Evidence for SARS-CoV-2 Delta and Omicron co-infections and recombination.

BA.1 Delta Omicron RNA virus SARS-CoV-2 Translation to patients alternative allele fraction breakpoint co-infection recombination sequencing

Journal

Med (New York, N.Y.)
ISSN: 2666-6340
Titre abrégé: Med
Pays: United States
ID NLM: 101769215

Informations de publication

Date de publication:
09 Dec 2022
Historique:
received: 25 04 2022
revised: 14 06 2022
accepted: 07 10 2022
pubmed: 5 11 2022
medline: 15 12 2022
entrez: 4 11 2022
Statut: ppublish

Résumé

Between November 2021 and February 2022, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta and Omicron variants co-circulated in the United States, allowing for co-infections and possible recombination events. We sequenced 29,719 positive samples during this period and analyzed the presence and fraction of reads supporting mutations specific to either the Delta or Omicron variant. We identified 18 co-infections, one of which displayed evidence of a low Delta-Omicron recombinant viral population. We also identified two independent cases of infection by a Delta-Omicron recombinant virus, where 100% of the viral RNA came from one clonal recombinant. In the three cases, the 5' end of the viral genome was from the Delta genome and the 3' end from Omicron, including the majority of the spike protein gene, though the breakpoints were different. Delta-Omicron recombinant viruses were rare, and there is currently no evidence that Delta-Omicron recombinant viruses are more transmissible between hosts compared with the circulating Omicron lineages. This research was supported by the NIH RADx initiative and by the Centers for Disease Control Contract 75D30121C12730 (Helix).

Sections du résumé

BACKGROUND BACKGROUND
Between November 2021 and February 2022, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta and Omicron variants co-circulated in the United States, allowing for co-infections and possible recombination events.
METHODS METHODS
We sequenced 29,719 positive samples during this period and analyzed the presence and fraction of reads supporting mutations specific to either the Delta or Omicron variant.
FINDINGS RESULTS
We identified 18 co-infections, one of which displayed evidence of a low Delta-Omicron recombinant viral population. We also identified two independent cases of infection by a Delta-Omicron recombinant virus, where 100% of the viral RNA came from one clonal recombinant. In the three cases, the 5' end of the viral genome was from the Delta genome and the 3' end from Omicron, including the majority of the spike protein gene, though the breakpoints were different.
CONCLUSIONS CONCLUSIONS
Delta-Omicron recombinant viruses were rare, and there is currently no evidence that Delta-Omicron recombinant viruses are more transmissible between hosts compared with the circulating Omicron lineages.
FUNDING BACKGROUND
This research was supported by the NIH RADx initiative and by the Centers for Disease Control Contract 75D30121C12730 (Helix).

Identifiants

pubmed: 36332633
pii: S2666-6340(22)00449-4
doi: 10.1016/j.medj.2022.10.002
pmc: PMC9581791
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

848-859.e4

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declarations of interests A.B., T.B., S.W., A.D.R., D.W., H.D., J.T.M., E.K., T.C., K.T., J.N., J.R., S.C., E.T.C., K.S.B., N.L.W., P.B.-F., S.J., E.S., D.B., J.T.L., M.I., W.L., and S.L. are all employees of Helix.

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Auteurs

Alexandre Bolze (A)

Helix, San Mateo, CA 94401, USA.

Tracy Basler (T)

Helix, San Mateo, CA 94401, USA.

Simon White (S)

Helix, San Mateo, CA 94401, USA.

Andrew Dei Rossi (A)

Helix, San Mateo, CA 94401, USA.

Dana Wyman (D)

Helix, San Mateo, CA 94401, USA.

Hang Dai (H)

Helix, San Mateo, CA 94401, USA.

Pavitra Roychoudhury (P)

Department of Laboratory Medicine and Pathology, University of Washington Medical Center, Seattle, WA 98195, USA.

Alexander L Greninger (AL)

Department of Laboratory Medicine and Pathology, University of Washington Medical Center, Seattle, WA 98195, USA.

Kathleen Hayashibara (K)

Thermo Fisher Scientific, South San Francisco, CA 94080, USA.

Mark Beatty (M)

County of San Diego Health and Human Services, San Diego, CA 92110, USA.

Seema Shah (S)

County of San Diego Health and Human Services, San Diego, CA 92110, USA.

Sarah Stous (S)

County of San Diego Health and Human Services, San Diego, CA 92110, USA.

John T McCrone (JT)

Helix, San Mateo, CA 94401, USA.

Eric Kil (E)

Helix, San Mateo, CA 94401, USA.

Tyler Cassens (T)

Helix, San Mateo, CA 94401, USA.

Kevin Tsan (K)

Helix, San Mateo, CA 94401, USA.

Jason Nguyen (J)

Helix, San Mateo, CA 94401, USA.

Jimmy Ramirez (J)

Helix, San Mateo, CA 94401, USA.

Scotty Carter (S)

Helix, San Mateo, CA 94401, USA.

Elizabeth T Cirulli (ET)

Helix, San Mateo, CA 94401, USA.

Kelly Schiabor Barrett (K)

Helix, San Mateo, CA 94401, USA.

Nicole L Washington (NL)

Helix, San Mateo, CA 94401, USA.

Pedro Belda-Ferre (P)

Helix, San Mateo, CA 94401, USA.

Sharoni Jacobs (S)

Helix, San Mateo, CA 94401, USA.

Efren Sandoval (E)

Helix, San Mateo, CA 94401, USA.

David Becker (D)

Helix, San Mateo, CA 94401, USA.

James T Lu (JT)

Helix, San Mateo, CA 94401, USA.

Magnus Isaksson (M)

Helix, San Mateo, CA 94401, USA.

William Lee (W)

Helix, San Mateo, CA 94401, USA.

Shishi Luo (S)

Helix, San Mateo, CA 94401, USA. Electronic address: shishi.luo@helix.com.

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Classifications MeSH