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首页> 外文期刊>Journal of bacteriology >The LysR-Type Virulence Activator AphB Regulates the Expression of Genes in Vibrio cholerae in Response to Low pH and Anaerobiosis
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The LysR-Type Virulence Activator AphB Regulates the Expression of Genes in Vibrio cholerae in Response to Low pH and Anaerobiosis

机译:LysR型毒力激活剂AphB调节霍乱弧菌中低pH和厌氧菌反应基因的表达。

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摘要

AphB is a LysR-type activator that initiates the expression of the virulence cascade in Vibrio cholerae by cooperating with the quorum-sensing-regulated activator AphA at the tcpPH promoter on the Vibrio pathogenicity island (VPI). To identify the ancestral chromosomal genes in V. cholerae regulated by AphB, we carried out a microarray analysis and show here that AphB influences the expression of a number of genes that are not associated with the VPI. One gene strongly activated by AphB is cadC, which encodes the ToxR-like transcriptional activator responsible for activating the expression of lysine decarboxylase, which plays an important role in survival at low pH. Other genes activated by AphB encode a Na+/H+ antiporter, a carbonic anhydrase, a member of the ClC family of chloride channels, and a member of the Gpr1/Fun34/YaaH family. AphB influences each of these genes directly by recognizing a conserved binding site within their promoters, as determined by gel mobility shift assays. Transcriptional lacZ fusions indicate that AphB activates the expression of these genes under aerobic conditions in response to low pH and also under anaerobic conditions at neutral pH. Further experiments show that the regulation of cadC by AphB in response to low pH and anaerobiosis is mirrored in the heterologous organism Escherichia coli, is independent of the global regulators Fnr and ArcAB, and depends upon the region of the promoter that contains the AphB binding site. These results raise the possibility that the activity of AphB is influenced by the pH and oxygen tension of the environment.
机译:AphB是一种LysR型激活剂,通过与 tcpPH 启动子上的群体感应调节激活剂AphA协同启动霍乱弧菌中的毒力级联表达。弧菌病原体岛(VPI)。为了鉴定 V中的祖染色体基因。由AphB调节的霍乱,我们进行了微阵列分析,并显示AphB影响许多与VPI无关的基因的表达。一个被AphB强烈激活的基因是 cadC ,它编码ToxR样转录激活因子,负责激活赖氨酸脱羧酶的表达,赖氨酸脱羧酶的表达在低pH条件下起着重要的作用。由AphB激活的其他基因编码Na + / H + 反向转运蛋白,碳酸酐酶,ClC氯化物通道的成员和Gpr1 / Fun34的成员/ YaaH家庭。 AphB通过识别其启动子内的保守结合位点直接影响这些基因中的每一个,如通过凝胶迁移率迁移分析所确定的。转录 lacZ 融合表明,AphB在有氧条件下响应低pH值以及在无氧条件下中性pH值下激活这些基因的表达。进一步的实验表明,异源生物大肠杆菌中反映了AphB响应低pH和厌氧菌而对 cadC 的调节,独立于全球调节剂Fnr和ArcAB,并且取决于包含AphB结合位点的启动子区域。这些结果增加了AphB的活性受环境的pH和氧张力影响的可能性。

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