Department of Microbiology and Environmental Toxicology, University of California - Santa Cruz, Santa Cruz, California, USA.
J Bacteriol. 2022 Sep 20;204(9):e0023122. doi: 10.1128/jb.00231-22. Epub 2022 Aug 16.
Many bacteria and archaea rely on chemotaxis signal transduction systems for optimal fitness. These complex, multiprotein signaling systems have core components found in all chemotactic microbes, as well as variable proteins found in only some species. We do not yet understand why these variations exist or whether there are specific niches that favor particular chemotaxis signaling organization. One variation is in the presence/absence of the chemotaxis methylation adaptation enzymes CheB and CheR. Genes for CheB and CheR are missing in the gastric pathogen Helicobacter pylori but present in related Helicobacter that colonize the liver or intestine. In this work, we asked whether there was a general pattern of CheB/CheR across multiple Helicobacter species. Helicobacter spp. all possess chemotactic behavior, based on the presence of genes for core signaling proteins CheA, CheW, and chemoreceptors. Genes for the CheB and CheR proteins, in contrast, were variably present. Niche mapping supported the idea that these genes were present in enterohepatic Helicobacter species and absent in gastric ones. We then analyzed whether there were differences between gastric and enterohepatic species in the CheB/CheR chemoreceptor target methylation sites. Indeed, these sites were less conserved in gastric species that lack CheB/CheR. Lastly, we determined that and could serve as markers to indicate whether an unknown Helicobacter species was of enterohepatic or gastric origin. Overall, these findings suggest the interesting idea that methylation-based adaptation is not required in specific environments, particularly the stomach. Chemotaxis signal transduction systems are common in the archaeal and bacterial world, but not all systems contain the same components. The rationale for this system variation remains unknown. In this report, comparative genomics analysis showed that the presence/absence of CheR and CheB is one main variation within the Helicobacter genus, and it is strongly associated with the niche of Helicobacter species: gastric Helicobacter species, which infect animal stomachs, have lost their CheB and CheR, while enterohepatic Helicobacter species, which infect the liver and intestine, retain them. This study not only provides an example that a chemotaxis system variant is associated with particular niches but also proposes that CheB and CheR are new markers distinguishing gastric from enterohepatic Helicobacter species.
许多细菌和古菌依赖于化学趋性信号转导系统以达到最佳适应性。这些复杂的、多蛋白的信号系统具有所有趋化微生物中都存在的核心成分,以及仅在某些物种中存在的可变性蛋白。我们还不清楚为什么会存在这些差异,或者是否存在特定的小生境偏好特定的趋化信号组织。一种变化是化学趋性甲基化适应酶 CheB 和 CheR 的存在/缺失。胃病原体幽门螺杆菌缺失 CheB 和 CheR 的基因,但在定植于肝脏或肠道的相关幽门螺杆菌中存在。在这项工作中,我们想知道在多个幽门螺杆菌物种中 CheB/CheR 是否存在普遍模式。基于核心信号蛋白 CheA、CheW 和化学感受器基因的存在,幽门螺杆菌属的所有物种都具有趋化行为。相反,CheB 和 CheR 蛋白的基因则存在可变性。小生境映射支持这样的观点,即这些基因存在于肠肝幽门螺杆菌物种中,而不存在于胃幽门螺杆菌物种中。然后,我们分析了在胃和肠肝物种中 CheB/CheR 化学感受器靶标甲基化位点是否存在差异。事实上,在缺乏 CheB/CheR 的胃物种中,这些位点的保守性较差。最后,我们确定 和 可以作为标记,表明未知的幽门螺杆菌物种是肠肝来源还是胃来源。总的来说,这些发现表明了一个有趣的观点,即甲基化适应在特定环境中并非必需,特别是在胃中。化学趋性信号转导系统在古菌和细菌世界中很常见,但并非所有系统都包含相同的成分。这种系统变异的原理仍然未知。在本报告中,比较基因组学分析表明,CheR 和 CheB 的存在/缺失是幽门螺杆菌属内的主要变异之一,并且与幽门螺杆菌物种的小生境强烈相关:感染动物胃的胃幽门螺杆菌物种已经失去了它们的 CheB 和 CheR,而感染肝脏和肠道的肠肝幽门螺杆菌物种则保留了它们。这项研究不仅提供了一个例子,即化学趋性系统的一个变体与特定小生境相关,还提出 CheB 和 CheR 是区分胃和肠肝幽门螺杆菌物种的新标记。