Gonzalo-Asensio Jesús, Soto Carlos Y, Arbués Ainhoa, Sancho Javier, del Carmen Menéndez María, García María J, Gicquel Brigitte, Martín Carlos
Departamento de Microbiología, Medicina Preventiva y Salud Pública, Facultad de Medicina, Universidad de Zaragoza, C/Domingo Miral s/n, 50009 Zaragoza, Spain.
J Bacteriol. 2008 Nov;190(21):7068-78. doi: 10.1128/JB.00712-08. Epub 2008 Aug 29.
The attenuated Mycobacterium tuberculosis H37Ra strain is an isogenic counterpart of the virulent paradigm strain H37Rv. Recently, a link between a point mutation in the PhoP transcriptional regulator and avirulence of H37Ra was established. Remarkably, a previous study demonstrated negative autoregulation of the phoP gene in H37Ra. These findings led us to study the transcriptional autoregulation of PhoP in the virulent H37Rv strain. In contrast to the negative autoregulation of PhoP previously published for H37Ra, our experiments using a phoP promoter-lacZ fusion showed that PhoP is positively autoregulated in both H37Rv and H37Ra compared with an H37Rv phoP deletion mutant constructed in this study. Using quantitative reverse transcription-PCR (RT-PCR) analysis, we showed that the phoP gene is transcribed at similar levels in H37Rv and H37Ra. Gel mobility shift and DNase I footprinting assays allowed us to identify the precise binding region of PhoP from H37Rv to the phoP promoter. We also carried out RT-PCR studies to demonstrate that phoP is transcribed together with the adjacent gene phoR, which codes for the cognate histidine kinase of the phoPR two-component system. In addition, quantitative RT-PCR studies showed that phoR is independently transcribed from a promoter possibly regulated by PhoP. Finally, we discuss the possible role in virulence of a single point mutation found in the phoP gene from the attenuated H37Ra strain but not in virulent members of the M. tuberculosis complex.
减毒结核分枝杆菌H37Ra菌株是强毒模式菌株H37Rv的同基因对应菌株。最近,已确定PhoP转录调节因子中的一个点突变与H37Ra的无毒力之间存在联系。值得注意的是,先前的一项研究证明了H37Ra中phoP基因的负自调控。这些发现促使我们研究PhoP在强毒H37Rv菌株中的转录自调控。与先前发表的关于H37Ra的PhoP负自调控不同,我们使用phoP启动子-lacZ融合的实验表明,与本研究构建的H37Rv phoP缺失突变体相比,PhoP在H37Rv和H37Ra中均为正自调控。使用定量逆转录PCR(RT-PCR)分析,我们表明phoP基因在H37Rv和H37Ra中的转录水平相似。凝胶迁移率变动分析和DNase I足迹分析使我们能够确定H37Rv的PhoP与phoP启动子的精确结合区域。我们还进行了RT-PCR研究,以证明phoP与相邻基因phoR一起转录,phoR编码phoPR双组分系统的同源组氨酸激酶。此外,定量RT-PCR研究表明phoR从可能受PhoP调控的启动子独立转录。最后,我们讨论了在减毒H37Ra菌株的phoP基因中发现但在结核分枝杆菌复合群的强毒株中未发现的单点突变在毒力中的可能作用。