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Virological characteristics of the SARS-CoV-2 XBB variant derived from recombination of two Omicron subvariants

Author

Listed:
  • Tomokazu Tamura

    (Hokkaido University
    Hokkaido University)

  • Jumpei Ito

    (The University of Tokyo)

  • Keiya Uriu

    (The University of Tokyo
    The University of Tokyo)

  • Jiri Zahradnik

    (Weizmann Institute of Science
    Charles University)

  • Izumi Kida

    (Hokkaido University)

  • Yuki Anraku

    (Hokkaido University)

  • Hesham Nasser

    (Kumamoto University
    Suez Canal University)

  • Maya Shofa

    (University of Miyazaki
    University of Miyazaki)

  • Yoshitaka Oda

    (Hokkaido University)

  • Spyros Lytras

    (Medical Research Council-University of Glasgow Centre for Virus Research)

  • Naganori Nao

    (Hokkaido University
    Hokkaido University)

  • Yukari Itakura

    (Hokkaido University
    Hokkaido University)

  • Sayaka Deguchi

    (Kyoto University)

  • Rigel Suzuki

    (Hokkaido University
    Hokkaido University)

  • Lei Wang

    (Hokkaido University
    Hokkaido University)

  • MST Monira Begum

    (Kumamoto University)

  • Shunsuke Kita

    (Hokkaido University)

  • Hisano Yajima

    (Kyoto University)

  • Jiei Sasaki

    (Kyoto University)

  • Kaori Sasaki-Tabata

    (Kyushu University)

  • Ryo Shimizu

    (Kumamoto University)

  • Masumi Tsuda

    (Hokkaido University
    Hokkaido University)

  • Yusuke Kosugi

    (The University of Tokyo
    The University of Tokyo)

  • Shigeru Fujita

    (The University of Tokyo
    The University of Tokyo)

  • Lin Pan

    (The University of Tokyo
    The University of Tokyo)

  • Daniel Sauter

    (The University of Tokyo
    University Hospital Tübingen)

  • Kumiko Yoshimatsu

    (Hokkaido University)

  • Saori Suzuki

    (Hokkaido University
    Hokkaido University)

  • Hiroyuki Asakura

    (Tokyo Metropolitan Institute of Public Health)

  • Mami Nagashima

    (Tokyo Metropolitan Institute of Public Health)

  • Kenji Sadamasu

    (Tokyo Metropolitan Institute of Public Health)

  • Kazuhisa Yoshimura

    (Tokyo Metropolitan Institute of Public Health)

  • Yuki Yamamoto

    (HiLung, Inc.)

  • Tetsuharu Nagamoto

    (HiLung, Inc.)

  • Gideon Schreiber

    (Weizmann Institute of Science)

  • Katsumi Maenaka

    (Hokkaido University
    Hokkaido University
    Hokkaido University
    Hokkaido University)

  • Takao Hashiguchi

    (Kyoto University
    CREST, Japan Science and Technology Agency)

  • Terumasa Ikeda

    (Kumamoto University)

  • Takasuke Fukuhara

    (Hokkaido University
    Hokkaido University
    AMED-CREST, Japan Agency for Medical Research and Development (AMED)
    Osaka University)

  • Akatsuki Saito

    (University of Miyazaki
    University of Miyazaki
    University of Miyazaki)

  • Shinya Tanaka

    (Hokkaido University
    Hokkaido University)

  • Keita Matsuno

    (Hokkaido University
    Hokkaido University
    Hokkaido University
    Hokkaido University)

  • Kazuo Takayama

    (Kyoto University
    CREST, Japan Science and Technology Agency)

  • Kei Sato

    (The University of Tokyo
    The University of Tokyo
    The University of Tokyo
    CREST, Japan Science and Technology Agency)

Abstract

In late 2022, SARS-CoV-2 Omicron subvariants have become highly diversified, and XBB is spreading rapidly around the world. Our phylogenetic analyses suggested that XBB emerged through the recombination of two cocirculating BA.2 lineages, BJ.1 and BM.1.1.1 (a progeny of BA.2.75), during the summer of 2022. XBB.1 is the variant most profoundly resistant to BA.2/5 breakthrough infection sera to date and is more fusogenic than BA.2.75. The recombination breakpoint is located in the receptor-binding domain of spike, and each region of the recombinant spike confers immune evasion and increases fusogenicity. We further provide the structural basis for the interaction between XBB.1 spike and human ACE2. Finally, the intrinsic pathogenicity of XBB.1 in male hamsters is comparable to or even lower than that of BA.2.75. Our multiscale investigation provides evidence suggesting that XBB is the first observed SARS-CoV-2 variant to increase its fitness through recombination rather than substitutions.

Suggested Citation

  • Tomokazu Tamura & Jumpei Ito & Keiya Uriu & Jiri Zahradnik & Izumi Kida & Yuki Anraku & Hesham Nasser & Maya Shofa & Yoshitaka Oda & Spyros Lytras & Naganori Nao & Yukari Itakura & Sayaka Deguchi & Ri, 2023. "Virological characteristics of the SARS-CoV-2 XBB variant derived from recombination of two Omicron subvariants," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-38435-3
    DOI: 10.1038/s41467-023-38435-3
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    References listed on IDEAS

    as
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    Cited by:

    1. Tomokazu Tamura & Takashi Irie & Sayaka Deguchi & Hisano Yajima & Masumi Tsuda & Hesham Nasser & Keita Mizuma & Arnon Plianchaisuk & Saori Suzuki & Keiya Uriu & Mst Monira Begum & Ryo Shimizu & Michae, 2024. "Virological characteristics of the SARS-CoV-2 Omicron XBB.1.5 variant," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    2. Orsolya Anna Pipek & Anna Medgyes-Horváth & József Stéger & Krisztián Papp & Dávid Visontai & Marion Koopmans & David Nieuwenhuijse & Bas B. Oude Munnink & István Csabai, 2024. "Systematic detection of co-infection and intra-host recombination in more than 2 million global SARS-CoV-2 samples," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    3. Dhiraj Mannar & James W. Saville & Chad Poloni & Xing Zhu & Alison Bezeruk & Keith Tidey & Sana Ahmed & Katharine S. Tuttle & Faezeh Vahdatihassani & Spencer Cholak & Laura Cook & Theodore S. Steiner , 2024. "Altered receptor binding, antibody evasion and retention of T cell recognition by the SARS-CoV-2 XBB.1.5 spike protein," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    4. Hisano Yajima & Yuki Anraku & Yu Kaku & Kanako Terakado Kimura & Arnon Plianchaisuk & Kaho Okumura & Yoshiko Nakada-Nakura & Yusuke Atarashi & Takuya Hemmi & Daisuke Kuroda & Yoshimasa Takahashi & Shu, 2024. "Structural basis for receptor-binding domain mobility of the spike in SARS-CoV-2 BA.2.86 and JN.1," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    5. Cassia Wagner & Kathryn E. Kistler & Garrett A. Perchetti & Noah Baker & Lauren A. Frisbie & Laura Marcela Torres & Frank Aragona & Cory Yun & Marlin Figgins & Alexander L. Greninger & Alex Cox & Hann, 2024. "Positive selection underlies repeated knockout of ORF8 in SARS-CoV-2 evolution," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

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