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Of mice and men: the host response to influenza virus infection
Influenza virus (IV) infections represent a very serious public health problem. At present, no established biomarkers exist to support diagnosis for respiratory viral infections and more importantly for severe IV disease. Studies in animal models are extremely important to understand the biological,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132725/ https://www.ncbi.nlm.nih.gov/pubmed/29947965 http://dx.doi.org/10.1007/s00335-018-9750-y |
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author | Kollmus, Heike Pilzner, Carolin Leist, Sarah R. Heise, Mark Geffers, Robert Schughart, Klaus |
author_facet | Kollmus, Heike Pilzner, Carolin Leist, Sarah R. Heise, Mark Geffers, Robert Schughart, Klaus |
author_sort | Kollmus, Heike |
collection | PubMed |
description | Influenza virus (IV) infections represent a very serious public health problem. At present, no established biomarkers exist to support diagnosis for respiratory viral infections and more importantly for severe IV disease. Studies in animal models are extremely important to understand the biological, genetic, and environmental factors that contribute to severe IV disease and to validate biomarker candidates from human studies. However, mouse human cross-species comparisons are often compromised by the fact that animal studies concentrate on the infected lungs, whereas in humans almost all studies use peripheral blood from patients. In addition, human studies do not consider genetic background as variable although human populations are genetically very diverse. Therefore, in this study, we performed a cross-species gene expression study of the peripheral blood from human patients and from the highly genetically diverse Collaborative Cross (CC) mouse population after IV infection. Our results demonstrate that changes of gene expression in individual genes are highly similar in mice and humans. The top-regulated genes in humans were also differentially regulated in mice. We conclude that the mouse is a highly valuable in vivo model system to validate and to discover gene candidates which can be used as biomarkers in humans. Furthermore, mouse studies allow confirmation of findings in humans in a well-controlled experimental system adding enormous value to the understanding of expression and function of human candidate genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00335-018-9750-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6132725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-61327252018-09-13 Of mice and men: the host response to influenza virus infection Kollmus, Heike Pilzner, Carolin Leist, Sarah R. Heise, Mark Geffers, Robert Schughart, Klaus Mamm Genome Article Influenza virus (IV) infections represent a very serious public health problem. At present, no established biomarkers exist to support diagnosis for respiratory viral infections and more importantly for severe IV disease. Studies in animal models are extremely important to understand the biological, genetic, and environmental factors that contribute to severe IV disease and to validate biomarker candidates from human studies. However, mouse human cross-species comparisons are often compromised by the fact that animal studies concentrate on the infected lungs, whereas in humans almost all studies use peripheral blood from patients. In addition, human studies do not consider genetic background as variable although human populations are genetically very diverse. Therefore, in this study, we performed a cross-species gene expression study of the peripheral blood from human patients and from the highly genetically diverse Collaborative Cross (CC) mouse population after IV infection. Our results demonstrate that changes of gene expression in individual genes are highly similar in mice and humans. The top-regulated genes in humans were also differentially regulated in mice. We conclude that the mouse is a highly valuable in vivo model system to validate and to discover gene candidates which can be used as biomarkers in humans. Furthermore, mouse studies allow confirmation of findings in humans in a well-controlled experimental system adding enormous value to the understanding of expression and function of human candidate genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00335-018-9750-y) contains supplementary material, which is available to authorized users. Springer US 2018-06-15 2018 /pmc/articles/PMC6132725/ /pubmed/29947965 http://dx.doi.org/10.1007/s00335-018-9750-y Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Kollmus, Heike Pilzner, Carolin Leist, Sarah R. Heise, Mark Geffers, Robert Schughart, Klaus Of mice and men: the host response to influenza virus infection |
title | Of mice and men: the host response to influenza virus infection |
title_full | Of mice and men: the host response to influenza virus infection |
title_fullStr | Of mice and men: the host response to influenza virus infection |
title_full_unstemmed | Of mice and men: the host response to influenza virus infection |
title_short | Of mice and men: the host response to influenza virus infection |
title_sort | of mice and men: the host response to influenza virus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132725/ https://www.ncbi.nlm.nih.gov/pubmed/29947965 http://dx.doi.org/10.1007/s00335-018-9750-y |
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