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Molecular characterization of swine leucocyte antigen class II genes in outbred pig populations

dc.contributor.authorHo, C. -S.en_US
dc.contributor.authorLunney, J. K.en_US
dc.contributor.authorLee, J. -H.en_US
dc.contributor.authorFranzo-Romain, M. H.en_US
dc.contributor.authorMartens, G. W.en_US
dc.contributor.authorRowland, R. R. R.en_US
dc.contributor.authorSmith, D. M.en_US
dc.date.accessioned2011-01-13T19:38:39Z
dc.date.available2011-01-13T19:38:39Z
dc.date.issued2010-08en_US
dc.identifier.citationHo, C.-S.; Lunney, J. K.; Lee, J.-H.; Franzo-Romain, M. H.; Martens, G. W.; Rowland, R. R. R.; Smith, D. M.; (2010). "Molecular characterization of swine leucocyte antigen class II genes in outbred pig populations." Animal Genetics 41(4): 428-432. <http://hdl.handle.net/2027.42/78611>en_US
dc.identifier.issn0268-9146en_US
dc.identifier.issn1365-2052en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/78611
dc.description.abstractThe highly polymorphic swine leucocyte antigen (SLA) genes are among the most important determinants of swine immune responses to disease and vaccines. Accurate and effective SLA genotyping methods are required to understand how SLA gene polymorphisms affect immunity, especially in outbred pigs with diverse genetic backgrounds. In this study, we present a simple and rapid molecular-based typing system for characterizing SLA class II alleles of the DRB1 , DQB1 and DQA loci. This system utilizes a set of 47 sequence-specific PCR primers developed to differentiate alleles by groups that share similar sequence motifs. We applied this typing method to investigate the SLA class II diversity in four populations of outbred pigs ( n  =   206) and characterized a total of 19 SLA class II haplotypes, six of which were shared by at least three of the sampled pig populations. We found that Lr-0.1 ( DRB1 *01XX– DQB1 *01XX– DQA *01XX) was the most prevalent haplotype with a combined frequency of 16.0%, followed by Lr-0.2 ( DRB1 *02XX– DQB1 *02XX– DQA *02XX) with 14.6% and Lr-0.15b ( DRB1 *04XX– DQB1 *0202– DQA *02XX) with 14.1%. Over 70% of the pigs ( n  =   147) had at least one copy of one of these three haplotypes. The PCR-based typing system described in this study demonstrates a reliable and unambiguous detection method for SLA class II alleles. It will be a valuable tool for studying the influence of SLA diversity on various immunological, pathological and physiological traits in outbred pigs.en_US
dc.format.extent44766 bytes
dc.format.extent3106 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.subject.otherGenotypingen_US
dc.subject.otherMajor Histocompatibility Complexen_US
dc.subject.otherOutbred Pigsen_US
dc.subject.otherPCR-SSPen_US
dc.subject.otherPolymorphismen_US
dc.subject.otherSLA Diversityen_US
dc.subject.otherSwine Leucocyte Antigenen_US
dc.titleMolecular characterization of swine leucocyte antigen class II genes in outbred pig populationsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationotherTransplant Immunology Laboratory, Department of Pathology, Baylor University Medical Center, Dallas, TX 75246, USAen_US
dc.contributor.affiliationotherInstitute of Biomedical Studies, Baylor University, Waco, TX 76798, USAen_US
dc.contributor.affiliationotherAnimal Parasitic Diseases Laboratory, BARC, ARS, USDA, Beltsville, MD 20705, USAen_US
dc.contributor.affiliationotherDivision of Animal Science and Resources, College of Agriculture and Life Sciences, Chungnam National University, Daejeon 305-764, Koreaen_US
dc.contributor.affiliationotherDepartment of Diagnostic Medicine and Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506, USAen_US
dc.identifier.pmid20121817en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/78611/1/AGE_2019_sm_suppinfo_tS3.pdf
dc.identifier.doi10.1111/j.1365-2052.2010.02019.xen_US
dc.identifier.sourceAnimal Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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