首页    期刊浏览 2025年02月28日 星期五
登录注册

文章基本信息

  • 标题:hipBA toxin-antitoxin systems mediate persistence in Caulobacter crescentus
  • 本地全文:下载
  • 作者:Charlie Y. Huang ; Carlos Gonzalez-Lopez ; Céline Henry
  • 期刊名称:Scientific Reports
  • 电子版ISSN:2045-2322
  • 出版年度:2020
  • 卷号:10
  • 期号:1
  • 页码:1-15
  • DOI:10.1038/s41598-020-59283-x
  • 出版社:Springer Nature
  • 摘要:Antibiotic persistence is a transient phenotypic state during which a bacterium can withstand otherwise lethal antibiotic exposure or environmental stresses. In Escherichia coli , persistence is promoted by the HipBA toxin-antitoxin system. The HipA toxin functions as a serine/threonine kinase that inhibits cell growth, while the HipB antitoxin neutralizes the toxin. E. coli HipA inactivates the glutamyl-tRNA synthetase GltX, which inhibits translation and triggers the highly conserved stringent response. Although hipBA operons are widespread in bacterial genomes, it is unknown if this mechanism is conserved in other species. Here we describe the functions of three hipBA modules in the alpha-proteobacterium Caulobacter crescentus . The HipA toxins have different effects on growth and macromolecular syntheses, and they phosphorylate distinct substrates. HipA 1 and HipA 2 contribute to antibiotic persistence during stationary phase by phosphorylating the aminoacyl-tRNA synthetases GltX and TrpS. The stringent response regulator SpoT is required for HipA-mediated antibiotic persistence, but persister cells can form in the absence of all hipBA operons or spoT , indicating that multiple pathways lead to persister cell formation in C. crescentus .
国家哲学社会科学文献中心版权所有