Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
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
_version_ 1782437284820287488
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
work_keys_str_mv AT koeppenkatja anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT hamptonthomash anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT jarekmichael anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT scharfemaren anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT gerberscotta anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT mielcarzdanielw anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT demerselorag anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT dolbenemilyl anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT hammondjohnh anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT hogandeboraha anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT stantonbrucea anovelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT koeppenkatja novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT hamptonthomash novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT jarekmichael novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT scharfemaren novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT gerberscotta novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT mielcarzdanielw novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT demerselorag novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT dolbenemilyl novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT hammondjohnh novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT hogandeboraha novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles
AT stantonbrucea novelmechanismofhostpathogeninteractionthroughsrnainbacterialoutermembranevesicles