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dc.contributor.authorAuray, Gaël
dc.contributor.authorLachance, Claude
dc.contributor.authorWang, Yingchao
dc.contributor.authorGagnon, Carl A.
dc.contributor.authorSegura, Mariela
dc.contributor.authorGottschalk, Marcelo
dc.date.accessioned2017-01-12T20:41:18Z
dc.date.availableNO_RESTRICTIONfr
dc.date.available2017-01-12T20:41:18Z
dc.date.issued2016-05-23
dc.identifier.urihttp://hdl.handle.net/1866/16379
dc.rightsCe document est mis à disposition selon les termes de la Licence Creative Commons Paternité 4.0 International. / This work is licensed Under a Creative Commons Attribution 4.0 International License.fr
dc.rights.urihttp://creativecommons.org/licenses/by/4.0en
dc.subjectMonocytesfr
dc.subjectMicroarraysfr
dc.subjectCo-infectionsfr
dc.subjectPhagocytosisfr
dc.subjectGene expressionfr
dc.subjectInflammationfr
dc.subjectIntracellular pathogensfr
dc.subjectStreptococcus suisfr
dc.titleTranscriptional analysis of PRRSV-infected porcine dendritic cell response to Streptococcus suis infection reveals up-regulation of inflammatory-related genes expressionfr
dc.typeArticlefr
dc.contributor.affiliationUniversité de Montréal. Faculté de médecine vétérinairefr
UdeM.statutProfesseur(e) / Professorfr
dc.identifier.doi10.1371/journal.pone.0156019
dcterms.abstractThe porcine reproductive and respiratory syndrome virus (PRRSV) is one of the most important swine pathogens and often serves as an entry door for other viral or bacterial pathogens, of which Streptococcus suis is one of the most common. Pre-infection with PRRSV leads to exacerbated disease caused by S. suis infection. Very few studies have assessed the immunological mechanisms underlying this higher susceptibility. Since antigen presenting cells play a major role in the initiation of the immune response, the in vitro transcriptional response of bone marrow-derived dendritic cells (BMDCs) and monocytes in the context of PRRSV and S. suis co-infection was investigated. BMDCs were found to be more permissive than monocytes to PRRSV infection; S. suis phagocytosis by PRRSV-infected BMDCs was found to be impaired, whereas no effect was found on bacterial intracellular survival. Transcription profile analysis, with a major focus on inflammatory genes, following S. suis infection, with and without pre-infection with PRRSV, was then performed. While PRRSV pre-infection had little effect on monocytes response to S. suis infection, a significant expression of several pro-inflammatory molecules was observed in BMDCs pre-infected with PRRSV after a subsequent infection with S. suis. While an additive effect could be observed for CCL4, CCL14, CCL20, and IL-15, a distinct synergistic up-regulatory effect was observed for IL-6, CCL5 and TNF-α after co-infection. This increased pro-inflammatory response by DCs could participate in the exacerbation of the disease observed during PRRSV and S. suis co-infection.fr
dcterms.isPartOfurn:ISSN:1932-6203
dcterms.languageengfr
UdeM.VersionRioxxVersion acceptée / Accepted Manuscript
oaire.citationTitlePLoS one
oaire.citationVolume11
oaire.citationIssue5


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Ce document est mis à disposition selon les termes de la Licence Creative Commons Paternité 4.0 International. / This work is licensed Under a Creative Commons Attribution 4.0 International License.
Usage rights : Ce document est mis à disposition selon les termes de la Licence Creative Commons Paternité 4.0 International. / This work is licensed Under a Creative Commons Attribution 4.0 International License.