Salmonella enterica subspecies I, serovar Typhimurium (S. typhimurium), is
a leading cause of human gastroenteritis, and is used as a mouse model of h
uman typhoid fever(1). The incidence of non-typhoid salmonellosis is increa
sing worldwide(2-4), causing millions of infections and many deaths in the
human population each year. Here we sequenced the 4,857-kilobase (kb) chrom
osome and 94-kb virulence plasmid of S. typhimurium strain LT2. The distrib
ution of close homologues of S. typhimurium LT2 genes in eight related ente
robacteria was determined using previously completed genomes of three relat
ed bacteria, sample sequencing of both S. enterica serovar Paratyphi A (S.
paratyphi A) and Klebsiella pneumoniae, and hybridization of three unsequen
ced genomes to a microarray of S. typhimurium LT2 genes. Lateral transfer o
f genes is frequent, with 11% of the S. typhimurium LT2 genes missing from
S. enterica serovar Typhi (S. typhi), and 29% missing from Escherichia coli
K12. The 352 gene homologues of S. typhimurium LT2 confined to subspecies
I of S. enterica- containing most mammalian and bird pathogens(5)- are usef
ul for studies of epidemiology, host specificity and pathogenesis. Most of
these homologues were previously unknown, and 50 may be exported to the per
iplasm or outer membrane, rendering them accessible as therapeutic or vacci
ne targets.