先天免疫系统
生物
铜绿假单胞菌
细菌外膜
免疫系统
核糖核酸
微生物学
小RNA
毒力
细胞生物学
核糖核酸酶P
基因
细菌
遗传学
大肠杆菌
作者
Zhen Xie,Xiao Wang,Yangyang Huang,Shukun Chen,Mohua Liu,Fuhua Zhang,Mengyuan Li,Xiao Wang,Yanchao Gu,Yadong Yang,Xihui Shen,Yao Wang,Xu Yang,Lei Xu
标识
DOI:10.1016/j.micpath.2024.106562
摘要
Bacterial outer membrane vesicles (OMVs) can package and deliver virulence factors into host cells, which is an important mechanism mediating host-pathogen interactions. It has been reported that small RNAs (sRNAs) can be packed into OMVs with varying relative abundance, which might affect the function and/or stability of host mRNAs. In this study, we used OptiPrep density gradient ultra-high-speed centrifugation to purify OMVs from Pseudomonas aeruginosa. Next, the sequences and abundance of sRNAs were detected by using Small RNA-Seq. In particular, sRNA4518698, sRNA2316613 and sRNA809738 were the three most abundant sRNAs in OMVs, which are all fragments of P. aeruginosa non-coding RNAs. sRNAs were shielded within the interior of OMVs and remained resistant to external RNase cleavage. The miRanda and RNAhybrid analysis demonstrated that those sRNAs could target a large number of host mRNAs, which were enriched in host immune responses by the functions of GO and KEGG enrichment. Experimentally, we demonstrated that the transfection of synthetic sRNA4518698, sRNA2316613, or sRNA809738 could reduce the expression of innate immune response genes in RAW264.7 cells. Together, we demonstrated that P. aeruginosa OMVs sRNAs can regulate innate immune responses. This study uncovered a mechanism in which the OMVs regulate host responses by transferring bacterial sRNAs.
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