Lee Jaejin, Shin Eunkyoung, Yeom Ji-Hyun, Park Jaeyoung, Kim Sunwoo, Lee Minho, Lee Kangseok
Department of Life Science, Chung-Ang University, Seoul, Republic of Korea.
Department of Microbiology, College of Medicine, Hallym University, Chuncheon, Republic of Korea.
Microb Pathog. 2022 Apr;165:105460. doi: 10.1016/j.micpath.2022.105460. Epub 2022 Feb 26.
RNase E-mediated RNA processing and degradation are involved in bacterial adaptation to environmental changes. The RraA regulatory protein, which is highly conserved in γ-proteobacteria, differentially modulates RNase E activity. Recent studies have revealed the association of Salmonella enterica serovar Typhimurium RNase E (STRNase E) with bacterial pathogenicity; however, the molecular mechanisms are unknown. Here, we show that the expression levels of STRraA, a protein regulator of STRNase E activity, affect S. Typhimurium pathogenicity. RNA-sequencing and RT-PCR analyses indicated positive effects of STRraA levels on the abundance of mRNA species from class II flagellar operons. Primer extension analysis further identified STRraA-regulated STRNase E cleavage in the 5' untranslated region of fliDST mRNA. The cleavage affected the stability of this polycistronic mRNA, suggesting that STRraA protects fliDST mRNA from STRNase E cleavage, leading to enhanced flagellar assembly. Accordingly, STRraA positively regulated flagellar assembly and motility. In addition, STrraA-deleted cells showed decreased invasion ability and cytotoxicity in infection of human cervical epithelial carcinoma cells and reduced mortality in a mouse infection model compared to wild-type cells. These results support an active role of STRraA in RNase E-mediated modulation of pathogenesis in S. Typhimurium.
核糖核酸酶E介导的RNA加工和降解参与细菌对环境变化的适应。RraA调节蛋白在γ-变形菌中高度保守,可差异性地调节核糖核酸酶E的活性。最近的研究揭示了鼠伤寒沙门氏菌核糖核酸酶E(STRNase E)与细菌致病性的关联;然而,其分子机制尚不清楚。在此,我们表明STRNase E活性的蛋白调节剂STRraA的表达水平影响鼠伤寒沙门氏菌的致病性。RNA测序和逆转录聚合酶链反应分析表明,STRraA水平对II类鞭毛操纵子的mRNA种类丰度有积极影响。引物延伸分析进一步确定了STRraA调节的STRNase E在fliDST mRNA的5'非翻译区的切割。这种切割影响了这种多顺反子mRNA的稳定性,表明STRraA保护fliDST mRNA免受STRNase E的切割,从而导致鞭毛组装增强。因此,STRraA正向调节鞭毛组装和运动性。此外,与野生型细胞相比,缺失STrraA的细胞在感染人宫颈癌细胞时显示出侵袭能力和细胞毒性降低,并且在小鼠感染模型中的死亡率降低。这些结果支持STRraA在鼠伤寒沙门氏菌中核糖核酸酶E介导的致病机制调节中发挥积极作用。
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