首页> 外文OA文献 >The minor pilin TcpB is located at the tip of the toxin co-regulated pilus of Vibrio cholerae and is the receptor for the filamentous phage CTXφ
【2h】

The minor pilin TcpB is located at the tip of the toxin co-regulated pilus of Vibrio cholerae and is the receptor for the filamentous phage CTXφ

机译:次要菌毛TcpB位于毒素共同调控的霍乱弧菌菌毛的尖端,并且是丝状噬菌体CTXφ的受体

摘要

Type IV pili are polymers of the major pilin subunit found on the surfaces of many Gram negative bacteria. They act like grappling hooks, undergoing cycles of polymerization, adhesion, and retraction, to mediate a diverse array of functions, including twitching motility, DNA uptake and adhesion. T4P possess several minor pilins, which are homologous to the major pilin but are produced in much lower quantities. Minor pilins prime Type IV pili assembly and have been proposed to localize to the tip of the pilus, but this has not been shown definitively. The Vibrio cholerae toxin co-regulated pilus (TCP) is a T4P that mediates microcolony formation, which is critical for the development of the gastrointestinal disease cholera. TCP is the primary receptor for the filamentous cholera toxin phage CTXφ, which binds to the pilus via its tip-associated protein, pIII. TCP possess a single minor pilin, TcpB, which initiates pilus assembly as well as retraction. We hypothesized that TcpB is located at the tip of the pilus and forms the binding site for CTXφ pIII. Here I use direct and competition ELISA to show that recombinantly expressed soluble TcpB and pIII interact. I show that CTXφ phage infection of V. cholerae is reduced 90 % in the presence of soluble TcpB or anti-TcpB antibody. Furthermore, gold-labeled anti-TcpB antibody binds to the tip of purified TCP, providing the first direct localization of a minor pilin to the tip of a T4P. Finally, I show that phage uptake is reduced 98 % in a retraction-deficient V. cholerae strain, demonstrating the role of pilus retraction in this process. My results define a two-step mechanism for CTXφ infection of V. cholerae, which involves (i) binding of CTX via its tip-associated pIII protein to its receptor, TcpB, at the tip of the pilus, and (ii) retraction of the pilus, which pulls CTXφ into the bacterial periplasm as if it were an extension of the pilus.
机译:IV型菌毛是许多革兰氏阴性细菌表面上发现的主要菌毛素亚基的聚合物。它们就像抓钩一样,经历聚合,粘附和缩回的循环,以介导各种功能,包括抽动,DNA吸收和粘附。 T4P具有几个次要菌毛素,与主要菌毛素同源,但产量要低得多。较小的菌毛是IV型菌毛的主要成分,有人提出将其定位在菌毛的尖端,但尚未明确显示。霍乱弧菌毒素共调节菌毛(TCP)是一种T4P,可介导小菌落的形成,这对于胃肠道疾病霍乱的发展至关重要。 TCP是丝状霍乱毒素噬菌体CTXφ的主要受体,它通过其尖端相关蛋白pIII与菌毛结合。 TCP拥有单个未成年人pilin TcpB,可启动菌毛组装和收回。我们假设TcpB位于菌毛的尖端,并形成CTXφpIII的结合位点。在这里,我使用直接竞争ELISA来显示重组表达的可溶性TcpB和pIII相互作用。我表明在可溶性TcpB或抗TcpB抗体存在下,霍乱弧菌的CTXφ噬菌体感染减少了90%。此外,金标记的抗TcpB抗体与纯化的TCP尖端结合,从而将次要菌毛蛋白首次直接定位在T4P的尖端。最后,我证明了在缺乏回缩力的霍乱弧菌菌株中噬菌体的吸收降低了98%,这表明菌毛回缩在此过程中的作用。我的结果定义了霍乱弧菌CTXφ感染的两步机制,其中包括(i)CTX通过其尖端相关的pIII蛋白与菌毛尖端的受体TcpB结合,以及(ii)收缩菌毛,将CTXφ拉入细菌的周质,就好像它是菌毛的延伸一样。

著录项

  • 作者

    Gutierrez Miguel Angel;

  • 作者单位
  • 年度 2017
  • 总页数
  • 原文格式 PDF
  • 正文语种
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号