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Isolation of Highly Persistent Mutants of Salmonella enterica Serovar Typhimurium Reveals a New Toxin-Antitoxin Module

机译:肠炎沙门氏菌鼠伤寒沙门氏菌高持久性突变株的分离揭示了一种新的毒素-抗毒素模块

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摘要

Bacterial persistence is characterized by the ability of a subpopulation within bacterial cultures to survive exposure to antibiotics and other lethal treatments. The surviving persisters are not the result of genetic changes but represent epigenetic variants that are in a physiological state where growth is inhibited. Since characterization of persisters has been performed mainly in Escherichia coli K-12, we sought to identify mechanisms of persistence in the pathogen Salmonella enterica serovar Typhimurium. Isolation of new highly persistent mutants revealed that the shpAB locus (Salmonella high persistence) imparted a 3- to 4-order-of-magnitude increase in survival after ampicillin exposure throughout its growth phase and protected the population against exposure to multiple antibiotics. Genetic characterization revealed that shpAB is a newly discovered toxin-antitoxin (TA) module. The high-persistence phenotype was attributed to a nonsense mutation in the 3′ end of the shpB gene encoding an antitoxin protein. Characteristic of other TA modules, shpAB is autoregulated, and high persistence depends on the Lon protease.
机译:细菌持久性的特征在于细菌培养物中的亚群在暴露于抗生素和其他致死性治疗中存活下来的能力。存活的坚持者不是遗传变化的结果,而是代表处于生长受抑制的生理状态的表观遗传变异。由于持久性的表征主要是在大肠杆菌K-12中进行的,因此我们试图确定在病原体小肠沙门氏菌血清鼠伤寒中的持久性机制。分离出新的高持久性突变体后发现,在整个生长阶段暴露于氨苄西林后,shpAB基因座(沙门氏菌高持久性)的存活率提高了3到4个数量级,并保护了人群免受多种抗生素的侵害。遗传特征表明shpAB是新发现的毒素-抗毒素(TA)模块。高持久性表型归因于编码抗毒素蛋白的shpB基因3'端的无意义突变。 shpAB是其他TA模块的特征,它是自动调节的,高持久性取决于Lon蛋白酶。

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