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Chikungunya patient transcriptional signatures faithfully recapitulated in a C57BL/6J mouse model
INTRODUCTION: An adult wild-type C57BL/6J mouse model of chikungunya virus (CHIKV) infection and disease has been extensively used to study the alphaviral arthritic immunopathology and to evaluate new interventions. How well mouse models recapitulate the gene expression profiles seen in humans remai...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791225/ https://www.ncbi.nlm.nih.gov/pubmed/36578476 http://dx.doi.org/10.3389/fimmu.2022.1092370 |
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author | Bishop, Cameron R. Caten, Felipe Ten Nakaya, Helder I. Suhrbier, Andreas |
author_facet | Bishop, Cameron R. Caten, Felipe Ten Nakaya, Helder I. Suhrbier, Andreas |
author_sort | Bishop, Cameron R. |
collection | PubMed |
description | INTRODUCTION: An adult wild-type C57BL/6J mouse model of chikungunya virus (CHIKV) infection and disease has been extensively used to study the alphaviral arthritic immunopathology and to evaluate new interventions. How well mouse models recapitulate the gene expression profiles seen in humans remains controversial. METHODS: Herein we perform a comparative transcriptomics analysis using RNA-Seq datasets from the C57BL/6J CHIKV mouse model with datasets obtained from adults and children acutely infected with CHIKV. RESULTS: Despite sampling quite different tissues, peripheral blood from humans and feet from mice, gene expression profiles were quite similar, with an overlap of up to ≈50% for up-regulated single copy orthologue differentially expressed genes. Furthermore, high levels of significant concordance between mouse and human were seen for immune pathways and signatures, which were dominated by interferons, T cells and monocyte/macrophages. Importantly, predicted responses to a series of anti-inflammatory drug and biologic treatments also showed cogent similarities between species. DISCUSSION: Comparative transcriptomics and subsequent pathway analysis provides a detailed picture of how a given model recapitulates human gene expression. Using this method, we show that the C57BL/6J CHIKV mouse model provides a reliable and representative system in which to study CHIKV immunopathology and evaluate new treatments. |
format | Online Article Text |
id | pubmed-9791225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97912252022-12-27 Chikungunya patient transcriptional signatures faithfully recapitulated in a C57BL/6J mouse model Bishop, Cameron R. Caten, Felipe Ten Nakaya, Helder I. Suhrbier, Andreas Front Immunol Immunology INTRODUCTION: An adult wild-type C57BL/6J mouse model of chikungunya virus (CHIKV) infection and disease has been extensively used to study the alphaviral arthritic immunopathology and to evaluate new interventions. How well mouse models recapitulate the gene expression profiles seen in humans remains controversial. METHODS: Herein we perform a comparative transcriptomics analysis using RNA-Seq datasets from the C57BL/6J CHIKV mouse model with datasets obtained from adults and children acutely infected with CHIKV. RESULTS: Despite sampling quite different tissues, peripheral blood from humans and feet from mice, gene expression profiles were quite similar, with an overlap of up to ≈50% for up-regulated single copy orthologue differentially expressed genes. Furthermore, high levels of significant concordance between mouse and human were seen for immune pathways and signatures, which were dominated by interferons, T cells and monocyte/macrophages. Importantly, predicted responses to a series of anti-inflammatory drug and biologic treatments also showed cogent similarities between species. DISCUSSION: Comparative transcriptomics and subsequent pathway analysis provides a detailed picture of how a given model recapitulates human gene expression. Using this method, we show that the C57BL/6J CHIKV mouse model provides a reliable and representative system in which to study CHIKV immunopathology and evaluate new treatments. Frontiers Media S.A. 2022-12-12 /pmc/articles/PMC9791225/ /pubmed/36578476 http://dx.doi.org/10.3389/fimmu.2022.1092370 Text en Copyright © 2022 Bishop, Caten, Nakaya and Suhrbier https://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 | Immunology Bishop, Cameron R. Caten, Felipe Ten Nakaya, Helder I. Suhrbier, Andreas Chikungunya patient transcriptional signatures faithfully recapitulated in a C57BL/6J mouse model |
title | Chikungunya patient transcriptional signatures faithfully recapitulated in a C57BL/6J mouse model |
title_full | Chikungunya patient transcriptional signatures faithfully recapitulated in a C57BL/6J mouse model |
title_fullStr | Chikungunya patient transcriptional signatures faithfully recapitulated in a C57BL/6J mouse model |
title_full_unstemmed | Chikungunya patient transcriptional signatures faithfully recapitulated in a C57BL/6J mouse model |
title_short | Chikungunya patient transcriptional signatures faithfully recapitulated in a C57BL/6J mouse model |
title_sort | chikungunya patient transcriptional signatures faithfully recapitulated in a c57bl/6j mouse model |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791225/ https://www.ncbi.nlm.nih.gov/pubmed/36578476 http://dx.doi.org/10.3389/fimmu.2022.1092370 |
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