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A functional polymorphism in IFNAR1 gene is associated with susceptibility and severity of HFMD with EV71 infection
Enterovirus 71 (EV71), one of the major pathogens of Hand, foot and mouth disease (HFMD), results in millions of infections and hundreds of deaths each year in Southeast Asia. Biased infection and variable clinical manifestations of EV71 HFMD indicated that host genetic background played an importan...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683517/ https://www.ncbi.nlm.nih.gov/pubmed/26679744 http://dx.doi.org/10.1038/srep18541 |
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author | Zou, Rongrong Zhang, Guoliang Li, Shaoyuan Wang, Wenfei Yuan, Jing Li, Jianming Wang, Yanrong Lin, Yimin Deng, Yong Zhou, Boping Gao, George Fu Liu, Yingxia |
author_facet | Zou, Rongrong Zhang, Guoliang Li, Shaoyuan Wang, Wenfei Yuan, Jing Li, Jianming Wang, Yanrong Lin, Yimin Deng, Yong Zhou, Boping Gao, George Fu Liu, Yingxia |
author_sort | Zou, Rongrong |
collection | PubMed |
description | Enterovirus 71 (EV71), one of the major pathogens of Hand, foot and mouth disease (HFMD), results in millions of infections and hundreds of deaths each year in Southeast Asia. Biased infection and variable clinical manifestations of EV71 HFMD indicated that host genetic background played an important role in the occurrence and development of the disease. We identified the mRNA profiles of EV71 HFMD patients, which type I interferon (IFN) pathway related genes were down-regulated. Four single nucleotide polymorphisms (SNPs) of type I IFN receptor 1 (IFNAR1) were chosen to analyze their relationships to EV71 infection. We found that genotype GG of promoter variant rs2843710 was associated with the susceptibility and severity to EV71 HFMD. In addition, we assessed the regulatory effects of rs2843710 to IFN stimulated genes (ISGs), and found that the expressions of IFNAR1, OAS1 and MX1 were significantly lower in patients with rs2843710 genotype GG. And rs2843710 allele G showed weaker transcriptional activity compared with allele C. Our study indicated that rs2843710 of IFNAR1 was associated with the susceptibility and severity of EV71 HFMD in Chinese Han populations, acting as a functional polymorphism by regulating ISGs expression, such as OAS1 and MX1. |
format | Online Article Text |
id | pubmed-4683517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46835172015-12-21 A functional polymorphism in IFNAR1 gene is associated with susceptibility and severity of HFMD with EV71 infection Zou, Rongrong Zhang, Guoliang Li, Shaoyuan Wang, Wenfei Yuan, Jing Li, Jianming Wang, Yanrong Lin, Yimin Deng, Yong Zhou, Boping Gao, George Fu Liu, Yingxia Sci Rep Article Enterovirus 71 (EV71), one of the major pathogens of Hand, foot and mouth disease (HFMD), results in millions of infections and hundreds of deaths each year in Southeast Asia. Biased infection and variable clinical manifestations of EV71 HFMD indicated that host genetic background played an important role in the occurrence and development of the disease. We identified the mRNA profiles of EV71 HFMD patients, which type I interferon (IFN) pathway related genes were down-regulated. Four single nucleotide polymorphisms (SNPs) of type I IFN receptor 1 (IFNAR1) were chosen to analyze their relationships to EV71 infection. We found that genotype GG of promoter variant rs2843710 was associated with the susceptibility and severity to EV71 HFMD. In addition, we assessed the regulatory effects of rs2843710 to IFN stimulated genes (ISGs), and found that the expressions of IFNAR1, OAS1 and MX1 were significantly lower in patients with rs2843710 genotype GG. And rs2843710 allele G showed weaker transcriptional activity compared with allele C. Our study indicated that rs2843710 of IFNAR1 was associated with the susceptibility and severity of EV71 HFMD in Chinese Han populations, acting as a functional polymorphism by regulating ISGs expression, such as OAS1 and MX1. Nature Publishing Group 2015-12-18 /pmc/articles/PMC4683517/ /pubmed/26679744 http://dx.doi.org/10.1038/srep18541 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zou, Rongrong Zhang, Guoliang Li, Shaoyuan Wang, Wenfei Yuan, Jing Li, Jianming Wang, Yanrong Lin, Yimin Deng, Yong Zhou, Boping Gao, George Fu Liu, Yingxia A functional polymorphism in IFNAR1 gene is associated with susceptibility and severity of HFMD with EV71 infection |
title | A functional polymorphism in IFNAR1 gene is associated with susceptibility and severity of HFMD with EV71 infection |
title_full | A functional polymorphism in IFNAR1 gene is associated with susceptibility and severity of HFMD with EV71 infection |
title_fullStr | A functional polymorphism in IFNAR1 gene is associated with susceptibility and severity of HFMD with EV71 infection |
title_full_unstemmed | A functional polymorphism in IFNAR1 gene is associated with susceptibility and severity of HFMD with EV71 infection |
title_short | A functional polymorphism in IFNAR1 gene is associated with susceptibility and severity of HFMD with EV71 infection |
title_sort | functional polymorphism in ifnar1 gene is associated with susceptibility and severity of hfmd with ev71 infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683517/ https://www.ncbi.nlm.nih.gov/pubmed/26679744 http://dx.doi.org/10.1038/srep18541 |
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