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About:
Mouse model of SARS-CoV-2 reveals inflammatory role of type I interferon signaling
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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
Mouse model of SARS-CoV-2 reveals inflammatory role of type I interferon signaling
Creator
Iwasaki, Akiko
Alfajaro, Mia
Wilen, Craig
Dong, Huiping
Homer, Robert
Israelow, Benjamin
Liu, Feimei
Lu, Peiwen
Mao, Tianyang
Meir, Amit
Ring, Aaron
Song, Eric
Wei, Jin
Source
BioRxiv; Medline; PMC; WHO
abstract
Severe Acute Respiratory Syndrome- Coronavirus 2 (SARS-Cov-2) has caused over 5,000,000 cases of Coronavirus disease (COVID-19) with significant fatality rate.(1–3) Due to the urgency of this global pandemic, numerous therapeutic and vaccine trials have begun without customary safety and efficacy studies.(4) Laboratory mice have been the stalwart of these types of studies; however, they do not support infection by SARS-CoV-2 due to the inability of its spike (S) protein to engage the mouse ortholog of its human entry receptor angiotensin-converting enzyme 2 (hACE2). While hACE2 transgenic mice support infection and pathogenesis,(5) these mice are currently limited in availability and are restricted to a single genetic background. Here we report the development of a mouse model of SARS-CoV-2 based on adeno associated virus (AAV)-mediated expression of hACE2. These mice support viral replication and antibody production and exhibit pathologic findings found in COVID-19 patients as well as non-human primate models. Moreover, we show that type I interferons are unable to control SARS-CoV2 replication and drive pathologic responses. Thus, the hACE2-AAV mouse model enables rapid deployment for in-depth analysis following robust SARS-CoV-2 infection with authentic patient-derived virus in mice of diverse genetic backgrounds. This represents a much-needed platform for rapidly testing prophylactic and therapeutic strategies to combat COVID-19.
has issue date
2020-05-27
(
xsd:dateTime
)
bibo:doi
10.1101/2020.05.27.118893
bibo:pmid
32577647
has license
cc-by-nc-nd
sha1sum (hex)
4e6c05be5e00d1f977ccf85a48372877fa522bf9
schema:url
https://doi.org/10.1101/2020.05.27.118893
resource representing a document's title
Mouse model of SARS-CoV-2 reveals inflammatory role of type I interferon signaling
has PubMed Central identifier
PMC7302201
has PubMed identifier
32577647
schema:publication
bioRxiv
resource representing a document's body
covid:4e6c05be5e00d1f977ccf85a48372877fa522bf9#body_text
is
schema:about
of
named entity 'numerous'
named entity 'models'
named entity 'global'
named entity 'pathogenesis'
named entity 'fatality rate'
named entity 'therapeutic'
named entity 'efficacy'
named entity 'safety'
named entity 'While'
named entity 'caused'
named entity 'receptor'
named entity 'authentic'
named entity 'AAV'
named entity 'AAV'
named entity 'support'
named entity 'support'
named entity 'pathologic'
named entity 'model'
named entity 'pathologic'
named entity 'type I interferons'
named entity 'AAV'
named entity 'non-human primate'
named entity 'mouse model'
named entity 'mouse model'
named entity 'Laboratory mice'
named entity 'COVID'
named entity 'vaccine'
named entity 'mice'
named entity 'Severe Acute Respiratory Syndrome'
named entity 'prophylactic'
named entity 'infection'
named entity 'type I interferon'
named entity 'SARS-CoV-2'
named entity 'Mouse model'
named entity 'inflammatory'
named entity 'PBS'
named entity 'virus'
named entity 'antibodies'
named entity 'mice'
named entity 'Supernatant'
named entity 'ketamine'
named entity 'immunocompromised'
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named entity 'SARS-CoV-2 virus'
named entity 'Meloxicam'
named entity 'mice'
named entity 'lung tissue'
named entity 'IRF3'
named entity 'COVID'
named entity 'cytokine'
named entity 'infection'
named entity '60 minutes'
named entity 'digestion'
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named entity 'IFNAR'
named entity 'SARS-CoV-1'
named entity 'gene'
named entity 'IRF3'
named entity 'IRF7'
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named entity 'infection'
named entity 'cellular processes'
named entity 'centrifugation'
named entity 'monocytes'
named entity 'lung'
named entity 'IRF3'
named entity 'monocyte-derived macrophages'
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