SLA-DRB1 and -DQB1 genotyping by the PCR-SSOP-Luminex method

Tissue Antigens. 2011 Jul;78(1):49-55. doi: 10.1111/j.1399-0039.2011.01669.x. Epub 2011 Apr 21.

Abstract

A simple and novel genotyping method was developed to detect alleles at the swine leukocyte antigen (SLA)-DRB1 and -DQB1 class II loci by using polymerase chain reaction (PCR)-fluorescently labeled sequence-specific oligonucleotide probes (SSOPs) and Luminex 100 xMAP detection. The PCR-SSOP-Luminex method exhibited accuracy of 95% for both SLA-DRB1 and -DQB1 in 6 homozygous and 16 heterozygous pig samples as confirmed by sequencing the PCR products of the same samples. In addition, 12 low-resolution SLA class II haplotypes consisting of 7 and 9 DRB1 and DQB1 alleles were identified, respectively, in one population of 283 Landrace pigs. This genotyping method facilitates the rapid and accurate identification of two- or four-digit alleles at the SLA-DRB1 and -DQB1 loci.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Frequency
  • Genetic Loci
  • Genotype
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II / genetics*
  • Histocompatibility Antigens Class II / immunology
  • Histocompatibility Testing / methods
  • Histocompatibility Testing / veterinary
  • Oligonucleotide Probes / genetics
  • Polymerase Chain Reaction / instrumentation
  • Polymerase Chain Reaction / methods*
  • Substrate Specificity / genetics
  • Swine / genetics*
  • Swine / immunology

Substances

  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • Oligonucleotide Probes
  • swine leukocyte antigen