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A Novel Mechanism of Host-Pathogen Interaction through sRNA in Bacterial Outer Membrane Vesicles
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 th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905634/ https://www.ncbi.nlm.nih.gov/pubmed/27295279 http://dx.doi.org/10.1371/journal.ppat.1005672 |
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author | Koeppen, Katja Hampton, Thomas H. Jarek, Michael Scharfe, Maren Gerber, Scott A. Mielcarz, Daniel W. Demers, Elora G. Dolben, Emily L. Hammond, John H. Hogan, Deborah A. Stanton, Bruce A. |
author_facet | Koeppen, Katja Hampton, Thomas H. Jarek, Michael Scharfe, Maren Gerber, Scott A. Mielcarz, Daniel W. Demers, Elora G. Dolben, Emily L. Hammond, John H. Hogan, Deborah A. Stanton, Bruce A. |
author_sort | Koeppen, Katja |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4905634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49056342016-06-28 A Novel Mechanism of Host-Pathogen Interaction through sRNA in Bacterial Outer Membrane Vesicles Koeppen, Katja Hampton, Thomas H. Jarek, Michael Scharfe, Maren Gerber, Scott A. Mielcarz, Daniel W. Demers, Elora G. Dolben, Emily L. Hammond, John H. Hogan, Deborah A. Stanton, Bruce A. PLoS Pathog Research Article 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. Public Library of Science 2016-06-13 /pmc/articles/PMC4905634/ /pubmed/27295279 http://dx.doi.org/10.1371/journal.ppat.1005672 Text en © 2016 Koeppen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Koeppen, Katja Hampton, Thomas H. Jarek, Michael Scharfe, Maren Gerber, Scott A. Mielcarz, Daniel W. Demers, Elora G. Dolben, Emily L. Hammond, John H. Hogan, Deborah A. Stanton, Bruce A. A Novel Mechanism of Host-Pathogen Interaction through sRNA in Bacterial Outer Membrane Vesicles |
title | A Novel Mechanism of Host-Pathogen Interaction through sRNA in Bacterial Outer Membrane Vesicles |
title_full | A Novel Mechanism of Host-Pathogen Interaction through sRNA in Bacterial Outer Membrane Vesicles |
title_fullStr | A Novel Mechanism of Host-Pathogen Interaction through sRNA in Bacterial Outer Membrane Vesicles |
title_full_unstemmed | A Novel Mechanism of Host-Pathogen Interaction through sRNA in Bacterial Outer Membrane Vesicles |
title_short | A Novel Mechanism of Host-Pathogen Interaction through sRNA in Bacterial Outer Membrane Vesicles |
title_sort | novel mechanism of host-pathogen interaction through srna in bacterial outer membrane vesicles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905634/ https://www.ncbi.nlm.nih.gov/pubmed/27295279 http://dx.doi.org/10.1371/journal.ppat.1005672 |
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