Low Environmental Temperature Exacerbates Severe Acute Respiratory Syndrome Coronavirus 2 Infection in Golden Syrian Hamsters

Author:

Chan Jasper Fuk-Woo1,Poon Vincent Kwok-Man1,Chan Chris Chung-Sing1,Chik Kenn Ka-Heng1,Tsang Jessica Oi-Ling1,Zou Zijiao1,Chan Chris Chun-Yiu1,Lee Andrew Chak-Yiu1,Li Can1,Liang Ronghui1,Cao Jianli1,Tang Kaiming1,Yuen Terrence Tsz-Tai1,Hu Bingjie1,Huang Xiner1,Chai Yue1,Shuai Huiping1,Luo Cuiting1,Cai Jian-Piao1,Chan Kwok-Hung1,Sridhar Siddharth1,Yin Feifei23,Kok Kin-Hang1,Chu Hin1,Zhang Anna Jinxia1,Yuan Shuofeng1,Yuen Kwok-Yung1345

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. Key Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, Hainan, China

3. Academician Workstation of Hainan Province, Hainan Medical University, Haikou, Hainan, China

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

5. Hainan Medical University-The University of Hong Kong Joint Laboratory of Tropical Infectious Diseases, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China

Abstract

Abstract Background The effect of low environmental temperature on viral shedding and disease severity of Coronavirus Disease 2019 (COVID-19) is uncertain. Methods We investigated the virological, clinical, pathological, and immunological changes in hamsters housed at room (21°C), low (12–15°C), and high (30–33°C) temperature after challenge by 105 plaque-forming units of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Results The nasal turbinate, trachea, and lung viral load and live virus titer were significantly higher (~0.5-log10 gene copies/β-actin, P < .05) in the low-temperature group at 7 days postinfection (dpi). The low-temperature group also demonstrated significantly higher level of tumor necrosis factor-α, interferon-γ (IFN-γ), interleukin-1β, and C-C motif chemokine ligand 3, and lower level of the antiviral IFN-α in lung tissues at 4 dpi than the other 2 groups. Their lungs were grossly and diffusely hemorrhagic, with more severe and diffuse alveolar and peribronchiolar inflammatory infiltration, bronchial epithelial cell death, and significantly higher mean total lung histology scores. By 7 dpi, the low-temperature group still showed persistent and severe alveolar inflammation and hemorrhage, and little alveolar cell proliferative changes of recovery. The viral loads in the oral swabs of the low-temperature group were significantly higher than those of the other two groups from 10 to 17 dpi by about 0.5–1.0 log10 gene copies/β-actin. The mean neutralizing antibody titer of the low-temperature group was significantly (P < .05) lower than that of the room temperature group at 7 dpi and 30 dpi. Conclusions This study provided in vivo evidence that low environmental temperature exacerbated the degree of virus shedding, disease severity, and tissue proinflammatory cytokines/chemokines expression, and suppressed the neutralizing antibody response of SARS-CoV-2-infected hamsters. Keeping warm in winter may reduce the severity of COVID-19.

Funder

Health and Medical Research Fund

Government of the Hong Kong Special Administrative Region

National Program on Key Research Project of China

Sanming Project of Medicine in Shenzhen, China

Major Science and Technology Program of Hainan Province

Hainan academician innovation platform

Hainan talent development project

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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