Genome‐based comparison between the recombinant SARS‐CoV‐2 XBB and its parental lineages

Author:

Scarpa Fabio1ORCID,Sanna Daria1,Azzena Ilenia12,Casu Marco2,Cossu Piero2,Fiori Pier Luigi13ORCID,Benvenuto Domenico4ORCID,Imperia Elena45,Giovanetti Marta67ORCID,Ceccarelli Giancarlo8ORCID,Cauda Roberto9,Cassone Antonio10,Pascarella Stefano11ORCID,Ciccozzi Massimo4ORCID

Affiliation:

1. Department of Biomedical Sciences University of Sassari Sassari Italy

2. Department of Veterinary Medicine University of Sassari Sassari Italy

3. Azienza Ospedaliera Universitaria (AOU) Sassari Sassari Italy

4. Units of Medical Statistics and Molecular Epidemiology University Campus Bio‐Medico of Rome Rome Italy

5. Unit of Gastroenterology, Department of Medicine University Campus Bio‐Medico of Rome Rome Italy

6. Laboratório de Flavivírus, Instituto Oswaldo Cruz Fundação Oswaldo Cruz Rio de Janeiro Brazil

7. Department of Science and Technology for Humans and the Environment University of Campus Bio‐Medico di Roma Rome Italy

8. Department of Public Health and Infectious Diseases, University Hospital Policlinico Umberto I Sapienza University of Rome Rome Italy

9. UOC Malattie Infettive, Department of Infectious Disease Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome Italy

10. Center of Genomic Genetic and Biology Siena Italy

11. Department of Biochemical Sciences “A. Rossi Fanelli” Sapienza Università di Roma Rome Italy

Abstract

AbstractRecombination is the main contributor to RNA virus evolution, and SARS‐CoV‐2 during the pandemic produced several recombinants. The most recent SARS‐CoV‐2 recombinant is the lineage labeled XBB, also known as Gryphon, which arose from BJ.1 and BM.1.1.1. Here we performed a genome‐based survey aimed to compare the new recombinant with its parental lineages that never became dominant. Genetic analyses indicated that the recombinant XBB and its first descendant XBB.1 show an evolutionary condition typical of an evolutionary blind background with no further epidemiologically relevant descendant. Genetic variability and expansion capabilities are slightly higher than parental lineages. Bayesian Skyline Plot indicates that XBB reached its plateau around October 6, 2022 and after an initial rapid growth the viral population size did not further expand, and around November 10, 2022 its levels of genetic variability decreased. Simultaneously with the reduction of the XBB population size, an increase of the genetic variability of its first sub‐lineage XBB.1 occurred, that in turn reached the plateau around November 9, 2022 showing a kind of vicariance with its direct progenitors. Structure analysis indicates that the affinity for ACE2 surface in XBB/XBB.1 RBDs is weaker than for BA.2 RBD. In conclusion, at present XBB and XBB.1 do not show evidence about a particular danger or high expansion capability. Genome‐based monitoring must continue uninterrupted to individuate if further mutations can make XBB more dangerous or generate new subvariants with different expansion capability.

Publisher

Wiley

Subject

Infectious Diseases,Virology

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