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High-Resolution HLA Typing of HLA-A, -B, -C, -DRB1, and -DQB1 in Kinh Vietnamese by Using Next-Generation Sequencing
Human leukocyte antigen (HLA) genotyping displays the particular characteristics of HLA alleles and haplotype frequencies in each population. Although it is considered the current gold standard for HLA typing, high-resolution sequence-based HLA typing is currently unavailable in Kinh Vietnamese popu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204072/ https://www.ncbi.nlm.nih.gov/pubmed/32425978 http://dx.doi.org/10.3389/fgene.2020.00383 |
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author | Do, Minh Duc Le, Linh Gia Hoang Nguyen, Vinh The Dang, Tran Ngoc Nguyen, Nghia Hoai Vu, Hoang Anh Mai, Thao Phuong |
author_facet | Do, Minh Duc Le, Linh Gia Hoang Nguyen, Vinh The Dang, Tran Ngoc Nguyen, Nghia Hoai Vu, Hoang Anh Mai, Thao Phuong |
author_sort | Do, Minh Duc |
collection | PubMed |
description | Human leukocyte antigen (HLA) genotyping displays the particular characteristics of HLA alleles and haplotype frequencies in each population. Although it is considered the current gold standard for HLA typing, high-resolution sequence-based HLA typing is currently unavailable in Kinh Vietnamese populations. In this study, high-resolution sequence-based HLA typing (3-field) was performed using an amplicon-based next-generation sequencing platform to identify the HLA-A, -B, -C, -DRB1, and -DQB1 alleles of 101 unrelated healthy Kinh Vietnamese individuals from southern Vietnam. A total of 28 HLA-A, 41 HLA-B, 21 HLA-C, 26 HLA-DRB1, and 25 HLA-DQB1 alleles were identified. The most frequently occurring HLA alleles were A(∗)11:01:01, B(∗)15:02:01, C(∗)07:02:01, DRB1(∗)12:02:01, and DQB1(∗)03:01:01. Haplotype calculation showed that A(∗)29:01:01∼B(∗)07:05:01, DRB1(∗)12:02:01∼DQB1(∗)3:01:01, A(∗)29:01:01∼C(∗)15:05:02∼B(∗)07:05:01, A(∗)33:03:01∼B(∗)58:01:01∼DRB1(∗)03:01:01, and A(∗)29:01:01∼C(∗)15:05:02∼B(∗)07:05:01∼DRB1(∗)10:01:01∼DQB1(∗)05:01:01 were the most common haplotypes in the southern Kinh Vietnamese population. Allele distribution and haplotype analyses demonstrated that the Vietnamese population shares HLA features with South-East Asians but retains unique characteristics. Data from this study will be potentially applicable in medicine and anthropology. |
format | Online Article Text |
id | pubmed-7204072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72040722020-05-18 High-Resolution HLA Typing of HLA-A, -B, -C, -DRB1, and -DQB1 in Kinh Vietnamese by Using Next-Generation Sequencing Do, Minh Duc Le, Linh Gia Hoang Nguyen, Vinh The Dang, Tran Ngoc Nguyen, Nghia Hoai Vu, Hoang Anh Mai, Thao Phuong Front Genet Genetics Human leukocyte antigen (HLA) genotyping displays the particular characteristics of HLA alleles and haplotype frequencies in each population. Although it is considered the current gold standard for HLA typing, high-resolution sequence-based HLA typing is currently unavailable in Kinh Vietnamese populations. In this study, high-resolution sequence-based HLA typing (3-field) was performed using an amplicon-based next-generation sequencing platform to identify the HLA-A, -B, -C, -DRB1, and -DQB1 alleles of 101 unrelated healthy Kinh Vietnamese individuals from southern Vietnam. A total of 28 HLA-A, 41 HLA-B, 21 HLA-C, 26 HLA-DRB1, and 25 HLA-DQB1 alleles were identified. The most frequently occurring HLA alleles were A(∗)11:01:01, B(∗)15:02:01, C(∗)07:02:01, DRB1(∗)12:02:01, and DQB1(∗)03:01:01. Haplotype calculation showed that A(∗)29:01:01∼B(∗)07:05:01, DRB1(∗)12:02:01∼DQB1(∗)3:01:01, A(∗)29:01:01∼C(∗)15:05:02∼B(∗)07:05:01, A(∗)33:03:01∼B(∗)58:01:01∼DRB1(∗)03:01:01, and A(∗)29:01:01∼C(∗)15:05:02∼B(∗)07:05:01∼DRB1(∗)10:01:01∼DQB1(∗)05:01:01 were the most common haplotypes in the southern Kinh Vietnamese population. Allele distribution and haplotype analyses demonstrated that the Vietnamese population shares HLA features with South-East Asians but retains unique characteristics. Data from this study will be potentially applicable in medicine and anthropology. Frontiers Media S.A. 2020-04-30 /pmc/articles/PMC7204072/ /pubmed/32425978 http://dx.doi.org/10.3389/fgene.2020.00383 Text en Copyright © 2020 Do, Le, Nguyen, Dang, Nguyen, Vu and Mai. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Do, Minh Duc Le, Linh Gia Hoang Nguyen, Vinh The Dang, Tran Ngoc Nguyen, Nghia Hoai Vu, Hoang Anh Mai, Thao Phuong High-Resolution HLA Typing of HLA-A, -B, -C, -DRB1, and -DQB1 in Kinh Vietnamese by Using Next-Generation Sequencing |
title | High-Resolution HLA Typing of HLA-A, -B, -C, -DRB1, and -DQB1 in Kinh Vietnamese by Using Next-Generation Sequencing |
title_full | High-Resolution HLA Typing of HLA-A, -B, -C, -DRB1, and -DQB1 in Kinh Vietnamese by Using Next-Generation Sequencing |
title_fullStr | High-Resolution HLA Typing of HLA-A, -B, -C, -DRB1, and -DQB1 in Kinh Vietnamese by Using Next-Generation Sequencing |
title_full_unstemmed | High-Resolution HLA Typing of HLA-A, -B, -C, -DRB1, and -DQB1 in Kinh Vietnamese by Using Next-Generation Sequencing |
title_short | High-Resolution HLA Typing of HLA-A, -B, -C, -DRB1, and -DQB1 in Kinh Vietnamese by Using Next-Generation Sequencing |
title_sort | high-resolution hla typing of hla-a, -b, -c, -drb1, and -dqb1 in kinh vietnamese by using next-generation sequencing |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204072/ https://www.ncbi.nlm.nih.gov/pubmed/32425978 http://dx.doi.org/10.3389/fgene.2020.00383 |
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