A Novel Mechanism of Host-Pathogen Interaction through sRNA in Bacterial Outer Membrane Vesicles

被引:365
作者
Koeppen, Katja [1 ]
Hampton, Thomas H. [1 ]
Jarek, Michael [2 ]
Scharfe, Maren [2 ]
Gerber, Scott A. [3 ,4 ,5 ]
Mielcarz, Daniel W. [5 ]
Demers, Elora G. [1 ]
Dolben, Emily L. [1 ]
Hammond, John H. [1 ]
Hogan, Deborah A. [1 ]
Stanton, Bruce A. [1 ]
机构
[1] Geisel Sch Med Dartmouth, Dept Microbiol & Immunol, Hanover, NH 03755 USA
[2] Genome Analyt Helmholtz Ctr Infect Res, Braunschweig, Lower Saxony, Germany
[3] Geisel Sch Med Dartmouth, Dept Genet, Hanover, NH USA
[4] Geisel Sch Med Dartmouth, Dept Biochem, Hanover, NH USA
[5] Norris Cotton Canc Ctr, Lebanon, NH USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
PSEUDOMONAS-AERUGINOSA; NONCODING RNAS; DNA; IDENTIFICATION; EXPRESSION; DIVERSITY; VIRULENCE; ASSOCIATE; PROTEINS; CELLS;
D O I
10.1371/journal.ppat.1005672
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacterial outer membrane vesicle (OMV)-mediated delivery of proteins to host cells is an important mechanism of host-pathogen communication. Emerging evidence suggests that OMVs contain differentially packaged short RNAs (sRNAs) with the potential to target host mRNA function and/or stability. In this study, we used RNA-Seq to characterize differentially packaged sRNAs in Pseudomonas aeruginosa OMVs, and to show transfer of OMV sRNAs to human airway cells. We selected one sRNA for further study based on its stable secondary structure and predicted mRNA targets. Our candidate sRNA (sRNA52320), a fragment of a P. aeruginosa methionine tRNA, was abundant in OMVs and reduced LPS-induced as well as OMV-induced IL-8 secretion by cultured primary human airway epithelial cells. We also showed that sRNA52320 attenuated OMV-induced KC cytokine secretion and neutrophil infiltration in mouse lung. Collectively, these findings are consistent with the hypothesis that sRNA52320 in OMVs is a novel mechanism of host-pathogen interaction whereby P. aeruginosa reduces the host immune response.
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页数:22
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