Cargando…
Outer Membrane Vesicle-Mediated Export of Processed PrtV Protease from Vibrio cholerae
BACKGROUND: Outer membrane vesicles (OMVs) are known to release from almost all Gram-negative bacteria during normal growth. OMVs carry different biologically active toxins and enzymes into the surrounding environment. We suggest that OMVs may therefore be able to transport bacterial proteases into...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4519245/ https://www.ncbi.nlm.nih.gov/pubmed/26222047 http://dx.doi.org/10.1371/journal.pone.0134098 |
_version_ | 1782383480407064576 |
---|---|
author | Rompikuntal, Pramod K. Vdovikova, Svitlana Duperthuy, Marylise Johnson, Tanya L. Åhlund, Monika Lundmark, Richard Oscarsson, Jan Sandkvist, Maria Uhlin, Bernt Eric Wai, Sun Nyunt |
author_facet | Rompikuntal, Pramod K. Vdovikova, Svitlana Duperthuy, Marylise Johnson, Tanya L. Åhlund, Monika Lundmark, Richard Oscarsson, Jan Sandkvist, Maria Uhlin, Bernt Eric Wai, Sun Nyunt |
author_sort | Rompikuntal, Pramod K. |
collection | PubMed |
description | BACKGROUND: Outer membrane vesicles (OMVs) are known to release from almost all Gram-negative bacteria during normal growth. OMVs carry different biologically active toxins and enzymes into the surrounding environment. We suggest that OMVs may therefore be able to transport bacterial proteases into the target host cells. We present here an analysis of the Vibrio cholerae OMV-associated protease PrtV. METHODOLOGY/PRINCIPAL FINDINGS: In this study, we demonstrated that PrtV was secreted from the wild type V. cholerae strain C6706 via the type II secretion system in association with OMVs. By immunoblotting and electron microscopic analysis using immunogold labeling, the association of PrtV with OMVs was examined. We demonstrated that OMV-associated PrtV was biologically active by showing altered morphology and detachment of cells when the human ileocecum carcinoma (HCT8) cells were treated with OMVs from the wild type V. cholerae strain C6706 whereas cells treated with OMVs from the prtV isogenic mutant showed no morphological changes. Furthermore, OMV-associated PrtV protease showed a contribution to bacterial resistance towards the antimicrobial peptide LL-37. CONCLUSION/SIGNIFICANCE: Our findings suggest that OMVs released from V. cholerae can deliver a processed, biologically active form of PrtV that contributes to bacterial interactions with target host cells. |
format | Online Article Text |
id | pubmed-4519245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45192452015-07-31 Outer Membrane Vesicle-Mediated Export of Processed PrtV Protease from Vibrio cholerae Rompikuntal, Pramod K. Vdovikova, Svitlana Duperthuy, Marylise Johnson, Tanya L. Åhlund, Monika Lundmark, Richard Oscarsson, Jan Sandkvist, Maria Uhlin, Bernt Eric Wai, Sun Nyunt PLoS One Research Article BACKGROUND: Outer membrane vesicles (OMVs) are known to release from almost all Gram-negative bacteria during normal growth. OMVs carry different biologically active toxins and enzymes into the surrounding environment. We suggest that OMVs may therefore be able to transport bacterial proteases into the target host cells. We present here an analysis of the Vibrio cholerae OMV-associated protease PrtV. METHODOLOGY/PRINCIPAL FINDINGS: In this study, we demonstrated that PrtV was secreted from the wild type V. cholerae strain C6706 via the type II secretion system in association with OMVs. By immunoblotting and electron microscopic analysis using immunogold labeling, the association of PrtV with OMVs was examined. We demonstrated that OMV-associated PrtV was biologically active by showing altered morphology and detachment of cells when the human ileocecum carcinoma (HCT8) cells were treated with OMVs from the wild type V. cholerae strain C6706 whereas cells treated with OMVs from the prtV isogenic mutant showed no morphological changes. Furthermore, OMV-associated PrtV protease showed a contribution to bacterial resistance towards the antimicrobial peptide LL-37. CONCLUSION/SIGNIFICANCE: Our findings suggest that OMVs released from V. cholerae can deliver a processed, biologically active form of PrtV that contributes to bacterial interactions with target host cells. Public Library of Science 2015-07-29 /pmc/articles/PMC4519245/ /pubmed/26222047 http://dx.doi.org/10.1371/journal.pone.0134098 Text en © 2015 Rompikuntal 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 Rompikuntal, Pramod K. Vdovikova, Svitlana Duperthuy, Marylise Johnson, Tanya L. Åhlund, Monika Lundmark, Richard Oscarsson, Jan Sandkvist, Maria Uhlin, Bernt Eric Wai, Sun Nyunt Outer Membrane Vesicle-Mediated Export of Processed PrtV Protease from Vibrio cholerae |
title | Outer Membrane Vesicle-Mediated Export of Processed PrtV Protease from Vibrio cholerae
|
title_full | Outer Membrane Vesicle-Mediated Export of Processed PrtV Protease from Vibrio cholerae
|
title_fullStr | Outer Membrane Vesicle-Mediated Export of Processed PrtV Protease from Vibrio cholerae
|
title_full_unstemmed | Outer Membrane Vesicle-Mediated Export of Processed PrtV Protease from Vibrio cholerae
|
title_short | Outer Membrane Vesicle-Mediated Export of Processed PrtV Protease from Vibrio cholerae
|
title_sort | outer membrane vesicle-mediated export of processed prtv protease from vibrio cholerae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4519245/ https://www.ncbi.nlm.nih.gov/pubmed/26222047 http://dx.doi.org/10.1371/journal.pone.0134098 |
work_keys_str_mv | AT rompikuntalpramodk outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae AT vdovikovasvitlana outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae AT duperthuymarylise outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae AT johnsontanyal outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae AT ahlundmonika outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae AT lundmarkrichard outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae AT oscarssonjan outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae AT sandkvistmaria outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae AT uhlinbernteric outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae AT waisunnyunt outermembranevesiclemediatedexportofprocessedprtvproteasefromvibriocholerae |