tetano
Editor, Senior Moderator
Emerg Microbes Infect
. 2020 Oct 17;1-19.
doi: 10.1080/22221751.2020.1838955. Online ahead of print.
Comparison of Transgenic and Adenovirus hACE2 Mouse Models for SARS-CoV-2 Infection
Raveen Rathnasinghe[SUP] 1 2 3 [/SUP], Shirin Strohmeier[SUP] 1 3 [/SUP], Fatima Amanat[SUP] 1 3 [/SUP], Virginia L Gillespie[SUP] 4 [/SUP], Florian Krammer[SUP] 1 [/SUP], Adolfo Garc?a-Sastre[SUP] 1 2 5 6 [/SUP], Lynda Coughlan[SUP] 1 7 [/SUP], Michael Schotsaert[SUP] 1 2 [/SUP], Melissa Uccellini[SUP] 1 2 [/SUP]
Affiliations
Abstract
Severe acute respiratory syndrome CoV-2 (SARS-CoV-2) is currently causing a worldwide pandemic with high morbidity and mortality. Development of animal models that recapitulate important aspects of coronavirus disease 2019 (COVID-19) is critical for the evaluation of vaccines and antivirals, and understanding disease pathogenesis. SARS-CoV-2 has been shown to use the same entry receptor as SARS-CoV-1, human angiotensin-converting enzyme 2 (hACE2)(1-3). Due to amino acid differences between murine and hACE2, inbred mouse strains fail to support high titer viral replication of SARS-CoV-2 virus. Therefore, a number of transgenic and knock-in mouse models, as well as viral vector-mediated hACE2 delivery systems have been developed. Here we compared the K18-hACE2 transgenic model to adenovirus-mediated delivery of hACE2 to the mouse lung. We show that K18-hACE2 mice replicate virus to high titers in the nasal turbinates, lung and brain, with high lethality, and cytokine/chemokine production. In contrast, adenovirus-mediated delivery results in viral replication to lower titers limited to the nasal turbinates and lung, and no clinical signs of infection with a challenge dose of 10[SUP]4[/SUP] plaque forming units. The K18-hACE2 model provides a stringent model for testing the ability of vaccines and antivirals to protect against disease, whereas the adenovirus delivery system has the flexibility to be used across multiple genetic backgrounds and modified mouse strains.
Keywords: ACE2; Adenovirus; COVID-19; SARS-CoV-2.
. 2020 Oct 17;1-19.
doi: 10.1080/22221751.2020.1838955. Online ahead of print.
Comparison of Transgenic and Adenovirus hACE2 Mouse Models for SARS-CoV-2 Infection
Raveen Rathnasinghe[SUP] 1 2 3 [/SUP], Shirin Strohmeier[SUP] 1 3 [/SUP], Fatima Amanat[SUP] 1 3 [/SUP], Virginia L Gillespie[SUP] 4 [/SUP], Florian Krammer[SUP] 1 [/SUP], Adolfo Garc?a-Sastre[SUP] 1 2 5 6 [/SUP], Lynda Coughlan[SUP] 1 7 [/SUP], Michael Schotsaert[SUP] 1 2 [/SUP], Melissa Uccellini[SUP] 1 2 [/SUP]
Affiliations
- PMID: 33073694
- DOI: 10.1080/22221751.2020.1838955
Abstract
Severe acute respiratory syndrome CoV-2 (SARS-CoV-2) is currently causing a worldwide pandemic with high morbidity and mortality. Development of animal models that recapitulate important aspects of coronavirus disease 2019 (COVID-19) is critical for the evaluation of vaccines and antivirals, and understanding disease pathogenesis. SARS-CoV-2 has been shown to use the same entry receptor as SARS-CoV-1, human angiotensin-converting enzyme 2 (hACE2)(1-3). Due to amino acid differences between murine and hACE2, inbred mouse strains fail to support high titer viral replication of SARS-CoV-2 virus. Therefore, a number of transgenic and knock-in mouse models, as well as viral vector-mediated hACE2 delivery systems have been developed. Here we compared the K18-hACE2 transgenic model to adenovirus-mediated delivery of hACE2 to the mouse lung. We show that K18-hACE2 mice replicate virus to high titers in the nasal turbinates, lung and brain, with high lethality, and cytokine/chemokine production. In contrast, adenovirus-mediated delivery results in viral replication to lower titers limited to the nasal turbinates and lung, and no clinical signs of infection with a challenge dose of 10[SUP]4[/SUP] plaque forming units. The K18-hACE2 model provides a stringent model for testing the ability of vaccines and antivirals to protect against disease, whereas the adenovirus delivery system has the flexibility to be used across multiple genetic backgrounds and modified mouse strains.
Keywords: ACE2; Adenovirus; COVID-19; SARS-CoV-2.