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Candidate Genes Associated with Susceptibility for SARS-Coronavirus

Assuming that no human had any previously acquired immunoprotection against severe acute respiratory syndrome coronavirus (SARS-CoV) during the 2003 SARS outbreak, the biological bases for possible difference in individual susceptibility are intriguing. However, this issue has never been fully eluci...

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Autores principales: Hsieh, Ying-Hen, Chen, Cathy W. S., Schmitz, Shu-Fang Hsu, King, Chwan-Chuan, Chen, Wei-Ju, Wu, Yi-Chun, Ho, Mei-Shang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089239/
https://www.ncbi.nlm.nih.gov/pubmed/19590927
http://dx.doi.org/10.1007/s11538-009-9440-8
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author Hsieh, Ying-Hen
Chen, Cathy W. S.
Schmitz, Shu-Fang Hsu
King, Chwan-Chuan
Chen, Wei-Ju
Wu, Yi-Chun
Ho, Mei-Shang
author_facet Hsieh, Ying-Hen
Chen, Cathy W. S.
Schmitz, Shu-Fang Hsu
King, Chwan-Chuan
Chen, Wei-Ju
Wu, Yi-Chun
Ho, Mei-Shang
author_sort Hsieh, Ying-Hen
collection PubMed
description Assuming that no human had any previously acquired immunoprotection against severe acute respiratory syndrome coronavirus (SARS-CoV) during the 2003 SARS outbreak, the biological bases for possible difference in individual susceptibility are intriguing. However, this issue has never been fully elucidated. Based on the premise that SARS patients belonging to a given genotype group having a significantly higher SARS infection rate than others would imply that genotype group being more susceptible, we make use of a compartmental model describing disease transmission dynamics and clinical and gene data of 100 laboratory confirmed SARS patients from Chinese Han population in Taiwan to estimate the infection rates of distinct candidate genotype groups among these SARS-infected individuals. The results show that CXCL10(−938AA) is always protective whenever it appears, but appears rarely and only jointly with either Fgl2(+158T/*) or HO-1(−497A/*), while (Fgl2)(+158T/*) is associated with higher susceptibility unless combined with CXCL10/IP-10(−938AA), when jointly is associated with lower susceptibility. The novel modeling approach proposed, which does not require sizable case and control gene datasets, could have important future public health implications in swiftly identifying potential high-risk groups associated with being highly susceptible to a particular infectious disease.
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spelling pubmed-70892392020-03-23 Candidate Genes Associated with Susceptibility for SARS-Coronavirus Hsieh, Ying-Hen Chen, Cathy W. S. Schmitz, Shu-Fang Hsu King, Chwan-Chuan Chen, Wei-Ju Wu, Yi-Chun Ho, Mei-Shang Bull Math Biol Original Article Assuming that no human had any previously acquired immunoprotection against severe acute respiratory syndrome coronavirus (SARS-CoV) during the 2003 SARS outbreak, the biological bases for possible difference in individual susceptibility are intriguing. However, this issue has never been fully elucidated. Based on the premise that SARS patients belonging to a given genotype group having a significantly higher SARS infection rate than others would imply that genotype group being more susceptible, we make use of a compartmental model describing disease transmission dynamics and clinical and gene data of 100 laboratory confirmed SARS patients from Chinese Han population in Taiwan to estimate the infection rates of distinct candidate genotype groups among these SARS-infected individuals. The results show that CXCL10(−938AA) is always protective whenever it appears, but appears rarely and only jointly with either Fgl2(+158T/*) or HO-1(−497A/*), while (Fgl2)(+158T/*) is associated with higher susceptibility unless combined with CXCL10/IP-10(−938AA), when jointly is associated with lower susceptibility. The novel modeling approach proposed, which does not require sizable case and control gene datasets, could have important future public health implications in swiftly identifying potential high-risk groups associated with being highly susceptible to a particular infectious disease. Springer-Verlag 2009-07-10 2010 /pmc/articles/PMC7089239/ /pubmed/19590927 http://dx.doi.org/10.1007/s11538-009-9440-8 Text en © Society for Mathematical Biology 2009 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 Article
Hsieh, Ying-Hen
Chen, Cathy W. S.
Schmitz, Shu-Fang Hsu
King, Chwan-Chuan
Chen, Wei-Ju
Wu, Yi-Chun
Ho, Mei-Shang
Candidate Genes Associated with Susceptibility for SARS-Coronavirus
title Candidate Genes Associated with Susceptibility for SARS-Coronavirus
title_full Candidate Genes Associated with Susceptibility for SARS-Coronavirus
title_fullStr Candidate Genes Associated with Susceptibility for SARS-Coronavirus
title_full_unstemmed Candidate Genes Associated with Susceptibility for SARS-Coronavirus
title_short Candidate Genes Associated with Susceptibility for SARS-Coronavirus
title_sort candidate genes associated with susceptibility for sars-coronavirus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089239/
https://www.ncbi.nlm.nih.gov/pubmed/19590927
http://dx.doi.org/10.1007/s11538-009-9440-8
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