Abbreviations
Abbreviations
i.m. intramuscular
i.v. intravenous
LPS lipopolysaccharide
Mp macrophages
Vi virulent (antigen)
v
Acknowledgements
We would like to thank the following for their participation in the preparation of
this document:
Dr M.K. Bhan, All India Institute of Medical Sciences, New Delhi, India
Dr Jeremy Farrar, Oxford University and the Hospital for Tropical Diseases,
Ho Chi Minh City, Viet Nam
Dr Pakleong Lim, Clinical Immunology Unit, The Prince of Wales Hospital, Shatin,
Hong Kong, People’s Republic of China
Dr Tikki Pang, Department of Evidence and Information for Policy, World Health
Organization, Geneva, Switzerland
vii
Dr Narain Punjabi, US NAMRU-2, Jakarta, Indonesia
and
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Chapter 1:
The organism, the disease
and transmission
S. typhi has several unique features, the genetic basis of many of which is known as
a result of early genetic studies and the recent sequencing of the whole genome.
Although many genes are shared with E. coli and at least 90% with S. typhimurium,
there are several unique clusters of genes known as pathogenicity islands and many
more single genes that seem to have been acquired by S. typhi during evolution.
S. typhi can be identified in the laboratory by several biochemical and serological tests
(see Chapter 2). One of the most specific is that of polysaccharide capsule Vi, which is
present in about 90% of all freshly isolated S. typhi and has a protective effect against
the bactericidal action of the serum of infected patients. This capsule provides the basis
for one of the commercially available vaccines (see Chapter 4). Vi antigen is present in
some other bacteria (Citrobacter freundii, Salmonella paratyphi C and Salmonella
dublin) but not in exactly the same genetic context. The ratio of disease caused by
S. typhi to that caused by S. paratyphi is about 10 to 1 in most of the countries where
this matter has been studied.
WHO/V&B/03.07 1