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Regulation of Metalloprotease Gene Expression in Vibrio vulnificus by a Vibrio harveyi LuxR Homologue

机译:哈氏弧菌LuxR同源物对创伤弧菌中金属蛋白酶基因表达的调节

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摘要

Expression of the Vibrio vulnificus metalloprotease gene, vvp, was turned up rapidly when bacterial growth reached the late log phase. A similar pattern of expression has been found in the metalloprotease gene of Vibrio cholerae, and this has been shown to be regulated by a Vibrio harveyi LuxR-like transcriptional activator. To find out whether a LuxR homologue exists in V. vulnificus, a gene library of this organism was screened by colony hybridization using a probe derived from a sequence that is conserved in various luxR-like genes of vibrios. A gene containing a 618-bp open reading frame was identified and found to be identical to the smcR gene of V. vulnificus reported previously. An isogenic SmcR-deficient (RD) mutant was further constructed by an in vivo allelic exchange technique. This mutant exhibited an extremely low level of vvp transcription compared with that of the parent strain. On the other hand, the cytolysin gene, vvhA, was expressed at a higher level in the RD mutant than in the parent strain during the log phase of growth. These data suggested that SmcR might not only be a positive regulator of the protease gene but might also be involved in negative regulation of the cytolysin gene. Virulence of the RD mutant in either normal or iron-overloaded mice challenged by intraperitoneal injection was comparable to that of the parent strain, indicating that SmcR is not required for V. vulnificus virulence in mice.
机译:当细菌生长达到对​​数晚期时,创伤弧菌金属蛋白酶基因vvp的表达迅速升高。在霍乱弧菌的金属蛋白酶基因中发现了类似的表达模式,并且已证明该表达模式受哈维弧菌LuxR样转录激活因子调控。为了找出V. vulnificus中是否存在LuxR同源物,使用衍生自在弧菌的各种luxR样基因中保守的序列的探针,通过菌落杂交筛选了该生物的基因库。鉴定出含有618bp开放阅读框的基因,发现该基因与先前报道的创伤弧菌的smcR基因相同。通过体内等位基因交换技术进一步构建了等基因SmcR缺陷(RD)突变体。与亲本菌株相比,该突变体表现出极低的vvp转录水平。另一方面,在对数生长期,RD突变体中的溶细胞素基因vvhA的表达水平高于亲本菌株。这些数据表明,SmcR不仅可能是蛋白酶基因的正调节剂,而且可能还参与了细胞溶素基因的负调节。腹膜内注射攻击的正常或铁负荷过重的小鼠中,RD突变体的毒力与亲本菌株的毒力相当,这表明SmcR对小鼠中的V. vulnificus毒力不是必需的。

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