Sequence and diversity of MHC DQA and DQB genes of the owl monkey Aotus nancymaae

被引:50
作者
Diaz, D
Naegeli, M
Rodriguez, R
Nino-Vasquez, JJ
Moreno, A
Patarroyo, ME
Pluschke, G
Daubenberger, CA
机构
[1] Swiss Trop Inst, CH-4002 Basel, Switzerland
[2] Univ Nacl Colombia, Hosp San Juan de Dios, Inst Inmunol, Bogota, DC, Colombia
关键词
Aotus nancymaae; MHC class II DQ genes; allelic lineages; polymorphism; peptide binding;
D O I
10.1007/s002510000189
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The New World primate Aotus nancymaae has been recommended by the World Health Organization (WHO) as a model for evaluation of malaria vaccine candidates, given its susceptibility to experimental infection with the human malaria parasites Plasmodium falciparum and Plasmodium vivax. We present here the nucleotide sequences of the complete cDNA of MHC-DQA1 and of the polymorphic exon 2 segments of MHC-DQB1/DQB2. In a group of three nonrelated animals captured in the wild, five alleles of MHC-DQA1 could be identified. They all belong to one lineage, namely Aona-DQA1*27. This lineage has not been described in any other New World monkey species studied. In a group of 19 unrelated animals, 14 Aona-DQB1 alleles could be identified which are grouped into the two lineages Aona-DQB1*22 and Aona-DQB1*23. These lineages have been described previously in the common marmoset and cotton-top tamarin. In addition, two Aona-DQB2 sequences could be identified which are highly similar to HLA-DQB2 sequences. Essential amino acid residues contributing to MHC DQ peptide binding pockets number 1 and 4 are conserved or semi-conserved between HLA-DQ and Aona-DQ molecules, indicating a capacity to bind similar peptide repertoires. These results fully support the use of Aotus monkeys as an animal model for evaluation of future subunit vaccine candidates.
引用
收藏
页码:528 / 537
页数:10
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