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MHC class I characterization of Indonesian cynomolgus macaques
Cynomolgus macaques (Macaca fascicularis) are quickly becoming a useful model for infectious disease and transplantation research. Even though cynomolgus macaques from different geographic regions are used for these studies, there has been limited characterization of full-length major histocompatibi...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2612123/ https://www.ncbi.nlm.nih.gov/pubmed/18504574 http://dx.doi.org/10.1007/s00251-008-0292-4 |
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author | Pendley, Chad J. Becker, Ericka A. Karl, Julie A. Blasky, Alex J. Wiseman, Roger W. Hughes, Austin L. O’Connor, Shelby L. O’Connor, David H. |
author_facet | Pendley, Chad J. Becker, Ericka A. Karl, Julie A. Blasky, Alex J. Wiseman, Roger W. Hughes, Austin L. O’Connor, Shelby L. O’Connor, David H. |
author_sort | Pendley, Chad J. |
collection | PubMed |
description | Cynomolgus macaques (Macaca fascicularis) are quickly becoming a useful model for infectious disease and transplantation research. Even though cynomolgus macaques from different geographic regions are used for these studies, there has been limited characterization of full-length major histocompatibility complex (MHC) class I immunogenetics of distinct geographic populations. Here, we identified 48 MHC class I cDNA nucleotide sequences in eleven Indonesian cynomolgus macaques, including 41 novel Mafa-A and Mafa-B sequences. We found seven MHC class I sequences in Indonesian macaques that were identical to MHC class I sequences identified in Malaysian or Mauritian macaques. Sharing of nucleotide sequences between these geographically distinct populations is also consistent with the hypothesis that Indonesia was a source of the Mauritian macaque population. In addition, we found that the Indonesian cDNA sequence Mafa-B*7601 is identical throughout its peptide binding domain to Mamu-B*03, an allele that has been associated with control of Simian immunodeficiency virus (SIV) viremia in Indian rhesus macaques. Overall, a better understanding of the MHC class I alleles present in Indonesian cynomolgus macaques improves their value as a model for disease research, and it better defines the biogeography of cynomolgus macaques throughout Southeast Asia. |
format | Text |
id | pubmed-2612123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-26121232008-12-30 MHC class I characterization of Indonesian cynomolgus macaques Pendley, Chad J. Becker, Ericka A. Karl, Julie A. Blasky, Alex J. Wiseman, Roger W. Hughes, Austin L. O’Connor, Shelby L. O’Connor, David H. Immunogenetics Original Paper Cynomolgus macaques (Macaca fascicularis) are quickly becoming a useful model for infectious disease and transplantation research. Even though cynomolgus macaques from different geographic regions are used for these studies, there has been limited characterization of full-length major histocompatibility complex (MHC) class I immunogenetics of distinct geographic populations. Here, we identified 48 MHC class I cDNA nucleotide sequences in eleven Indonesian cynomolgus macaques, including 41 novel Mafa-A and Mafa-B sequences. We found seven MHC class I sequences in Indonesian macaques that were identical to MHC class I sequences identified in Malaysian or Mauritian macaques. Sharing of nucleotide sequences between these geographically distinct populations is also consistent with the hypothesis that Indonesia was a source of the Mauritian macaque population. In addition, we found that the Indonesian cDNA sequence Mafa-B*7601 is identical throughout its peptide binding domain to Mamu-B*03, an allele that has been associated with control of Simian immunodeficiency virus (SIV) viremia in Indian rhesus macaques. Overall, a better understanding of the MHC class I alleles present in Indonesian cynomolgus macaques improves their value as a model for disease research, and it better defines the biogeography of cynomolgus macaques throughout Southeast Asia. Springer-Verlag 2008-05-27 2008 /pmc/articles/PMC2612123/ /pubmed/18504574 http://dx.doi.org/10.1007/s00251-008-0292-4 Text en © Springer-Verlag 2008 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Paper Pendley, Chad J. Becker, Ericka A. Karl, Julie A. Blasky, Alex J. Wiseman, Roger W. Hughes, Austin L. O’Connor, Shelby L. O’Connor, David H. MHC class I characterization of Indonesian cynomolgus macaques |
title | MHC class I characterization of Indonesian cynomolgus macaques |
title_full | MHC class I characterization of Indonesian cynomolgus macaques |
title_fullStr | MHC class I characterization of Indonesian cynomolgus macaques |
title_full_unstemmed | MHC class I characterization of Indonesian cynomolgus macaques |
title_short | MHC class I characterization of Indonesian cynomolgus macaques |
title_sort | mhc class i characterization of indonesian cynomolgus macaques |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2612123/ https://www.ncbi.nlm.nih.gov/pubmed/18504574 http://dx.doi.org/10.1007/s00251-008-0292-4 |
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