The Omicron Sub-Variant BA.4 Displays a Remarkable Lack of Clinical Signs in a Golden Syrian Hamster Model of SARS-CoV-2 Infection

Author:

Davies Elizabeth R.1ORCID,Ryan Kathryn A.1ORCID,Bewley Kevin R.1ORCID,Coombes Naomi S.1ORCID,Salguero Francisco J.1ORCID,Carnell Oliver T.1ORCID,Biddlecombe Sarah1,Charlton Michael1,Challis Amy1,Cross Eleanor S.1,Handley Alastair1,Ngabo Didier1,Weldon Thomas M.1,Hall Yper1,Funnell Simon G. P.123ORCID

Affiliation:

1. UKHSA Porton, Vaccine Development and Evaluation Centre, UK Health Security Agency, Manor Farm Road, Salisbury SP4 0JG, UK

2. Quadram Institute Bioscience, Norwich Research Park, Norwich NR4 7UQ, UK

3. World Health Organization, Appia 20, 1211 Geneva, Switzerland

Abstract

The ongoing emergence of SARS-CoV-2 virus variants remains a source of concern because it is accompanied by the potential for increased virulence as well as evasion of immunity. Here we show that, although having an almost identical spike gene sequence as another Omicron variant (BA.5.2.1), a BA.4 isolate lacked all the typical disease characteristics of other isolates seen in the Golden Syrian hamster model despite replicating almost as effectively. Animals infected with BA.4 had similar viral shedding profiles to those seen with BA.5.2.1 (up to day 6 post-infection), but they all failed to lose weight or present with any other significant clinical signs. We hypothesize that this lack of detectable signs of disease during infection with BA.4 was due to a small (nine nucleotide) deletion (∆686–694) in the viral genome (ORF1ab) responsible for the production of non-structural protein 1, which resulted in the loss of three amino acids (aa 141–143).

Funder

Coalition for Epidemic Preparedness Innovations

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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