Evidence map›Paper›PMID 38057313›Full record

ArticleNature communications2023

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

Khadija Khan, Gila Lustig, Cornelius Römer, Kajal Reedoy, Zesuliwe Jule, Farina Karim, Yashica Ganga, Mallory Bernstein, Zainab Baig, Laurelle Jackson and 19 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
18.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

62 citing papers in PubMed, 96 citations in OpenAlex.

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2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

29 authors at 7 institutions in 3 countries.

Khadija KhanAfrica Health Research Institute, Durban, South Africa.ORCID 0000-0001-7565-7400
Gila LustigCentre for the AIDS Programme of Research in South Africa, Durban, South Africa.
Cornelius RömerBiozentrum, University of Basel, Basel, Switzerland.ORCID 0000-0002-6138-6539
Kajal ReedoyAfrica Health Research Institute, Durban, South Africa.
Zesuliwe JuleAfrica Health Research Institute, Durban, South Africa.
Farina KarimAfrica Health Research Institute, Durban, South Africa.
Yashica GangaAfrica Health Research Institute, Durban, South Africa.
Mallory BernsteinAfrica Health Research Institute, Durban, South Africa.ORCID 0000-0001-7498-2391
Zainab BaigAfrica Health Research Institute, Durban, South Africa.
Laurelle JacksonAfrica Health Research Institute, Durban, South Africa.
Boitshoko MahlanguCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service, Johannesburg, South Africa.
Anele MnguniCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service, Johannesburg, South Africa.ORCID 0000-0002-1854-5573
Ayanda NzimandeCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service, Johannesburg, South Africa.
Nadine StockCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service, Johannesburg, South Africa.
Dikeledi KekanaCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service, Johannesburg, South Africa.
Buhle NtoziniCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service, Johannesburg, South Africa.
Cindy van DeventerAmpath Molecular Biology, Centurion, South Africa.
Terry MarshallAmpath Molecular Biology, Centurion, South Africa.
Nithendra ManickchundDepartment of Infectious Diseases, Nelson R. Mandela School of Clinical Medicine, University of KwaZulu-Natal, Durban, South Africa.
Bernadett I GosnellDepartment of Infectious Diseases, Nelson R. Mandela School of Clinical Medicine, University of KwaZulu-Natal, Durban, South Africa.ORCID 0000-0002-6336-7489
Richard J LessellsCentre for the AIDS Programme of Research in South Africa, Durban, South Africa.ORCID 0000-0003-0926-710X
Quarraisha Abdool KarimCentre for the AIDS Programme of Research in South Africa, Durban, South Africa.ORCID 0000-0002-0985-477X
Salim S Abdool KarimCentre for the AIDS Programme of Research in South Africa, Durban, South Africa.ORCID 0000-0002-4986-2133
Mahomed-Yunus S MoosaDepartment of Infectious Diseases, Nelson R. Mandela School of Clinical Medicine, University of KwaZulu-Natal, Durban, South Africa.ORCID 0000-0001-6191-4023
Tulio de OliveiraCentre for the AIDS Programme of Research in South Africa, Durban, South Africa.ORCID 0000-0002-3027-5254
Anne von GottbergCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service, Johannesburg, South Africa.ORCID 0000-0002-0243-7455
Nicole WolterCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, a Division of the National Health Laboratory Service, Johannesburg, South Africa.ORCID 0000-0002-9526-0133
Richard A NeherBiozentrum, University of Basel, Basel, Switzerland.ORCID 0000-0003-2525-1407
Alex SigalAfrica Health Research Institute, Durban, South Africa. alex.sigal@ahri.org.ORCID 0000-0001-8571-2004
Africa Health Research Institute · ZANational Health Laboratory Service · ZACentre for the AIDS Programme of Research in South Africa · ZAUniversity of KwaZulu-Natal · ZAEducation Labour Relations Council · ZASIB Swiss Institute of Bioinformatics · CHUniversity of Washington · US

Funding

ACL HHS U01IP001048NCIRD CDC HHS U01 IP001048Wellcome Trust
6 · The paper itself

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.

Indexed as

COVID-19SARS-CoV-2Africa, SouthernAntibodies, NeutralizingAntibodies, ViralHumansAntibodies, NeutralizingAntibodies, Viral

Identifiers

PMID38057313
PMCPMC10700484
OpenAlexW4389398845

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.