RpoS levels at low temperature in Salmonella has not previously been investigated, however, the lack of a growth phenotype in the rpoS mutant in the current study corresponds well with previous results, AC220 supplier showing that an rpoS mutant of S. Typhimurium SL1344 was only slightly sensitive to low temperature [20]. In contrast to results from Listeria monocytogenes, where clpP is expressed at elevated level when grown at 10°C [21], temperature

down shift did not cause increased clpP BIX 1294 ic50 transcription in S. Typhimurium (data not shown), and we interpret this as a further indication that the effect of ClpP deletion on growth a low temperature is indirect, i.e. caused by too high levels of RpoS. The csrA gene is essential for growth at low temperature independent of clpP and rpoS The csrA gene was first identified in a screen of factors affecting glycogen accumulation [22], and a FHPI mouse csrA mutant accumulates high amounts of glycogen [23]. More recently, it was found that glycogen accumulation is involved in protection against environmental stress similar to other sugar components [24]. The csrA system has been found to be important for numerous cell functions affecting virulence, motility and stress adaptation [25–27], and both deletion and over-expression of this gene have been shown to affect the cell morphology in Legionella pneumophila and E. coli [22,28,29]. Mutation

of csrA causes severe growth defects at 37°C and suppressor mutants arise spontaneously [30,31]. To overcome the uncertainty of working with a mixed population of original and spontaneous suppressor mutants, we have previously chosen to work with a ΔcsrA::kan suppressor mutant [13], and the same well-characterized suppressor mutant was used in the present study. The csrA (sup) mutant Tolmetin was severely impaired in colony formation on LB agar already at 21°C (Figure 1A)

as well as during growth in LB broth at 10°C (Figure 2D). This phenotype could be reversed by complementation of the csrA gene (Figure 2D) and further by using an arabinose inducible promoter (Additional file 1: Figure S1). Unlike the clpP/rpoS double mutant, the rpoS/csrA (sup) mutant did not grow at 21°C nor at lower temperatures (Figure 1A), indicating that the csrA gene was essential for growth at low temperature independent from RpoS levels. Growth of the clpP/csrA mutant was similarly impaired, however, the ability of this strain to grow a low temperature increased slightly compared to the csrA (sub) mutant (growth possible at 21°C and a 15°C). This improvement disappeared when rpoS was mutated in addition to clpP and csrA (Figures 1 and 2). As both the mutation in clpP and csrA cause increased RpoS level, one could have expected growth to be more affected. We investigated if the level of RpoS was increased in the double mutant.