Single, double and triple mutants of Salmonella enterica serovar Typhimurium degP ( htrA), degQ ( hhoA) and degS ( hhoB) have diverse phenotypes on exposure to elevated temperature and their growth in vivo is attenuated to different extents
DegP (HtrA) is a well-studied protease involved in survival of bacteria under stress conditions in vitro and in vivo. There are two paralogues of DegP in the Salmonella enterica serovar Typhimurium genome, DegQ and DegS. In order to understand more about the biological significance of this gene fami...
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Veröffentlicht in: | Microbial pathogenesis 2006-10, Vol.41 (4), p.174-182 |
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Zusammenfassung: | DegP (HtrA) is a well-studied protease involved in survival of bacteria under stress conditions in vitro and in vivo. There are two paralogues of DegP in the
Salmonella enterica serovar Typhimurium genome, DegQ and DegS. In order to understand more about the biological significance of this gene family, a series of
deg-deletion mutants was generated in
S. Typhimurium strain SL3261 by allelic replacement. At elevated temperature in vitro, the viability of
degP and
degS mutants was reduced when compared with the parent strain whereas the viability of a
degQ mutant was not significantly affected. The viability of a double
degP-
degS mutant at elevated temperature was severely decreased when compared with the respective single mutants or, interestingly, with a triple
degP-degQ-
degS mutant.
All the
deg deletions were transduced into the mouse-virulent strain SL1344 and the resultant mutants were injected intravenously into BALB/c mice to test virulence.
degP and
degS single mutants and all combinations of double and triple mutants were attenuated to different degrees, whereas the single
degQ mutant was as virulent as the wild-type strain. Thus, within this gene family,
degP and
degS appear important for survival at elevated temperature and are necessary for full virulence, whereas a single
degQ deletion appears to have no clear role in survival and growth at elevated temperature or in mice. |
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ISSN: | 0882-4010 1096-1208 |
DOI: | 10.1016/j.micpath.2006.07.004 |