Department of Microbiology and Immunobiology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA; College of Life Science, Nankai University, 94 Weijin Road, Tianjin 300071, China.
Department of Microbiology and Immunobiology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA; Division of Infectious Disease, Brigham & Women's Hospital, and Howard Hughes Medical Institute, Boston, MA 02115, USA.
Cell Host Microbe. 2013 Dec 11;14(6):652-63. doi: 10.1016/j.chom.2013.11.001.
Analysis of genes required for host infection will provide clues to the drivers of evolutionary fitness of pathogens like Vibrio cholerae, a mounting threat to global heath. We used transposon insertion site sequencing (Tn-seq) to comprehensively assess the contribution of nearly all V. cholerae genes toward growth in the infant rabbit intestine. Four hundred genes were identified as critical to V. cholerae in vivo fitness. These included most known colonization factors and several new genes affecting the bacterium's metabolic properties, resistance to bile, and ability to synthesize cyclic AMP-GMP. Notably, a mutant carrying an insertion in tsiV3, encoding immunity to a bacteriocidal type VI secretion system (T6SS) effector VgrG3, exhibited a colonization defect. The reduced in vivo fitness of tsiV3 mutants depends on their cocolonization with bacterial cells carrying an intact T6SS locus and VgrG3 gene, suggesting that the V. cholerae T6SS is functional and mediates antagonistic interbacterial interactions during infection.
分析宿主感染所需的基因将为霍乱弧菌等病原体进化适应力的驱动因素提供线索,霍乱弧菌是全球健康的一个日益严重的威胁。我们使用转座子插入位点测序(Tn-seq)技术,全面评估了近所有霍乱弧菌基因在婴儿兔肠道内生长的贡献。鉴定出 400 个对霍乱弧菌体内适应性至关重要的基因。这些基因包括大多数已知的定植因子和几个影响细菌代谢特性、胆汁抗性和合成环 AMP-GMP 能力的新基因。值得注意的是,携带 tsiV3 插入突变的突变体,该基因编码对杀菌性 VI 型分泌系统(T6SS)效应物 VgrG3 的免疫,表现出定植缺陷。tsiV3 突变体体内适应性降低取决于它们与携带完整 T6SS 基因座和 VgrG3 基因的细菌细胞的共定植,这表明霍乱弧菌的 T6SS 是功能性的,并在感染过程中介导细菌间的拮抗相互作用。