Abstract
The SARS-CoV-2 epidemic in southern Africa has been characterized by three distinct waves. The first was associated with a mix of SARS-CoV-2 lineages, while the second and third waves were driven by the Beta (B.1.351) and Delta (B.1.617.2) variants, respectively1–3. In November 2021, genomic surveillance teams in South Africa and Botswana detected a new SARS-CoV-2 variant associated with a rapid resurgence of infections in Gauteng province, South Africa. Within three days of the first genome being uploaded, it was designated a variant of concern (Omicron, B.1.1.529) by the World Health Organization and, within three weeks, had been identified in 87 countries. The Omicron variant is exceptional for carrying over 30 mutations in the spike glycoprotein, which are predicted to influence antibody neutralization and spike function4. Here we describe the genomic profile and early transmission dynamics of Omicron, highlighting the rapid spread in regions with high levels of population immunity.
Original language | English (US) |
---|---|
Pages (from-to) | 679-686 |
Number of pages | 8 |
Journal | Nature |
Volume | 603 |
Issue number | 7902 |
DOIs | |
State | Published - Mar 24 2022 |
All Science Journal Classification (ASJC) codes
- General
Access to Document
Other files and links
Fingerprint
Dive into the research topics of 'Rapid epidemic expansion of the SARS-CoV-2 Omicron variant in southern Africa'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver
}
Rapid epidemic expansion of the SARS-CoV-2 Omicron variant in southern Africa. / Viana, Raquel; Moyo, Sikhulile; Amoako, Daniel G. et al.
In: Nature, Vol. 603, No. 7902, 24.03.2022, p. 679-686.Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Rapid epidemic expansion of the SARS-CoV-2 Omicron variant in southern Africa
AU - Viana, Raquel
AU - Moyo, Sikhulile
AU - Amoako, Daniel G.
AU - Tegally, Houriiyah
AU - Scheepers, Cathrine
AU - Althaus, Christian L.
AU - Anyaneji, Ugochukwu J.
AU - Bester, Phillip A.
AU - Boni, Maciej F.
AU - Chand, Mohammed
AU - Choga, Wonderful T.
AU - Colquhoun, Rachel
AU - Davids, Michaela
AU - Deforche, Koen
AU - Doolabh, Deelan
AU - du Plessis, Louis
AU - Engelbrecht, Susan
AU - Everatt, Josie
AU - Giandhari, Jennifer
AU - Giovanetti, Marta
AU - Hardie, Diana
AU - Hill, Verity
AU - Hsiao, Nei Yuan
AU - Iranzadeh, Arash
AU - Ismail, Arshad
AU - Joseph, Charity
AU - Joseph, Rageema
AU - Koopile, Legodile
AU - Kosakovsky Pond, Sergei L.
AU - Kraemer, Moritz U.G.
AU - Kuate-Lere, Lesego
AU - Laguda-Akingba, Oluwakemi
AU - Lesetedi-Mafoko, Onalethatha
AU - Lessells, Richard J.
AU - Lockman, Shahin
AU - Lucaci, Alexander G.
AU - Maharaj, Arisha
AU - Mahlangu, Boitshoko
AU - Maponga, Tongai
AU - Mahlakwane, Kamela
AU - Makatini, Zinhle
AU - Marais, Gert
AU - Maruapula, Dorcas
AU - Masupu, Kereng
AU - Matshaba, Mogomotsi
AU - Mayaphi, Simnikiwe
AU - Mbhele, Nokuzola
AU - Mbulawa, Mpaphi B.
AU - Mendes, Adriano
AU - Mlisana, Koleka
AU - Mnguni, Anele
AU - Mohale, Thabo
AU - Moir, Monika
AU - Moruisi, Kgomotso
AU - Mosepele, Mosepele
AU - Motsatsi, Gerald
AU - Motswaledi, Modisa S.
AU - Mphoyakgosi, Thongbotho
AU - Msomi, Nokukhanya
AU - Mwangi, Peter N.
AU - Naidoo, Yeshnee
AU - Ntuli, Noxolo
AU - Nyaga, Martin
AU - Olubayo, Lucier
AU - Pillay, Sureshnee
AU - Radibe, Botshelo
AU - Ramphal, Yajna
AU - Ramphal, Upasana
AU - San, James E.
AU - Scott, Lesley
AU - Shapiro, Roger
AU - Singh, Lavanya
AU - Smith-Lawrence, Pamela
AU - Stevens, Wendy
AU - Strydom, Amy
AU - Subramoney, Kathleen
AU - Tebeila, Naume
AU - Tshiabuila, Derek
AU - Tsui, Joseph
AU - van Wyk, Stephanie
AU - Weaver, Steven
AU - Wibmer, Constantinos K.
AU - Wilkinson, Eduan
AU - Wolter, Nicole
AU - Zarebski, Alexander E.
AU - Zuze, Boitumelo
AU - Goedhals, Dominique
AU - Preiser, Wolfgang
AU - Treurnicht, Florette
AU - Venter, Marietje
AU - Williamson, Carolyn
AU - Pybus, Oliver G.
AU - Bhiman, Jinal
AU - Glass, Allison
AU - Martin, Darren P.
AU - Rambaut, Andrew
AU - Gaseitsiwe, Simani
AU - von Gottberg, Anne
AU - de Oliveira, Tulio
N1 - Funding Information: Acknowledgements We thank L. de Gouveia, A. Buys, C. Fourie, N. Duma, M. Ndlovu and other members of the NICD Centre for Respiratory Diseases and Meningitis and Sequencing Core Facility; N. Govender, G. Ntshoe, A. Moipone Shonhiwa, D. Muganhiri, I. Matiea, E. Mathatha, F. Gavhi, T. Mashudu Lamola, M. Makhubele, M. Matjokotja, S. Mdleleni, M. Makhubela from the national SARS-CoV-2 NICD surveillance team for NMCSS case data; F. Mckenna, T. Graham Bell, N. Munava, S. Kwenda, M. Raza Bano and J. Khosa from NICD IT for NMCSS case and test data (in particular, SGTF data); and the following people from the diagnostic laboratories for their assistance: K. Reddy, L. Gounder and C. Naicker from NHLS Inkosi Albert Luthuli Central Hospital Laboratory, S. Korsman from the NHLS Groote Schuur Laboratory, and A. Enoch at NHLS Green Point Laboratory; the staff at the global laboratories who generated and made public the SARS-CoV-2 sequences (through GISAID) used as reference dataset in this study (a complete list of individual contributors of sequences is provided in Supplementary Table 1). The research reported in this publication was supported by the Strategic Health Innovation Partnerships Unit of the South African Medical Research Council, with funds received from the South African Department of Science and Innovation. Sequencing activities at KRISP and CERI were supported in part by the WHO, the National Institutes of Health (NIH) (U01 AI151698) for the United World Antivirus Research Network (UWARN), and the Rockefeller Foundation (grants 2021 HTH 017 and 2020 HTH 062). C.L.A. received funding from the European Union’s Horizon 2020 research and innovation programme, project EpiPose (no. 101003688). D.P.M. was funded by the Wellcome Trust (222574/Z/21/Z). R.C. and A.R. acknowledge support from the Wellcome Trust (Collaborators Award 206298/Z/17/Z, ARTIC network) and A.R. from the European Research Council (no. 725422, ReservoirDOCS). V.H. was supported by the Biotechnology and Biological Sciences Research Council (BBSRC) (grant no. BB/M010996/1). A.E.Z., J.T., M.U.G.K. and O.G.P. acknowledge support from the Oxford Martin School. M.U.G.K. acknowledges support from the Rockefeller Foundation, Google.org, and the European Horizon 2020 programme MOOD (no. 874850). M.V. and the members of the Zoonotic Arbo and Respiratory Virus Program, UP was funded through the ANDEMIA G7 Global Health Concept: contributions to improvement of International Health, COVID-19 funds through the Robert Koch Institute. The genomic sequencing at UCT/NHLS is funded from the South African Medical Research Council and Department of Science and Innovation; and by the Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa), which is supported by core funding from the Wellcome Trust (203135/Z/16/Z and 222754). C.W. and J.B. are funded by the EDCTP (RADIATES Consortium; RIA2020EF-3030). Sequencing activities at the NICD were supported by a conditional grant from the South African National Department of Health as part of the emergency COVID-19 response; a cooperative agreement between the National Institute for Communicable Diseases of the National Health Laboratory Service and the United States Centers for Disease Control and Prevention (no. 5U01IP001048-05-00); the African Society of Laboratory Medicine (ASLM) and Africa Centers for Disease Control and Prevention through a subaward from the Bill and Melinda Gates Foundation grant no. INV-018978; the UK Foreign, Commonwealth and Development Office and Wellcome (no. 221003/Z/20/Z); the South African Medical Research Council (SHIPNCD 76756); the UK Department of Health and Social Care, managed by the Fleming Fund and performed under the auspices of the SEQAFRICA project. The genomic sequencing in Botswana was supported by the Foundation for Innovative New Diagnostics and Fogarty International Center (5D43TW009610), NIH (5K24AI131924-04; 5K24AI131928-05) and support from the Botswana government through the Ministry of Health & Wellness and Presidential COVID-19 Task Force. S. Moyo. was supported in part by the Bill & Melinda Gates Foundation (036530). Under the grant conditions of the Foundation, a Creative Commons Attribution 4.0 Generic License has already been assigned to the Author Accepted Manuscript version that might arise from this submission. Funding Information: We thank L. de Gouveia, A. Buys, C. Fourie, N. Duma, M. Ndlovu and other members of the NICD Centre for Respiratory Diseases and Meningitis and Sequencing Core Facility; N. Govender, G. Ntshoe, A. Moipone Shonhiwa, D. Muganhiri, I. Matiea, E. Mathatha, F. Gavhi, T. Mashudu Lamola, M. Makhubele, M. Matjokotja, S. Mdleleni, M. Makhubela from the national SARS-CoV-2 NICD surveillance team for NMCSS case data; F. Mckenna, T. Graham Bell, N. Munava, S. Kwenda, M. Raza Bano and J. Khosa from NICD IT for NMCSS case and test data (in particular, SGTF data); and the following people from the diagnostic laboratories for their assistance: K. Reddy, L. Gounder and C. Naicker from NHLS Inkosi Albert Luthuli Central Hospital Laboratory, S. Korsman from the NHLS Groote Schuur Laboratory, and A. Enoch at NHLS Green Point Laboratory; the staff at the global laboratories who generated and made public the SARS-CoV-2 sequences (through GISAID) used as reference dataset in this study (a complete list of individual contributors of sequences is provided in Supplementary Table 1). The research reported in this publication was supported by the Strategic Health Innovation Partnerships Unit of the South African Medical Research Council, with funds received from the South African Department of Science and Innovation. Sequencing activities at KRISP and CERI were supported in part by the WHO, the National Institutes of Health (NIH) (U01 AI151698) for the United World Antivirus Research Network (UWARN), and the Rockefeller Foundation (grants 2021 HTH 017 and 2020 HTH 062).?C.L.A. received funding from the European Union?s Horizon 2020 research and innovation programme, project EpiPose (no. 101003688). D.P.M. was funded by the Wellcome Trust (222574/Z/21/Z). R.C. and A.R. acknowledge support from the Wellcome Trust (Collaborators Award 206298/Z/17/Z, ARTIC network) and A.R. from the European Research Council (no. 725422, ReservoirDOCS). V.H. was supported by the Biotechnology and Biological Sciences Research Council (BBSRC) (grant no. BB/M010996/1). A.E.Z., J.T., M.U.G.K. and O.G.P. acknowledge support from the Oxford Martin School. M.U.G.K. acknowledges support from the Rockefeller Foundation, Google.org, and the European Horizon 2020 programme MOOD (no. 874850). M.V. and the members of the Zoonotic Arbo and Respiratory Virus Program, UP was funded through the ANDEMIA G7 Global Health Concept: contributions to improvement of International Health, COVID-19 funds through the Robert Koch Institute. The genomic sequencing at UCT/NHLS is funded from the South African Medical Research Council and Department of Science and Innovation; and by the Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa), which is supported by core funding from the Wellcome Trust (203135/Z/16/Z and 222754). C.W. and J.B. are funded by the EDCTP (RADIATES Consortium; RIA2020EF-3030). Sequencing activities at the NICD were supported by a conditional grant from the South African National Department of Health as part of the emergency COVID-19 response; a cooperative agreement between the National Institute for Communicable Diseases of the National Health Laboratory Service and the United States Centers for Disease Control and Prevention (no. 5U01IP001048-05-00); the African Society of Laboratory Medicine (ASLM) and Africa Centers for Disease Control and Prevention through a subaward from the Bill and Melinda Gates Foundation grant no. INV-018978; the UK Foreign, Commonwealth and Development Office and Wellcome (no. 221003/Z/20/Z); the South African Medical Research Council (SHIPNCD 76756); the UK Department of Health and Social Care, managed by the Fleming Fund and performed under the auspices of the SEQAFRICA project. The genomic sequencing in Botswana was supported by the Foundation for Innovative New Diagnostics and Fogarty International Center (5D43TW009610), NIH (5K24AI131924-04; 5K24AI131928-05) and support from the Botswana government through the Ministry of Health & Wellness and Presidential COVID-19 Task Force. S.?Moyo. was supported in part by the Bill & Melinda Gates Foundation (036530).?Under the grant conditions of the Foundation, a Creative Commons Attribution 4.0 Generic License has already been assigned to the Author Accepted Manuscript version that might arise from this submission. Publisher Copyright: © 2022, The Author(s).
PY - 2022/3/24
Y1 - 2022/3/24
N2 - The SARS-CoV-2 epidemic in southern Africa has been characterized by three distinct waves. The first was associated with a mix of SARS-CoV-2 lineages, while the second and third waves were driven by the Beta (B.1.351) and Delta (B.1.617.2) variants, respectively1–3. In November 2021, genomic surveillance teams in South Africa and Botswana detected a new SARS-CoV-2 variant associated with a rapid resurgence of infections in Gauteng province, South Africa. Within three days of the first genome being uploaded, it was designated a variant of concern (Omicron, B.1.1.529) by the World Health Organization and, within three weeks, had been identified in 87 countries. The Omicron variant is exceptional for carrying over 30 mutations in the spike glycoprotein, which are predicted to influence antibody neutralization and spike function4. Here we describe the genomic profile and early transmission dynamics of Omicron, highlighting the rapid spread in regions with high levels of population immunity.
AB - The SARS-CoV-2 epidemic in southern Africa has been characterized by three distinct waves. The first was associated with a mix of SARS-CoV-2 lineages, while the second and third waves were driven by the Beta (B.1.351) and Delta (B.1.617.2) variants, respectively1–3. In November 2021, genomic surveillance teams in South Africa and Botswana detected a new SARS-CoV-2 variant associated with a rapid resurgence of infections in Gauteng province, South Africa. Within three days of the first genome being uploaded, it was designated a variant of concern (Omicron, B.1.1.529) by the World Health Organization and, within three weeks, had been identified in 87 countries. The Omicron variant is exceptional for carrying over 30 mutations in the spike glycoprotein, which are predicted to influence antibody neutralization and spike function4. Here we describe the genomic profile and early transmission dynamics of Omicron, highlighting the rapid spread in regions with high levels of population immunity.
UR - http://www.scopus.com/inward/record.url?scp=85122882393&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85122882393&partnerID=8YFLogxK
U2 - 10.1038/s41586-022-04411-y
DO - 10.1038/s41586-022-04411-y
M3 - Article
C2 - 35042229
AN - SCOPUS:85122882393
SN - 0028-0836
VL - 603
SP - 679
EP - 686
JO - Nature
JF - Nature
IS - 7902
ER -