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PLoS One. 2008;3(12):e3829. doi: 10.1371/journal.pone.0003829. Epub 2008 Dec 3.

Differentially evolved genes of Salmonella pathogenicity islands: insights into the mechanism of host specificity in Salmonella.

Author information

1
Department of Microbiology and Cell Biology, Centre for Infectious Disease Research and Biosafety Laboratories, Indian Institute of Science, Bangalore, India.

Abstract

BACKGROUND:

The species Salmonella enterica (S. enterica) includes many serovars that cause disease in avian and mammalian hosts. These serovars differ greatly in their host range and their degree of host adaptation. The host specificity of S. enterica serovars appears to be a complex phenomenon governed by multiple factors acting at different stages of the infection process, which makes identification of the cause/s of host specificity solely by experimental methods difficult.

METHODOLOGY/PRINCIPAL FINDINGS:

In this study, we have employed a molecular evolution and phylogenetics based approach to identify genes that might play important roles in conferring host specificity to different serovars of S. enterica. These genes are 'differentially evolved' in different S. enterica serovars. This list of 'differentially evolved' genes includes genes that encode translocon proteins (SipD, SseC and SseD) of both Salmonella pathogenicity islands 1 and 2 encoded type three secretion systems, sptP, which encodes an effector protein that inhibits the mitogen-activated protein kinase pathway of the host cell, and genes which encode effector proteins (SseF and SifA) that are important in placing the Salmonella-containing vacuole in a juxtanuclear position.

CONCLUSIONS/SIGNIFICANCE:

Analysis of known functions of these 'differentially evolved genes' indicates that the products of these genes directly interact with the host cell and manipulate its functions and thereby confer host specificity, at least in part, to different serovars of S. enterica that are considered in this study.

PMID:
19050757
PMCID:
PMC2585142
DOI:
10.1371/journal.pone.0003829
[Indexed for MEDLINE]
Free PMC Article
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