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Emergence and phenotypic characterization of the global SARS-CoV-2 C.1.2 lineage

Author

Listed:
  • Cathrine Scheepers

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of the Witwatersrand)

  • Josie Everatt

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS))

  • Daniel G. Amoako

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS))

  • Houriiyah Tegally

    (University of KwaZulu-Natal
    Stellenbosch University)

  • Constantinos Kurt Wibmer

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS))

  • Anele Mnguni

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS))

  • Arshad Ismail

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS))

  • Boitshoko Mahlangu

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS))

  • Bronwen E. Lambson

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of the Witwatersrand)

  • Darren P. Martin

    (University of Cape Town)

  • Eduan Wilkinson

    (University of KwaZulu-Natal
    Stellenbosch University)

  • James Emmanuel San

    (University of KwaZulu-Natal
    Stellenbosch University)

  • Jennifer Giandhari

    (University of KwaZulu-Natal)

  • Nelia Manamela

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of the Witwatersrand)

  • Noxolo Ntuli

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS))

  • Prudence Kgagudi

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of the Witwatersrand)

  • Sandile Cele

    (Africa Health Research Institute
    University of KwaZulu-Natal)

  • Simone I. Richardson

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of the Witwatersrand)

  • Sureshnee Pillay

    (University of KwaZulu-Natal)

  • Thabo Mohale

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS))

  • Upasana Ramphal

    (University of KwaZulu-Natal)

  • Yeshnee Naidoo

    (University of KwaZulu-Natal
    Stellenbosch University)

  • Zamantungwa T. Khumalo

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of Pretoria)

  • Gaurav Kwatra

    (University of the Witwatersrand
    Christian Medical College)

  • Glenda Gray

    (South African Medical Research Council)

  • Linda-Gail Bekker

    (Desmond Tutu HIV Centre)

  • Shabir A. Madhi

    (University of the Witwatersrand)

  • Vicky Baillie

    (University of the Witwatersrand)

  • Wesley C. Voorhis

    (University of Washington)

  • Florette K. Treurnicht

    (National Health Laboratory Service (NHLS)
    University of the Witwatersrand)

  • Marietjie Venter

    (University of Pretoria)

  • Koleka Mlisana

    (University of KwaZulu-Natal
    National Health Laboratory Service (NHLS)
    Faulty of Health Sciences, University of Witwatersrand)

  • Nicole Wolter

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of the Witwatersrand)

  • Alex Sigal

    (Africa Health Research Institute
    University of KwaZulu-Natal
    Max Planck Institute for Infection Biology)

  • Carolyn Williamson

    (University of Cape Town
    National Health Laboratory Service (NHLS)
    Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa))

  • Nei-yuan Hsiao

    (University of Cape Town
    National Health Laboratory Service (NHLS)
    Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa))

  • Nokukhanya Msomi

    (National Health Laboratory Service (NHLS)
    University of KwaZulu-Natal)

  • Tongai Maponga

    (Stellenbosch University)

  • Wolfgang Preiser

    (National Health Laboratory Service (NHLS)
    Stellenbosch University)

  • Zinhle Makatini

    (National Health Laboratory Service (NHLS)
    University of the Witwatersrand)

  • Richard Lessells

    (University of KwaZulu-Natal)

  • Penny L. Moore

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of the Witwatersrand
    University of Cape Town
    Centre for the AIDS Programme of Research in South Africa (CAPRISA))

  • Tulio Oliveira

    (University of KwaZulu-Natal
    Stellenbosch University)

  • Anne Gottberg

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of the Witwatersrand
    University of Cape Town)

  • Jinal N. Bhiman

    (National Institute for Communicable Diseases (NICD) of the National Health Laboratory Service (NHLS)
    University of the Witwatersrand)

Abstract

Global genomic surveillance of SARS-CoV-2 has identified variants associated with increased transmissibility, neutralization resistance and disease severity. Here we report the emergence of the PANGO lineage C.1.2, detected at low prevalence in South Africa and eleven other countries. The initial C.1.2 detection is associated with a high substitution rate, and includes changes within the spike protein that have been associated with increased transmissibility or reduced neutralization sensitivity in SARS-CoV-2 variants of concern or variants of interest. Like Beta and Delta, C.1.2 shows significantly reduced neutralization sensitivity to plasma from vaccinees and individuals infected with the ancestral D614G virus. In contrast, convalescent donors infected with either Beta or Delta show high plasma neutralization against C.1.2. These functional data suggest that vaccine efficacy against C.1.2 will be equivalent to Beta and Delta, and that prior infection with either Beta or Delta will likely offer protection against C.1.2.

Suggested Citation

  • Cathrine Scheepers & Josie Everatt & Daniel G. Amoako & Houriiyah Tegally & Constantinos Kurt Wibmer & Anele Mnguni & Arshad Ismail & Boitshoko Mahlangu & Bronwen E. Lambson & Darren P. Martin & Eduan, 2022. "Emergence and phenotypic characterization of the global SARS-CoV-2 C.1.2 lineage," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-29579-9
    DOI: 10.1038/s41467-022-29579-9
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    References listed on IDEAS

    as
    1. Baisheng Li & Aiping Deng & Kuibiao Li & Yao Hu & Zhencui Li & Yaling Shi & Qianling Xiong & Zhe Liu & Qianfang Guo & Lirong Zou & Huan Zhang & Meng Zhang & Fangzhu Ouyang & Juan Su & Wenzhe Su & Jing, 2022. "Viral infection and transmission in a large, well-traced outbreak caused by the SARS-CoV-2 Delta variant," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    2. Bryan A. Johnson & Xuping Xie & Adam L. Bailey & Birte Kalveram & Kumari G. Lokugamage & Antonio Muruato & Jing Zou & Xianwen Zhang & Terry Juelich & Jennifer K. Smith & Lihong Zhang & Nathen Bopp & C, 2021. "Loss of furin cleavage site attenuates SARS-CoV-2 pathogenesis," Nature, Nature, vol. 591(7849), pages 293-299, March.
    3. Allison J. Greaney & Tyler N. Starr & Christopher O. Barnes & Yiska Weisblum & Fabian Schmidt & Marina Caskey & Christian Gaebler & Alice Cho & Marianna Agudelo & Shlomo Finkin & Zijun Wang & Daniel P, 2021. "Mapping mutations to the SARS-CoV-2 RBD that escape binding by different classes of antibodies," Nature Communications, Nature, vol. 12(1), pages 1-14, December.
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