State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Molecular Microbiology and Technology of the Ministry of Education, Department of Microbiology, College of Life Sciences, Nankai University, Tianjin, China.
Department of Molecular Genetics, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, Netherlands.
mBio. 2020 Jun 30;11(3):e00659-20. doi: 10.1128/mBio.00659-20.
Posttranscriptional regulation plays an essential role in the quick adaptation of pathogenic bacteria to host environments, and RNases play key roles in this process by modifying small RNAs and mRNAs. We find that the endonuclease YbeY is required for rRNA processing and the bacterial virulence in a murine acute pneumonia model. Transcriptomic analyses reveal that knocking out the gene results in downregulation of oxidative stress response genes, including the catalase genes and Consistently, the mutant is more susceptible to HO and neutrophil-mediated killing. Overexpression of restores the bacterial tolerance to HO and neutrophil killing as well as virulence. We further find that the downregulation of the oxidative stress response genes is due to defective expression of the stationary-phase sigma factor RpoS. We demonstrate an autoregulatory mechanism of RpoS and find that mutation increases the level of a small RNA, ReaL, which directly represses the translation of through the 5' UTR of its mRNA and subsequently reduces the expression of the oxidative stress response genes. assays demonstrate direct degradation of ReaL by YbeY. Deletion of or overexpression of in the mutant restores the bacterial tolerance to oxidative stress and the virulence. We also demonstrate that YbeZ binds to YbeY and is involved in the 16S rRNA processing and regulation of and as well as the bacterial virulence. Overall, our results reveal pleiotropic roles of YbeY and the YbeY-mediated regulation of through ReaL. The increasing bacterial antibiotic resistance imposes a severe threat to human health. For the development of effective treatment and prevention strategies, it is critical to understand the mechanisms employed by bacteria to grow in the human body. Posttranscriptional regulation plays an important role in bacterial adaptation to environmental changes. RNases and small RNAs are key players in this regulation. In this study, we demonstrate critical roles of the RNase YbeY in the virulence of the pathogenic bacterium We further identify the small RNA ReaL as the direct target of YbeY and elucidate the YbeY-regulated pathway on the expression of bacterial virulence factors. Our results shed light on the complex regulatory network of and indicate that inference with the YbeY-mediated regulatory pathway might be a valid strategy for the development of a novel treatment strategy.
转录后调控在致病菌快速适应宿主环境中起着至关重要的作用,而核糖核酸酶(RNases)通过修饰小 RNA 和 mRNA 来在这个过程中发挥关键作用。我们发现内切核酸酶 YbeY 是细菌 rRNA 加工和小鼠急性肺炎模型中细菌毒力所必需的。转录组分析显示,基因缺失导致氧化应激反应基因下调,包括过氧化氢酶基因和。一致地,突变体对 HO 和中性粒细胞介导的杀伤更为敏感。过表达可恢复细菌对 HO 和中性粒细胞杀伤以及毒力的耐受性。我们进一步发现,氧化应激反应基因的下调是由于静止期σ因子 RpoS 的表达缺陷所致。我们证明了 RpoS 的自我调控机制,并发现突变增加了一种小 RNA ReaL 的水平,该 RNA 通过其 mRNA 的 5'UTR 直接抑制的翻译,从而降低氧化应激反应基因的表达。实验证明了 YbeY 对 ReaL 的直接降解。在突变体中缺失或过表达可恢复细菌对氧化应激的耐受性和毒力。我们还证明 YbeZ 结合 YbeY,并参与 16S rRNA 加工以及和的调控以及细菌毒力。总的来说,我们的结果揭示了 YbeY 的多效性作用以及通过 ReaL 对的 YbeY 介导的调控。不断增加的细菌抗生素耐药性对人类健康构成了严重威胁。为了制定有效的治疗和预防策略,了解细菌在人体中生长的机制至关重要。转录后调控在细菌适应环境变化中起着重要作用。核糖核酸酶和小 RNA 是这种调控的关键参与者。在这项研究中,我们证明了核糖核酸酶 YbeY 在致病菌毒力中的关键作用。我们进一步将小 RNA ReaL 鉴定为 YbeY 的直接靶标,并阐明了 YbeY 调控的细菌毒力因子表达途径。我们的结果揭示了的复杂调控网络,并表明干扰 YbeY 介导的调控途径可能是开发新治疗策略的有效策略。