Virological features and pathogenicity of SARS-CoV-2 Omicron BA.2

Jasper Fuk Woo Chan, Bingjie Hu, Yue Chai, Huiping Shuai, Huan Liu, Jialu Shi, Yuanchen Liu, Chaemin Yoon, Jinjin Zhang, Jing Chu Hu, Yuxin Hou, Xiner Huang, Terrence Tsz Tai Yuen, Tianrenzheng Zhu, Wenjun Li, Jian Piao Cai, Cuiting Luo, Cyril Chik Yan Yip, Anna Jinxia Zhang, Jie ZhouShuofeng Yuan, Bao Zhong Zhang, Jian Dong Huang, Kelvin Kai Wang To, Kwok Yung Yuen, Hin Chu

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34 Citations (Scopus)

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron BA.2 was a dominant circulating SARS-CoV-2 variant worldwide. Recent reports hint that BA.2 is similarly potent regarding antibody evasion but may be more transmissible than BA.1. The pathogenicity of BA.2 remains unclear and is of critical public health significance. Here we investigated the virological features and pathogenicity of BA.2 with in vitro and in vivo models. We show that BA.2 is less dependent on transmembrane protease serine 2 (TMPRSS2) for virus entry in comparison with BA.1 in vitro. In K18-hACE2 mice, BA.2 replicates more efficiently than BA.1 in the nasal turbinates and replicates marginally less efficiently in the lungs, leading to decreased body weight loss and improved survival. Our study indicates that BA.2 is similarly attenuated in lungs compared with BA.1 but is potentially more transmissible because of its better replication at the nasal turbinates.

Original languageEnglish
Article number100743
JournalCell Reports Medicine
Volume3
Issue number9
DOIs
Publication statusPublished - Sept 20 2022
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2022 The Author(s)

ASJC Scopus Subject Areas

  • General Biochemistry,Genetics and Molecular Biology

Keywords

  • BA.1
  • BA.2
  • COVID-19
  • Omicron
  • SARS-CoV-2
  • TMPRSS2
  • pathogenicity
  • replication

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