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dc.contributor.authorDang, Yuan
dc.contributor.authorLachance, Claude
dc.contributor.authorWang, Yingchao
dc.contributor.authorGagnon, Carl A.
dc.contributor.authorSavard, Christian
dc.contributor.authorSegura, Mariela
dc.contributor.authorGrenier, Daniel
dc.contributor.authorGottschalk, Marcelo
dc.date.accessioned2015-07-02T18:43:48Z
dc.date.availableNO_RESTRICTIONfr
dc.date.available2015-07-02T18:43:48Z
dc.date.issued2014-04
dc.identifier.citationDang, Y., Lachance, C., Wang, Y., Gagnon, C.A, Savard, C., Segura M., Grenier D. et Gottschalk, M. (2014, April). Transcriptional approach to study porcine tracheal epithelial cells individually or dually infected with swine influenza virus and Streptococcus suis. BMC Veterinary Research, 10.fr
dc.identifier.urihttp://hdl.handle.net/1866/12187
dc.subjectStreptococcus suisfr
dc.subjectSwine Influenza virusfr
dc.subjectCo-infectionfr
dc.subjectMicroarrayfr
dc.subjectCytokines/chemokines inductionfr
dc.subjectPorcine tracheal epithelial cellsfr
dc.titleTranscriptional approach to study porcine tracheal epithelial cells individually or dually infected with swine influenza virus and Streptococcus suisfr
dc.typeArticlefr
dc.contributor.affiliationUniversité de Montréal. Faculté de médecine vétérinairefr
UdeM.statutProfesseur(e) / Professorfr
dcterms.abstractBackground: Swine influenza is a highly contagious viral infection in pigs affecting the respiratory tract that can have significant economic impacts. Streptococcus suis serotype 2 is one of the most important post-weaning bacterial pathogens in swine causing different infections, including pneumonia. Both pathogens are important contributors to the porcine respiratory disease complex. Outbreaks of swine influenza virus with a significant level of co-infections due to S. suis have lately been reported. In order to analyze, for the first time, the transcriptional host response of swine tracheal epithelial (NPTr) cells to H1N1 swine influenza virus (swH1N1) infection, S. suis serotype 2 infection and a dual infection, we carried out a comprehensive gene expression profiling using a microarray approach. Results: Gene clustering showed that the swH1N1 and swH1N1/S. suis infections modified the expression of genes in a similar manner. Additionally, infection of NPTr cells by S. suis alone resulted in fewer differentially expressed genes compared to mock-infected cells. However, some important genes coding for inflammatory mediators such as chemokines, interleukins, cell adhesion molecules, and eicosanoids were significantly upregulated in the presence of both pathogens compared to infection with each pathogen individually. This synergy may be the consequence, at least in part, of an increased bacterial adhesion/invasion of epithelial cells previously infected by swH1N1, as recently reported. Conclusion: Influenza virus would replicate in the respiratory epithelium and induce an inflammatory infiltrate comprised of mononuclear cells and neutrophils. In a co-infection situation, although these cells would be unable to phagocyte and kill S. suis, they are highly activated by this pathogen. S. suis is not considered a primary pulmonary pathogen, but an exacerbated production of proinflammatory mediators during a co-infection with influenza virus may be important in the pathogenesis and clinical outcome of S. suis-induced respiratory diseases.fr
dcterms.bibliographicCitationBMC veterinary research ; vol. 10
dcterms.isPartOfurn:ISSN:1746-6148
dcterms.languageengfr
UdeM.VersionRioxxVersion acceptée / Accepted Manuscript


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