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Abstracts (complete list) - Wissenschaft Online

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Barbara C. Rütgen, Wilhelm Gerner, Armin Saalmüller, Sabine E. Hammer<br />

MHC typing in swine: The SLA-haplotype repertoire of<br />

Austrian Large White, Landrace, and Pietrain breeding stocks<br />

MHC (major histocompatibility complex) genes encode cell surface glycoproteins which<br />

bind and present antigenic peptides to T cells. The genes within this complex are highly<br />

polymorphic, suggesting that diversity in MHC genes is a good measure of population<br />

fitness. Resource herds of swine leukocyte antigen (SLA)-characterized pigs are<br />

valuable large animal models for biomedical research in terms of immune responses,<br />

disease resistance, and production traits. This study represents the initial<br />

characterization of founder haplotypes of commercial pigs in Austria which are F2<br />

descendants of purebred Large White, Landrace, and Pietrain populations. The<br />

respective founder SLA-haplotypes were detected by a reverse transcription-polymerase<br />

chain reaction (RT-PCR)-based SLA typing method to clone and DNA sequence the<br />

putative alleles at four SLA class Ia loci, designated as SLA-1, SLA-2, SLA-3, and SLA-6<br />

and four SLA class II loci, SLA-DQA1, SLA-DQB1, SLA-DRA1, and SLA-DRB1. The data<br />

obtained so far indicate that the Large White, Landrace, and Pietrain pigs have at least<br />

four SLA class Ia founder haplotypes (4a.0, 4b.0, 13.0, 5.0) and three SLA class II<br />

founder haplotypes (0.4, 0.2, 0.9). Furthermore, the analyzed specimen point toward<br />

the occurrence of at least three novel SLA class Ia haplotypes. The newly generated<br />

sequences will be used to design allele-specific primers for establishing a rapid SLA<br />

typing assay to discriminate each allele using PCR with sequence-specific primers (PCR-<br />

SSP). To check the PCR screening approach for false negatives, positive control primers<br />

were also designed to amplify a portion of the alpha-actin gene and multiplexed with<br />

the allele-specific primers. By applying a combination of SLA typing by cloning and DNA<br />

sequencing together with PCR-SSP, we will be able to characterize the entire Large<br />

White, Landrace, and Pietrain breeding stocks and to identify the SLA haplotype<br />

distribution present in the respective breeds.

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