Secretable Small RNAs via Outer Membrane Vesicles in Periodontal Pathogens

生物 牙密螺旋体 聚集放线菌 小RNA 小RNA 牙龈卟啉单胞菌 细菌外膜 阿尔戈瑙特 细胞生物学 小核仁RNA 核糖核酸 基因 非编码RNA 计算生物学 细菌 遗传学 RNA干扰 大肠杆菌
作者
Ji-Woong Choi,S.-C. Kim,Su‐Hyung Hong,Heon‐Jin Lee
出处
期刊:Journal of Dental Research [SAGE]
卷期号:96 (4): 458-466 被引量:151
标识
DOI:10.1177/0022034516685071
摘要

MicroRNAs (miRNAs) have been shown to be major regulators of eukaryotic gene expression. However, bacterial RNAs comparable in size to eukaryotic miRNAs (18-22 nucleotides) have received little attention. Recently, a novel class of small RNAs similar in size to miRNAs (miRNA-size, small RNAs or msRNAs) have also been found in several bacteria. Like miRNAs, msRNAs are approximately 15 to 25 nucleotides in length, and their precursors are predicted to form a hairpin loop secondary structure. Here, we identified msRNAs in the periodontal pathogens Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, and Treponema denticola. We examined these msRNAs using a deep sequencing method and characterized dozens of msRNAs through bioinformatic analysis. Highly expressed msRNAs were selected for further validation. The findings suggest that this class of small RNAs is well conserved across the domains of life. Indeed, msRNAs secreted via bacterial outer membrane vesicles (OMVs) were detected. The ability of bacterial OMVs to deliver RNAs into eukaryotic cells was also observed. These msRNAs in OMVs allowed us to identify their potential human immune-related target genes. Furthermore, we found that exogenous msRNAs could suppress expression of certain cytokines in Jurkat T cells. We propose msRNAs may function as novel bacterial signaling molecules that mediate bacteria-to-human interactions. Furthermore, this study may provide fresh insight into bacterial pathogenic mechanisms of periodontal diseases.
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