Cargando…
Establishment of a Novel Primary Human Skeletal Myoblast Cellular Model for Chikungunya Virus Infection and Pathogenesis
Chikungunya virus (CHIKV) is a re-emerging arbovirus known to cause chronic myalgia and arthralgia and is now considered endemic in countries across Asia and Africa. The tissue tropism of CHIKV infection in humans remains, however, ill-defined. Due to the fact that myositis is commonly observed in m...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759813/ https://www.ncbi.nlm.nih.gov/pubmed/26892458 http://dx.doi.org/10.1038/srep21406 |
_version_ | 1782416787315359744 |
---|---|
author | Hussain, Khairunnisa’ Mohamed Lee, Regina Ching Hua Ng, Mary Mah-Lee Chu, Justin Jang Hann |
author_facet | Hussain, Khairunnisa’ Mohamed Lee, Regina Ching Hua Ng, Mary Mah-Lee Chu, Justin Jang Hann |
author_sort | Hussain, Khairunnisa’ Mohamed |
collection | PubMed |
description | Chikungunya virus (CHIKV) is a re-emerging arbovirus known to cause chronic myalgia and arthralgia and is now considered endemic in countries across Asia and Africa. The tissue tropism of CHIKV infection in humans remains, however, ill-defined. Due to the fact that myositis is commonly observed in most patients infected with CHIKV, we sought to develop a clinically relevant cellular model to better understand the pathogenesis of CHIKV infection. In this study, primary human skeletal muscle myoblasts (HSMM) were established as a novel human primary cell line that is highly permissive to CHIKV infection, with maximal amounts of infectious virions observed at 16 hours post infection. Genome-wide microarray profiling analyses were subsequently performed to identify and map genes that are differentially expressed upon CHIKV infection. Infection of HSMM cells with CHIKV resulted in altered expressions of host genes involved in skeletal- and muscular-associated disorders, innate immune responses, cellular growth and death, host metabolism and virus replication. Together, this study has shown the establishment of a clinically relevant primary human cell model that paves the way for the further analysis of host factors and their involvement in the various stages of CHIKV replication cycle and viral pathogenesis. |
format | Online Article Text |
id | pubmed-4759813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47598132016-02-29 Establishment of a Novel Primary Human Skeletal Myoblast Cellular Model for Chikungunya Virus Infection and Pathogenesis Hussain, Khairunnisa’ Mohamed Lee, Regina Ching Hua Ng, Mary Mah-Lee Chu, Justin Jang Hann Sci Rep Article Chikungunya virus (CHIKV) is a re-emerging arbovirus known to cause chronic myalgia and arthralgia and is now considered endemic in countries across Asia and Africa. The tissue tropism of CHIKV infection in humans remains, however, ill-defined. Due to the fact that myositis is commonly observed in most patients infected with CHIKV, we sought to develop a clinically relevant cellular model to better understand the pathogenesis of CHIKV infection. In this study, primary human skeletal muscle myoblasts (HSMM) were established as a novel human primary cell line that is highly permissive to CHIKV infection, with maximal amounts of infectious virions observed at 16 hours post infection. Genome-wide microarray profiling analyses were subsequently performed to identify and map genes that are differentially expressed upon CHIKV infection. Infection of HSMM cells with CHIKV resulted in altered expressions of host genes involved in skeletal- and muscular-associated disorders, innate immune responses, cellular growth and death, host metabolism and virus replication. Together, this study has shown the establishment of a clinically relevant primary human cell model that paves the way for the further analysis of host factors and their involvement in the various stages of CHIKV replication cycle and viral pathogenesis. Nature Publishing Group 2016-02-19 /pmc/articles/PMC4759813/ /pubmed/26892458 http://dx.doi.org/10.1038/srep21406 Text en Copyright © 2016, 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 Hussain, Khairunnisa’ Mohamed Lee, Regina Ching Hua Ng, Mary Mah-Lee Chu, Justin Jang Hann Establishment of a Novel Primary Human Skeletal Myoblast Cellular Model for Chikungunya Virus Infection and Pathogenesis |
title | Establishment of a Novel Primary Human Skeletal Myoblast Cellular Model for Chikungunya Virus Infection and Pathogenesis |
title_full | Establishment of a Novel Primary Human Skeletal Myoblast Cellular Model for Chikungunya Virus Infection and Pathogenesis |
title_fullStr | Establishment of a Novel Primary Human Skeletal Myoblast Cellular Model for Chikungunya Virus Infection and Pathogenesis |
title_full_unstemmed | Establishment of a Novel Primary Human Skeletal Myoblast Cellular Model for Chikungunya Virus Infection and Pathogenesis |
title_short | Establishment of a Novel Primary Human Skeletal Myoblast Cellular Model for Chikungunya Virus Infection and Pathogenesis |
title_sort | establishment of a novel primary human skeletal myoblast cellular model for chikungunya virus infection and pathogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759813/ https://www.ncbi.nlm.nih.gov/pubmed/26892458 http://dx.doi.org/10.1038/srep21406 |
work_keys_str_mv | AT hussainkhairunnisamohamed establishmentofanovelprimaryhumanskeletalmyoblastcellularmodelforchikungunyavirusinfectionandpathogenesis AT leereginachinghua establishmentofanovelprimaryhumanskeletalmyoblastcellularmodelforchikungunyavirusinfectionandpathogenesis AT ngmarymahlee establishmentofanovelprimaryhumanskeletalmyoblastcellularmodelforchikungunyavirusinfectionandpathogenesis AT chujustinjanghann establishmentofanovelprimaryhumanskeletalmyoblastcellularmodelforchikungunyavirusinfectionandpathogenesis |