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A novel hamster model of SARS-CoV-2 respiratory infection using a pseudotyped virus.
Yamada, Hiroshi; Sasaki, So-Ichiro; Tani, Hideki; Somekawa, Mayu; Kawasuji, Hitoshi; Saga, Yumiko; Yoshida, Yoshihiro; Yamamoto, Yoshihiro; Hayakawa, Yoshihiro; Morinaga, Yoshitomo.
  • Yamada H; Department of Microbiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.
  • Sasaki SI; Section of Host Defences, Institute of Natural Medicine, University of Toyama, Toyama, Japan.
  • Tani H; Department of Virology, Toyama Institute of Health, Toyama, Japan.
  • Somekawa M; Department of Microbiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.
  • Kawasuji H; Department of Clinical Infectious Diseases, Toyama University Graduate School of Medicine and Pharmaceutical Sciences, Toyama, Japan.
  • Saga Y; Department of Virology, Toyama Institute of Health, Toyama, Japan.
  • Yoshida Y; Department of Microbiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.
  • Yamamoto Y; Department of Clinical Infectious Diseases, Toyama University Graduate School of Medicine and Pharmaceutical Sciences, Toyama, Japan.
  • Hayakawa Y; Section of Host Defences, Institute of Natural Medicine, University of Toyama, Toyama, Japan.
  • Morinaga Y; Department of Microbiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan. morinaga@med.u-toyama.ac.jp.
Sci Rep ; 12(1): 11125, 2022 07 01.
Article in English | MEDLINE | ID: covidwho-2028698
ABSTRACT
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a biosafety level (BSL)-3 pathogen; therefore, its research environment is limited. Pseudotyped viruses that mimic the infection of SARS-CoV-2 have been widely used for in vitro evaluation because they are available in BSL-2 containment laboratories. However, in vivo application is inadequate. Therefore, animal models instigated with animal BSL-2 will provide opportunities for in vivo evaluation. Hamsters (6-10-week-old males) were intratracheally inoculated with luciferase-expressing vesicular stomatitis virus (VSV)-based SARS-CoV-2 pseudotyped virus. The lungs were harvested 24-72 h after inoculation and luminescence was measured using an in vivo imaging system. Lung luminescence after inoculation with the SARS-CoV-2 pseudotyped virus increased in a dose-dependent manner and peaked at 48 h. The VSV-G (envelope G) pseudotyped virus also induced luminescence; however, a 100-fold concentration was required to reach a level similar to that of the SARS-CoV-2 pseudotyped virus. The SARS-CoV-2 pseudotyped virus is applicable to SARS-CoV-2 respiratory infections in a hamster model. Because of the single-round infectious virus, the model can be used to study the steps from viral binding to entry, which will be useful for future research on SARS-CoV-2 entry without using live SARS-CoV-2 or transgenic animals.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies Limits: Animals Language: English Journal: Sci Rep Year: 2022 Document Type: Article Affiliation country: S41598-022-15258-8

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies Limits: Animals Language: English Journal: Sci Rep Year: 2022 Document Type: Article Affiliation country: S41598-022-15258-8