Pathogenicity, transmissibility, and fitness of SARS-CoV-2 Omicron in Syrian hamsters

The in vivo pathogenicity, transmissibility, and fitness of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron (B.1.1.529) variant are not well understood. We compared these virological attributes of this new variant of concern (VOC) with those of the Delta (B.1.617.2) variant...

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Published inScience (American Association for the Advancement of Science) Vol. 377; no. 6604; pp. 428 - 433
Main Authors Yuan, Shuofeng, Ye, Zi-Wei, Liang, Ronghui, Tang, Kaiming, Zhang, Anna Jinxia, Lu, Gang, Ong, Chon Phin, Man Poon, Vincent Kwok, Chan, Chris Chung-Sing, Mok, Bobo Wing-Yee, Qin, Zhenzhi, Xie, Yubin, Chu, Allen Wing-Ho, Chan, Wan-Mui, Ip, Jonathan Daniel, Sun, Haoran, Tsang, Jessica Oi-Ling, Yuen, Terrence Tsz-Tai, Chik, Kenn Ka-Heng, Chan, Chris Chun-Yiu, Cai, Jian-Piao, Luo, Cuiting, Lu, Lu, Yip, Cyril Chik-Yan, Chu, Hin, To, Kelvin Kai-Wang, Chen, Honglin, Jin, Dong-Yan, Yuen, Kwok-Yung, Chan, Jasper Fuk-Woo
Format Journal Article
LanguageEnglish
Published Washington The American Association for the Advancement of Science 22.07.2022
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Abstract The in vivo pathogenicity, transmissibility, and fitness of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron (B.1.1.529) variant are not well understood. We compared these virological attributes of this new variant of concern (VOC) with those of the Delta (B.1.617.2) variant in a Syrian hamster model of COVID-19. Omicron-infected hamsters lost significantly less body weight and exhibited reduced clinical scores, respiratory tract viral burdens, cytokine and chemokine dysregulation, and lung damage than Delta-infected hamsters. Both variants were highly transmissible through contact transmission. In noncontact transmission studies Omicron demonstrated similar or higher transmissibility than Delta. Delta outcompeted Omicron without selection pressure, but this scenario changed once immune selection pressure with neutralizing antibodies—active against Delta but poorly active against Omicron—was introduced. Next-generation vaccines and antivirals effective against this new VOC are therefore urgently needed. There is growing evidence that the Omicron variant of concern (VOC) is more transmissible and infectious than previous iterations of severe acute respiratory syndrome coronavirus 2. Yuan et al . compared Syrian hamsters exposed to either Omicron or Delta VOCs. Animals infected with Omicron showed lower respiratory tract viral burdens and reduced clinical severity. Nevertheless, Omicron was at least as transmissible as Delta, if not more so. When animals were challenged with a mixture of both variants, Delta outcompeted Omicron in naïve hamsters. This competitive advantage disappeared, however, in vaccinated animals. Moreover, vaccinated hamsters were better than unvaccinated animals at transmitting Omicron to co-housed companions. This work helps to clarify how Omicron might have gone on to become the predominant strain in populations with high rates of previous infection and vaccination. —STS Less pathogenic but highly transmissible, SARS-CoV-2 Omicron can outcompete Delta under immune selection pressure.
AbstractList The in vivo pathogenicity, transmissibility, and fitness of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron (B.1.1.529) variant are not well understood. We compared these virological attributes of this new variant of concern (VOC) with those of the Delta (B.1.617.2) variant in a Syrian hamster model of COVID-19. Omicron-infected hamsters lost significantly less body weight and exhibited reduced clinical scores, respiratory tract viral burdens, cytokine and chemokine dysregulation, and lung damage than Delta-infected hamsters. Both variants were highly transmissible through contact transmission. In noncontact transmission studies Omicron demonstrated similar or higher transmissibility than Delta. Delta outcompeted Omicron without selection pressure, but this scenario changed once immune selection pressure with neutralizing antibodies-active against Delta but poorly active against Omicron-was introduced. Next-generation vaccines and antivirals effective against this new VOC are therefore urgently needed.The in vivo pathogenicity, transmissibility, and fitness of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron (B.1.1.529) variant are not well understood. We compared these virological attributes of this new variant of concern (VOC) with those of the Delta (B.1.617.2) variant in a Syrian hamster model of COVID-19. Omicron-infected hamsters lost significantly less body weight and exhibited reduced clinical scores, respiratory tract viral burdens, cytokine and chemokine dysregulation, and lung damage than Delta-infected hamsters. Both variants were highly transmissible through contact transmission. In noncontact transmission studies Omicron demonstrated similar or higher transmissibility than Delta. Delta outcompeted Omicron without selection pressure, but this scenario changed once immune selection pressure with neutralizing antibodies-active against Delta but poorly active against Omicron-was introduced. Next-generation vaccines and antivirals effective against this new VOC are therefore urgently needed.
Delta and Omicron go toe to toeThere is growing evidence that the Omicron variant of concern (VOC) is more transmissible and infectious than previous iterations of severe acute respiratory syndrome coronavirus 2. Yuan et al. compared Syrian hamsters exposed to either Omicron or Delta VOCs. Animals infected with Omicron showed lower respiratory tract viral burdens and reduced clinical severity. Nevertheless, Omicron was at least as transmissible as Delta, if not more so. When animals were challenged with a mixture of both variants, Delta outcompeted Omicron in naïve hamsters. This competitive advantage disappeared, however, in vaccinated animals. Moreover, vaccinated hamsters were better than unvaccinated animals at transmitting Omicron to co-housed companions. This work helps to clarify how Omicron might have gone on to become the predominant strain in populations with high rates of previous infection and vaccination. —STS
The in vivo pathogenicity, transmissibility, and fitness of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron (B.1.1.529) variant are not well understood. We compared these virological attributes of this new variant of concern (VOC) with those of the Delta (B.1.617.2) variant in a Syrian hamster model of COVID-19. Omicron-infected hamsters lost significantly less body weight and exhibited reduced clinical scores, respiratory tract viral burdens, cytokine and chemokine dysregulation, and lung damage than Delta-infected hamsters. Both variants were highly transmissible through contact transmission. In noncontact transmission studies Omicron demonstrated similar or higher transmissibility than Delta. Delta outcompeted Omicron without selection pressure, but this scenario changed once immune selection pressure with neutralizing antibodies—active against Delta but poorly active against Omicron—was introduced. Next-generation vaccines and antivirals effective against this new VOC are therefore urgently needed. There is growing evidence that the Omicron variant of concern (VOC) is more transmissible and infectious than previous iterations of severe acute respiratory syndrome coronavirus 2. Yuan et al . compared Syrian hamsters exposed to either Omicron or Delta VOCs. Animals infected with Omicron showed lower respiratory tract viral burdens and reduced clinical severity. Nevertheless, Omicron was at least as transmissible as Delta, if not more so. When animals were challenged with a mixture of both variants, Delta outcompeted Omicron in naïve hamsters. This competitive advantage disappeared, however, in vaccinated animals. Moreover, vaccinated hamsters were better than unvaccinated animals at transmitting Omicron to co-housed companions. This work helps to clarify how Omicron might have gone on to become the predominant strain in populations with high rates of previous infection and vaccination. —STS Less pathogenic but highly transmissible, SARS-CoV-2 Omicron can outcompete Delta under immune selection pressure.
Author Luo, Cuiting
Sun, Haoran
Jin, Dong-Yan
Chan, Jasper Fuk-Woo
Chan, Wan-Mui
Zhang, Anna Jinxia
Xie, Yubin
To, Kelvin Kai-Wang
Chan, Chris Chung-Sing
Tsang, Jessica Oi-Ling
Chan, Chris Chun-Yiu
Mok, Bobo Wing-Yee
Lu, Gang
Yuan, Shuofeng
Qin, Zhenzhi
Chen, Honglin
Chu, Allen Wing-Ho
Ip, Jonathan Daniel
Ye, Zi-Wei
Cai, Jian-Piao
Yuen, Kwok-Yung
Chu, Hin
Tang, Kaiming
Chik, Kenn Ka-Heng
Liang, Ronghui
Lu, Lu
Ong, Chon Phin
Yuen, Terrence Tsz-Tai
Man Poon, Vincent Kwok
Yip, Cyril Chik-Yan
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  givenname: Shuofeng
  orcidid: 0000-0001-7996-1119
  surname: Yuan
  fullname: Yuan, Shuofeng
  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
– sequence: 2
  givenname: Zi-Wei
  orcidid: 0000-0002-6446-4299
  surname: Ye
  fullname: Ye, Zi-Wei
  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  givenname: Ronghui
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  givenname: Kaiming
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  surname: Tang
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  givenname: Anna Jinxia
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  givenname: Gang
  orcidid: 0000-0003-4695-2325
  surname: Lu
  fullname: Lu, Gang
  organization: Key Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, Hainan, China., Academician Workstation of Hainan Province, Hainan Medical University-The University of Hong Kong Joint Laboratory of Tropical Infectious Diseases, Hainan Medical University, Haikou, Hainan, China; and The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  givenname: Chon Phin
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  surname: Ong
  fullname: Ong, Chon Phin
  organization: School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
– sequence: 8
  givenname: Vincent Kwok
  orcidid: 0000-0002-7737-8912
  surname: Man Poon
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong Special Administrative Region, China
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  givenname: Chris Chung-Sing
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  surname: Chan
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong Special Administrative Region, China
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  givenname: Bobo Wing-Yee
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  surname: Mok
  fullname: Mok, Bobo Wing-Yee
  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
– sequence: 11
  givenname: Zhenzhi
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  givenname: Yubin
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  surname: Xie
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
– sequence: 13
  givenname: Allen Wing-Ho
  surname: Chu
  fullname: Chu, Allen Wing-Ho
  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
– sequence: 14
  givenname: Wan-Mui
  surname: Chan
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  givenname: Jonathan Daniel
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  orcidid: 0000-0001-6488-6531
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  organization: Department of Infectious Disease and Microbiology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong Province, China
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  givenname: Jessica Oi-Ling
  surname: Tsang
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong Special Administrative Region, China
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  givenname: Chris Chun-Yiu
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  givenname: Jian-Piao
  orcidid: 0000-0003-4077-3852
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
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  givenname: Cuiting
  surname: Luo
  fullname: Luo, Cuiting
  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China
– sequence: 23
  givenname: Lu
  surname: Lu
  fullname: Lu, Lu
  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong Special Administrative Region, China
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  givenname: Cyril Chik-Yan
  surname: Yip
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  organization: Department of Infectious Disease and Microbiology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong Province, China
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  givenname: Hin
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  givenname: Kelvin Kai-Wang
  orcidid: 0000-0002-1921-5824
  surname: To
  fullname: To, Kelvin Kai-Wang
  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong Special Administrative Region, China., Department of Infectious Disease and Microbiology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong Province, China., Department of Microbiology, Queen Mary Hospital, Pokfulam, Hong Kong Special Administrative Region, China., Guangzhou Laboratory, Guangdong Province, China
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  givenname: Honglin
  orcidid: 0000-0001-5108-8338
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  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong Special Administrative Region, China., Department of Infectious Disease and Microbiology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong Province, China., Guangzhou Laboratory, Guangdong Province, China
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  givenname: Dong-Yan
  orcidid: 0000-0002-2778-3530
  surname: Jin
  fullname: Jin, Dong-Yan
  organization: School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Guangzhou Laboratory, Guangdong Province, China
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  givenname: Kwok-Yung
  orcidid: 0000-0001-8700-4570
  surname: Yuen
  fullname: Yuen, Kwok-Yung
  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Academician Workstation of Hainan Province, Hainan Medical University-The University of Hong Kong Joint Laboratory of Tropical Infectious Diseases, Hainan Medical University, Haikou, Hainan, China; and The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong Special Administrative Region, China., Department of Infectious Disease and Microbiology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong Province, China., Department of Microbiology, Queen Mary Hospital, Pokfulam, Hong Kong Special Administrative Region, China
– sequence: 30
  givenname: Jasper Fuk-Woo
  orcidid: 0000-0001-6336-6657
  surname: Chan
  fullname: Chan, Jasper Fuk-Woo
  organization: State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Academician Workstation of Hainan Province, Hainan Medical University-The University of Hong Kong Joint Laboratory of Tropical Infectious Diseases, Hainan Medical University, Haikou, Hainan, China; and The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China., Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong Special Administrative Region, China., Department of Infectious Disease and Microbiology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong Province, China., Department of Microbiology, Queen Mary Hospital, Pokfulam, Hong Kong Special Administrative Region, China
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Snippet The in vivo pathogenicity, transmissibility, and fitness of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron (B.1.1.529) variant are...
Delta and Omicron go toe to toeThere is growing evidence that the Omicron variant of concern (VOC) is more transmissible and infectious than previous...
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SubjectTerms Animals
Coronaviruses
Hamsters
Pathogenicity
Pathogens
Respiratory diseases
Respiratory tract
Severe acute respiratory syndrome coronavirus 2
Vaccination
Viral diseases
Title Pathogenicity, transmissibility, and fitness of SARS-CoV-2 Omicron in Syrian hamsters
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