Evolution of Influenza A(H3N2) Viruses in 2 Consecutive Seasons of Genomic Surveillance, 2021–2023

Author:

Fall Amary1,Han Lijie1,Yunker Madeline1,Gong Yu-Nong2345ORCID,Li Tai-Jung23,Norton Julie M1,Abdullah Omar1,Rothman Richard E6,Fenstermacher Katherine Z J6,Morris C Paul17,Pekosz Andrew68,Klein Eili69,Mostafa Heba H1

Affiliation:

1. Division of Medical Microbiology, Department of Pathology, Johns Hopkins School of Medicine , Baltimore, Maryland , USA

2. Research Center for Emerging Viral Infections, College of Medicine, Chang Gung University , Taoyuan , Taiwan

3. International Master Degree Program for Molecular Medicine in Emerging Viral Infections, College of Medicine, Chang Gung University , Taoyuan , Taiwan

4. Department of Laboratory Medicine, Linkou Chang Gung Memorial Hospital , Taoyuan , Taiwan

5. National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes , Zhunan , Taiwan

6. Department of Emergency Medicine, Johns Hopkins School of Medicine , Baltimore, Maryland , USA

7. Integrated Research Facility, Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Frederick, Maryland , USA

8. W.Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health , Baltimore, Maryland , USA

9. Center for Disease Dynamics, Economics, and Policy , Washington, District of Columbia , USA

Abstract

Abstract Background The circulation and the genomic evolution of influenza A(H3N2) viruses during the 2021/2022 and 2022/2023 seasons were studied and associated with infection outcomes. Methods Remnant influenza A–positive samples following standard-of-care testing from patients across the Johns Hopkins Health System (JHHS) were used for the study. Samples were randomly selected for whole viral genome sequencing. The sequence-based pEpitope model was used to estimate the predicted vaccine efficacy (pVE) for circulating H3N2 viruses. Clinical data were collected and associated with viral genomic data. Results A total of 121 683 respiratory specimens were tested for influenza at JHHS between 1 September 2021 and 31 December 2022. Among them, 6071 (4.99%) tested positive for influenza A. Of these, 805 samples were randomly selected for sequencing, with hemagglutinin (HA) segments characterized for 610 samples. Among the characterized samples, 581 were H3N2 (95.2%). Phylogenetic analysis of HA segments revealed the exclusive circulation of H3N2 viruses with HA segments of the 3C.2a1b.2a.2 clade. Analysis of a total of 445 complete H3N2 genomes revealed reassortments; 200 of 227 of the 2022/2023 season genomes (88.1%) were found to have reassorted with clade 3C.2a1b.1a. The pVE was estimated to be −42.53% for the 2021/2022 season and 30.27% for the 2022/2023 season. No differences in clinical presentations or admissions were observed between the 2 seasons. Conclusions The increased numbers of cases and genomic diversity of influenza A(H3N2) during the 2022/2023 season were not associated with a change in disease severity compared to the previous influenza season.

Funder

Johns Hopkins Center of Excellence in Influenza Research and Surveillance

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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