Distinct Cell Transcriptomic Landscapes Upon Henipavirus Infections

Hendra virus (HeV) and Cedar virus (CedV) are henipaviruses, which fall into the Paramyxoviridae family of single-stranded, negative-sense RNA viruses. HeV is classified as a Biosafety Level-4 (BSL-4) agent, as it is highly pathogenic and is often fatal to humans. To date, no HeV prevention or treat...

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Main Authors: Mingyue Chen, Mary Tachedjian, Glenn A. Marsh, Jie Cui, Lin-Fa Wang
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-05-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2020.00986/full
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author Mingyue Chen
Mingyue Chen
Mingyue Chen
Mary Tachedjian
Glenn A. Marsh
Jie Cui
Jie Cui
Lin-Fa Wang
Lin-Fa Wang
author_facet Mingyue Chen
Mingyue Chen
Mingyue Chen
Mary Tachedjian
Glenn A. Marsh
Jie Cui
Jie Cui
Lin-Fa Wang
Lin-Fa Wang
author_sort Mingyue Chen
collection DOAJ
description Hendra virus (HeV) and Cedar virus (CedV) are henipaviruses, which fall into the Paramyxoviridae family of single-stranded, negative-sense RNA viruses. HeV is classified as a Biosafety Level-4 (BSL-4) agent, as it is highly pathogenic and is often fatal to humans. To date, no HeV prevention or treatment methods for human are available. In contrast, previous experimental infection studies have suggested that CedV is non-pathogenic. Flying foxes (pteropid bats) in Australia are the natural reservoirs of both viruses, but the cellular responses of bats to these viral infections remain unclear. Here, we infected bat and human cells with these viruses. We then examined the total transcriptomic landscapes of the cells at 6 or 24 h post infection. Unexpectedly, despite the close phylogenetic relationship between HeV and CedV, there was a dramatic difference in cellular gene expression patterns in response to the two different infections. It is likely that minor differences in the phosphoprotein (P) gene coding strategy between the two viruses cause the observed incongruence in host transcriptomic divergence and viral lethality. This study greatly expands our understanding of the pathogenic mechanisms of henipaviruses.
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spelling doaj.art-61fa85021cc34bc1a0de1d661d8641e12022-12-22T00:16:02ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2020-05-011110.3389/fmicb.2020.00986528301Distinct Cell Transcriptomic Landscapes Upon Henipavirus InfectionsMingyue Chen0Mingyue Chen1Mingyue Chen2Mary Tachedjian3Glenn A. Marsh4Jie Cui5Jie Cui6Lin-Fa Wang7Lin-Fa Wang8Key Laboratory of Fermentation Engineering, National 111 Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, ChinaCAS Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, ChinaCenter for Biosafety Mega-Science, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, ChinaCAS Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, ChinaAustralian Animal Health Laboratory, CSIRO Health and Biosecurity, Geelong, VIC, AustraliaCAS Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, ChinaCenter for Biosafety Mega-Science, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, ChinaAustralian Animal Health Laboratory, CSIRO Health and Biosecurity, Geelong, VIC, AustraliaProgramme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, SingaporeHendra virus (HeV) and Cedar virus (CedV) are henipaviruses, which fall into the Paramyxoviridae family of single-stranded, negative-sense RNA viruses. HeV is classified as a Biosafety Level-4 (BSL-4) agent, as it is highly pathogenic and is often fatal to humans. To date, no HeV prevention or treatment methods for human are available. In contrast, previous experimental infection studies have suggested that CedV is non-pathogenic. Flying foxes (pteropid bats) in Australia are the natural reservoirs of both viruses, but the cellular responses of bats to these viral infections remain unclear. Here, we infected bat and human cells with these viruses. We then examined the total transcriptomic landscapes of the cells at 6 or 24 h post infection. Unexpectedly, despite the close phylogenetic relationship between HeV and CedV, there was a dramatic difference in cellular gene expression patterns in response to the two different infections. It is likely that minor differences in the phosphoprotein (P) gene coding strategy between the two viruses cause the observed incongruence in host transcriptomic divergence and viral lethality. This study greatly expands our understanding of the pathogenic mechanisms of henipaviruses.https://www.frontiersin.org/article/10.3389/fmicb.2020.00986/fullbats (Chiroptera)Hendra virus (HeV)Cedar virustranscriptomaticscell infection
spellingShingle Mingyue Chen
Mingyue Chen
Mingyue Chen
Mary Tachedjian
Glenn A. Marsh
Jie Cui
Jie Cui
Lin-Fa Wang
Lin-Fa Wang
Distinct Cell Transcriptomic Landscapes Upon Henipavirus Infections
Frontiers in Microbiology
bats (Chiroptera)
Hendra virus (HeV)
Cedar virus
transcriptomatics
cell infection
title Distinct Cell Transcriptomic Landscapes Upon Henipavirus Infections
title_full Distinct Cell Transcriptomic Landscapes Upon Henipavirus Infections
title_fullStr Distinct Cell Transcriptomic Landscapes Upon Henipavirus Infections
title_full_unstemmed Distinct Cell Transcriptomic Landscapes Upon Henipavirus Infections
title_short Distinct Cell Transcriptomic Landscapes Upon Henipavirus Infections
title_sort distinct cell transcriptomic landscapes upon henipavirus infections
topic bats (Chiroptera)
Hendra virus (HeV)
Cedar virus
transcriptomatics
cell infection
url https://www.frontiersin.org/article/10.3389/fmicb.2020.00986/full
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