Staphylococcus aureus and Virulence-Related Small RNA

Rudra Mishra, Bhama Mishra Awdhesh Kumar Mishra, Nalini Easwaran, K. Gothandam
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Abstract

Staphylococcus aureus causes a wide range of diseases, including both community-associated and hospital-acquired infections such as abscesses, wound infections, osteomyelitis, endocarditis and septicemia. Regulation of the expression of various virulence factors is initiated through complex coordination between two-component systems, transcriptional regulatory proteins and regulatory small RNAs (sRNAs). S.aureus uses many sRNA and RNA–RNA interactions mediated the regulation of the expression of genes post-transcriptionally, but it uses few sigma factors to initiate the transcription function. sRNA transcripts are encoded within intergenic regions or in antisense orientation to mRNA transcripts, and sRNA regulation plays a central role in the response to stress stimuli encountered by pathogens during infection. One of the most intriguing examples of sRNA-mediated post-transcriptional regulation is RNAIII from S.aureus, which interacts with and regulates various RNA targets involved in virulence. Several genes known to be regulated by RNAIII have been demonstrated to be regulated by the sarA locus, independent of its effect on the expression of RNAIII. We discuss the potential role of small RNA (sRNA) in the pathogenesis and virulence factors production of Staphylococcus aureus.
金黄色葡萄球菌及其毒力相关小RNA
金黄色葡萄球菌引起多种疾病,包括社区相关感染和医院获得性感染,如脓肿、伤口感染、骨髓炎、心内膜炎和败血症。各种毒力因子的表达调控是通过双组分系统、转录调控蛋白和调控小rna (sRNAs)之间的复杂协调启动的。金黄色葡萄球菌通过多种sRNA和RNA-RNA相互作用介导转录后基因表达的调控,但很少使用sigma因子启动转录功能。sRNA转录本编码在基因间区或mRNA转录本的反义取向,并且sRNA调控在感染期间病原体对应激刺激的反应中起着核心作用。srna介导的转录后调控的最有趣的例子之一是来自金黄色葡萄球菌的RNAIII,它与参与毒力的各种RNA靶点相互作用并调节。一些已知受RNAIII调控的基因已被证明受sarA位点调控,而不受其对RNAIII表达的影响。我们讨论了小RNA (sRNA)在金黄色葡萄球菌发病机制和毒力因子产生中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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