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Replication of SARS-CoV-2 Omicron BA.2 Variant in Ex Vivo Cultures of the Human Upper and Lower Respiratory Tract

33 Pages Posted: 30 May 2022

See all articles by Kenrie PY Hui

Kenrie PY Hui

The University of Hong Kong - School of Public Health

Ka-Chun Ng

The University of Hong Kong - School of Public Health

John CW Ho

The University of Hong Kong - School of Public Health

Hin-Wo Yeung

The University of Hong Kong - School of Public Health

Rachel HH Ching

The University of Hong Kong - School of Public Health

Haogao Gu

The University of Hong Kong - School of Public Health

Joseph CK Chung

The University of Hong Kong - Department of Surgery

Velda LY Chow

The University of Hong Kong - Department of Surgery

Ko-Yung Sit

The University of Hong Kong - Department of Surgery

Michael KY Hsin

The University of Hong Kong - Department of Surgery

Timmy WK Au

The University of Hong Kong - Department of Surgery

Leo LM Poon

The University of Hong Kong - School of Public Health

J.S. Malik Peiris

The University of Hong Kong - School of Public Health

John M. Nicholls

The University of Hong Kong - Department of Pathology

Michael CW Chan

The University of Hong Kong - School of Public Health

More...

Abstract

Background: The Omicron BA.2 sublineage has replaced BA.1 worldwide and has comparable levels of immune evasion to BA.1. These observations suggest that enhanced antibody evasion is not related to increased transmissibility of BA.2.

Methods: Here, we characterized the replication competence and tissue tropism of three Omicron BA.1, BA.1.1, BA.2 variants in comparison with the wild-type virus and Delta variants, in human nasal, bronchial and lung tissues cultured ex vivo.

Findings: BA.2 replicated more efficiently in nasal and bronchial tissues at 33°C than wild-type, Delta and BA.1. Both BA.2 and BA.1 had higher replication competence than wild-type and Delta viruses in bronchial tissues at 37°C. BA.1, BA.1.1 and BA.2 replicated less well in lung parenchymal tissues compared to wild-type and Delta viruses.

Interpretation: Higher replication competence of Omicron BA.2 in the human upper airway at 33°C than BA.1 may help to explain the current expansion of BA.2 over BA.1. A lower replication level of the tested Omicron variants in human lung tissues is in line with the clinical manifestations of decreased disease severity of patients infected with the Omicron strain compared with other ancestral strains.

Funding Information: This work was supported by US National Institute of Allergy and Infectious Diseases and the Theme-Based Research Scheme under University Grants Committee of Hong Kong Special Administrative Region, China.

Declaration of Interests: The authors declare no competing financial interests.

Ethics Approval Statement: All experiments were carried out in a Bio-safety Level 3 (BSL-3) facility. Informed consent was obtained from all subjects and approval was granted by the Institutional Review Board (IRB) of the University of Hong Kong and the Hospital Authority (Hong Kong West) (IRB approval no: UW 20-862 and UW 20-588).

Keywords: SARS-CoV-2, Omicron BA.2, Nasal tissue, Bronchial tissue, Transmission, Pathogenicity

Suggested Citation

Hui, Kenrie PY and Ng, Ka-Chun and Ho, John CW and Yeung, Hin-Wo and Ching, Rachel HH and Gu, Haogao and Chung, Joseph CK and Chow, Velda LY and Sit, Ko-Yung and Hsin, Michael KY and Au, Timmy WK and Poon, Leo LM and Peiris, J.S. Malik and Nicholls, John M. and Chan, Michael CW, Replication of SARS-CoV-2 Omicron BA.2 Variant in Ex Vivo Cultures of the Human Upper and Lower Respiratory Tract. Available at SSRN: https://ssrn.com/abstract=4123178 or http://dx.doi.org/10.2139/ssrn.4123178

Kenrie Py Hui

The University of Hong Kong - School of Public Health ( email )

Ka-Chun Ng

The University of Hong Kong - School of Public Health ( email )

John Cw Ho

The University of Hong Kong - School of Public Health ( email )

Hin-Wo Yeung

The University of Hong Kong - School of Public Health ( email )

Rachel Hh Ching

The University of Hong Kong - School of Public Health ( email )

Haogao Gu

The University of Hong Kong - School of Public Health ( email )

Joseph Ck Chung

The University of Hong Kong - Department of Surgery ( email )

Velda Ly Chow

The University of Hong Kong - Department of Surgery ( email )

Ko-Yung Sit

The University of Hong Kong - Department of Surgery ( email )

Michael Ky Hsin

The University of Hong Kong - Department of Surgery ( email )

Timmy Wk Au

The University of Hong Kong - Department of Surgery ( email )

Leo Lm Poon

The University of Hong Kong - School of Public Health ( email )

Hong Kong, Pokfulam
China

J.S. Malik Peiris

The University of Hong Kong - School of Public Health ( email )

Hong Kong, Pokfulam
China

John M. Nicholls

The University of Hong Kong - Department of Pathology ( email )

Michael Cw Chan (Contact Author)

The University of Hong Kong - School of Public Health ( email )

Hong Kong, Pokfulam
China
(852) 3917-9800 (Phone)
(852) 2855-9587 (Fax)

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