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Evolution and neutralization escape of the SARS-CoV-2 BA.2.86 subvariant

Author

Listed:
  • Khadija Khan

    (Africa Health Research Institute
    University of KwaZulu-Natal)

  • Gila Lustig

    (Centre for the AIDS Programme of Research in South Africa)

  • Cornelius Römer

    (Biozentrum, University of Basel
    Swiss Institute of Bioinformatics)

  • Kajal Reedoy

    (Africa Health Research Institute)

  • Zesuliwe Jule

    (Africa Health Research Institute)

  • Farina Karim

    (Africa Health Research Institute
    University of KwaZulu-Natal)

  • Yashica Ganga

    (Africa Health Research Institute)

  • Mallory Bernstein

    (Africa Health Research Institute)

  • Zainab Baig

    (Africa Health Research Institute)

  • Laurelle Jackson

    (Africa Health Research Institute)

  • Boitshoko Mahlangu

    (Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service)

  • Anele Mnguni

    (Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service)

  • Ayanda Nzimande

    (Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service)

  • Nadine Stock

    (Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service)

  • Dikeledi Kekana

    (Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service)

  • Buhle Ntozini

    (Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service)

  • Cindy Deventer

    (Ampath Molecular Biology)

  • Terry Marshall

    (Ampath Molecular Biology)

  • Nithendra Manickchund

    (University of KwaZulu-Natal)

  • Bernadett I. Gosnell

    (University of KwaZulu-Natal)

  • Richard J. Lessells

    (Centre for the AIDS Programme of Research in South Africa
    KwaZulu-Natal Research Innovation and Sequencing Platform)

  • Quarraisha Abdool Karim

    (Centre for the AIDS Programme of Research in South Africa
    Columbia University)

  • Salim S. Abdool Karim

    (Centre for the AIDS Programme of Research in South Africa
    Columbia University)

  • Mahomed-Yunus S. Moosa

    (University of KwaZulu-Natal)

  • Tulio Oliveira

    (Centre for the AIDS Programme of Research in South Africa
    KwaZulu-Natal Research Innovation and Sequencing Platform
    Stellenbosch University
    University of Washington)

  • Anne Gottberg

    (Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service
    University of the Witwatersrand)

  • Nicole Wolter

    (Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service
    University of the Witwatersrand)

  • Richard A. Neher

    (Biozentrum, University of Basel
    Swiss Institute of Bioinformatics)

  • Alex Sigal

    (Africa Health Research Institute
    University of KwaZulu-Natal
    Centre for the AIDS Programme of Research in South Africa)

Abstract

Omicron BA.2.86 subvariant differs from Omicron BA.2 as well as recently circulating variants by over 30 mutations in the spike protein alone. Here we report on the isolation of the live BA.2.86 subvariant from a diagnostic swab collected in South Africa which we tested for escape from neutralizing antibodies and viral replication properties in cell culture. We found that BA.2.86 does not have significantly more escape relative to Omicron XBB.1.5 from neutralizing immunity elicited by either Omicron XBB-family subvariant infection or from residual neutralizing immunity of recently collected sera from the South African population. BA.2.86 does have extensive escape relative to ancestral virus with the D614G substitution (B.1 lineage) when neutralized by sera from pre-Omicron vaccinated individuals and relative to Omicron BA.1 when neutralized by sera from Omicron BA.1 infected individuals. BA.2.86 and XBB.1.5 show similar viral infection dynamics in the VeroE6-TMPRSS2 and H1299-ACE2 cell lines. We also investigate the relationship of BA.2.86 to BA.2 sequences. The closest BA.2 sequences are BA.2 samples from Southern Africa circulating in early 2022. Similarly, many basal BA.2.86 sequences were sampled in Southern Africa. This suggests that BA.2.86 potentially evolved in this region, and that unobserved evolution led to escape from neutralizing antibodies similar in scale to recently circulating strains of SARS-CoV-2.

Suggested Citation

  • Khadija Khan & Gila Lustig & Cornelius Römer & Kajal Reedoy & Zesuliwe Jule & Farina Karim & Yashica Ganga & Mallory Bernstein & Zainab Baig & Laurelle Jackson & Boitshoko Mahlangu & Anele Mnguni & Ay, 2023. "Evolution and neutralization escape of the SARS-CoV-2 BA.2.86 subvariant," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43703-3
    DOI: 10.1038/s41467-023-43703-3
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    References listed on IDEAS

    as
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    1. Daming Zhou & Piyada Supasa & Chang Liu & Aiste Dijokaite-Guraliuc & Helen M. E. Duyvesteyn & Muneeswaran Selvaraj & Alexander J. Mentzer & Raksha Das & Wanwisa Dejnirattisai & Nigel Temperton & Paul , 2024. "The SARS-CoV-2 neutralizing antibody response to SD1 and its evasion by BA.2.86," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    2. Delphine Planas & Isabelle Staropoli & Vincent Michel & Frederic Lemoine & Flora Donati & Matthieu Prot & Francoise Porrot & Florence Guivel-Benhassine & Banujaa Jeyarajah & Angela Brisebarre & Océane, 2024. "Distinct evolution of SARS-CoV-2 Omicron XBB and BA.2.86/JN.1 lineages combining increased fitness and antibody evasion," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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