RNA sequencing differential gene expression analysis of isolated perfused bovine udders experimentally inoculated with Streptococcus agalactiae

dc.contributor.authorSbardella, A. P. [UNESP]
dc.contributor.authorWeller, M. M.D.C.A.
dc.contributor.authorFonseca, I.
dc.contributor.authorStafuzza, N. B. [UNESP]
dc.contributor.authorBernardes, P. A. [UNESP]
dc.contributor.authore Silva, F. F.
dc.contributor.authorda Silva, M. V.G.B.
dc.contributor.authorMartins, M. F.
dc.contributor.authorMunari, D. P. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)
dc.contributor.institutionUniversidade Federal de Viçosa (UFV)
dc.date.accessioned2019-10-06T16:11:27Z
dc.date.available2019-10-06T16:11:27Z
dc.date.issued2019-02-01
dc.description.abstractThe aim of this study was to elucidate the differential gene expression in the RNA sequencing transcriptome of isolated perfused udders collected from 4 slaughtered Holstein × Zebu crossbred dairy cows experimentally inoculated with Streptococcus agalactiae. We studied 3 different statistical tools (edgeR, baySeq, and Cuffdiff 2). In summary, 2 quarters of each udder were experimentally inoculated with Strep. agalactiae and the other 2 were used as a control. Mammary tissue biopsies were collected at times 0 and 3 h after infection. The total RNA was extracted and sequenced on an Illumina HiSeq 2000 (Illumina Inc., San Diego, CA). Transcripts were assembled from the reads aligned to the bovine UMD 3.1 reference genome, and the statistical analyses were performed using the previously mentioned tools (edgeR, baySeq, and Cuffdiff 2). Finally, the identified genes were submitted to pathway enrichment analysis. A total of 1,756, 1,161, and 3,389 genes with differential gene expression were identified when using edgeR, baySeq, and Cuffdiff 2, respectively. A total of 122 genes were identified by the overlapping of the 3 methods; however, only the platelet activation presented a significantly enriched pathway. From the results, we suggest the FCER1G, GNAI2, ORAI1, and VASP genes shared among the 3 methods in this pathway for posterior biological validation.en
dc.description.affiliationDepartamento de Ciências Exatas Universidade Estadual Paulista—UNESP/FCAV
dc.description.affiliationEmpresa Brasileira de Pesquisa Agropecuária—Embrapa Gado de Leite
dc.description.affiliationDepartamento de Zootecnia Universidade Federal de Viçosa
dc.description.affiliationUnespDepartamento de Ciências Exatas Universidade Estadual Paulista—UNESP/FCAV
dc.format.extent1761-1767
dc.identifierhttp://dx.doi.org/10.3168/jds.2018-15516
dc.identifier.citationJournal of Dairy Science, v. 102, n. 2, p. 1761-1767, 2019.
dc.identifier.doi10.3168/jds.2018-15516
dc.identifier.issn1525-3198
dc.identifier.issn0022-0302
dc.identifier.scopus2-s2.0-85059037453
dc.identifier.urihttp://hdl.handle.net/11449/188541
dc.language.isoeng
dc.relation.ispartofJournal of Dairy Science
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectbaySeq
dc.subjectcrossbred dairy cow
dc.subjectCuffdiff 2
dc.subjectedgeR
dc.titleRNA sequencing differential gene expression analysis of isolated perfused bovine udders experimentally inoculated with Streptococcus agalactiaeen
dc.typeArtigo
unesp.departmentCiências Exatas - FCAVpt

Arquivos