Vallet Simon-Ulysse, Hansen Lykke Haastrup, Bistrup Freja Cecillie, Laursen Signe Aagaard, Chapalay Julien Bortoli, Chambon Marc, Turcatti Gerardo, Viollier Patrick H, Kirkpatrick Clare L
Department of Microbiology and Molecular Medicine, Institute of Genetics and Genomics in Geneva (iG3), Faculty of Medicine/CMU, University of Geneva, Geneva, Switzerland.
Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.
mBio. 2020 May 5;11(3):e00538-20. doi: 10.1128/mBio.00538-20.
Rod-shaped bacteria frequently localize proteins to one or both cell poles in order to regulate processes such as chromosome replication or polar organelle development. However, the roles of polar factors in responses to extracellular stimuli have been generally unexplored. We employed chemical-genetic screening to probe the interaction between one such factor from , TipN, and extracellular stress and found that TipN is required for normal resistance of cell envelope-directed antibiotics, including vancomycin which does not normally inhibit growth of Gram-negative bacteria. Forward genetic screening for suppressors of vancomycin sensitivity in the absence of TipN revealed the TonB-dependent receptor ChvT as the mediator of vancomycin sensitivity. Loss of ChvT improved resistance to vancomycin and cefixime in the otherwise sensitive Δ strain. The activity of the two-component system regulating ChvT (ChvIG) was increased in Δ cells relative to the wild type under some, but not all, cell wall stress conditions that this strain was sensitized to, in particular cefixime and detergent exposure. Together, these results indicate that TipN contributes to cell envelope stress resistance in addition to its roles in intracellular development, and its loss influences signaling through the ChvIG two-component system which has been co-opted as a sensor of cell wall stress in Maintenance of an intact cell envelope is essential for free-living bacteria to protect themselves against their environment. In the case of rod-shaped bacteria, the poles of the cell are potential weak points in the cell envelope due to the high curvature of the layers and the need to break and reform the cell envelope at the division plane as the cells divide. We have found that TipN, a factor required for correct division and cell pole development in , is also needed for maintaining normal levels of resistance to cell wall-targeting antibiotics such as vancomycin and cefixime, which interfere with peptidoglycan synthesis. Since TipN is normally located at the poles of the cell and at the division plane just before cells complete division, our results suggest that it is involved in stabilization of these weak points of the cell envelope as well as its other roles inside the cell.
杆状细菌经常将蛋白质定位到一个或两个细胞极,以调节诸如染色体复制或极性细胞器发育等过程。然而,极性因子在应对细胞外刺激中的作用通常尚未得到探索。我们采用化学遗传学筛选来探究来自的一种此类因子TipN与细胞外应激之间的相互作用,发现TipN是对包括万古霉素在内的针对细胞壁的抗生素产生正常抗性所必需的,万古霉素通常不会抑制革兰氏阴性菌的生长。在没有TipN的情况下对万古霉素敏感性的抑制子进行正向遗传学筛选,发现TonB依赖性受体ChvT是万古霉素敏感性的介导因子。ChvT的缺失提高了对万古霉素和头孢克肟的抗性,而在其他情况下敏感的Δ菌株中则不然。在该菌株对其敏感的一些但并非所有细胞壁应激条件下,特别是头孢克肟和去污剂暴露时,相对于野生型,调节ChvT的双组分系统(ChvIG)在Δ细胞中的活性增加。总之,这些结果表明TipN除了在细胞内发育中的作用外,还对细胞壁应激抗性有贡献,并且其缺失会影响通过ChvIG双组分系统的信号传导,该系统已被用作细胞壁应激的传感器。维持完整的细胞壁对于自由生活的细菌保护自身免受环境影响至关重要。对于杆状细菌而言,由于各层的高曲率以及细胞分裂时在分裂平面处需要破坏和重新形成细胞壁,细胞极是细胞壁中的潜在弱点。我们发现,TipN是中正确分裂和细胞极发育所必需的因子,对于维持对干扰肽聚糖合成的诸如万古霉素和头孢克肟等针对细胞壁的抗生素的正常抗性水平也是必需的。由于TipN通常位于细胞极以及细胞即将完成分裂前所在的分裂平面处,我们的结果表明它参与了细胞壁这些弱点处的稳定以及其在细胞内的其他作用。