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Comparative transcriptome analysis reveals the intensive early-stage responses of host cells to SARS-CoV-2 infection
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schema:ScholarlyArticle
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Comparative transcriptome analysis reveals the intensive early-stage responses of host cells to SARS-CoV-2 infection
Creator
Wang, Ming
Sheng, Jie
Tan, Wenjie
Huang, Baoying
Ye, Fei
Jiang, Taijiao
Wu, Aiping
Mao, Longfei
Pan, Mei
Sun, Jiya
Yang, Ren
Zhu, Wenjie
Source
BioRxiv
abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a widespread outbreak of highly pathogenic COVID-19. It is therefore important and timely to characterize interactions between the virus and host cell at the molecular level to understand its disease pathogenesis. To gain insights, we performed high-throughput sequencing that generated time-series data simultaneously for bioinformatics analysis of virus genomes and host transcriptomes implicated in SARS-CoV-2 infection. Our analysis results showed that the rapid growth of the virus was accompanied by an early intensive response of host genes. We also systematically compared the molecular footprints of the host cells in response to SARS-CoV-2, SARS-CoV and MERS-CoV. Upon infection, SARS-CoV-2 induced hundreds of up-regulated host genes hallmarked by a significant cytokine production followed by virus-specific host antiviral responses. While the cytokine and antiviral responses triggered by SARS-CoV and MERS-CoV were only observed during the late stage of infection, the host antiviral responses during the SARS-CoV-2 infection were gradually enhanced lagging behind the production of cytokine. The early rapid host responses were potentially attributed to the high efficiency of SARS-CoV-2 entry into host cells, underscored by evidence of a remarkably up-regulated gene expression of TPRMSS2 soon after infection. Taken together, our findings provide novel molecular insights into the mechanisms underlying the infectivity and pathogenicity of SARS-CoV-2.
has issue date
2020-05-01
(
xsd:dateTime
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bibo:doi
10.1101/2020.04.30.071274
has license
biorxiv
sha1sum (hex)
23c8b3c03d7e8df89898145ddcac6944e941ffe5
schema:url
https://doi.org/10.1101/2020.04.30.071274
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Comparative transcriptome analysis reveals the intensive early-stage responses of host cells to SARS-CoV-2 infection
schema:publication
bioRxiv
resource representing a document's body
covid:23c8b3c03d7e8df89898145ddcac6944e941ffe5#body_text
is
schema:about
of
named entity 'Our'
named entity 'performed'
named entity 'high-throughput sequencing'
named entity 'COVID-19'
named entity 'transcriptome'
named entity 'cells'
named entity 'responses'
covid:arg/23c8b3c03d7e8df89898145ddcac6944e941ffe5
named entity 'disease'
named entity 'SARS-CoV-2'
named entity 'virus'
named entity 'pathogenesis'
named entity 'host'
named entity 'molecular'
named entity 'caused'
named entity 'Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)'
named entity 'cell'
named entity 'Comparative'
named entity 'Severe acute respiratory syndrome coronavirus 2'
named entity 'SARS-CoV-2'
named entity 'host cells'
named entity 'host cells'
named entity 'SARS-CoV-2'
named entity 'hpi'
named entity 'gene expression'
named entity 'hpi'
named entity 'innate immune responses'
named entity 'MERS-CoV'
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named entity 'RNA-Seq'
named entity 'cDNA libraries'
named entity 'China'
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named entity 'SARS-CoV-2'
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named entity 'SARS-CoV'
named entity 'Differentially Expressed Genes'
named entity 'upper respiratory tract'
named entity 'host cells'
named entity 'interferon'
named entity 'IRF9'
named entity 'cell lines'
named entity 'coronavirus infections'
named entity 'penicillin'
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named entity 'DDX58'
named entity 'hpi'
named entity 'host response'
named entity 'metabolism'
named entity 'pathology'
named entity 'Coronavirus disease 2019'
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