0 3 log10 decline in CFU/ml from 60 to 120 min after the heat sho

0.3 log10 decline in CFU/ml from 60 to 120 min after the heat shock onset. In contrast, Doramapimod mouse CFU counts revealed that S. aureus cultures exposed to 43°C or 37°C showed equivalent growth and survival profiles. These data allowed defining 43°C and 48°C as sub-lethal and eventually lethal temperatures, respectively. We also observed that

S. aureus cultures continually exposed to 43°C or 37°C showed marginally different growth kinetics, while those continuously exposed to 48°C remained growth-arrested at least for a 5 h-period (Figure 1) followed by a significant viability decline at 18 h (data not shown). Figure 1 Comparison of S. aureus ISP794 growth rates at 37°C, 43°C, or 48°C. Viable counts (CFU/ml) of bacterial cultures, grown on Mueller-Hinton broth at the indicated temperatures, were estimated by agar plating of serially diluted samples. To verify that the marginal CFU decline during S. aureus heat stress at 48°C did not reflect heat-induced aggregation of the bacterial culture, we also evaluated bacterial

viability by fluorescence microscopy, using the Live/Dead BacLight Bacterial Viability assay (see Methods). No significant aggregation was induced by www.selleckchem.com/products/GSK690693.html heat exposure and the proportion of propidium iodide-stained, red bacteria increased slowly over time, in agreement with the slowly declining viable counts (data not shown). Finally, the extent of cell lysis was also estimated by the percentage of extracellularly released ATP before and after up-shift from 37°C to 48°C. The results showed nearly equivalent, low contents of extracellular ATP at the different temperatures, which represented <10% of intracellular ATP assayed in parallel and confirmed the marginal cell lysis (data not shown). Additional heat-stress transcriptomic responses from various metabolic

pathways A large proportion of genes whose transcript levels showed ≥ 2-fold changes after up-shifts to either 43°C or 48°C belonged either to additional stress response pathways that were not regulated by CtsR-, HrcA-, and/or SigB, or to major metabolic pathways that likely contributed to the physiological Etoposide clinical trial adjustment and survival of heat-stress exposed bacteria. The Additional file 4 shows selected examples of up- or down-regulated genes representative of the different metabolic categories. A more exhaustive list of relevant gene transcripts and pathways is presented in the Additional file 2, which also includes altered genes of general function prediction only or unknown function. Regulation of osmotic balance Some heat-induced genes likely contributed to osmotolerance, such as those encoding glycine betaine transporter (opuD), choline dehydrogenase (betA), and glycine GS-9973 aldehyde dehydrogenase (gbsA).

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