ESSENTIAL ROLES OF CORE STARVATION-STRESS RESPONSE LOCI IN CARBON-STARVATION-INDUCIBLE CROSS-RESISTANCE AND HYDROGEN PEROXIDE-INDUCIBLE ADAPTIVE RESISTANCE TO OXIDATIVE CHALLENGE IN SALMONELLA-TYPHIMURIUM
Rl. Seymour et al., ESSENTIAL ROLES OF CORE STARVATION-STRESS RESPONSE LOCI IN CARBON-STARVATION-INDUCIBLE CROSS-RESISTANCE AND HYDROGEN PEROXIDE-INDUCIBLE ADAPTIVE RESISTANCE TO OXIDATIVE CHALLENGE IN SALMONELLA-TYPHIMURIUM, Molecular microbiology, 20(3), 1996, pp. 497-505
The starvation-stress response (SSR) of Salmonella typhimurium encompa
sses the physiological changes that occur upon starvation for an essen
tial nutrient, e.g, C-source, A subset of SSR genes, known as core SSR
genes, are required for the long-term starvation survival of the bact
eria, Four core SSR loci have been identified in S, typhimurium: rpoS,
stiA, stiB, and stiC, Here we report that in S, typhimurium C-starvat
ion induced a greater and more sustainable cross-resistance to oxidati
ve challenge (15 mM hydrogen peroxide (H2O2) for 40 min) than either N
- or P-starvation, Of the four core SSR loci, only rpoS and stiC mutan
ts exhibited a defective C-starvation-inducible cross-resistance to H2
O2 challenge, Interestingly, (unadapted) log-phase S. typhimurium rpoS
and stiA mutants were very sensitive to oxidative challenge, Based on
this, we determined if these core SSR loci were important for H2O2 re
sistance developed during a 60 min adaptive exposure to 60 mu M H2O2 (
adapted cells), Both unadapted and adapted rpoS and stiA mutants were
hypersensitive to a H2O2 challenge, in addition, a stiB mutant exhibit
ed normal adaptive resistance for the first 20 mins of H2O2 challenge
but then rapidly lost viability, declining to a level of about 1.5% of
the wild-type strain, The results of these experiments indicate that:
(i) the rpoS and stiC loci are essential for the development of C-sta
rvation-inducible cross-resistance to oxidative challenge, and (ii) th
e rpoS, stiA, and, in a delayed effect, stiB loci are needed for H2O2-
inducible adaptive resistance to oxidative challenge, Moreover, we fou
nd that both stiA and stiB are induced by a 60 mu M H2O2 exposure, but
only stiA was regulated (repressed) by (reduced form) OxyR.