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IFITM3 Rs12252-C Variant Increases Potential Risk for Severe Influenza Virus Infection in Chinese Population
Background: Interferon Inducible Transmembrane 3 (IFITM3) is a key factor in interferon pathway and it involves host's immune response against multiple viruses. IFITM3 rs12252-C was associated with severe influenza virus infection in several studies, however whether this association is universa...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491636/ https://www.ncbi.nlm.nih.gov/pubmed/28713779 http://dx.doi.org/10.3389/fcimb.2017.00294 |
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author | Pan, Yang Yang, Peng Dong, Tao Zhang, Yi Shi, Weixian Peng, Xiaomin Cui, Shujuan Zhang, Daitao Lu, Guilan Liu, Yimeng Wu, Shuangsheng Wang, Quanyi |
author_facet | Pan, Yang Yang, Peng Dong, Tao Zhang, Yi Shi, Weixian Peng, Xiaomin Cui, Shujuan Zhang, Daitao Lu, Guilan Liu, Yimeng Wu, Shuangsheng Wang, Quanyi |
author_sort | Pan, Yang |
collection | PubMed |
description | Background: Interferon Inducible Transmembrane 3 (IFITM3) is a key factor in interferon pathway and it involves host's immune response against multiple viruses. IFITM3 rs12252-C was associated with severe influenza virus infection in several studies, however whether this association is universal to all types of influenza virus or diverse ethnic populations remain controversial. Method: A case-control genetic association study was performed from September 2013 to April 2014 and September 2014 to April 2015. All samples were tested for influenza using RT-PCR, and genotyped by High Resolution Melting assay. Results: A total of 65 healthy people, 165 mild influenza-like illness (ILI) cases and 315 severe acute respiratory infection (SARI) cases were enrolled in this study. The frequency of CC genotype was much higher in SARI cases with IVI than that in ILI cases with IVI (61.59 vs. 27.16%), leading a 4.67-fold greater risk for severe IVI than other two genotypes. Moreover, the risk of IFITM3 rs12252-C variant for severe IVI was specific for both influenza A and influenza B. Conclusion: IFITM3 rs12252 CC genotype was associated with severity rather than susceptibility of IVI in Chinese population, and this strong effect was observed in all subtypes of seasonal influenza infection. |
format | Online Article Text |
id | pubmed-5491636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54916362017-07-14 IFITM3 Rs12252-C Variant Increases Potential Risk for Severe Influenza Virus Infection in Chinese Population Pan, Yang Yang, Peng Dong, Tao Zhang, Yi Shi, Weixian Peng, Xiaomin Cui, Shujuan Zhang, Daitao Lu, Guilan Liu, Yimeng Wu, Shuangsheng Wang, Quanyi Front Cell Infect Microbiol Microbiology Background: Interferon Inducible Transmembrane 3 (IFITM3) is a key factor in interferon pathway and it involves host's immune response against multiple viruses. IFITM3 rs12252-C was associated with severe influenza virus infection in several studies, however whether this association is universal to all types of influenza virus or diverse ethnic populations remain controversial. Method: A case-control genetic association study was performed from September 2013 to April 2014 and September 2014 to April 2015. All samples were tested for influenza using RT-PCR, and genotyped by High Resolution Melting assay. Results: A total of 65 healthy people, 165 mild influenza-like illness (ILI) cases and 315 severe acute respiratory infection (SARI) cases were enrolled in this study. The frequency of CC genotype was much higher in SARI cases with IVI than that in ILI cases with IVI (61.59 vs. 27.16%), leading a 4.67-fold greater risk for severe IVI than other two genotypes. Moreover, the risk of IFITM3 rs12252-C variant for severe IVI was specific for both influenza A and influenza B. Conclusion: IFITM3 rs12252 CC genotype was associated with severity rather than susceptibility of IVI in Chinese population, and this strong effect was observed in all subtypes of seasonal influenza infection. Frontiers Media S.A. 2017-06-30 /pmc/articles/PMC5491636/ /pubmed/28713779 http://dx.doi.org/10.3389/fcimb.2017.00294 Text en Copyright © 2017 Pan, Yang, Dong, Zhang, Shi, Peng, Cui, Zhang, Lu, Liu, Wu and Wang. 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) or licensor 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 | Microbiology Pan, Yang Yang, Peng Dong, Tao Zhang, Yi Shi, Weixian Peng, Xiaomin Cui, Shujuan Zhang, Daitao Lu, Guilan Liu, Yimeng Wu, Shuangsheng Wang, Quanyi IFITM3 Rs12252-C Variant Increases Potential Risk for Severe Influenza Virus Infection in Chinese Population |
title | IFITM3 Rs12252-C Variant Increases Potential Risk for Severe Influenza Virus Infection in Chinese Population |
title_full | IFITM3 Rs12252-C Variant Increases Potential Risk for Severe Influenza Virus Infection in Chinese Population |
title_fullStr | IFITM3 Rs12252-C Variant Increases Potential Risk for Severe Influenza Virus Infection in Chinese Population |
title_full_unstemmed | IFITM3 Rs12252-C Variant Increases Potential Risk for Severe Influenza Virus Infection in Chinese Population |
title_short | IFITM3 Rs12252-C Variant Increases Potential Risk for Severe Influenza Virus Infection in Chinese Population |
title_sort | ifitm3 rs12252-c variant increases potential risk for severe influenza virus infection in chinese population |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491636/ https://www.ncbi.nlm.nih.gov/pubmed/28713779 http://dx.doi.org/10.3389/fcimb.2017.00294 |
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