SARS-CoV CH.1.1 Variant: Genomic and Structural Insight

Author:

Bazzani Liliana1ORCID,Imperia Elena23,Scarpa Fabio4ORCID,Sanna Daria4ORCID,Casu Marco5ORCID,Borsetti Alessandra6ORCID,Pascarella Stefano7ORCID,Petrosillo Nicola8ORCID,Cella Eleonora9ORCID,Giovanetti Marta110,Ciccozzi Massimo2ORCID

Affiliation:

1. Sciences and Technologies for Sustainable Development and One Health, University Campus Bio-Medico of Rome, 00128 Rome, Italy

2. Unit of Medical Statistics and Molecular Epidemiology, University Campus Bio-Medico of Rome, 00128 Rome, Italy

3. Unit of Gastroenterology, Department of Medicine, University Campus Bio-Medico of Rome, 00128 Rome, Italy

4. Department of Biomedical Sciences, University of Sassari, 07100 Sassari, Italy

5. Department of Veterinary Medicine, University of Sassari, 07100 Sassari, Italy

6. National HIV/AIDS Research Center (CNAIDS), National Institute of Health, 00161 Rome, Italy

7. Department of Biochemical Sciences “A. Rossi Fanelli”, Sapienza University of Rome, 00185 Rome, Italy

8. Infection Prevention and Control—Infectious Disease Service, Fondazione Policlinico Universitario Campus Bio-Medico, 00128 Rome, Italy

9. Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL 32816, USA

10. Instituto Rene Rachou Fundação Oswaldo Cruz, Belo Horizonte 30190-002, MG, Brazil

Abstract

In early February 2023, the Omicron subvariant XBB.1.5, also known as “Kraken”, accounted for more than 44% of new COVID-19 cases worldwide, whereas a relatively new Omicron subvariant named CH.1.1, deemed “Orthrus”, accounted for less than 6% of new COVID-19 cases during the subsequent weeks. This emerging variant carries a mutation, L452R, previously observed in the highly pathogenic Delta and the highly transmissible BA.4 and BA.5 variants, necessitating a shift to active surveillance to assure adequate preparedness for likely future epidemic peaks. We provide a preliminary understanding of the global distribution of this emerging SARS-CoV-2 variant by combining genomic data with structural molecular modeling. In addition, we shield light on the number of specific point mutations in this lineage that may have functional significance, thereby increasing the risk of disease severity, vaccine resistance, and increased transmission. This variant shared about 73% of the mutations with Omicron-like strains. Our homology modeling analysis revealed that CH.1.1 may have a weakened interaction with ACE2 and that its electrostatic potential surface appears to be more positive than that of the reference ancestral virus. Finally, our phylogenetic analysis revealed that this likely-emerging variant was already cryptically circulating in European countries prior to its first detection, highlighting the importance of having access to whole genome sequences for detecting and controlling emerging viral strains.

Publisher

MDPI AG

Subject

Infectious Diseases

Reference26 articles.

1. (2023, May 03). World Health Organization. Available online: https://covid19.who.int/.

2. Emergence of SARS-CoV-2 B.1.1.7 Lineage—United States, December 29, 2020–January 12, 2021;Galloway;Morb. Mortal. Wkly. Rep.,2021

3. Genomic epidemiology of the SARS-CoV-2 epidemic in Brazil;Giovanetti;Nat. Microbiol.,2022

4. Detection of a SARS-CoV-2 variant of concern in South Africa;Tegally;Nature,2021

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