A major factor in the resilience of is the alternative sigma factor B (σ). Type II Toxin/Antitoxin (TA) systems are also known to have a role in the bacterial stress response upon activation via the ClpP or Lon proteases. Directly upstream of the σ operon in is the TA system , which can cleave mRNA at UACMU sites. In this study, we showed that the TA locus does not affect the level of persister formation during treatment with antibiotics in lethal doses, but exerts different effects according to the sub-inhibitory stress added. Growth of a Δ mutant was enhanced relative to the wildtype in the presence of sub-inhibitory norfloxacin and at 42 °C, but was decreased when challenged with ampicillin and gentamicin. In contrast to studies in , we found that the locus did not affect transcription of genes within the σ operon, but MazEF effected the expression of the σ-dependent genes and , with a 0.22 and 0.05 fold change, respectively, compared to the wildtype under sub-inhibitory norfloxacin conditions. How exactly this system operates remains an open question, however, our data indicates it is not analogous to the system of , suggesting a novel mode of action for MazEF in
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308263 | PMC |
http://dx.doi.org/10.3390/toxins9010031 | DOI Listing |
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