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Actinobacillus pleuropneumoniae two-component system QseB/QseC regulates the transcription of PilM, an important determinant of bacterial adherence and virulence

机译:胸膜肺炎放线杆菌两组分系统QseB / QseC调节PilM的转录,PilM是细菌粘附和毒力的重要决定因素

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摘要

QseB/QseC is one of the five predicted two-component systems (TCSs) in Actinobacillus pleuropneumoniae. To understand the roles of this TCS in A. pleuropneumoniae, a markerless gene-deletion mutant Delta qseBC was constructed. Differentially expressed (DE) genes in Delta qseBC were filtered by microarray analysis. A total of 44 DE genes were found to be regulated by QseB/QseC system. The transcriptional profile of A. pleuropneumoniae Delta qseBC was compared with that of Delta luxS and catecholamine (CA) stimulations, 13 genes regulated by QseB/QseC were found also regulated by LuxS, and 3 Qse-regulons were co-regulated by CA stimulations, respectively. Binding of QseB to the promoters of three regulons (pilM, glpK and hugZ), which were co-regulated by QseB/QseC and LuxS, was evaluated by electrophoretic mobility-shift assay. Results indicated that pilM was directly regulated by phosphorylated-QseB. Then the pilM deletion mutant Delta pilM was constructed and characterized. Data presented here revealed that adherence ability of Delta pilM to St. Jude porcine lung cells was significantly decreased, and Delta pilM exhibited reduced virulence in pigs, suggesting PilM contributes to the process of A. pleuropneumoniae infection. (C) 2015 Elsevier B.V. All rights reserved.
机译:QseB / QseC是胸膜肺炎放线杆菌中五个预测的两组分系统(TCS)之一。为了了解该TCS在胸膜肺炎链球菌中的作用,构建了无标记基因缺失突变体Delta qseBC。通过微阵列分析过滤Delta qseBC中的差异表达(DE)基因。发现总共44个DE基因受QseB / QseC系统调控。比较了胸膜肺炎链球菌Delta qseBC与Delta luxS和儿茶酚胺(CA)刺激的转录谱,发现13个受QseB / QseC调控的基因也受LuxS调控,而3个Qse调控子受CA刺激共调控,分别。通过电泳迁移率漂移分析评估了QseB与三个被qseB / QseC和LuxS共同调节的调节子(pilM,glpK和hugZ)的启动子的结合。结果表明,pilM直接受磷酸化QseB调控。然后构建并鉴定了pilM缺失突变体Delta pilM。此处提供的数据表明,Delta pilM对St. Jude猪肺细胞的粘附能力显着降低,并且Delta pilM在猪中的毒力降低,表明PilM有助于胸膜肺炎链球菌感染。 (C)2015 Elsevier B.V.保留所有权利。

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