首页> 美国卫生研究院文献>Journal of Bacteriology >A Vibrio cholerae Relaxed (relA) Mutant Expresses Major Virulence Factors Exhibits Biofilm Formation and Motility and Colonizes the Suckling Mouse Intestine
【2h】

A Vibrio cholerae Relaxed (relA) Mutant Expresses Major Virulence Factors Exhibits Biofilm Formation and Motility and Colonizes the Suckling Mouse Intestine

机译:霍乱弧菌松弛(relA)突变体表达主要毒力因子表现出生物膜形成和运动并定居在乳鼠肠道

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We have constructed a relaxed mutant of El Tor biotype Vibrio cholerae strain C7258 by disruption of the RelA catalytic domain. The ability of the V. cholerae relaxed mutant to biosynthesize guanosine tetraphosphate and pentaphosphate was severely affected; the mutant showed a reduced growth rate in minimal medium that could be reversed by the addition of Casamino Acids, and it was thermosensitive. Contrary to published findings, the new relA mutant still produced significant cholera toxin and toxin-coregulated pilus. The V. cholerae relA mutant was motile, produced normal biofilms, and colonized the suckling mouse intestine. Our data suggest that levels of basal guanosine nucleotides pppGpp and ppGpp, rather than the availability of a stringent response, could influence expression of virulence factors, depending on strain and culture conditions. Production of hemagglutinin (HA)/protease, which requires HapR, RpoS, and the cyclic AMP receptor protein, was not strongly affected. Nevertheless, overexpression of RelA protein from an isopropyl-β-d-thiogalactopyranoside-inducible promoter posttranscriptionally diminished production of HA/protease.
机译:我们通过破坏RelA催化结构域构建了一个轻松的El Tor生物型霍乱弧菌菌株C7258突变体。霍乱弧菌松弛突变体生物合成鸟苷四磷酸和五磷酸的能力受到严重影响。该突变体在基本培养基中显示出降低的生长速率,可以通过添加酪蛋白氨基酸来逆转,并且具有热敏感性。与已发表的发现相反,新的relA突变体仍产生大量霍乱毒素和毒素结合菌毛。霍乱弧菌的relA突变体是能动的,产生正常的生物膜,并定居在乳鼠的小肠中。我们的数据表明基础鸟苷核苷酸pppGpp和ppGpp的水平,而不是严格的响应的可用性,可能会影响毒力因子的表达,具体取决于菌株和培养条件。血凝素(HA)/蛋白酶(需要HapR,RpoS和环状AMP受体蛋白)的产生并未受到严重影响。然而,从异丙基-β-d-硫代吡喃半乳糖苷诱导的启动子中过表达RelA蛋白在转录后减少了HA /蛋白酶的产生。

著录项

相似文献

  • 外文文献
  • 中文文献
代理获取

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