Cargando…
Sodium Taurocholate Stimulates Campylobacter jejuni Outer Membrane Vesicle Production via Down-Regulation of the Maintenance of Lipid Asymmetry Pathway
Campylobacter jejuni outer membrane vesicles (OMVs) contain numerous virulence-associated proteins including the cytolethal distending toxin and three serine proteases. As C. jejuni lacks the classical virulence-associated secretion systems of other enteric pathogens that deliver effectors directly...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549495/ https://www.ncbi.nlm.nih.gov/pubmed/31192166 http://dx.doi.org/10.3389/fcimb.2019.00177 |
_version_ | 1783424019426443264 |
---|---|
author | Davies, Cadi Taylor, Aidan J. Elmi, Abdi Winter, Jody Liaw, Janie Grabowska, Anna D. Gundogdu, Ozan Wren, Brendan W. Kelly, David J. Dorrell, Nick |
author_facet | Davies, Cadi Taylor, Aidan J. Elmi, Abdi Winter, Jody Liaw, Janie Grabowska, Anna D. Gundogdu, Ozan Wren, Brendan W. Kelly, David J. Dorrell, Nick |
author_sort | Davies, Cadi |
collection | PubMed |
description | Campylobacter jejuni outer membrane vesicles (OMVs) contain numerous virulence-associated proteins including the cytolethal distending toxin and three serine proteases. As C. jejuni lacks the classical virulence-associated secretion systems of other enteric pathogens that deliver effectors directly into target cells, OMVs may have a particularly important role in virulence. C. jejuni OMV production is stimulated by the presence of physiological concentrations of the bile salt sodium taurocholate (ST) through an unknown mechanism. The maintenance of lipid asymmetry (MLA) pathway has been implicated in a novel mechanism for OMV biogenesis, open to regulation by host signals. In this study we investigated the role of the MLA pathway in C. jejuni OMV biogenesis with ST as a potential regulator. OMV production was quantified by analyzing protein and lipid concentrations of OMV preparations and OMV particle counts produced by nanoparticle tracking analysis. Mutation of mlaA which encodes the outer membrane component of the MLA pathway significantly increased OMV production compared to the wild-type strain. Detergent sensitivity and membrane permeability assays confirmed the increased OMV production was not due to changes in membrane stability. The presence of 0.2% (w/v) ST increased wild-type OMV production and reduced OMV size, but did not further stimulate mlaA mutant OMV production or significantly alter mlaA mutant OMV size. qRT-PCR analysis demonstrated that the presence of ST decreased expression of both mlaA and mlaC in C. jejuni wild-type strains 11168 and 488. Collectively the data in this study suggests C. jejuni can regulate OMV production in response to host gut signals through changes in expression of the MLA pathway. As the gut bile composition is dependent on both diet and the microbiota, this study highlights the potential importance of diet and lifestyle factors on the varying disease presentations associated with gut pathogen infection. |
format | Online Article Text |
id | pubmed-6549495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65494952019-06-12 Sodium Taurocholate Stimulates Campylobacter jejuni Outer Membrane Vesicle Production via Down-Regulation of the Maintenance of Lipid Asymmetry Pathway Davies, Cadi Taylor, Aidan J. Elmi, Abdi Winter, Jody Liaw, Janie Grabowska, Anna D. Gundogdu, Ozan Wren, Brendan W. Kelly, David J. Dorrell, Nick Front Cell Infect Microbiol Cellular and Infection Microbiology Campylobacter jejuni outer membrane vesicles (OMVs) contain numerous virulence-associated proteins including the cytolethal distending toxin and three serine proteases. As C. jejuni lacks the classical virulence-associated secretion systems of other enteric pathogens that deliver effectors directly into target cells, OMVs may have a particularly important role in virulence. C. jejuni OMV production is stimulated by the presence of physiological concentrations of the bile salt sodium taurocholate (ST) through an unknown mechanism. The maintenance of lipid asymmetry (MLA) pathway has been implicated in a novel mechanism for OMV biogenesis, open to regulation by host signals. In this study we investigated the role of the MLA pathway in C. jejuni OMV biogenesis with ST as a potential regulator. OMV production was quantified by analyzing protein and lipid concentrations of OMV preparations and OMV particle counts produced by nanoparticle tracking analysis. Mutation of mlaA which encodes the outer membrane component of the MLA pathway significantly increased OMV production compared to the wild-type strain. Detergent sensitivity and membrane permeability assays confirmed the increased OMV production was not due to changes in membrane stability. The presence of 0.2% (w/v) ST increased wild-type OMV production and reduced OMV size, but did not further stimulate mlaA mutant OMV production or significantly alter mlaA mutant OMV size. qRT-PCR analysis demonstrated that the presence of ST decreased expression of both mlaA and mlaC in C. jejuni wild-type strains 11168 and 488. Collectively the data in this study suggests C. jejuni can regulate OMV production in response to host gut signals through changes in expression of the MLA pathway. As the gut bile composition is dependent on both diet and the microbiota, this study highlights the potential importance of diet and lifestyle factors on the varying disease presentations associated with gut pathogen infection. Frontiers Media S.A. 2019-05-29 /pmc/articles/PMC6549495/ /pubmed/31192166 http://dx.doi.org/10.3389/fcimb.2019.00177 Text en Copyright © 2019 Davies, Taylor, Elmi, Winter, Liaw, Grabowska, Gundogdu, Wren, Kelly and Dorrell. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Davies, Cadi Taylor, Aidan J. Elmi, Abdi Winter, Jody Liaw, Janie Grabowska, Anna D. Gundogdu, Ozan Wren, Brendan W. Kelly, David J. Dorrell, Nick Sodium Taurocholate Stimulates Campylobacter jejuni Outer Membrane Vesicle Production via Down-Regulation of the Maintenance of Lipid Asymmetry Pathway |
title | Sodium Taurocholate Stimulates Campylobacter jejuni Outer Membrane Vesicle Production via Down-Regulation of the Maintenance of Lipid Asymmetry Pathway |
title_full | Sodium Taurocholate Stimulates Campylobacter jejuni Outer Membrane Vesicle Production via Down-Regulation of the Maintenance of Lipid Asymmetry Pathway |
title_fullStr | Sodium Taurocholate Stimulates Campylobacter jejuni Outer Membrane Vesicle Production via Down-Regulation of the Maintenance of Lipid Asymmetry Pathway |
title_full_unstemmed | Sodium Taurocholate Stimulates Campylobacter jejuni Outer Membrane Vesicle Production via Down-Regulation of the Maintenance of Lipid Asymmetry Pathway |
title_short | Sodium Taurocholate Stimulates Campylobacter jejuni Outer Membrane Vesicle Production via Down-Regulation of the Maintenance of Lipid Asymmetry Pathway |
title_sort | sodium taurocholate stimulates campylobacter jejuni outer membrane vesicle production via down-regulation of the maintenance of lipid asymmetry pathway |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549495/ https://www.ncbi.nlm.nih.gov/pubmed/31192166 http://dx.doi.org/10.3389/fcimb.2019.00177 |
work_keys_str_mv | AT daviescadi sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway AT tayloraidanj sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway AT elmiabdi sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway AT winterjody sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway AT liawjanie sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway AT grabowskaannad sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway AT gundogduozan sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway AT wrenbrendanw sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway AT kellydavidj sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway AT dorrellnick sodiumtaurocholatestimulatescampylobacterjejunioutermembranevesicleproductionviadownregulationofthemaintenanceoflipidasymmetrypathway |