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Syrian hamsters as a small animal model for SARS-CoV-2 infection and countermeasure development

Authors :
Yuri Furusawa
Noriko Kinoshita
Noriko Nakajima
Tadaki Suzuki
Aaron Balogh
Tokiko Watanabe
Peter Halfmann
Samantha Loeber
Moe Okuda
Mutsumi Ito
Seiya Yamayoshi
Makoto Takeda
Lizheng Guan
Florian Krammer
Shufang Fan
Kenta Takahashi
Kiyoko Iwatsuki-Horimoto
Masaki Imai
Hiroshi Ueki
Tammy Armbrust
Masato Hatta
Shin-ichiro Hattori
Tiago J. S. Lopes
Atsuhiro Yasuhara
Shiho Chiba
Yuko Sakai-Tagawa
Norio Ohmagari
Shinya Yamada
Hiroaki Mitsuya
Makoto Kuroda
Michiko Ujie
Yoshihiro Kawaoka
Maki Kiso
Kosuke Takada
Source :
Proceedings of the National Academy of Sciences of the United States of America, Proceedings of the National Academy of Sciences
Publication Year :
2020

Abstract

Significance Since SARS-CoV-2 emerged in China, it has spread rapidly around the world. Effective vaccines and therapeutics for SARS-CoV-2−induced disease (coronavirus disease 2019;COVID-19) are urgently needed. We found that SARS-CoV-2 isolates replicate efficiently in the lungs of Syrian hamsters and cause severe pathological lesions in the lungs of these animals similar to commonly reported imaging features of COVID-19 patients with pneumonia. SARS-CoV-2−infected hamsters mounted neutralizing antibody responses and were protected against rechallenge with SARS-CoV-2. Moreover, passive transfer of convalescent serum to naïve hamsters inhibited virus replication in their lungs. Syrian hamsters are a useful small animal model for the evaluation of vaccines, immunotherapies, and antiviral drugs.<br />At the end of 2019, a novel coronavirus (severe acute respiratory syndrome coronavirus 2; SARS-CoV-2) was detected in Wuhan, China, that spread rapidly around the world, with severe consequences for human health and the global economy. Here, we assessed the replicative ability and pathogenesis of SARS-CoV-2 isolates in Syrian hamsters. SARS-CoV-2 isolates replicated efficiently in the lungs of hamsters, causing severe pathological lung lesions following intranasal infection. In addition, microcomputed tomographic imaging revealed severe lung injury that shared characteristics with SARS-CoV-2−infected human lung, including severe, bilateral, peripherally distributed, multilobular ground glass opacity, and regions of lung consolidation. SARS-CoV-2−infected hamsters mounted neutralizing antibody responses and were protected against subsequent rechallenge with SARS-CoV-2. Moreover, passive transfer of convalescent serum to naïve hamsters efficiently suppressed the replication of the virus in the lungs even when the serum was administrated 2 d postinfection of the serum-treated hamsters. Collectively, these findings demonstrate that this Syrian hamster model will be useful for understanding SARS-CoV-2 pathogenesis and testing vaccines and antiviral drugs.

Details

ISSN :
10916490
Volume :
117
Issue :
28
Database :
OpenAIRE
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Accession number :
edsair.doi.dedup.....5f0539f8aab636401be64a8deaca8e30