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Activation of the Two-Component System LisRK Promotes Cell Adhesion and High Ampicillin Tolerance in Listeria monocytogenes

机译:双组分系统LISRK促进细胞粘附和高氨苄青霉素耐受性在<斜视>李斯特菌单核细胞增生中

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Listeria monocytogenes is a foodborne pathogen which can survive in harsh environmental conditions. It responds to external stimuli through an array of two-component systems (TCS) that sense external cues. Several TCS, including LisRK, have been linked to Listeria ’s ability to grow at slightly elevated antibiotic levels. The aim of this study was to determine if the TCS LisRK is also involved in acquiring the high antibiotic tolerance that is characteristic of persister cells. LisRK activates a response that leads to remodeling of the cell envelope, and we therefore hypothesized that activation of LisRK could also increase in the cells’ adhesiveness and initiate the first step in biofilm formation. We used a Δ lisR mutant to study antibiotic tolerance in the presence and absence of LisRK, and a GFP reporter strain to visualize the activation of LisRK in L. monocytogenes LO28 at a single-cell level. LisRK was activated in most cells in stationary phase cultures. Antimicrobial susceptibility tests showed that LisRK was required for the generation of ampicillin tolerance under these conditions. The wildtype strain tolerated exposure to ampicillin at 1,000 × inhibitory levels for 24 h, and the fraction of surviving cells was 20,000-fold higher in the wildtype strain compared to the Δ lisR mutant. The same protection was not offered to other antibiotics (vancomycin, gentamicin, tetracycline), and the mechanism for antibiotic tolerance is thus highly specific. Furthermore, quantification of bacterial attachment rates and attachment force also revealed that the absence of a functional LisRK rendered the cells less adhesive. Hence, LisRK TCS promotes multiple protective mechanisms simultaneously. Graphical Abstract Listeria monocytogenes activates the two-component system LisRK under stress, and becomes more adhesive and highly tolerant to ampicillin.
机译:Listeria单核细胞增生是一种食物中的病原体,可以在恶劣的环境条件下存活。它通过感测外部提示的两组分量系统(TCS)阵列响应外部刺激。包括LISRK在内的几个TCS与李斯特菌的抗生素水平略高的能力有关。本研究的目的是确定TCS LISRK是否还参与获取具有抗泄漏细胞特征的高抗生素耐受性。 LISRK激活导致细胞包膜重塑的反应,因此我们假设LISRK的激活也可能增加细胞的粘合性并引发生物膜形成的第一步。我们使用了δLISR突变体在LISRK的存在和不存在下研究抗生素耐受性,以及GFP报告菌株以在单细胞水平下可视化L.单核细胞增生LO28中的LISRK活化。在固定相培养物中的大多数细胞中被激活了LISRK。抗微生物易感性试验表明,在这些条件下,氨苄青霉素耐受性需要LISRK。与δLISR突变体相比,野生型菌株在1,000×抑制水平下暴露于氨苄青霉素的抑制水平,并且与δLISR突变体相比,野生型菌株中存活细胞的级分高出20,000倍。其他抗生素(万古霉素,庆大霉素,四环素)没有提供相同的保护,因此抗生素耐受的机制是高度特异性的。此外,细菌附着速率和附着力的定量也显示出函数式锂的不存在使细胞较少的粘合剂。因此,LISRK TCS同时促进多种保护机制。图形摘要李斯特菌单核细胞增生在应力下激活双组分系统LISRK,并变得更加粘附,高度耐受氨苄青霉素。

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