Roborovski hamster (Phodopus roborovskii) strain SH101 as a systemic infection model of SARS-CoV-2

Virulence. 2021 Dec;12(1):2430-2442. doi: 10.1080/21505594.2021.1972201.

Abstract

Severe acute respiratory syndrome CoV-2 (SARS-CoV-2) is currently causing a worldwide threat with its unusually high transmission rates and rapid evolution into diverse strains. Unlike typical respiratory viruses, SARS-CoV-2 frequently causes systemic infection by breaking the boundaries of the respiratory systems. The development of animal models recapitulating the clinical manifestations of COVID-19 is of utmost importance not only for the development of vaccines and antivirals but also for understanding the pathogenesis. However, there has not been developed an animal model for systemic infection of SARS-CoV-2 representing most aspects of the clinical manifestations of COVID-19 with systemic symptoms. Here we report that a Roborovski hamster strain SH101, a laboratory inbred hamster strain of P. roborovskii, displayed most symptoms of systemic infection upon SARS-CoV-2 infection as in the case of the human counterpart, unlike current COVID-19 animal models. Roborovski hamster strain SH101 post-infection of SARS-CoV-2 represented most clinical symptoms of COVID-19 such as snuffling, labored breathing, dyspnea, cough, hunched posture, progressive weight loss, ruffled fur, and high fever following shaking chills. Histological examinations also revealed initial right-predominated pneumonia as well as slight organ damages in the brain and liver, manifesting systemic COVID-19 cases. Considering the merit of a small animal as well as its clinical manifestations of SARS-CoV-2 infection in human, this hamster model seems to provide an ideal tool to investigate COVID-19.

Keywords: COVID-19 animal model; Phodopus roborovskii SH101; SARS-CoV-2; roborovski hamster.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Temperature
  • Brain / pathology
  • COVID-19* / pathology
  • COVID-19* / physiopathology
  • Cricetinae / classification*
  • Disease Models, Animal*
  • Female
  • Liver / pathology
  • Lung / pathology
  • Male
  • Mesocricetus
  • Mice
  • Mice, Transgenic
  • SARS-CoV-2*

Grants and funding

This research was supported by JINIS BDRD Research Institute of JINIS Biopharmaceuticals Inc. (Initial of authors who received fund: S. H.) and the Korea Basic Science Institute (KBSI) [grant C130000] (Initial of authors who received fund: H. J. C.).