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Endoribonuclease YbeY Is Essential for RNA Processing and Virulence in Pseudomonas aeruginosa

机译:Neulibonuclease Ybey对于RNA加工和毒力是必不可少的<命名含量含量型=“属型”>假单胞菌铜绿假单胞菌

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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 Pseudomonas aeruginosa endonuclease YbeY is required for rRNA processing and the bacterial virulence in a murine acute pneumonia model. Transcriptomic analyses reveal that knocking out the ybeY gene results in downregulation of oxidative stress response genes, including the catalase genes katA and katB . Consistently, the ybeY mutant is more susceptible to H _(2)O _(2) and neutrophil-mediated killing. Overexpression of katA restores the bacterial tolerance to H _(2)O _(2) 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 ybeY mutation increases the level of a small RNA, ReaL, which directly represses the translation of rpoS through the 5′ UTR of its mRNA and subsequently reduces the expression of the oxidative stress response genes. In vitro assays demonstrate direct degradation of ReaL by YbeY. Deletion of reaL or overexpression of rpoS in the ybeY 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 reaL and rpoS as well as the bacterial virulence. Overall, our results reveal pleiotropic roles of YbeY and the YbeY-mediated regulation of rpoS through ReaL.
机译:后术中规例在快速适应宿主环境中的快速调整中起重要作用,并且通过修改小RNA和MRNA,RNASES在该过程中起主要角色。我们发现假鼠铜绿假单胞菌核酸酶Ybey是rRNA加工和小鼠急性肺炎模型中的细菌毒力所必需的。转录组分析表明,敲出ybey基因导致氧化应激反应基因的下调,包括过氧化酶基因Kata和Katb。始终如一地,YBEY突变体更容易受到H _(2)O _(2)和中性粒细胞介导的杀伤。 kata的过度表达恢复了对H _(2)O _(2)和中性粒细胞杀伤以及毒力的细菌耐受性。我们进一步发现氧化应激响应基因的下调是由于静止相σ因子RPO的表达缺陷。我们证明了RPO的自动调节机制,并发现YBEY突变增加了小RNA,真实的水平,该水平直接通过其mRNA的5'UTR直接抑制RPO的翻译,随后降低了氧化应激反应基因的表达。体外测定表现出Ybey的真实的直接降解。 ybey突变体中RPO的真实或过度表达的缺失恢复了对氧化应激和毒力的细菌耐受性。我们还证明YBEZ与YBEY结合,并且参与了16S rRNA处理和对实际和RPO的调节以及细菌毒力。总体而言,我们的结果揭示了尤比和Ybey-Mediated对RPO的调节的热爱ropic作用。

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