Häse C C, Mekalanos J J
Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 1998 Jan 20;95(2):730-4. doi: 10.1073/pnas.95.2.730.
The production of several virulence factors in Vibrio cholerae O1, including cholera toxin and the pilus colonization factor TCP (toxin-coregulated pilus), is strongly influenced by environmental conditions. To specifically identify membrane proteins involved in these signal transduction events, we examined a transposon library of V. cholerae generated by Tnbla mutagenesis for cells that produce TCP when grown under various nonpermissive conditions. To select for TCP-producing cells we used the recently described bacteriophage CTX phi-Kan, which uses TCP as its receptor and carries a gene encoding resistance to kanamycin. Among the isolated mutants was a transposon insertion in a gene homologous to nqrB from Vibrio alginolyticus, which encodes a subunit of a Na(+)-translocating NADH:ubiquinone oxidoreductase, and tcpI, encoding a chemo-receptor previously implicated in the negative regulation of TCP production. A third transposon mutant had an insertion in tcpP, which is in an operon with tcpH, a known positive regulator of TCP production. However, TcpP was shown to be essential for TCP production in V. cholerae, as a tcpP-deletion strain was deficient in pili production. The amino-terminal region of TcpP shows sequence homology to the DNA-binding domains of several regulatory proteins, including ToxR from V. cholerae and PsaE from Yersinia pestis. Like ToxR, TcpP activates transcription of the toxT gene, an essential activator of tcp operon transcription. Furthermore, TcpH, with its large periplasmic domain and inner membrane anchor, has a structure similar to that of ToxS and was shown to enhance the activity of TcpP. We propose that TcpP/TcpH constitute a pair of regulatory proteins functionally similar to ToxR/ToxS and PsaE/PsaF that are required for toxT transcription in V. cholerae.
霍乱弧菌O1中几种毒力因子的产生,包括霍乱毒素和菌毛定植因子TCP(毒素共调节菌毛),受到环境条件的强烈影响。为了具体鉴定参与这些信号转导事件的膜蛋白,我们检查了通过Tnbla诱变产生的霍乱弧菌转座子文库,以寻找在各种非允许条件下生长时产生TCP的细胞。为了筛选产生TCP的细胞,我们使用了最近描述的噬菌体CTX phi-Kan,它以TCP作为其受体,并携带一个编码对卡那霉素抗性的基因。在分离出的突变体中,有一个转座子插入到与溶藻弧菌的nqrB同源的基因中,该基因编码Na(+)-转运NADH:泛醌氧化还原酶的一个亚基,还有tcpI,它编码一种先前被认为参与TCP产生负调控的化学感受器。第三个转座子突变体在tcpP中发生了插入,tcpP与tcpH处于同一个操纵子中,tcpH是已知的TCP产生的正调控因子。然而,TcpP被证明对霍乱弧菌中TCP的产生至关重要,因为一个tcpP缺失菌株缺乏菌毛产生。TcpP的氨基末端区域与几种调节蛋白的DNA结合结构域具有序列同源性,包括霍乱弧菌的ToxR和鼠疫耶尔森菌的PsaE。与ToxR一样,TcpP激活toxT基因的转录,toxT基因是tcp操纵子转录的必需激活因子。此外,TcpH具有大的周质结构域和内膜锚定结构,其结构与ToxS相似,并被证明能增强TcpP的活性。我们提出,TcpP/TcpH构成了一对功能上类似于ToxR/ToxS和PsaE/PsaF的调节蛋白,它们是霍乱弧菌中toxT转录所必需的。