Department of Microbiology, University of Georgia, Athens, Georgia, USA.
Department of Microbiology, University of Georgia, Athens, Georgia, USA
Microbiol Mol Biol Rev. 2020 Jan 29;84(1). doi: 10.1128/MMBR.00092-19. Print 2020 Feb 19.
Pathogenic microorganisms use various mechanisms to conserve energy in host tissues and environmental reservoirs. One widespread but often overlooked means of energy conservation is through the consumption or production of molecular hydrogen (H). Here, we comprehensively review the distribution, biochemistry, and physiology of H metabolism in pathogens. Over 200 pathogens and pathobionts carry genes for hydrogenases, the enzymes responsible for H oxidation and/or production. Furthermore, at least 46 of these species have been experimentally shown to consume or produce H Several major human pathogens use the large amounts of H produced by colonic microbiota as an energy source for aerobic or anaerobic respiration. This process has been shown to be critical for growth and virulence of the gastrointestinal bacteria serovar Typhimurium, , , and (including carcinogenic strains). H oxidation is generally a facultative trait controlled by central regulators in response to energy and oxidant availability. Other bacterial and protist pathogens produce H as a diffusible end product of fermentation processes. These include facultative anaerobes such as , Typhimurium, and , which persist by fermentation when limited for respiratory electron acceptors, as well as obligate anaerobes, such as , , and , that produce large amounts of H during growth. Overall, there is a rich literature on hydrogenases in growth, survival, and virulence in some pathogens. However, we lack a detailed understanding of H metabolism in most pathogens, especially obligately anaerobic bacteria, as well as a holistic understanding of gastrointestinal H transactions overall. Based on these findings, we also evaluate H metabolism as a possible target for drug development or other therapies.
病原微生物利用各种机制在宿主组织和环境储库中保存能量。一种广泛但经常被忽视的能量保存方式是通过消耗或产生分子氢(H)。在这里,我们全面回顾了病原体中 H 代谢的分布、生物化学和生理学。超过 200 种病原体和共生病原体携带氢化酶基因,这些酶负责 H 的氧化和/或产生。此外,至少有 46 种这些物种已被实验证明消耗或产生 H。几种主要的人类病原体利用结肠微生物群产生的大量 H 作为有氧或无氧呼吸的能源。已经表明,这个过程对于胃肠道细菌血清型 Typhimurium、、、和(包括致癌菌株)的生长和毒力至关重要。H 氧化通常是一种兼性特征,由中央调节剂根据能量和氧化剂可用性进行控制。其他细菌和原生动物病原体将 H 作为发酵过程的可扩散终产物产生。这些包括兼性厌氧菌,如、Typhimurium 和,当受到呼吸电子受体限制时通过发酵来维持生存,以及严格厌氧菌,如、、和,在生长过程中会产生大量 H。总的来说,关于 H 在一些病原体的生长、存活和毒力中的作用有丰富的文献。然而,我们对大多数病原体,特别是严格厌氧菌中的 H 代谢缺乏详细的了解,也缺乏对胃肠道 H 整体交易的了解。基于这些发现,我们还评估了 H 代谢作为药物开发或其他疗法的可能靶点。