Shanghai Institute of Infectious Disease and Biosecurity, School of Public Health, Fudan University, Shanghai, China.
Shanghai Institute of Infectious Disease and Biosecurity, School of Public Health, Fudan University, Shanghai, China; Clinical Research Center, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Trends Microbiol. 2024 Jan;32(1):79-92. doi: 10.1016/j.tim.2023.07.002. Epub 2023 Aug 2.
The retransmissions of SARS-CoV-2 from several mammals - primarily mink and white-tailed deer - to humans have raised concerns for the emergence of a new animal-derived SARS-CoV-2 variant to worsen the pandemic. Here, we discuss animal species that are susceptible to natural or experimental infection with SARS-CoV-2 and can transmit the virus to mates or humans. We describe cutting-edge techniques to assess the impact of a mutation in the viral spike (S) protein on its receptor and on antibody binding. Our review of spike sequences of animal-derived viruses identified nine unique amino acid exchanges in the receptor-binding domain (RBD) that are not present in any variant of concern (VOC). These mutations are present in SARS-CoV-2 found in companion animals such as dogs and cats, and they exhibit a higher frequency in SARS-CoV-2 found in mink and white-tailed deer, suggesting that sustained transmissions may contribute to maintaining novel mutations. Four of these exchanges, such as Leu452Met, could undermine acquired immune protection in humans while maintaining high affinity for the human angiotensin-converting enzyme 2 (ACE2) receptor. Finally, we discuss important avenues of future research into animal-derived viruses with public health risks.
几种哺乳动物(主要是水貂和白尾鹿)向人类传播的 SARS-CoV-2 再感染引起了人们对新的源自动物的 SARS-CoV-2 变体出现以加重大流行的担忧。在这里,我们讨论了易受自然或实验性 SARS-CoV-2 感染的动物物种,这些动物可以将病毒传播给配偶或人类。我们描述了评估病毒刺突(S)蛋白突变对其受体和抗体结合的影响的尖端技术。我们对源自动物的病毒的刺突序列的综述确定了受体结合域(RBD)中九个独特的氨基酸交换,这些交换在任何关注的变体(VOC)中都不存在。这些突变存在于伴侣动物(如狗和猫)中的 SARS-CoV-2 中,并且在水貂和白尾鹿中发现的 SARS-CoV-2 中更为常见,这表明持续传播可能有助于维持新的突变。这四个交换中的 Leu452Met 等交换可能破坏人类获得的免疫保护,同时保持对人类血管紧张素转换酶 2(ACE2)受体的高亲和力。最后,我们讨论了对具有公共卫生风险的源自动物的病毒进行未来研究的重要途径。