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Sensitization of Non-permissive Laboratory Mice to SARS-CoV-2 with a Replication-Deficient Adenovirus Expressing Human ACE2
Journal article   Open access   Peer reviewed

Sensitization of Non-permissive Laboratory Mice to SARS-CoV-2 with a Replication-Deficient Adenovirus Expressing Human ACE2

Lok-Yin Roy Wong, Kun Li, Jing Sun, Zhen Zhuang, Jincun Zhao, Paul B McCray and Stanley Perlman
STAR Protocols, Vol.1(3), pp.100169-100169
12/18/2020
DOI: 10.1016/j.xpro.2020.100169
PMID: 33377063
url
https://doi.org/10.1016/j.xpro.2020.100169View
Published (Version of record) Open Access

Abstract

Common laboratory mice such as BALB/c and C57BL/6 mice are not permissive to SARS-CoV2 infection. Sensitization of laboratory mice with Adenovirus expressing human ACE2 (Ad5-hACE2) provides a rapid model for testing viral intervention in vivo. Despite the lack of lethal outcome, Ad5-hACE2-sensitized mice show 20% weight loss on average upon viral challenge with infectious virus being detected at the site of sensitization. This protocol describes the sensitization and subsequent infection of common laboratory mice for use in testing anti-viral interventions. For complete details on the use and execution of this protocol, please refer to Sun et al. (2020). [Display omitted] •Sensitization of non-permissive laboratory mice to SARS-CoV-2 infection by Ad5-hACE2•A mouse model for SARS-CoV-2 infection for testing anti-viral interventions•Rapid model applicable to mice with different genetic backgrounds Common laboratory mice such as BALB/c and C57BL/6 mice are not permissive to SARS-CoV-2 infection. Sensitization of laboratory mice with Adenovirus expressing human ACE2 (Ad5-hACE2) provides a rapid model for testing viral intervention in vivo. Despite the lack of lethal outcome, Ad5-hACE2-sensitized mice show 20% weight loss on average upon viral challenge with infectious virus being detected at the site of sensitization. This protocol describes the sensitization and subsequent infection of common laboratory mice for use in testing anti-viral interventions.
Model Organisms Immunology

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