Department of Molecular Biology and Microbiology and Howard Hughes Medical Institute, Tufts University School of Medicine, Boston, MA 02111, USA.
Int Microbiol. 2017 Sep;20(3):116-120. doi: 10.2436/20.1501.01.292.
This review highlights recent findings on the evolutionary arms race between the causative agent of cholera Vibrio cholerae and virulent bacteriophages (phages) ICP1, ICP2, and ICP3 isolated from cholera patient stool samples. We discuss mechanisms of phage resistance such as a unique phage-inhibitory chromosomal island and mutations that affect phage receptor expression. We also discuss the molecular characterization of ICP1 and its unique CRISPR-Cas system, which it uses to combat the phage-inhibitory chromosomal island. The role of phages in the life cycle of V. cholerae has been increasingly recognized and investigated in the past decade. This article will review hypotheses as to how the predator-prey relationship may have an impact on infections within individuals and on the self-limiting nature of cholera epidemics. In addition, we put forth a strategy of using phages as an intervention to reduce household transmission of cholera within a community.
这篇综述强调了最近在霍乱弧菌(Vibrio cholerae)与从霍乱患者粪便样本中分离出来的烈性噬菌体(噬菌) ICP1、ICP2 和 ICP3 之间的进化军备竞赛方面的发现。我们讨论了噬菌体抗性的机制,如独特的噬菌体抑制性染色体岛和影响噬菌体受体表达的突变。我们还讨论了 ICP1 的分子特征及其独特的 CRISPR-Cas 系统,该系统用于对抗噬菌体抑制性染色体岛。在过去十年中,噬菌体在霍乱弧菌生命周期中的作用越来越受到重视和研究。本文将综述捕食者-猎物关系如何影响个体感染以及霍乱流行的自限性的假说。此外,我们提出了一种利用噬菌体作为干预措施来减少社区内霍乱家庭传播的策略。