Abstract

The highly polymorphic swine major histocompatibility complex (MHC), termed swine leukocyte antigen (SLA), is associated with different levels of immunologic responses to infectious diseases, vaccines, and transplantation. Pig breeds with known SLA haplotypes are important genetic resources for biomedical research. Canadian Yorkshire and Landrace pigs represent the current specific pathogen-free (SPF) breeding stock maintained in the isolation environment at the Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences. In this study, we identified 61 alleles at five polymorphic SLA loci (SLA-1, SLA-2, SLA-3, DRB1, and DQB1) representing 17 class I haplotypes and 11 class II haplotypes using reverse transcription-polymerase chain reaction (RT-PCR) sequence-based typing and PCR-sequence specific primers methods in 367 Canadian SPF Yorkshire and Landrace pigs. The official designation of the alleles has been assigned by the SLA Nomenclature Committee of the International Society for Animal Genetics and released in updated Immuno Polymorphism Database-MHC SLA sequence database [Release 2.0.0.3 (2016-11-03)]. The submissions confirmed some unassigned alleles and standardized nomenclatures of many previously unconfirmed alleles in the GenBank database. Three class I haplotypes, Hp-37.0, 63.0, and 73.0, appeared to be novel and have not previously been reported in other pig populations. One crossover within the class I region and two between class I and class II regions were observed, resulting in three new recombinant haplotypes. The presence of the duplicated SLA-1 locus was confirmed in three class I haplotypes Hp-28.0, Hp-35.0, and Hp-63.0. Furthermore, we also analyzed the functional diversities of 19 identified frequent SLA class I molecules in this study and confirmed the existence of four supertypes using the MHCcluster method. These results will be useful for studying the adaptive immune response and immunological phenotypic differences in pigs, screening potential T-cell epitopes, and further developing the more effective vaccines.

Highlights

  • Swine major histocompatibility complex (MHC), which codes for swine leukocyte antigen (SLA), has been mapped to pig chromosome 7 spanning the centromere

  • The nucleotide sequences of SLA1*rh[03] (AF074427), SLA-2*05rh[03] (AF074428), DRB1*06sL47 (L08847), DQB1*0203 (AB012093, AF113970), and DQB1*0204 (L08844, EU039916) had previously been submitted to the IPDMHC database and were identical to the partial coding sequences that we identified in specific pathogen-free (SPF) Yorkshire and Landrace pigs

  • The SLA-1*09:01 allele was not detected by sequence-based typing (SBT) method using the full-length locus-specific primers SLA1-F/SLA1-R in seven Landrace pigs with Hp-28.0

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Summary

Introduction

Swine major histocompatibility complex (MHC), which codes for swine leukocyte antigen (SLA), has been mapped to pig chromosome 7 spanning the centromere. SLA genes are highly polymorphic comprising classical class I, II, and III genes (1). SLA class I and class II proteins are involved in the adaptive immune response through their respective presentations of endogenous and exogenous peptide antigens to circulating T lymphocytes (2). Class III molecules include many important immune-defense genes, such as the tumor necrosis factor gene families and components of the complement cascade (3). Among SLA class I and class II genes, SLA-1, SLA-2, SLA-3, DRB1, and DQB1 are highly polymorphic. 192 classical SLA class I alleles (69 SLA-1, 87 SLA-2, and 36 SLA-3) and 145 polymorphic class II alleles (91 DRB1 and 54 DQB1) have been designated by the SLA Nomenclature Committee of the International Society for Animal Genetics (ISAG) in the Immuno Polymorphism Database (IPD)-MHC SLA sequence database.[1]

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