Unknown,Transcriptomics,Genomics,Proteomics

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Transcription profiling of Listeria monocytogenes wild type and cadC deletion mutant grown in BHI at 37ºC

ABSTRACT: CadC is the transcriptional regulator of CadA, an efflux pump conferring cadmium resistance. We previously showed that during in vivo infection, Listeria monocytogenes uses CadC to directly repress the expression of the LspB lipoprotein signal peptidase, avoiding the exposure of the lipoprotein LpeA to the host immune system, impairing inflammatory cytokine expression and promoting intramacrophage survival and virulence. Here, to assess if CadC could be a widespread virulence regulator, we searched for other genes regulated by CadC using Listeria monocytogenes tiling arrays.

ORGANISM(S): Listeria monocytogenes EGD-e

SUBMITTER: Didier Cabanes

PROVIDER: E-MTAB-7857 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Project description:In several gram-positive bacterial genera including Bacillus, Staphylococcus, and Listeria, sigma B (σB) has been identified as a stress-responsive alternative sigma factor responsible for initiating transcription of genes (the σB regulon) involved in response to stress-inducing environmental conditions. In L. monocytogenes, a foodborne pathogen of considerable threat to public health and the food industry, σB is involved in regulation of stress response and virulence gene expression. We have defined the σB regulon in L. monocytogenes during early stationary phase and under salt stress (0.3M NaCl) conditions using whole-genome microarrays, identifying 168 genes that generated ≥2.0-fold higher signals in the parental strain 10403S than in an isogenic sigB null mutant (ΔsigB), categorized into nine functional groups including stress-response genes (12), virulence genes (5), and genes related to transport (26) and metabolism (45). To gain a broader biological perspective of the σB stress response system, we applied these microarrays to Listeria innocua under the same environmental conditions. Our studies revealed 64 candidates in the L. innocua σB regulon with ≥2.0-fold higher signals in the parent than in a ΔsigB mutant; 49 of the 64 genes overlap with the L. monocytogenes σB regulon, indicating extensive overlap in σB-controlled genes between the two species. Further transcriptional analysis using TaqMan quantitative real time RT-PCR was performed for selected genes that displayed contrasting fold changes among the four microarray data sets (two stress conditions per species). We report novel members of the L. monocytogenes σB regulon, as well as the initial definition of the L. innocua σB regulon. Our comparative studies of the σB stress response systems in L. monocytogenes and L. innocua revealed features of the σB regulon that are conserved and unique to the two species. Keywords: Listeria monocytogenes, Listeria innocua, SigB regulon, salt stress, stationary phase

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Transcription profiling of Listeria monocytogenes wild type and cadC deletion mutant grown in BHI at 37ºC

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