Emergence and dissemination of SARS-CoV-2 XBB.1.5 in New York

Author:

Gámbaro Fabiana1,Duerr Ralf234ORCID,Dimartino Dacia5,Marier Christian5,Iturrate Eduardo3,Mulligan Mark J234,Heguy Adriana56ORCID,Dellicour Simon17ORCID

Affiliation:

1. Spatial Epidemiology Lab (SpELL), Université Libre de Bruxelles , Brussels 1050, Belgium

2. Department of Medicine, Division of Infectious Diseases and Immunology, NYU Grossman School of Medicine , 10016, USA

3. Vaccine Center, NYU Grossman School of Medicine , New York, NY 10016, USA

4. Department of Microbiology, NYU Grossman School of Medicine , 10016, USA

5. Genome Technology Center, Office of Science and Research, NYU Langone Health , 10016, USA

6. Department of Pathology, NYU Grossman School of Medicine , 10016, USA

7. Department of Microbiology, Immunology and Transplantation, Rega Institute, Laboratory for Clinical and Epidemiological Virology, KU Leuven , Leuven 3000, Belgium

Abstract

Abstract The recombinant SARS-CoV-2 Omicron XBB.1.5 variant was first detected in New York City (NYC) and rapidly became the predominant variant in the area by early 2023. The increased occurrence of circulating variants within the SARS-CoV-2 XBB-sublineage prompted the modification of COVID-19 mRNA vaccines by Moderna and Pfizer-BioNTech. This update, implemented in mid-September 2023, involved the incorporation of a monovalent XBB.1.5 component. Considering that NYC probably played a central role in the emergence of the XBB.1.5 variant, we conducted phylogeographic analysis to investigate the emergence and spread of this variant in the metropolitan area. Our analysis confirms that XBB.1.5 emerged within or near the NYC area and indicates that XBB.1.5 had a diffusion velocity similar to that of the variant Alpha in the same study area. Additionally, the analysis of 2,392 genomes collected in the context of the genomic surveillance program at NYU Langone Health system showed that there was no increased proportion of XBB.1.5, relative to all cocirculating variants, in the boosted compared to unvaccinated individuals. This study provides a comprehensive description of the emergence and dissemination of XBB.1.5.

Funder

Cancer Center Support Grant, USA

European Union Horizon 2020 project MOOD

Fonds National de la Recherche Scientifique

Division of Microbiology and Infectious Diseases

Clinical Center

Fonds voor Wetenschappelijk Onderzoek — Vlaanderen, FWO, Belgium

Publisher

Oxford University Press (OUP)

Reference8 articles.

1. Variant-specific Introduction and Dispersal Dynamics of SARS-CoV-2 in New York City – From Alpha To Omicron;Dellicour;PLoS Pathogens,2023

2. Selective Adaptation of SARS-CoV-2 Omicron under Booster Vaccine Pressure: A Multicentre Observational Study;Duerr;eBioMedicine,2023

3. ECDC Classifies XBB.1.5-like Lineages with the Amino Acid Change F456L as Variants of Interest Following an Increase in SARS-CoV-2 Transmission in EU/EEA Countries and Abroad;European Centre for Disease Prevention and Control,2023

4. Profound Neutralization Evasion and Augmented Host Cell Entry are Hallmarks of the Fast-spreading SARS-CoV-2 Lineage XBB.1.5;Hoffmann;Cellular and Molecular Immunology,2023

5. GISAID’s Role in Pandemic Response;Khare;China CDC Weekly,2021

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