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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调节霍乱弧菌基因在低pH和厌氧菌反应中的表达▿

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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,它通过与弧菌病原性岛(VPI)上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毒力级联的表达。为了鉴定由AphB调节的霍乱弧菌的祖先染色体基因,我们进行了微阵列分析,并在这里显示AphB影响许多与VPI不相关的基因的表达。 AphB强烈激活的一个基因是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,赖氨酸脱羧酶在低pH条件下的存活中起着重要作用。由AphB激活的其他基因编码Na + / H +反转运蛋白,碳酸酐酶,ClC氯离子通道家族成员和Gpr1 / Fun34 / YaaH家族成员。 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,如凝胶迁移率移动分析所确定。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,AphB对低pH和厌氧菌的响应对cadC的调节在异源生物大肠杆菌中反映出来,独立于全局调节剂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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