Cargando…
The antigen recognition portion of African buffalo class I MHC is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurations
African buffalo (Syncerus caffer) have been distinct from the Auroch lineage leading to domestic cattle for 5 million years, and are reservoirs of multiple pathogens, that affect introduced domestic cattle. To date, there has been no analysis of the class I MHC locus in African buffalo. We present t...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039833/ https://www.ncbi.nlm.nih.gov/pubmed/36512055 http://dx.doi.org/10.1007/s00251-022-01287-0 |
_version_ | 1784912353507147776 |
---|---|
author | Obara, Isaiah Nijhof, Ard Atimnedi, Patrick Mijele, Domnic Nanteza, Anne Elati, Khawla Bishop, Richard |
author_facet | Obara, Isaiah Nijhof, Ard Atimnedi, Patrick Mijele, Domnic Nanteza, Anne Elati, Khawla Bishop, Richard |
author_sort | Obara, Isaiah |
collection | PubMed |
description | African buffalo (Syncerus caffer) have been distinct from the Auroch lineage leading to domestic cattle for 5 million years, and are reservoirs of multiple pathogens, that affect introduced domestic cattle. To date, there has been no analysis of the class I MHC locus in African buffalo. We present the first data on African buffalo class I MHC, which demonstrates that gene and predicted protein coding sequences are approximately 86–87% similar to that of African domestic cattle in the peptide binding region. The study also shows concordance in the distribution of codons with elevated posterior probabilities of positive selection in the buffalo class I MHC and known antigen binding sites in cattle. Overall, the diversity in buffalo class I sequences appears greater than that in cattle, perhaps related to a more complex pathogen challenge environment in Africa. However, application of NetMHCpan suggested broad clustering of peptide binding specificities between buffalo and cattle. Furthermore, in the case of at least 20 alleles, critical peptide-binding residues appear to be conserved with those of cattle, including at secondary anchor residues. Alleles with six different length transmembrane regions were detected. This preliminary analysis suggests that like cattle, but unlike most other mammals, African buffalo appears to exhibit configuration (haplotype) variation in which the loci are expressed in distinct combinations. |
format | Online Article Text |
id | pubmed-10039833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-100398332023-03-27 The antigen recognition portion of African buffalo class I MHC is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurations Obara, Isaiah Nijhof, Ard Atimnedi, Patrick Mijele, Domnic Nanteza, Anne Elati, Khawla Bishop, Richard Immunogenetics Original Article African buffalo (Syncerus caffer) have been distinct from the Auroch lineage leading to domestic cattle for 5 million years, and are reservoirs of multiple pathogens, that affect introduced domestic cattle. To date, there has been no analysis of the class I MHC locus in African buffalo. We present the first data on African buffalo class I MHC, which demonstrates that gene and predicted protein coding sequences are approximately 86–87% similar to that of African domestic cattle in the peptide binding region. The study also shows concordance in the distribution of codons with elevated posterior probabilities of positive selection in the buffalo class I MHC and known antigen binding sites in cattle. Overall, the diversity in buffalo class I sequences appears greater than that in cattle, perhaps related to a more complex pathogen challenge environment in Africa. However, application of NetMHCpan suggested broad clustering of peptide binding specificities between buffalo and cattle. Furthermore, in the case of at least 20 alleles, critical peptide-binding residues appear to be conserved with those of cattle, including at secondary anchor residues. Alleles with six different length transmembrane regions were detected. This preliminary analysis suggests that like cattle, but unlike most other mammals, African buffalo appears to exhibit configuration (haplotype) variation in which the loci are expressed in distinct combinations. Springer Berlin Heidelberg 2022-12-13 2023 /pmc/articles/PMC10039833/ /pubmed/36512055 http://dx.doi.org/10.1007/s00251-022-01287-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Obara, Isaiah Nijhof, Ard Atimnedi, Patrick Mijele, Domnic Nanteza, Anne Elati, Khawla Bishop, Richard The antigen recognition portion of African buffalo class I MHC is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurations |
title | The antigen recognition portion of African buffalo class I MHC is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurations |
title_full | The antigen recognition portion of African buffalo class I MHC is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurations |
title_fullStr | The antigen recognition portion of African buffalo class I MHC is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurations |
title_full_unstemmed | The antigen recognition portion of African buffalo class I MHC is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurations |
title_short | The antigen recognition portion of African buffalo class I MHC is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurations |
title_sort | antigen recognition portion of african buffalo class i mhc is highly polymorphic, consistent with a complex pathogen challenge environment, and the 3’ region suggests distinct haplotype configurations |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039833/ https://www.ncbi.nlm.nih.gov/pubmed/36512055 http://dx.doi.org/10.1007/s00251-022-01287-0 |
work_keys_str_mv | AT obaraisaiah theantigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT nijhofard theantigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT atimnedipatrick theantigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT mijeledomnic theantigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT nantezaanne theantigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT elatikhawla theantigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT bishoprichard theantigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT obaraisaiah antigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT nijhofard antigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT atimnedipatrick antigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT mijeledomnic antigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT nantezaanne antigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT elatikhawla antigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations AT bishoprichard antigenrecognitionportionofafricanbuffaloclassimhcishighlypolymorphicconsistentwithacomplexpathogenchallengeenvironmentandthe3regionsuggestsdistincthaplotypeconfigurations |