Payelleville Amaury, Brillard Julien
DGIMI, INRAE, Univ. Montpellier, Montpellier, France.
Cellular and Molecular Microbiology, Faculté des Sciences, Université Libre de Bruxelles, Gosselies, Belgium.
Front Microbiol. 2021 May 14;12:685670. doi: 10.3389/fmicb.2021.685670. eCollection 2021.
DNA methylation can be part of epigenetic mechanisms, leading to cellular subpopulations with heterogeneous phenotypes. While prokaryotic phenotypic heterogeneity is of critical importance for a successful infection by several major pathogens, the exact mechanisms involved in this phenomenon remain unknown in many cases. Powerful sequencing tools have been developed to allow the detection of the DNA methylated bases at the genome level, and they have recently been extensively applied on numerous bacterial species. Some of these tools are increasingly used for metagenomics analysis but only a limited amount of the available methylomic data is currently being exploited. Because newly developed tools now allow the detection of subpopulations differing in their genome methylation patterns, it is time to emphasize future strategies based on a more extensive use of methylomic data. This will ultimately help to discover new epigenetic gene regulations involved in bacterial phenotypic heterogeneity, including during host-pathogen interactions.
DNA甲基化可以是表观遗传机制的一部分,导致具有异质表型的细胞亚群。虽然原核生物的表型异质性对于几种主要病原体的成功感染至关重要,但在许多情况下,这一现象所涉及的确切机制仍然未知。已经开发出强大的测序工具,用于在基因组水平上检测DNA甲基化碱基,并且最近它们已被广泛应用于众多细菌物种。其中一些工具越来越多地用于宏基因组学分析,但目前仅利用了有限的可用甲基化组数据。由于新开发的工具现在能够检测基因组甲基化模式不同的亚群,因此现在是时候强调基于更广泛使用甲基化组数据的未来策略了。这最终将有助于发现参与细菌表型异质性的新的表观遗传基因调控,包括在宿主 - 病原体相互作用期间。