Spike destabilization attenuates Mink Cluster 5 SARS-CoV-2

J Julia N. Faraone (Center for Retrovirus Research, The Ohio State University) P Pei Li (Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, P. R. China) J Junping Hong (Center for Retrovirus Research, The Ohio State University) J Jinkai Zang (Center for Retrovirus Research, The Ohio State University) Y Yajie Liu (Center for Retrovirus Research, The Ohio State University) Y Yan Xu P Panke Qu (Center for Retrovirus Research, The Ohio State University) J John P. Evans (Center for Retrovirus Research, The Ohio State University) J Jie Chen Y Yi-Min Zheng (Center for Retrovirus Research, The Ohio State University) P Phylip Chen (Center for Microbe and Immunity Research, The Abigail Wexner Research Institute at Nationwide Children’s Hospital) M Mark E. Peeples (Center for Microbe and Immunity Research, The Abigail Wexner Research Institute at Nationwide Children’s Hospital) K Kai Xu S Shan-Lu Liu (Center for Retrovirus Research, The Ohio State University)

Abstract

Throughout the COVID-19 pandemic, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has shown the capacity to infect a wide range of nonhuman hosts, including farmed mink. In early 2020, a mink-associated variant, termed mink cluster 5 (MC5V), emerged in Denmark and spread to mink farmers and their household contacts but failed to cause a sustained outbreak and eventually disappeared. Here, we demonstrate that the spike protein (S) of MC5V is intrinsically unstable and impaired in processing, leading to markedly attenuated infectivity and fusogenicity. Remarkably, these defects are primarily driven by a single mutation, I692V, located in the S2 subunit of S, with additional contribution from the Y453F substitution in the receptor-binding domain. Structural analyses indicate that I692V induces conformational instability in S, promoting spontaneous S1 shedding and impairing spike incorporation into virions. These findings reveal that spike instability constrains viral fitness and emphasize the importance of monitoring zoonotic SARS-CoV-2 variants and other emerging viral pathogens.

Article Details

Volume / Issue Vol. 123, Issue 10
Published March 10, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (14)

J

Julia N. Faraone

Center for Retrovirus Research, The Ohio State University

P

Pei Li

Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, P. R. China

J

Junping Hong

Center for Retrovirus Research, The Ohio State University

J

Jinkai Zang

Center for Retrovirus Research, The Ohio State University

Y

Yajie Liu

Center for Retrovirus Research, The Ohio State University

Y

Yan Xu

P

Panke Qu

Center for Retrovirus Research, The Ohio State University

J

John P. Evans

Center for Retrovirus Research, The Ohio State University

J

Jie Chen

Y

Yi-Min Zheng

Center for Retrovirus Research, The Ohio State University

P

Phylip Chen

Center for Microbe and Immunity Research, The Abigail Wexner Research Institute at Nationwide Children’s Hospital

M

Mark E. Peeples

Center for Microbe and Immunity Research, The Abigail Wexner Research Institute at Nationwide Children’s Hospital

K

Kai Xu

S

Shan-Lu Liu

Center for Retrovirus Research, The Ohio State University