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      • Acid stress activation of the &sgr;<sup>E</sup> stress response in <i>Salmonella enterica</i> serovar Typhimurium

        Muller, Cé,cile,Bang, Iel-Soo,Velayudhan, Jyoti,Karlinsey, Joyce,Papenfort, Kai,Vogel, Jö,rg,Fang, Ferric C. Blackwell Publishing Ltd 2009 Molecular microbiology Vol.71 No.5

        <P>Summary</P><P>The alternative sigma factor &sgr;<SUP>E</SUP> is activated by unfolded outer membrane proteins (OMPs) and plays an essential role in <I>Salmonella</I> pathogenesis. The canonical pathway of &sgr;<SUP>E</SUP> activation in response to envelope stress involves sequential proteolysis of the anti-sigma factor RseA by the PDZ proteases DegS and RseP. Here we show that &sgr;<SUP>E</SUP> in <I>Salmonella enterica</I> sv. Typhimurium can also be activated by acid stress. A &sgr;<SUP>E</SUP>-deficient mutant exhibits increased susceptibility to acid pH and reduced survival in an acidified phagosomal vacuole. Acid activation of &sgr;<SUP>E</SUP>-dependent gene expression is independent of the unfolded OMP signal or the DegS protease but requires processing of RseA by RseP. The RseP PDZ domain is indispensable for acid induction, suggesting that acid stress may disrupt an inhibitory interaction between RseA and the RseP PDZ domain to allow RseA proteolysis in the absence of antecedent action of DegS. These observations demonstrate a novel environmental stimulus and activation pathway for the &sgr;<SUP>E</SUP> regulon that appear to be critically important during <I>Salmonella</I>–host cell interactions.</P>

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