Simulation of the Clinical and Pathological Manifestations of Coronavirus Disease 2019 (COVID-19) in a Golden Syrian Hamster Model: Implications for Disease Pathogenesis and Transmissibility

Author:

Chan Jasper Fuk-Woo123,Zhang Anna Jinxia1,Yuan Shuofeng1,Poon Vincent Kwok-Man1,Chan Chris Chung-Sing1,Lee Andrew Chak-Yiu1,Chan Wan-Mui1,Fan Zhimeng1,Tsoi Hoi-Wah1,Wen Lei1,Liang Ronghui1,Cao Jianli1,Chen Yanxia1,Tang Kaiming1,Luo Cuiting1,Cai Jian-Piao1,Kok Kin-Hang1,Chu Hin1,Chan Kwok-Hung1,Sridhar Siddharth123,Chen Zhiwei1,Chen Honglin1,To Kelvin Kai-Wang123,Yuen Kwok-Yung123

Affiliation:

1. State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China

2. Department of Clinical Microbiology and Infection Control, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China

3. Department of Microbiology, Queen Mary Hospital, Pokfulam, Hong Kong Special Administrative Region, China

Abstract

Abstract Background A physiological small-animal model that resembles COVID-19 with low mortality is lacking. Methods Molecular docking on the binding between angiotensin-converting enzyme 2 (ACE2) of common laboratory mammals and the receptor-binding domain of the surface spike protein of SARS-CoV-2 suggested that the golden Syrian hamster is an option. Virus challenge, contact transmission, and passive immunoprophylaxis studies were performed. Serial organ tissues and blood were harvested for histopathology, viral load and titer, chemokine/cytokine level, and neutralizing antibody titer. Results The Syrian hamster could be consistently infected by SARS-CoV-2. Maximal clinical signs of rapid breathing, weight loss, histopathological changes from the initial exudative phase of diffuse alveolar damage with extensive apoptosis to the later proliferative phase of tissue repair, airway and intestinal involvement with viral nucleocapsid protein expression, high lung viral load, and spleen and lymphoid atrophy associated with marked chemokine/cytokine activation were observed within the first week of virus challenge. The mean lung virus titer was between 105 and 107 TCID50/g. Challenged index hamsters consistently infected naive contact hamsters housed within the same cages, resulting in similar pathology but not weight loss. All infected hamsters recovered and developed mean serum neutralizing antibody titers ≥1:427 14 days postchallenge. Immunoprophylaxis with early convalescent serum achieved significant decrease in lung viral load but not in lung pathology. No consistent nonsynonymous adaptive mutation of the spike was found in viruses isolated from the infected hamsters. Conclusions Besides satisfying Koch’s postulates, this readily available hamster model is an important tool for studying transmission, pathogenesis, treatment, and vaccination against SARS-CoV-2.

Funder

Sanming Project of Medicine in Shenzhen, China

High Level-Hospital Program, Health Commission of Guangdong Province, China

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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