Miscellaneous Viruses
Miscellaneous Viruses
Miscellaneous Viruses
us
s
Papova
Parvo
Rubella
Rota
SARS
Slow viruses (Prions)
PAPOVAviruse
s
Papillomavirus &
Polyomavirus
Polyomaviruses
Polyomaviruses latent infection in
mice
cultures
l
onl
y
Human Papilloma
Virus
(HPV)
and feet
Verruca vulgaris
seen on hands
children HPV 1, 2, 3, 4
Condyloma acuminatum
of
soft
moist,
pedunculated
warts on ext. genitalia,
transmitted, may turn malignant- 6, 1
sexually
HPV
1
HPV 6, 11 intraepithelial neoplasia
HPV 16, 18 Ca Cx
Common
warts
type 1-4
HPV s
t.
n-
when
Parvovirus
Very small single stranded viru
DNA
s
Parvovirus B19
Infection
2nd/3rd trimester
haem.
anaemia
during
Detection
of virus in blood early/ Ab
later
Erythema infectiosum-Parvovirus
B19
Slapped cheek
appearance
Typical rash of
erythema infectiosum
Rubella ( German
Measles)
Gregg 1941- congenital
cataract
st trimester congenital
1
Inf. early in pregnancy- fetal death
malformations
Congenital
rubella cardiac defects,
cataract,
deafness
post
.
Congenital Rubella
Classical triad
Congenital cataract
Deafness
Cardiac defects
Congenit Rubell
al
a
Viral diarrhea
Rota-Wheel (latin)
Characteristic
appearance
-wheel with radiating
spokes
Rotavirus
Mode of spread
-Feco oral
2-5days
Maximal shedding of virus
occurs after onset of diarrhea
The virus can withstand drying, hence
can
survive on hands, fomites, toys etc.,
Outbreaks-Preschool and daycare centres
A)
Laboratorydiagnosi
Detection of viral antigen-ELISA
A LA
s
Direct observation-El m/e
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Mode of infection
Clinical features
Fever,cough,dyspnea,occ.diarrhea
3-30% fatality
Death is due to respiratory failure
Caused by an
abnormal protein called
PrPsc
It is devoid of nucleic
acid and highly
resistant
Prusiner to chemical
the
and
physical
coined
term agents
these
proteinaceous
PRION
forparticle.
infectious
Stanley Prusiner
Nobel Laureate(1997)
PRION diseases
HUMAN
CJD (Creutzfeldt-
Jacob
disease)
GSS (Gerstmann
straussler-Scheinker)
FFI (Fatal familial
insomnia)
Kuru
ANIMAL
Scrapie
(BSE) Bovine
spongiform
encephalopathy
Transmissible
mink
encephalopathy etc.,
Scrapie
Natural disease
Irritable with
intense pruritis
Finally paralysis and
death
Transmission
Via infected tissue, or syndrome may be
inherited
-cuts in skin
-transplantation of contaminated
tissue (cornea)
PRION diseases
Pathogenesis
The abnormal Prion protein accumulates in the brain
neuronal damage ensues
spongiform degeneration results
NormalGray matter
Vacuolisation in BSE
CJD
-Progressive dementia
-can occur in
-Sporadic forms
-Inherited forms
-Iatrogenic (foll. corneal transplant etc.,)
-variant CJD affects younger people
-?due to eating of BSE infected meat
-has atypical features (psychiatric symptoms
etc.,)
31
Kuru
Seen
Modes of control
For CJD & GSS
All neurosurgical tools to be disinfected in
5% hypochlorite solution or 2M NaOH
or autoclaving at131oC for 11/2 hrs.
For vCJD
Avoid eating infected meat products
34
Than
k
yo
u
35