Your browser doesn't support javascript.
Human angiotensin-converting enzyme 2 transgenic mice infected with SARS-CoV-2 develop severe and fatal respiratory disease.
Golden, Joseph W; Cline, Curtis R; Zeng, Xiankun; Garrison, Aura R; Carey, Brian D; Mucker, Eric M; White, Lauren E; Shamblin, Joshua D; Brocato, Rebecca L; Liu, Jun; Babka, April M; Rauch, Hypaitia B; Smith, Jeffrey M; Hollidge, Bradley S; Fitzpatrick, Collin; Badger, Catherine V; Hooper, Jay W.
  • Golden JW; Virology Division.
  • Cline CR; Pathology.
  • Zeng X; Pathology.
  • Garrison AR; Virology Division.
  • Carey BD; Diagnostic Systems Division, and.
  • Mucker EM; Virology Division.
  • White LE; Veterinary Medicine Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Maryland, USA.
  • Shamblin JD; Veterinary Medicine Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Maryland, USA.
  • Brocato RL; Virology Division.
  • Liu J; Pathology.
  • Babka AM; Pathology.
  • Rauch HB; Diagnostic Systems Division, and.
  • Smith JM; Virology Division.
  • Hollidge BS; Virology Division.
  • Fitzpatrick C; Virology Division.
  • Badger CV; Virology Division.
  • Hooper JW; Virology Division.
JCI Insight ; 5(19)2020 10 02.
Article in English | MEDLINE | ID: covidwho-1388620
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
See preprint
ABSTRACT
The emergence of SARS-CoV-2 has created an international health crisis, and small animal models mirroring SARS-CoV-2 human disease are essential for medical countermeasure (MCM) development. Mice are refractory to SARS-CoV-2 infection owing to low-affinity binding to the murine angiotensin-converting enzyme 2 (ACE2) protein. Here, we evaluated the pathogenesis of SARS-CoV-2 in male and female mice expressing the human ACE2 gene under the control of the keratin 18 promoter (K18). In contrast to nontransgenic mice, intranasal exposure of K18-hACE2 animals to 2 different doses of SARS-CoV-2 resulted in acute disease, including weight loss, lung injury, brain infection, and lethality. Vasculitis was the most prominent finding in the lungs of infected mice. Transcriptomic analysis from lungs of infected animals showed increases in transcripts involved in lung injury and inflammatory cytokines. In the low-dose challenge groups, there was a survival advantage in the female mice, with 60% surviving infection, whereas all male mice succumbed to disease. Male mice that succumbed to disease had higher levels of inflammatory transcripts compared with female mice. To our knowledge, this is the first highly lethal murine infection model for SARS-CoV-2 and should be valuable for the study of SARS-CoV-2 pathogenesis and for the assessment of MCMs.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Cause of Death / Coronavirus Infections / Peptidyl-Dipeptidase A / Disease Progression / Severe Acute Respiratory Syndrome Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Limits: Animals / Female / Humans / Male Language: English Year: 2020 Document Type: Article

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Cause of Death / Coronavirus Infections / Peptidyl-Dipeptidase A / Disease Progression / Severe Acute Respiratory Syndrome Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Limits: Animals / Female / Humans / Male Language: English Year: 2020 Document Type: Article