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The SARS-CoV-2 Omicron (B.1.1.529) variant exhibits altered pathogenicity, transmissibility, and fitness in the golden Syrian hamster model
Shuofeng Yuan; Zi-Wei Ye; Ronghui Liang; Kaiming Tang; Anna Jinxia Zhang; Gang Lu; Chon Phin Ong; Vincent Kwok-Man Poon; Chris Chung-Sing Chan; Bobo Wing Yee Mok; Zhenzhi Qin; Yubin Xie; Haoran Sun; Jessica Oi-Ling Tsang; Terrence Tsz-Tai Yuen; Kenn Ka-Heng Chik; Chris Chun-Yiu Chan; Jian-Piao Cai; Cuiting Luo; Lu Lu; Cyril Chik-Yan Yip; Hin Chu; Kelvin Kai-Wang To; Honglin Chen; Dong-Yan Jin; Kwok-Yung Yuen; Jasper F.W. Chan.
Affiliation
  • Shuofeng Yuan; The University of Hong Kong
  • Zi-Wei Ye; The University of Hong Kong
  • Ronghui Liang; The University of Hong Kong
  • Kaiming Tang; The University of Hong Kong
  • Anna Jinxia Zhang; The University of Hong Kong
  • Gang Lu; Hainan Medical College
  • Chon Phin Ong; The University of Hong Kong
  • Vincent Kwok-Man Poon; The University of Hong Kong
  • Chris Chung-Sing Chan; The University of Hong Kong
  • Bobo Wing Yee Mok; University of Hong Kong
  • Zhenzhi Qin; The University of Hong Kong
  • Yubin Xie; The University of Hong Kong
  • Haoran Sun; The University of Hong Kong
  • Jessica Oi-Ling Tsang; The University of Hong Kong
  • Terrence Tsz-Tai Yuen; The University of Hong Kong
  • Kenn Ka-Heng Chik; The University of Hong Kong
  • Chris Chun-Yiu Chan; The University of Hong Kong
  • Jian-Piao Cai; The University of Hong Kong
  • Cuiting Luo; The University of Hong Kong
  • Lu Lu; The University of Hong Kong
  • Cyril Chik-Yan Yip; The University of Hong Kong
  • Hin Chu; The University of Hong Kong
  • Kelvin Kai-Wang To; University of Hong Kong
  • Honglin Chen; The University of Hong Kong
  • Dong-Yan Jin; The University of Hong Kong
  • Kwok-Yung Yuen; The University of Hong Kong
  • Jasper F.W. Chan; University of Hong Kong
Preprint in English | bioRxiv | ID: ppbiorxiv-476031
ABSTRACT
The newly emerging SARS-CoV-2 Omicron (B.1.1.529) variant first identified in South Africa in November 2021 is characterized by an unusual number of amino acid mutations in its spike that renders existing vaccines and therapeutic monoclonal antibodies dramatically less effective. The in vivo pathogenicity, transmissibility, and fitness of this new Variant of Concerns are unknown. We investigated these virological attributes of the Omicron variant in comparison with those of the currently dominant Delta (B.1.617.2) variant in the golden Syrian hamster COVID-19 model. Omicron-infected hamsters developed significantly less body weight losses, clinical scores, respiratory tract viral burdens, cytokine/chemokine dysregulation, and tissue damages than Delta-infected hamsters. The Omicron and Delta variant were both highly transmissible (100% vs 100%) via contact transmission. Importantly, the Omicron variant consistently demonstrated about 10-20% higher transmissibility than the already-highly transmissible Delta variant in repeated non-contact transmission studies (overall 30/36 vs 24/36, 83.3% vs 66.7%). The Delta variant displayed higher fitness advantage than the Omicron variant without selection pressure in both in vitro and in vivo competition models. However, this scenario drastically changed once immune selection pressure with neutralizing antibodies active against the Delta variant but poorly active against the Omicron variant were introduced, with the Omicron variant significantly outcompeting the Delta variant. Taken together, our findings demonstrated that while the Omicron variant is less pathogenic than the Delta variant, it is highly transmissible and can outcompete the Delta variant under immune selection pressure. Next-generation vaccines and antivirals effective against this new VOC are urgently needed. One Sentence SummaryThe novel SARS-CoV-2 Omicron variant, though less pathogenic, is highly transmissible and outcompetes the Delta variant under immune selection pressure in the golden Syrian hamster COVID-19 model.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2022 Document type: Preprint
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