Aslan Hüsnü, Petersen Maiken Engelbrecht, De Berardinis Alberto, Zacho Brunhede Maja, Khan Nasar, Vergara Alberto, Kallipolitis Birgitte, Meyer Rikke Louise
Faculty of Natural Sciences, Interdisciplinary Nanoscience Center, Aarhus University, Aarhus, Denmark.
Faculty of Veterinary Medicine, University of Teramo, Teramo, Italy.
Front Microbiol. 2021 Jan 27;12:618174. doi: 10.3389/fmicb.2021.618174. eCollection 2021.
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 '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 mutant to study antibiotic tolerance in the presence and absence of LisRK, and a GFP reporter strain to visualize the activation of LisRK in 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 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.
是一种食源性病原体,能够在恶劣的环境条件下存活。它通过一系列感知外部线索的双组分系统(TCS)对外部刺激做出反应。包括LisRK在内的几种TCS与在略高抗生素水平下生长的能力有关。本研究的目的是确定TCS LisRK是否也参与获得持久性细胞特有的高抗生素耐受性。LisRK激活一种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附性并启动生物膜形成的第一步。我们使用Δ突变体研究在有和没有LisRK的情况下的抗生素耐受性,并使用GFP报告菌株在单细胞水平上可视化LO28中LisRK的激活。LisRK在稳定期培养物中的大多数细胞中被激活。抗菌药敏试验表明,在这些条件下产生氨苄青霉素耐受性需要LisRK。野生型菌株能够耐受1000倍抑制水平的氨苄青霉素暴露24小时,与Δ突变体相比,野生型菌株中存活细胞的比例高出20000倍。对其他抗生素(万古霉素、庆大霉素、四环素)没有同样的保护作用,因此抗生素耐受性机制具有高度特异性。此外,对细菌附着率和附着力的定量分析还表明,缺乏功能性LisRK会使细胞的粘附性降低。因此,LisRK TCS同时促进多种保护机制。