses in nature, perhaps with special signicance
to overwintering of viruses.
Similarly, natural infection of bats by dengue
virus was suggested by a serological study in Costa
Rica and Ecuador, and more convincingly by positive RT-PCR of the brains of Rousettus leschenaulti
bats in southern China [56,57]. Kyasanur Forest
disease is a aviviral haemorrhagic fever mainly
seen in western India. The virus is mainly transmitted between rodents and insectivores via ixodid
ticks. Isolation of the virus from bats (Rhinolophus
rouxii and Cynopterus sphinx) had been reported
on two occasions from India. The role of bats in
the ecology of these medically important aviviruses is unknown [58,59]. Antibody against the
yellow fever virus was described in a bat in one
study, though primates are still believed to be
the most important reservoir of sylvatic yellow
fever [23]. A virus named Montana Myotis leukoencephalitis (MML) virus was initially isolated in the
1960s from Myotis lucifugus [60]. Subsequent genome analysis placed it into the family Flaviviridae
[61]. No arthropod vectors have been identied
for this virus and the virus can be transmitted
directly to mice from bat bites. The Rio Bravo virus
was isolated from the salivary glands of Brazilian
free-tailed bats (Tadarida brasiliensis) in the USA
and Mexico and also from Molossus ater in Trinidad
[62,63]. It has no known arthropod vectors and is
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv

believed to be transmitted amongst bats by direct
contact or aerosols. Human infections by the Rio
Bravo virus, including cases of laboratory-acquired
infections (resulting in meningitis, orchitis or
oophoritis), have been documented [64]. Other
aviviruses that have been described in bats
include the Ilheus virus, Tamana bat virus, and
Yokose virus [23,63,65]. The Ilheus virus causes an
acute febrile illness in humans in Latin America
and cases of encephalitis have been reported but
without mortalities. The main reservoir hosts are
birds and it is transmitted by mosquitoes.
It is evident that bats can be infected by numerous aviviruses in nature. It is also biologically
plausible that they have the potential to serve as
reservoir hosts in certain situations, such as overwintering of viruses. However, as pointed out by
Scott, evidence of viral infection in a vertebrate
host does not equate to a signicant role for
them in the natural ecology of the viruses [66].
Virological proles of infected animals, density
of vectors, feeding habits of vectors and their
vectorial capacity are all essential factors to be
considered in this regard.
Orthomyxoviridae
Isolation of inuenza virus A/H3N2 from Nyctalus
noctula bats in Kazakhstan was reported in the
1970s in the Russian literature [67]. Subsequently,
serological evidence of inuenza A/H2N2 and A/
H3N2 infections of various bat species was found
in India [68]. Although bats are likely to be susceptible to inuenza virus infection, current epidemiological studies do not consider them a
signicant reservoir of the viruses in nature.
Paramyxoviridae
Paramyxoviruses are common pathogens of
humans. Important human pathogens include
Respirovirus (human parainuenza viruses 1 and
3), Rubulavirus (human parainuenza viruses 2
and 4, mumps virus), Morbillivirus (measles virus),
and Metapneumovirus. The rst nding of a paramyxovirus in bats was described in 1966 [69,70].
A parainuenza virus type 2 was isolated from
the frugivorus bat Rousettus leschenaulti in India.
The Mapuera virus was the second paramyxovirus
isolated from the yellow-shouldered bat (Sturnira
lilium) in Brazil in 1979 [71]. Both have not been
found to cause human infections. The signicance
of paramyxoviruses in bats, however, became
79
evident in the 1990s with the occurrence of two
outbreaks in humans and animals. The new genus
Henipavirus was proposed to encompass two of
the three zoonotic paramyxoviruses that are
pathogenic to humans, namely Hendra and Nipah
viruses. Whether the Indian type 2 parainuenza
virus is related to the newly described paramyxoviruses is unknown.
In 1994, an outbreak of fatal hyperacute respiratory illness occurred in horses in Queensland,
Australia. Two human contacts of the index horse
were infected and developed an inuenza-like illness. One of them died of pneumonitis, respiratory
failure, and renal failure and a virus was isolated
from both the fatal patient and the horses [72]. The
virus was initially called equine morbillivirus and
later named Hendra virus. In the 1995 outbreak in
Queensland, another patient died of encephalitis
after Hendra virus infection [73]. Following the
initial outbreaks of Hendra virus infection, a serological survey in Australia involving 5264 sera
from 46 terrestrial animal species failed to show
any evidence of infection by this new virus. However, seropositivity was detected in the spectacled
fruit bat (Pteropus conspicillatus), black fruit bat (P.
alecto), little red (P. scapulatus), and grey-headed
bat (P. poliocephalus) [74]. Subsequently, Hendra
virus was isolated from the viscera and fetuses
of P. policephalus and P. alecto [75]. Retrospective
analysis of bat sera showed that the virus was present in Australian ying foxes as early as 1982 and
in some surveys, seroprevalence as high as 47%
had been documented [76]. As is the case for
many other bat-associated infections, Hendra
virus does not cause disease or pathology in
bats, and transplacental transmission to the fetus
is possible. The route of transmission from ying
foxes to horses has not been directly documented,
though exposure to infected urine has been considered possible [76]. In addtion to horses, cats
and guinea pigs are also susceptible to Hendra
virus infection and these animals can shed the
virus in urine [77]. Humans acquired the infection
solely from horses to date and not from ying
foxes. The route of transmission to humans probably occur through contact with the respiratory
secretions of the infected horses.
From September 1998 to June 1999, an outbreak
of encephalitis occurred amongst pig-farmers in
Malaysia. The aetiology of the disease is a novel
paramyxovirus name Nipah virus isolated from
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv
80
the cerebrospinal uid of the patients [78,79].
There were 265 patients involved in the outbreak,
with a case fatality rate of 39.6% and 15% of the
survivors had residual neurological decits
[79,80]. The outbreak in humans was preceded
by sudden and massive deaths of the pigs due to
acute respiratory distress syndrome and encephalitis, and close contacts with pigs was conrmed to
be the major risk factor for acquisition of the infection in a case-control study [80]. The presence of
the virus in the respiratory secretions and urine
of infected pigs suggested that contact with these
secretions is the likely route of transmission.
About 8% of the patients did not have a contact
history with sick pigs; dogs were suspected to be
another possible vector for transmission as they
can also be infected by Nipah virus. Culling of
over 1 million pigs was needed to terminate the
outbreak. Singapore was concurrently hit by an
outbreak of Nipah encephalitis in March 1999
which affected 11 abbatoir workers who handled
pigs imported from Malaysia [81]. Contact with
live pigs was again conrmed to be a major risk
factor for infection [82]. No interpersonal or nosocomial transmission of Nipah virus infection was
noted in these two outbreaks [83].
A search for the reservoir hosts of Nipah virus
found that in addition to pigs, wild boars (Sus
scrofa), domestic dogs (Canis lupus) and rodents
(Rattus rattus) could be secondarily infected. But
the main natural reservoir of the virus appears to
be ying foxes. Serological studies showed that,
in Malaysia, a number of bat species are seropositive, with the majority of the animals belonging to
the Megachiroptera [84]. The highest seroprevalence was found in Pteropus hypomelanus (31% seropositive), followed by Pteropus vampyrus (17%),
Eonycteris spelaea (5%), Cynopterus brachyotis (4%),
and the Microchiropteran Scotophilus kuhlii (3%).
Subsequently, Nipah virus was cultured from the
urine of the ying fox P. hypomelanus [85]. It was
postulated that the combination of anthropogenic
deforestation and drought caused by the El Nino
Southern Oscillation drove the frugivorous ying
foxes from their natural habitats into orchard plantations. The close proximity between the bats and
pigs thus created, resulted in the cross-species
infection of the pigs and subsequently humans [86].
There was no epidemiological evidence to suggest that Nipah virus was transmitted from ying
foxes to humans directly and no person-to-person
S. Wong et al.
transmission of the infection has been conrmed
in the outbreaks in Malaysia and Singapore.
Nevertheless, the presence of the virus in the
respiratory secretions and urine of infected
humans has been documented, suggesting that
the risk of interpersonal spread may not be zero
[87]. Although the number of cases that has been
studied was small, it appeared that the presence
of Nipah virus in respiratory secretions and urine
is conned to the rst week of illness before the
appearance of IgM antibodies.
In 2001 and 2003, outbreaks of a febrile neurological disease occurred in Bangladesh. Retrospective studies showed that the outbreak was
again caused by Nipah virus infection [88,89].
The Bangladeshi outbreaks are notable in two
aspects. Firstly, pig populations were very
small in Bangladesh and there were no reports of
massive animal deaths in the vicinity of the
affected villages. Direct bat-to-human transmission
through accidental exposures to bats or bat secretions was suspected. Secondly, there were familial
clusters of cases suggesting the possibility of interpersonal spread through contact with the patients
secretions. Nipah virus antibodies were found in
two ying foxes (Pteropus giganteus) in Bangladesh.
A similar outbreak of encephalitis occurred in the
northeastern part of India in 2001 and retrospective
studies again conrmed Nipah virus as the cause
of encephalitis [90]. Animal studies were not performed in the Indian outbreak but nosocomial
spread of the infection was observed.
In Cambodia, Pteropus lylei has a 11.512.3%
seroprevalence for Nipah virus but only 0.26%
of the urine samples were culture positive,
suggesting a transient infection of the ying foxes
by the virus [91,92]. In Thailand, seroprevalence
among Pteropus hypomelanus, P. lylei, P. vampyrus,
and Hipposideros larvatus ranged from 1.3% to
15.4%, and the virus was detectable by RT-PCR
in P. lylei (saliva and urine) and H. larvatus (saliva)
bats [93]. Recently, serological evidence of infection by Henipavirus was also reported among
Pteropus vampyrus in Indonesia [94]. Phylogenetic
analysis of the nucleocapsid gene sequence
suggested that there are three lineages of Nipah
virus, with NipahBangladesh and NipahIndia
being closer to each other than NipahMalaysia
and NipahCambodia [88,90].
From April to September in 1997, sows in New
South Wales, Australia, were found to have
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv

decreased pregnancy rate and litter size. There
was an increase in mummied, stillborn, and
deformed piglets. The affected stillborn piglets
were found to have severe degeneration of the central nervous system and some had myocarditis.
Subsequently a new viruslater named the
Menangle viruswas isolated from the infected
piglets [95]. Among 251 persons with contact
with the pigs in the piggeries, 2 were seropositive
for the virus [96]. Both of the patients developed a
febrile illness with headache, malaise, myalgia,
and skin rashes with no long term sequelae. The
ying foxes Pteropus policephalus and P. alecto
were seropositive for the Menangle virus [95].
The route of transmission of menangle virus
from ying foxes to pigs, amongst pigs, and
from pigs to human is unknown. The complete
genome of the Menangle was reported which conrmed its position in the family Paramyxoviridae
[97].
As a result of enhanced surveillance for batassociated viruses in Southeast Asia, the Tioman
virus was discovered. Tioman virus is a novel
paramyxovirus isolated from the urine of the ying fox Pteropus hypomelanus in Malaysia and the
genome of the virus has been published. It was
placed under the genus Rubulavirus by genomic
analysis [98,99]. Human infections due to Tioman
virus have not been described.
Reoviridae
Two reoviruses have been isolated from bats. They
include the Nelson Bay virus and Pulau virus
[100,101]. The transmissibility and pathogenicity
of these viruses to humans are unknown.
Retroviridae
By searching through the mouse (Mus musculus)
and rat (Rattus norvegicus) genomes, genetic elements belonging to betaretroviruses were discovered in these rodents. In the same study,
sequences similar to the env gene of an endogenous retrovirus CpERV-5_AC138156 was found
in the genome of the Sebas short-tail bat (Carrollia
perspicillata) [102].
Rhabdoviridae
The Rhabdoviridae contains six genera, Vesiculovirus, Lyssavirus, Ephemerovirus, Novirhabdovirus,
Cytorhabdovirus, Nucleorhabdovirus, the last two
being plant viruses. Vesicular stomatitis (VesiculoCopyright # 2006 John Wiley & Sons, Ltd.
81
virus) occurs in horses, cattle, and pigs in the Western Hemisphere. It produces a disease in livestock
similar to foot-and-mouth disease. Seroprevalence
amongst humans can be high in enzootic areas but
human infection is generally mild or asymptomatic. Bats have been implicated, but not proven,
as a possible carrier for vesicular stomatitis virus
[103]. In contrast, the Chandipura virus, another
Vesiculovirus, causes a much more severe encephalitis, sometimes in large outbreaks, in India [104].
Sandies were believed to be the vector of Chandipura virus but it has not been found in association
with bats. Mount Elgon bat virus was another
rhabdovirus isolated from Rhinolophus hildebrandtii
eloquens and described in 1969 [105]. It has not
been associated with human infections.
The lyssaviruses are arguably the most important of all bat-associated viruses. The Lyssavirus
species include rabies virus, (genotype 1), Lagos
bat virus (genotype 2), Mokola virus (genotype
3), Duvenhage virus (genotype 4), European bat
lyssaviruses 1 and 2 (genotypes 5 and 6, respectively), Australian bat lyssavirus (genotype 7),
and four newly described genotypes found in Eurasia, Aravan (isolated in 1991), Khujand (isolated
in 2001), Irkut (isolated in 2002), and West Caucasian bat viruses (isolated in 2002) [106,107,108].
These four Eurasian genotypes and the Lagos bat
virus have not been shown to cause human infections to date [109]. There had only been one
reported case of human infections caused by the
Duvenhage virus to date which occurred in South
Africa in 1970 [110,111]. Miniopterus schreibersii
was considered to be the host associated with the
infection and the virus was isolated once from a
Nycteris thebaica bat [111].
The lyssaviruses differ from each other not only
in their genotypes (based on nucleoprotein gene
sequences), but also in their pathogenicity in animals and cross-neutralisation by antibodies. Based
on the transmembrane glycoprotein sequence,
these seven lyssavirus genotypes were further
divided into two phylogroups [112]. Phylogroup
I consists of genotypes 1, 4, 5, 6 and 7 while phylogroup II consists of genotypes 2 and 3. Phylogenetic analyses of the four Eurasian lyssaviruses
using the glycoprotein, nucleocapsid and phosphoprotein gene sequences has also been published [113]. Aravan, Irkut, Khujand and West
Caucasian bat viruses are considered to be separate genotypes according to nucleoprotein gene
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv
82
sequences. Aravan, Irkut and Khujand viruses are
related to each other and to genotypes 4, 5 and 6
viruses, and these six viruses are believed to represent a phylogroup of Old World bat lyssaviruses.
The West Caucasian bat virus is the most divergent of all known lyssaviruses.
All the above lyssaviruses have been isolated
from bats except Mokola virus which is mainly
isolated from cats and occasionally from rodents
and shrews. For the bat-associated lyssaviruses,
only rabies virus is also associated with other terrestrial animals (especially carnivores); all the
others have bats as the sole natural reservoir hosts.
Rabies virus has a worldwide distribution while
the other lyssaviruses are relatively restricted geographically. A large number of animals are susceptible to infection by the classical rabies virus.
However, only mammals of the orders Chiroptera
and Carnivora transmit the virus efciently in nature. In countries which are free from canine rabies,
bats are the most important source for human
rabies. The evolution of rabies virus has been studied in detail. Phylogenetic studies showed that
the different genotypes of lyssaviruses are clearly
distinct from each other and that, within genotype
1, distinct lineages with respect to the reservoir
host range can be recognised [114]. The chiropteran rabies viruses are likely to be older than the carnivoran viruses, and the current rabies viruses
amongst carnivores probably arose as a result of
two cross-species spillover events from bats to carnivores. One of the events resulted in the North
American raccoon and skunk rabies virus lineage
while the other resulted in the carnivore rabies
lineage in the rest of the world. Cross-species
transmission of rabies virus still occurs today but
all these incidents are the result of bat-to-terrestrial
animals spillover not the reverse [115]. Phylogenetic division of bat rabies viruses was clearly
shown to be associated with clustering of specic
bat species in two studies, suggesting that some
rabies viruses co-segregate with their bat hosts
[116,117]. In Canada, for example colonial and
non-migratory Myotis bats are associated with
rabies virus clades that are distinct from those assicated with solitary, tree-dwelling and migratory
Lasiurus bats [117].
The vast majority of human rabies in the world
is acquired from canine sources. In some countries,
however, bats carrying variants of the genotype 1
rabies virus are equally, if not more important,
S. Wong et al.
causes of human infections. From 1958 to 2000,
bat rabies accounted for 32 of the 35 indigenous
cases of rabies in the USA [118]. In 26 of the
patients, there was no history of bat bites. Nineteen of these 26 cryptic rabies were associated
with two species, Lasionycteris noctivagans and
Pipistrellus subavus. Similarly in Latin America,
bat rabies is as important as canine rabies in causing disease in humans and livestocks. In Brazil,
analysis showed that canine- and bat-related
rabies viruses reside in distinct groups, reinforcing
the hypothesis that different rabies virus strains
are preferentially related to different mammalian
hosts [119,120].
Bat rabies viruses are associated with a large
number of bat species, both frugivorous, insectivorous, and sanguivorous. In the Latin America,
Desmodus rotundus, Artibeus lituratus, Artibeus
planirostris, Tadarida brasiliensis, Nyctinomops laticaudatus, Eumops auripendulus, Eptesicus furinalis,
Lasiurus borealis, Molossus spp. are often encountered [119,120,121,122]. In North America,
Eptesicus fuscus, is one of the commonest rabid
bat species, followed by Myostis spp. (e.g. M.
lucifugus), Lasionycteris noctivagans, Lasiurus spp.
(e.g. L. cinereus, L. borealis, L. intermedius, L. seminolus), Tadarida brasiliensis and Pipistrellus subavus
[117,118,123,124]. Pteropus bats have been found
to be infected by rabies virus in India [125]. Rabid
bats may become sick, though most of the animals
will remain healthy and asymptomatic. Transmission of rabies virus among bats likely occurs orally
and through biting. Although aerosolisation of bat
rabies virus in saliva or excreta has been postulated as a possible means of transmission, humans
are mainly infected via percutaneous or mucosal
contacts with infected bats.
European bat lyssaviruses 1 and 2 are found in a
number of European countries including Denmark, Finland, France, Germany, Hungary,
Lithuania, the Netherlands, Poland, the Russian
Federation, Slovakia, Spain, Switzerland, Ukraine
and the United Kingdom [126]. European bat lyssaviruses are generally restricted to bats. They
only rarely infect other mammalian species including one stone marten (Martes foina), two sheep, and
three human beings [127]. One of the three human
infections was due to European bat lyssavirus 1
(1985, Ukraine) and two due to European bat lyssavirus 2 (1985, diagnosed in Finland but had
exposures in Finland, Switzerland and Asia;
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv

2002, Scotland) [126]. A fouth case occurred in
1977 in Ukraine and the isolate was believed to
be European bat lyssavirus 1, but the strain was
not genetically typed [128]. European bat lyssavirus 1 is the commoner of the two types and is
mainly associated with Eptesicus serotinus
[19,129,130,131]. Asymptomatic infection of a zoo
bat Rousettus aegyptiacus has been reported [132].
The sole reservoirs of European bat lyssavirus 2
to date are the Myotis bats (M. daubentonii and M.
dasycneme) [128,130,133,134].
Australian bat lyssavirus was rst recovered
from Pteropus alecto in New South Wales, Australia,
and later also found in other bat species [135]. Two
fatal human infections in Australia have been
reported, both had sustained bat-related injuries
prior to onset of disease [136,137]. Post-exposure
prophylaxis with rabies vaccine and immunoglobulin were given in subsequent potential exposures to Australian bat lyssavirus and no human
cases have ever been described [138,139]. In contrast to other bat-associated pathogens, Australian
bat lyssavirus can cause encephalitis in infected
bats [138,139]. Surveillance using immunouorescent staining of bat brains showed that healthy ying foxes have a lower positive rate than sick and
injured animals ( < 1% vs. 6.5%, respectively) [139].
Bat-associated lyssaviruses have also been
increasingly recognised in Asian countries. In
India, the ying fox Pteropus policephalus was
found to be infected by rabies virus using direct
immunouorescent staining of brain tissue [125].
In the Philippines, no lyssaviruses were detected
in the brains of 821 bats, but 9.5% of the bats in
six species possessed neutralising antibodies
against Australian bat lyssavirus, especially
among Miniopterus schreibersi [140]. In Cambodia,
neutralising antibodies were detected against a
number of lyssaviruses, including rabies virus,
European bat lyssavirus 1, Australian bat lyssavirus, and Lagos bat virus [141]. A similar picture
was seen in Thailand in which serological evidence of infection by Aravan, Khujand, Irkit
and Australian bat lyssavirus was found in 3.8%
(all from Pteropus lylei and Hipposideros armiger)
of the bat samples [142]. Neutralising antibodies against Aravan and Khujand viruses were
detected in three Pteropus giganteus samples in
Bangladesh [143]. In these latter four Asian surveys, no lyssaviruses were detected in the brains
of the bats by direct immunouorescence and/or
83
mouse inoculation. Although serological assays
per se may be complicated by cross-reactions
between different lyssaviruses, the studies do raise
the possibility that these lyssavirus species may
have a broader geographical distribution than previously described.
In addition to the natural route of zoonotic
transmission of rabies virus to humans, organ
transplantation has in recent years been recognised as an iatrogenic route of transmission. The
rst report of such transmission occurred in Texas
in 2004 when four recipients received organs from
a donor who died of subarachnoid haemorrhage.
The organs transplanted included iliac artery, liver
and two kidneys. All four recipients subsequently
developed rabies encephalitis within 30 days of
infection and all succumbed to the infection. In retrospect, the donor was found to have been bitten
by a bat before his death [18]. In 2005, a similar
incident occurred in Germany. A 26-year old
woman visited India in October in 2004 and died
in Germany in late 2004. Three recipients received
lungs, combined kidney/pancreas and kidney,
and all of them died of rabies. Subsequent examination of the donors brain showed typical pathological features of rabies including Negri bodies
and positive immunohistochemical staining [144].
The three recipients of liver and cornea remained
asymptomatic as of February 2005. Such incidents
highlight the importance of excluding rare and
exotic diseases in potential organ donors and the
novel iatrogenic routes of transmitting batassociated pathogens.
The prognosis of human rabies after the onset of
symptoms is extremely poor with almost 100%
mortality. The only useful specic post-exposure
management, apart from local wound cleansing,
is the use of rabies vaccine and immunoglobulin
(local inltration and systemic injection). Although
no useful antiviral agent is available to date, one
recent report showed that a potent anti-excitotoxic
therapy led to the survival of a patient. A 15-year
old girl who sustained a laceration from a bat
developed clinical rabies without post-exposure
prophylaxis. A regimen of high doses of midazolam, barbiturates, diazepam and ketamine,
together with ribavirin and amantadine, appeared
to tide over the acute phase of infection before the
development of immunity, and the patient eventually regained consciousness, albeit with some
neurological decits [145]. The currently available
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv
84
rabies vaccines are extremely effective for pre- and
post-exposure prophylaxis of rabies virus infections. Failures occur only in situations of delayed
vaccination and multiple severe animal bites to
the head. There are no controlled clinical trials
on the efcacy of rabies vaccines or immunoglobulins towards other lyssaviruses. However, vaccines
and immunoglobulin have been given to persons
exposed to European and Australian bat lyssaviruses without failure so far. Animal studies of
rabies vaccines against European bat lyssaviruses
have yielded variable results depending on the
vaccine strains used and the host species. In a
recent study in mice, human diploid cell vaccine
conferred cross-protection against both European
and Australian bat lyssaviruses, thus providing
some experimental evidence for the protective efcacy against these phylogroup I lyssaviruses [146].
Vaccine efcacy against Lagos bat virus is likely to
be low. The efcacy of human rabies vaccines and
immunoglobulin against the Eurasian genotypes
appears to be unsatisfactory, and the degree of
protection is related to the phylogenetic distance
from the rabies virus [147].
Togaviridae
The two genera of togaviruses contain several
important human pathogens. Examples of Alphavirus include Barmah Forest virus, Chikungunya
virus, eastern equine encephalitis virus, Onyongnyong virus, Ross River virus, Semliki Forest
virus, Sindbis virus, Venezuelan equine encephalitis virus, and western equine encephalitis virus.
Eastern, western, and Venezuelan equine encephalitis viruses are primarily associated with encephalitis, while chikungunya, Onyong-nyong, Ross
River, sinbis, and Barmah Forest viruses commonly present as fever, rash and arthritis. Rubella
virus is the only example of Rubivirus for which
human is the only natural host.
All alphaviruses are transmitted by arthropods,
especially mosquitoes. Evidence of infection by
chikungunya, eastern and Venezuelan equine
encephalitis viruses have been found in bats. Chikungunya virus causes recurrent and explosive
outbreaks in many tropical countries. The most
recent outbreak occurred in the southwest Indian
Ocean involving La Reunion, Mauritius, Seychelles, Mayotte, Maldives and India. Since March
2005, there have been more than 3000 conrmed
cases and an estimated infected population of
S. Wong et al.
over 200 000 [148]. The urban cycle of chikungunya
is maintained by human-to-human transmission
via mosquitoes (mainly Aedes aegypti but also Aedes
albopictus), while a rural cycle is maintained
between non-human primates. Bats have occasionally been found to be infected by chikungunya
virus, though the potential of the bat for further
transmission requires conrmation [149]. The
reservoir of eastern equine encephalitis virus is
primarily birds, but other animals such as rodents,
marsupials, and bats are often infected in Latin
America. Serological evidence for bat infection by
eastern equine encephalitis virus was documented
in Trinidad and Guatemala [23,150]. Venezualan
equine encephalitis virus has a broad host range
including rodents, bats, horses, sheep, dogs and
birds, but the main sylvatic reservoir is believed
to be rodents. Horses are efcient amplifying hosts
and human infections and outbreaks mostly
resulted from equine infections [151]. Several
species of bats have serological evidence of infection by the Venezualan equine encephalitis virus
in Guatemala and positive viral cultures have
been obtained from Carollia perspicillata, Desmodus
rotundus and Uroderma bilobatum [152,153,154].
Bats might have been infected through mosquito
bites, ingesting infected mosquitoes, or feeding
on the blood of viraemic animals in the case of
vampire bats. They may play a role in geographical dispersal of the virus and as an alternative
reservoir for the virus [151,152]. The ying foxes
(Pteropus poliocephalus and Pteropus pscapulatus)
are considered to be unimportant reservoirs of
Ross River virus in one study [155].
IMPLICATIONS
To prevent transmission of bat-associated zoonoses to humans, the key is to gain a better understanding of the ecology of bats and the range of
infectious agents associated with them. Surveillance of bat-associated viruses is based on passive
surveillance in many countries of the world, in
part because of the conservation status of bats.
Passive surveillance usually targets towards sick,
injured or dead animals, which may bias the
results. To better understand the prevalence of
old and new pathogens, active surveillance is
obviously preferable.
The primary preventive measure against batassociated infections is conservation of the natural
habitats of bats. The intrusion of Nipah virus to the
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv

pig population and subsequently to humans
serves as the most recent example. In Latin America, outbreaks of human rabies from vampire bats
almost always followed the destruction of the bats
habitats, forcing the animals to feed on humans
and livestock. In situations where exposure to
bats is unavoidable, measures to reduce contact
between bats and humans may be considered,
such as bat-proong of houses in the endemic
areas and the use of personal protective equipment for workers and scientists in frequent contact
with bats. In Latin America, application of anticoagulants to bats and cattle have been utilised to control the vampire bat population. This approach,
however, has not achieved much success and
may have adverse effects on the ecology of bats
or other fauna and ora. With the excellent results
from the use of oral rabies vaccine to control rabies
in wildlife in Europe and North America, oral
vaccines against bat rabies were being tested in
vampire bats with satisfactory experimental
results [156,157]. Pre- and post-exposure prophylaxis using rabies vaccines appears to be effective
against genotypes of lyssavirus that are known to
cause human infections despite the antigenic differences from classical rabies virus. Pre-exposure
vaccination is especially important for persons
with constant exposure to bats such as bat biologists. The value of vaccines against other bat-associated viruses remains unknown mainly because
of the lack of effective vaccines (e.g. against
Henipavirus) or the uncertain role of bats in the
transmission of infections (e.g. Japanese encephalitis virus).
As depicted in the Supplementary Table, the
known and potential viral pathogens are distributed in numerous families of bats. However, one
thing that stands out from the table is that
most of the important pathogens are often associated with four families: Pteropodidae, Molossidae,
Phyllostomidae and Vespertilionidae. This could be
due to a greater biodiversity of these species, better known biological features, or indeed, a co-evolution of the main pathogens with specic bat
species. The understanding of the association
between viruses and bat families could also be
useful to predict the likelihood of transmission or
dissemination to humans. For example, many of
the ying foxes (Pteropodidae) are relatively large
animals and, being strong yers, they could reach
relatively long distances from their roosting sites.
85
Being frugivorous bats, Pteropus spp. often
encroach onto fruit plantations and hence may
bring them into closer contacts with humans. The
big brown bat (Eptesicus fuscus, Vespertilionidae), an
insectivorous species, likewise is relatively close to
humans in that it often roosts in buildings and
man-made structures in cities or rural areas. The
serotine bat (Eptesicus serotinus) is equally at
home in buildings. The carriage of lyssaviruses
by these bats is an obvious concern to man.
Although bats are currently not considered the
most dominant group of mammals giving rise to
emerging or re-emerging infections in humans,
this could reect a relative paucity of studies on
this important group of mammals [2]. In the last
decade, a number of new infections have caused
outbreaks in different parts of the world. Some
of these causative agents, such as the henipavirus
and SARS coronavirus, have been found to have a
reservoir in bats. Bats have also been proven to be
a natural host for enigmatic viruses such as the
Ebola virus and their signicance in the natural
ecology of loviruses remains to be uncovered. It
is interesting to note that many of the bat-associated pathogens do not cause any clinicopathological damage to the bats, and coupling with the
longevity and migratory habits of the bats, make
this animal a potentially important reservoir for
emerging and re-emerging infections.
It can be seen from the above checklist of viruses
that very often the geographical distribution and
host range of many bat-associated infections
broadens as more surveillance was performed in
different parts of the world and when more bat
species were studied. Examples include coronaviruses, Henipavirus and lyssaviruses. In lyssaviruses, for example surveys of South and
Southeast Asian bats showed that Australian bat
lyssavirus and the Eurasian lyssaviruses may
indeed have a broader distribution than previously known. Many of the new viruses were discovered in bats following recent human or animal
outbreaks of infectious diseases and enhanced surveillance in wild animals. A variety of coronaviruses were discovered in southern China after
the SARS epidemic in diverse bat species. The
outbreak of Nipah encephalitis in Malaysia and
the association of the virus with ying foxes
prompted enhanced surveillance of bats. This led
to the discovery of the new Tioman and Pulau
viruses. The nding of these new viruses is the
Rev. Med. Virol. 2007; 17: 6791.
DOI: 10.1002/rmv
S. Wong et al.
86
result of a systematic and targeted surveillance of
bats, which underscores the importance of such an
approach in the future study of zoonotic agents. It
is therefore hardly surprising to predict that more
viruses will be discovered in bats in the future.
However, one should not forget that the mere isolation of a virus from bats does not necessarily
implicate an active role of bats in the natural ecology of the microbe. Whether bats are incidental
and dead-end hosts or actively support the maintenance of the viruses need to be investigated in
more vigorous studies. Anthropogenic and natural
changes in the environment due to deforestation,
alteration of habitats of bats, alterations in animal
diversity, and climatic events may shift the ecology of bats and expose humans to new pathogens.
A long-term systematic surveillance of bats is
essential to unravel the complex ecology between
bats, humans, other animals, arthropod vectors
and the environment. Such studies will benet
not only humans, but also conservation of wildlife
and biodiversity.
ACKNOWLEDGEMENT
The authors are grateful to the generous support of
the Providence Foundation Limited in memory of
the late Dr Lui Hac Minh, and that of Mr Fred WC
Chan and Ms Dorcas Suen on our research work
on emerging infections. This work is partly
supported by the Research Grant Council and
the Research Fund for the Control of Infectious
Diseases of the Health, Welfare and Food Bureau
of the Hong Kong Special Administrative Region
Government. The authors give special thanks
to the Mammal Working Group, Agriculture,
Fisheries and Conservation Department for
their help in taking the photographs of Chinese
horseshoe bats.
REFERENCES
1. Palmer SR, Lord Soulsby, Simpson DIH. (eds).
Zoonoses: Biology, Clinical Practice, and Public Health
Control. Oxford University Press: Oxford, 1998.
2. Woolhouse ME, Gowtage-Sequeria S. Host range
and emerging and reemerging pathogens. Emerg
Infect Dis 2005; 11: 18421847.
3. Food and Agriculture Organization of the
United Nations. 2005. FAO Statistical Databases.
http://faostat.fao.org/faostat/form?collection
Production. Livestock.Stocks&Domain Production
&servlet 1&hasbulk &version ext&language
language EN. [13 April, 2006.]
4. Kalish ML, Wolfe ND, Ndongmo CB, et al. Hunters

exposed to simian immunodeciency virus. Emerg
Infect Dis 2005; 12: 19281930.
5. Wolfe ND, Daszak P, Kilpatrick AM, Burke DS.
Bushmeat hunting, deforestation, and prediction
of zoonotic disease emergence. Emerg Infect Dis
2005; 12: 18221827.
6. Wolfe ND, Switzer WM, Carr JK, et al. Naturally
acquired simian retrovirus infections in central
African hunters. Lancet 2004; 363: 932937.
7. Integrated Taxonomic Information System. http://
itis.gbif.net. [14 April, 2006.]
8. Nowak RM. Walkers Bats of the World. Johns
Hopkins University Press: Baltimore, 1994.
9. Kunz TH, Lumsden LF. Ecology of cavity and
foliage roosting bats. In Bat Ecology, Kunz TH,
Fenton MB (eds). The University of Chicago Press:
Chicago, 2003; 389.
10. Neuweiler G. The Biology of the Bats. Oxford University Press: Oxford, 2000.
11. Barclay RMR, Harder LD. Life histories of bats: life
in the slow lane. In Bat Ecology, Kunz TH, Fenton
MB (eds). The University of Chicago Press:
Chicago, 2003; 209253.
12. Speakman JR, Thomas DW. Physiological ecology
and energetics of bats. In Bat Ecology, Kunz TH,
Fenton MB (eds). The University of Chicago Press:
Chicago, 2003; 430490.
13. Fleming TH, Eby P. Ecology of bat migration. In Bat
Ecology, Kunz TH, Fenton MB (eds). The University
of Chicago Press: Chicago, 2003; 156208.
14. Goncalves MA, Sa-Neto RJ, Brazil TK. Outbreak of
aggressions and transmission of rabies in human
beings by vampire bats in northeastern Brazil. Rev
Soc Bras Med Trop 2002; 35: 461464.
15. Schneider MC, Aron J, Santos-Burgoa C, Uieda W,
Ruiz-Velazco S. Common vampire bat attacks on
humans in a village of the Amazon region of Brazil.
Cad Saude Publica 2001; 17: 15311536.
16. Cross JH, Lien JC, Huang WC, Lien SC, Chiu SF.
Japanese encephalitis virus surveillance in Taiwan.
II. Isolations from mosquitoes and bats in Taipei
area 19691970. Taiwan Yi Xue Hui Za Zhi 1971; 70:
681686.
17. Lampo M, Feliciangeli MD, Marquez LM, Bastidas
C, Lau P. A possible role of bats as a blood source
for the Leishmania vector Lutzomyia longipalpis (Diptera: Psychodidae). Am J Trop Med Hyg 2000; 62: 718
719.
18. Srinivasan A, Burton EC, Kuehnert MJ, et al. Transmission of rabies virus from an organ donor to four
transplant recipients. N Engl J Med 2005; 352: 1103
1111.
19. Daszak P, Cunningham AA, Hyatt AD. Anthropogenic environmental change and the emergence of
Rev. Med. Virol. 2007; 17: 6791.

DOI: 10.1002/rmv
20.
21.
22.
23.
24.
25.
26.
27.
28.
29.
30.
31.
32.
33.
infectious diseases in wildlife. Acta Trop 2001; 78:

103116.
Weiss RA, McMichael AJ. Social and environmental
risk factors in the emergence of infectious diseases.
Nat Med 2004; 10(12 Suppl): S7076.
Constantine DG. Geographic translocation of bats:
known and potential problems. Emerg Infect Dis
2003; 9: 1721.
Downs WG, Anderson CR, Spence L, Aitken THG,
Greenhall AG. Tacaribe virus, a new agent isolated
from Artibeus bats and mosquitoes in Trinidad,
West Indies. Am J Trop Med Hyg 1963; 12: 640646.
Price JL. Serological evidence of infection of Tacaribe virus and arboviruses in Trinidadian bats. Am J
Trop Med Hyg 1978; 27: 162167.
Williams JE, Imlarp S, Top FH Jr , Cavanaugh DC,
Russell PK. Kaeng Khoi virus from naturally
infected bedbugs (Cimicidae) and immature freetailed bats. Bull World Health Organ 1976; 53: 365
369.
Osborne JC, Rupprecht CE, Olson JG, et al. Isolation
of Kaeng Khoi virus from dead Chaerephon plicata
bats in Cambodia. J Gen Virol 2003; 84: 26852689.
Charrel RN, Gallian P, Navarro-Mar JM, et al.
Emergence of Toscana virus in Europe. Emerg Infect
Dis 2005; 11: 16571663.
Verani P, Ciufolini MG, Caciolli S, et al. Ecology of
viruses isolated from sand ies in Italy and characterized of a new Phlebovirus (Arabia virus). Am J
Trop Med Hyg 1988; 38: 433439.
Zhong NS, Zheng BJ, Li YM, et al. Epidemiology
and cause of severe acute respiratory syndrome
(SARS) in Guangdong, Peoples Republic of China,
in February, 2003. Lancet 2003; 362: 13531358.
Guan Y, Zheng BJ, He YQ, et al. Isolation and characterization of viruses related to the SARS coronavirus from animals in southern China. Science
2003; 302: 276278.
Guan Y, Zheng BJ, He YQ, et al. Isolation and characterization of viruses related to the SARS coronavirus from animals in southern China. Science
2003; 302: 276278.
Leung GM, Lim WW, Ho LM, et al. Seroprevalence
of IgG antibodies to SARS-coronavirus in asymptomatic or subclinical population groups. Epidemiol
Infect 2006; 134: 211221.
Che XY, Di B, Zhao GP, et al. A patient with asymptomatic severe acute respiratory syndrome (SARS)
and antigenemia from the 20032004 community
outbreak of SARS in Guangzhou, China. Clin Infect
Dis 2006; 43: e15.
World Health Organization. Consensus document
on the epidemiology of severe acute respiratory
syndrome (SARS): 2003. http://www.who.int/csr/
sars/en/WHOconsensus.pdf.
87
34. Kuiken T, Fouchier RA, Schutten M, et al. Newly
discovered coronavirus as the primary cause of
severe acute respiratory syndrome. Lancet 2003;
362: 263270.
35. Martina BE, Haagmans BL, Kuiken T, et al. SARS
virus infection of cats and ferrets. Nature 2003;
425: 915.
36. Greenough TC, Carville A, Coderre J, et al. Pneumonitis and multi-organ system disease in common
marmosets (Callithrix jacchus) infected with the
severe acute respiratory syndrome-associated coronavirus. Am J Pathol 2005; 167: 455463.
37. Roberts A, Vogel L, Guarner J, et al. Severe acute
respiratory syndrome coronavirus infection of
golden Syrian hamsters. J Virol 2005; 79: 503511.
38. McAuliffe J, Vogel L, Roberts A, et al. Replication of
SARS coronavirus administered into the respiratory tract of African Green, rhesus and cynomolgus
monkeys. Virology 2004; 330: 815.
39. Lau SK, Woo PC, Li KS, et al. Severe acute respiratory syndrome coronavirus-like virus in Chinese
horseshoe bats. Proc Natl Acad Sci USA 2005; 102:
1404014045.
40. Poon LL, Chu DK, Chan KH, et al. Identication of a
novel coronavirus in bats. J Virol 2005; 79: 20012009.
41. Woo PCY, Lau SKP, Li KSM, et al. Molecular diversity of coronaviruses in bats. Virology 2006; 351: 180
187.
42. Li W, Shi Z, Yu M, et al. Bats are natural reservoirs of
SARS-like coronaviruses. Science 2005; 310: 676679.
43. World Health Organization. Marburg haemorrhagic fever in Angola update 25. 24 August, 2005.
http://www.who.int/csr/don/2005_08_24/en/index.
html [13 April, 2006.]
44. World Health Organization. Ebola haemorrhagic
fever in the Republic of the Congo update 2. 16
June, 2005. http://www.who.int/csr/don/2005_
06_16/en/index.html [13 April, 2006.]
45. Pourrut X, Kumulungui B, Wittmann T, et al. The
natural history of Ebola virus in Africa. Microb Infect
2005; 7: 10051014.
46. Leroy EM, Kumulungui B, Pourrut X, et al. Fruit
bats as reservoirs of Ebola virus. Nature 2005; 438:
575576.
47. Paul SD, Rajagopalan PK, Sreenivasan MA. Isolation of the West Nile virus from the frugivorous
bat, Rousettus leschenaulti. Indian J Med Res 1970;
58: 11691171.
48. Centers for Disease Control and Prevention (CDC).
West Nile virus activityUnited States, September
29 October 5, 2004. MMWR Morb Mortal Wkly Rep
2004; 53: 922923.
49. Marn AA, Petersen LR, Eidson M, et al. Widespread West Nile virus activity, eastern United
States, 2000. Emerg Infect Dis 2001; 7: 730735.
Rev. Med. Virol. 2007; 17: 6791.

DOI: 10.1002/rmv
88
50. Pilipski JD, Pilipski LM, Risley LS. West Nile virus
antibodies in bats from New Jersey and New York.
J Wildl Dis 2004; 40: 335337.
51. Sulkin SE, Allen R, Sims R. Studies of arthropodborne viruse infections in Chiroptera. I. Susceptibility of insectivorous species to experimental infection with Japanese B and St. Louis encephalitis
viruses. Am J Trop Med Hyg 1963; 12: 800814.
52. Sulkin SE, Allen R, Sims R. Studies of arthropodborne virus infections in Chiroptera. III. Inuence
of environmental temperature on experimental
infection with Japanese B and St. Louis encephalitis
viruses. Am J Trop Med Hyg 1966; 15: 406417.
53. Sulkin SE, Sims R, Allen R. Studies of arthropodborne virus infections in Chiroptera. II. Experiments with Japanese B and St. Louis encephalitis
viruses in the gravid bat. Evidence of transplacental
transmission. Am J Trop Med Hyg 1964; 13: 475481.
54. Herbold JR, Heuschele WP, Berry RL, Parsons MA.
Reservoir of St. Louis encephalitis virus in Ohio
bats. Am J Vet Res 1983; 44: 18891893.
55. Sulkin SE, Allen R, Miura T, Toyokawa K. Studies
of arthropod-borne virus infections in chiroptera.
VI. Isolation of Japanese B encephalitis virus from
naturally infected bats. Am J Trop Med Hyg 1970;
19: 7787.
56. Platt KB, Mangiaco JA, Rocha OJ, et al. Detection
of dengue virus neutralising antibodies in bats from
Costa Rica and Ecuador. J Med Entomol 2000; 37:
965967.
57. Zhang H, Yang X, Li G. Detection of dengue virus
genome RNA in some kinds of animals caught from
dengue fever endemic areas in Hainan Island with
reverse transcription-polymerase chain reaction.
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za
Zhi 1998; 12: 226228.
58. Pavri KM, Singh KR. Kyasanur Forest disease virus
infection in the frugivorous bat, Cynopterus sphinx.
Indian J Med Res 1968; 56: 12021204.
59. Rajagopalan PK, Paul SD, Sreenivasan MA. Isolation
of Kyasanur Forest disease virus from the insectivorous bat, Rhinolophus rouxi and from Ornithodoros
ticks. Indian J Med Res 1969; 57: 805808.
60. Bell JF, Thomas LA. A new virus, MML, enzootic in
bats (Myotis lucifugus) of Montana. Am J Trop Med
Hyg 1964; 13: 607612.
61. Charlier N, Leyssen P, Pleij CWA, et al. Complete
genome sequence of Montana Myotis leukoencephalitis virus, phylogenetic analysis and comparative study of the 30 untranslated region of
aviviruses with no known vector. J Gen Virol
2002; 83: 18751885.
62. Baer GM, Woodall DF. Bat salivary gland virus carrier state in a naturally infected Mexican freetail
bat. Am J Trop Med 1966; 15: 769771.
S. Wong et al.
63. Price JL. Isolation of Rio Bravo and a hitherto undescribed agent, Tamana bat virus, from insectivorous
bats in Trinidad, with serological evidence of infection in bats and man. Am J Trop Med Hyg 1978; 27:
153161.
64. Burke DS, Monath TP. Flaviviruses. In Fields
Virology (4th ed) Knipe DM, Howley PM (eds).
Lippincott Williams & Wilkins: Philadelphia,
2001; 10431125.
65. Tajima S, Takasaki T, Matsuno S, Nakayama M,
Kurane I. Genetic characterization of Yokose virus,
a avivirus isolated from the bat in Japan. Virology
2005; 332: 3844.
66. Scott TW. Are bats really involved in dengue virus
transmission? J Med Entomol 2001; 38: 771772.
67. Lvov DK, Easterday B, Hinshow W, Dandurov I,
Arkhipov PN. Isolation of strains of the Hong Kong
complex (H3N2) inuenza virus from Nyctalus noctula bats in Kazakhstan. Vopr Virusol 1979; 4: 338341.
68. Kelkar SD, Kadam SS, Banerjee K. Haemagglutination inhibition antibodies against inuenza virus in
bats. Indian J Med Res 1981; 74: 147152.
69. Hollinger FB, Pavri KM. Bat parainuenza virus.
Immunological, chemical, and physical properties.
Am J Trop Med Hyg 1971; 20: 131138.
70. Pavri KM, Singh KR, Hollinger FB. Isolation of a
new parainuenza virus from a frugivorous bat,
Rousettus leschenaulti, collected at Poona, India.
Am J Trop Med Hyg 1971; 20: 125130.
71. Henderson GW, Laird C, Dermott E, Rima BK. Characterization of Mapuera virus: structure, proteins
and nucleotide sequence of the gene encoding the
nucleocapsid protein. J Gen Virol 1995; 76: 25092518.
72. Selvey LA, Wells RM, McCormack JG, et al. Infection of humans and horses by a newly described
morbillivirus. Med J Aust 1995; 162: 642645.
73. OSullivan JD, Allworth AM, Paterson DL, et al.
Fatal encephalitis due to novel paramyxovirus
transmitted from horses. Lancet 1997; 349: 9395.
74. Young PL, Halpin K, Selleck PW, et al. Serologic evidence for the presence in Pteropus bats of a paramyxovirus related to equine morbillivirus. Emerg
Infect Dis 1996; 2: 239240.
75. Halpin K, Young PL, Field HE, Mackenzie JS. Isolation of Hendra virus from pteropid bats: a natural
reservoir of Hendra virus. J Gen Virol 2000; 81:
19271932.
76. Field H, Young P, Yob JM, Mills J, Hall L,
Mackenzie J. The natural history of Hendra and
Nipah viruses. Microbes Infect 2001; 3: 307314.
77. Barclay AJ, Paton DJ. Hendra (equine morbillivirus). Vet J 2000; 160: 169176.
78. Chua KB, Goh KJ, Wong KT, et al. Fatal encephalitis
due to Nipah virus among pig-farmers in Malaysia.
Lancet 1999; 354: 12571259.
Rev. Med. Virol. 2007; 17: 6791.

DOI: 10.1002/rmv

79. Goh KJ, Tan CT, Chew NK, et al. Clinical features of
Nipah virus encephalitis among pig farmers in
Malaysia. N Engl J Med 2000; 342: 12291235.
80. Parashar UD, Sunn LM, Ong F, et al. Case-control
study of risk factors for human infection with a
new zoonotic paramyxovirus, Nipah virus, during
a 19981999 outbreak of severe encephalitis in
Malaysia. J Infect Dis 2000; 181: 17551759.
81. Paton NI, Leo YS, Zaki SR, et al. Outbreak of Nipahvirus infection among abattoir workers in Singapore. Lancet 1999; 354: 12531256.
82. Chew MH, Arguin PM, Shay DK, et al. Risk factors
for Nipah virus infection among abattoir workers in
Singapore. J Infect Dis 2000; 181: 17601763.
83. Mounts AW, Kaur H, Parashar UD, et al. A cohort
study of health care workers to assess nosocomial
transmissibility of Nipah virus, Malaysia, 1999. J
Infect Dis 2001; 183: 810813.
84. Yob JM, Field H, Rashdi AM, et al. Nipah virus
infection in bats (order Chiroptera) in peninsular
Malaysia. Emerg Infect Dis 2001; 7: 439441.
85. Chua KB, Koh CL, Hooi PS, et al. Isolation of Nipah
virus from Malaysian Island ying-foxes. Microbes
Infect 2002; 4: 145151.
86. Chua KB, Chua BH, Wang CW. Anthropogenic
deforestation, El Nino and the emergence of
Nipah virus in Malaysia. Malays J Pathol 2002; 24:
1521.
87. Chua KB, Lam SK, Goh KJ, et al. The presence of
Nipah virus in respiratory secretions and urine of
patients during an outbreak of Nipah virus encephalitis in Malaysia J Infect 2001; 42: 4043.
88. Harcourt BH, Lowe L, Tamin A, et al. Genetic characterization of Nipah virus, Bangladesh, 2004.
Emerg Infect Dis 2005; 11: 15941597.
89. Hsu VP, Hossain MJ, Parashar UD, et al. Nipah
virus encephalitis reemergence, Bangladesh. Emerg
Infect Dis 2004; 10: 20822087.
90. Chadha MS, Comer JA, Lowe L, et al. Nipah virusassociated encephalitis outbreak, Siliguri, India.
Emerg Infect Dis 2006; 12: 235240.
91. Olson JG, Rupprecht C, Rollin PE, et al. Antibodies
to Nipah-like virus in bats (Pteropus lylei), Cambodia. Emerg Infect Dis 2002; 8: 987988.
92. Reynes JM, Counor D, Ong S, et al. Nipah virus in
Lyles ying foxes, Cambodia. Emerg Infect Dis
2005; 11: 10421047.
93. Wacharapluesadee S, Lumlertdacha B, Boongird K,
et al. Bat Nipah virus, Thailand. Emerg Infect Dis
2005; 11: 19491951.
94. Sendow I, Field HE, Curran J, et al. Henipavirus in
Pteropus vampyrus bats, Indonesia. Emerg Infect Dis
2006; 12: 711712.
95. Philbey AW, Kirkland PD, Ross AD, et al. An apparently new virus (family Paramyxoviridae) infectious
89
96.
97.
98.
99.
100.
101.
102.
103.
104.
105.
106.
107.
108.
109.
for pigs, humans, and fruit bats. Emerg Infect Dis

1998; 4: 269271.
Chant K, Chan R, Smith M, Dwyer DE, Kirkland P.
Probable human infection with a newly described
virus in the family Paramyxoviridae. Emerg Infect
Dis 1998; 4: 273275.
Bowden TR, Boyle DB. Completion of the fulllength genome sequence of Menangle virus:
characterization of the polymerase gene and
genomic 5 trailer region. Arch Virol 2005; 150:
21252137.
Chua KB, Wang LF, Lam SK, et al. Tioman virus, a
novel paramyxovirus isolated from fruit bats in
Malaysia. Virology 2001; 283: 215229.
Chua KB, Wang LF, Lam SK, Eaton BT. Full length
genome sequence of Tioman virus, a novel paramyxovirus in the genus Rubulavirus isolated from
fruit bats in Malaysia. Arch Virol 2002; 147: 1323
1348.
Gard GP, Compans RW. Structure and cytopathic
effects of Nelson Bay virus. J Virol 1970; 6: 100106.
Pritchard LI, Chua KB, Cummins D, et al. Pulau
virus: a new member of the Nelson Bay orthoreovirus species isolated from fruit bats in Malaysia.
Arch Virol 2006; 151: 229239.
Baillie GJ, van de Lagemaat LN, Baust C, Mager DL.
Multiple groups of endogenous betaretroviruses in
mice, rats, and other mammals. J Virol 2004; 78:
57845798.
Donaldson AI. Bats as possible maintenance hosts
for vesicular stomatitis virus. Am J Epidemiol 1970;
92: 132136.
Rao BL, Basu A, Wairagkar NS, et al. A large outbreak of acute encephalitis with high fatality rate
in children in Andhra Pradesh, India, in 2003, associated with Chandipura virus. Lancet 2004; 364:
869874.
Murphy FA, Shope RE, Metselaar D, Simpson DI.
Characterization of Mount Elgon bat virus, a new
member of the rhabdovirus group. Virology 1970;
40: 288297.
Arai YT, Kuzmin IV, Kameoka Y, Botvinkin AD.
New lyssavirus genotype from the lesser mouseeared bat (Myotis blythi), Kyrghyzstan. Emerg Infect
Dis 2003; 9: 333337.
Botvinkin AD, Poleschuk EM, Kuzmin IV, et al.
Novel lyssaviruses isolated from bats in Russia.
Kuzmin IV, Orciari LA, Arai YT, et al. Bat lyssaviruses (Aravan and Khujand) from Central Asia:
phylogenetic relationships according to N, P and
G gene sequences. Virus Res 2003; 97: 6579.
Markotter W, Randles J, Rupprecht CE, et al. Lagos
Bat Virus, South Africa. Emerg Infect Dis 2006; 12:
504506.
Rev. Med. Virol. 2007; 17: 6791.

DOI: 10.1002/rmv
90
110. Meredith CD, Rossouw AP, Koch HP. An unusual
case of human rabies thought to be of chiropteran
origin. S Afr Med J 1971; 45: 767769.
111. King AA, Meredith CD, Thomson GR. The biology
of southern African lyssavirus variants. Curr Top
Microbiol Immunol 1994; 187: 267295.
112. Badrane H, Bahloul C, Perrin P, Tordo N. Evidence of
two Lyssavirus phylogroups with distinct pathogenicity and immunogenicity. J Virol 2001; 75: 32683276.
113. Kuzmin IV, Hughes GJ, Botvinkin AD, Orciari LA,
Rupprecht CE. Phylogenetic relationships of Irkut
and West Caucasian bat viruses within the Lyssavirus genus and suggested quantitative criteria
based on the N gene sequence for lyssavirus genotype denition. Virus Res 2005; 111: 2843.
114. Badrane H, Tordo N. Host switching in Lyssavirus
history from the Chiroptera to the Carnivora
orders. J Virol 2001; 75: 80968104.
115. Shankar V, Orciari LA, de Mattos C, et al. Genetic
divergence of rabies viruses from bat species of Colorado, USA. Vector Borne Zoonotic Dis 2005; 5: 330
341.
116. Davis PL, Bourhy H, Holmes EC. The evolutionary
history and dynamics of bat rabies virus. Infect
Genet Evol 2006 (In press).
117. Nadin-Davis SA, Huang W, Armstrong J, et al. Antigenic and genetic divergence of rabies viruses from
bat species indigenous to Canada. Virus Res 2001;
74: 139156.
118. Messenger SL, Smith JS, Rupprecht CE. Emerging
epidemiology of bat-associated cryptic cases of
rabies in humans in the United States. Clin Infect
Dis 2002; 35: 738747.
119. Ito M, Arai YT, Itou T, et al. Genetic characterization
and geographic distribution of rabies virus isolates
in Brazil: identication of two reservoirs, dogs and
vampire bats. Virology 2001; 284: 214222.
120. Kobayashi Y, Sato G, Shoji Y, et al. Molecular epidemiological analysis of bat rabies viruses in Brazil.
J Vet Med Sci 2005; 67: 647652.
121. Cisterna D, Bonaventura R, Caillou S, et al. Antigenic and molecular characterization of rabies virus
in Argentina. Virus Res 2005; 109: 139147.
122. de Mattos CA, Favi M, Yung V, Pavletic C, de Mattos CC. Bat rabies in urban centers in Chile. J Wildl
Dis 2000; 36: 231240.
123. Nadin-Davis SA, Loza-Rubio E. The molecular epidemiology of rabies associated with chiropteran
hosts in Mexico. Virus Res 2006; 117: 215226.
124. Schowalter DB. Characteristics of bat rabies in
Alberta. Can J Comp Med 1980; 44: 7076.
125. Pal SR, Arora B, Chhuttani PN, et al. Rabies virus
infection of a ying fox bat, Pteropus policephalus
in Chandigarh, Northern India. Trop Geogr Med
1980; 32: 265267.
S. Wong et al.
126. Stantic-Pavlinic M. Public health concerns in bat
rabies across Europe. Euro Surveill 2005; 10: 217220.
127. Muller T, Cox J, Peter W, et al. Spill-over of European bat lyssavirus type 1 into a stone marten
(Martes foina) in Germany. J Vet Med B Infect Dis
Vet Public Health 2004; 51: 4954.
128. Fooks AR, Brookes SM, Johnson N, McElhinney
LM, Hutson AM. European bat lyssaviruses: an
emerging zoonosis. Epidemiol Infect 2003; 131:
10291039.
129. Bourhy H, Kissi B, Lafon M, Sacramento D, Tordo N.
Antigenic and molecular characterization of bat
rabies virus in Europe. J Clin Microbiol 1992; 30:
24192426.
130. Serra-Cobo J, Amengual B, Abellan C, Bourhy H.
European bat lyssavirus infection in Spanish bat
populations. Emerg Infect Dis 2002; 8: 413420.
131. van der Poel WH, van der Heide R, Verstraten ER,
et al. European bat lyssaviruses, The Netherlands.
Emerg Infect Dis 2005; 11: 18541859.
132. Rnsholt L, Srensen KJ, Bruschke CJM, et al. Clinical silent rabies infection in (zoo) bats. Vet Rec 1998;
142: 519520.
133. Brookes SM, Aegerter JN, Smith GC, et al. European
bat lyssavirus in Scottish bats. Emerg Infect Dis 2005;
11: 572578.
134. Johnson N, Selden D, Parsons G, et al. Isolation of a
European bat lyssavirus type 2 from a Daubentons
bat in the United Kingdom. Vet Rec 2003; 152: 383
387.
135. Fraser GC, Hooper PT, Lunt RA, et al. Encephalitis
caused by a Lyssavirus in fruit bats in Australia.
136. Allworth A, Murray K, Morgan J. A human case of
encephalitis due to a lyssavirus recently identied
in fruit bats. Commun Dis Intell 1996; 20: 504.
137. Mackenzie JS. Emerging viral diseases: an Australian perspective. Emerg Infect Dis 1999; 5: 18.
138. McCall BJ, Epstein JH, Neill AS, et al. Potential
exposure to Australian bat lyssavirus, Queensland,
19961999. Emerg Infect Dis 2000; 6: 259264.
139. McCall BJ, Field HE, Smith GA, Storie GJ, Harrower
BJ. Dening the risk of human exposure to Australian bat lyssavirus through potential non-bat animal infection. Commun Dis Intell 2005; 29: 202205.
140. Arguin PM, Murray-Lillibridge K, Miranda ME,
Smith JS, Calaor AB, Rupprecht CE. Serologic
evidence of Lyssavirus infections among bats, the
Philippines. Emerg Infect Dis 2002; 8: 258262.
141. Reynes JM, Molia S, Audry L, et al. Serologic evidence of lyssavirus infection in bats, Cambodia.
Emerg Infect Dis 2004; 10: 22312234.
142. Lumlertdacha B, Boongird K, Wanghongsa S, et al.
Survey for bat lyssaviruses, Thailand. Emerg Infect
Dis 2005; 11: 232236.
Rev. Med. Virol. 2007; 17: 6791.

DOI: 10.1002/rmv

143. Kuzmin IV, Niezgoda M, Carroll DS, et al. Lyssavirus surveillance in bats, Bangladesh. Emerg Infect
Dis 2005; 12: 486488.
144. Hellenbrand W, Meyer C, Rasch G, Steffens I,
Ammon A. E-alert 18 February: cases of rabies in
Germany following organ transplantation. Euro.
Surveill. 10:E050224.6. http://www.eurosurveillance.
org/ew/2005/ 050224.asp#6. [3 May, 2006.]
145. Willoughby Jr. RE, Tieves KS, Hoffman GM, et al.
Survival after treatment of rabies with induction
of coma. N Engl J Med 2005; 352: 25082514.
146. Brookes SM, Parsons G, Johnson N, McElhinney
LM, Fooks AR. Rabies human diploid cell
vaccine elicits cross-neutralising and cross-protecting immune responses against European and
Australian bat lyssaviruses. Vaccine 2005; 23:
41014109.
147. Hanlon CA, Kuzmin IV, Blanton JD, Weldon WC,
Manangan JS, Rupprecht CE. Efcacy of rabies biologics against new lyssaviruses from Eurasia. Virus
Res 2005; 111: 4454.
148. World Health Organization. Chikungunya and
Dengue in the south west Indian Ocean. http://
www.who.int/csr/don/2006_03_17/en/index.html.
[20 April, 2006.]
149. Diallo M, Thonnon J, Traore-Lamizana M, Fontenille D. Vectors of Chikungunya virus in Senegal:
current data and transmission cycles. Am J Trop
Med Hyg 1999; 60: 281286.
150. Ubico SR, McLean RG. Serologic survey of neotropical bats in Guatemala for virus antibodies. J Wildl
Dis 1995; 31: 19.
91
151. Weaver SC, Ferro C, Barrera R, Boshell J, Navarro
JC. Venezuelan equine encephalitis. Annu Rev Entomol 2004; 49: 141174.
152. Seymour C, Dickerman RW, Martin MS. Venezuelan encephalitis virus infection in neotropical bats.
I. Natural infection in a Guatemalan enzootic focus.
Am J Trop Med Hyg 1978; 27: 290296.
153. Correa-Giron P, Calisher CH, Baer GM. Epidemic
strain of Venezuelan equine encephalomyelitis
virus from a vampire bat captured in Oaxaca,
Mexico, 1970. Science 1972; 175: 546547.
154. Calisher CH, Kinney RM, de Souza Lopes O, Trent
DW, Monath TP, Francy DB. Identication of a new
Venezuelan equine encephalitis virus from Brazil.
Am J Trop Med Hyg 1982; 31: 12601272.
155. Ryan PA, Martin L, Mackenzie JS, Kay BH.
Investigation of gray-headed ying foxes (Pteropus
poliocephalus) (Megachiroptera: Pteropodidae) and
mosquitoes in the ecology of Ross River virus in
Australia. Am J Trop Med Hyg 1997; 57: 476482.
156. Almeida MF, Martorelli LF, Aires CC, Sallum PC,
Massad E. Indirect oral immunization of captive
vampires, Desmodus rotundus. Virus Res 2005; 111:
7782.
157. Setien AA, Brochier B, Tordo N, et al. Experimental
rabies infection and oral vaccination in vampire bats
(Desmodus rotundus). Vaccine 1998; 16: 11221126.
158. Wanzeller AL, Diniz JA, Gomes ML, et al. Ultrastructural, antigenic and physicochemical characterization of the Moju dos Campos (Bunyavirus)
isolated from bat in the Brazilian Amazon region.
Mem Inst Oswaldo Cruz 2002; 97: 307311.
Rev. Med. Virol. 2007; 17: 6791.

DOI: 10.1002/rmv

Wong Et Al. (2007)

Uploaded by

Copyright:

Available Formats

Wong Et Al. (2007)

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Wong Et Al. (2007)

Uploaded by

Copyright:

Available Formats

Reviews in Medical Virology

Rev. Med. Virol. 2007; 17: 6791.

Bats as a continuing source of emerging

Copyright # 2006 John Wiley & Sons, Ltd.

have large populations reared in relatively

Copyright # 2006 John Wiley & Sons, Ltd.

Nil (direct bat-tohuman transmission)

Nil (direct bat-tohuman transmission);

Biologist and other

Biologist and other

Close contacts with

Sporadic cases only

Palm civets and

Table 1. Transmission dynamics of selected bat-associated viruses

Nil; rarely through

Health care facilities

Health care facilities,

Health care facilities

Bats and emerging infection

Rev. Med. Virol. 2007; 17: 6791.

Table 2. Summary of bat families (7,8)

Tropical Asia, Australia,

Horseshoe bats and Old

Old World, tropical and

family Phyllostomidae and found only in Latin

and bat rabies viruses to humans and Ebola virus

Bats and emerging infection

Copyright # 2006 John Wiley & Sons, Ltd.

Rev. Med. Virol. 2007; 17: 6791.

Bats and emerging infection

Table 3. Risk ranking of bat-associated viruses in causing human infectionsa

Copyright # 2006 John Wiley & Sons, Ltd.

Rev. Med. Virol. 2007; 17: 6791.

European bat lyssavirus 1

This is especially common in families such as

serology [22,23]. It has not been found to infect

Bats and emerging infection

Bats and emerging infection

RT-PCR) in three species of bats captured in

become easier. These ndings have important

Bats and emerging infection

Bats and emerging infection

Bats and emerging infection

Bats and emerging infection

Copyright # 2006 John Wiley & Sons, Ltd.

4. Kalish ML, Wolfe ND, Ndongmo CB, et al. Hunters

Rev. Med. Virol. 2007; 17: 6791.

Bats and emerging infection

infectious diseases in wildlife. Acta Trop 2001; 78:

Copyright # 2006 John Wiley & Sons, Ltd.

Rev. Med. Virol. 2007; 17: 6791.

Copyright # 2006 John Wiley & Sons, Ltd.

Rev. Med. Virol. 2007; 17: 6791.

Bats and emerging infection

Copyright # 2006 John Wiley & Sons, Ltd.

for pigs, humans, and fruit bats. Emerg Infect Dis

Rev. Med. Virol. 2007; 17: 6791.

Copyright # 2006 John Wiley & Sons, Ltd.

Rev. Med. Virol. 2007; 17: 6791.