Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program.

COVID-19 Centers for Disease Control Cycle threshold Lineage Next generation sequencing Reverse transcription polymerase chain reaction SARS-CoV-2 Variant

Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
25 Apr 2022
Historique:
received: 01 12 2021
accepted: 11 04 2022
entrez: 26 4 2022
pubmed: 27 4 2022
medline: 28 4 2022
Statut: epublish

Résumé

The Centers for Disease Control and Prevention contracted with laboratories to sequence the SARS-CoV-2 genome from positive samples across the United States to enable public health officials to investigate the impact of variants on disease severity as well as the effectiveness of vaccines and treatment. Herein we present the initial results correlating RT-PCR quality control metrics with sample collection and sequencing methods from full SARS-CoV-2 viral genomic sequencing of 24,441 positive patient samples between April and June 2021. RT-PCR confirmed (N Gene Ct value < 30) positive patient samples, with nucleic acid extracted from saliva, nasopharyngeal and oropharyngeal swabs were selected for viral whole genome SARS-CoV-2 sequencing. Sequencing was performed using Illumina COVIDSeq™ protocol on either the NextSeq550 or NovaSeq6000 systems. Informatic variant calling, and lineage analysis were performed using DRAGEN COVID Lineage applications on Illumina's Basespace cloud analytical system. All sequence data and variant calls were uploaded to NCBI and GISAID. An association was observed between higher sequencing coverage, quality, and samples with a lower Ct value, with < 27 being optimal, across both sequencing platforms and sample collection methods. Both nasopharyngeal swabs and saliva samples were found to be optimal samples of choice for SARS-CoV-2 surveillance sequencing studies, both in terms of strain identification and sequencing depth of coverage, with NovaSeq 6000 providing higher coverage than the NextSeq 550. The most frequent variants identified were the B.1.617.2 Delta (India) and P.1 Gamma (Brazil) variants in the samples sequenced between April 2021 and June 2021. At the time of submission, the most common variant > 99% of positives sequenced was Omicron. These initial analyses highlight the importance of sequencing platform, sample collection methods, and RT-PCR Ct values in guiding surveillance efforts. These surveillance studies evaluating genetic changes of SARS-CoV-2 have been identified as critical by the CDC that can affect many aspects of public health including transmission, disease severity, diagnostics, therapeutics, and vaccines.

Sections du résumé

BACKGROUND BACKGROUND
The Centers for Disease Control and Prevention contracted with laboratories to sequence the SARS-CoV-2 genome from positive samples across the United States to enable public health officials to investigate the impact of variants on disease severity as well as the effectiveness of vaccines and treatment. Herein we present the initial results correlating RT-PCR quality control metrics with sample collection and sequencing methods from full SARS-CoV-2 viral genomic sequencing of 24,441 positive patient samples between April and June 2021.
METHODS METHODS
RT-PCR confirmed (N Gene Ct value < 30) positive patient samples, with nucleic acid extracted from saliva, nasopharyngeal and oropharyngeal swabs were selected for viral whole genome SARS-CoV-2 sequencing. Sequencing was performed using Illumina COVIDSeq™ protocol on either the NextSeq550 or NovaSeq6000 systems. Informatic variant calling, and lineage analysis were performed using DRAGEN COVID Lineage applications on Illumina's Basespace cloud analytical system. All sequence data and variant calls were uploaded to NCBI and GISAID.
RESULTS RESULTS
An association was observed between higher sequencing coverage, quality, and samples with a lower Ct value, with < 27 being optimal, across both sequencing platforms and sample collection methods. Both nasopharyngeal swabs and saliva samples were found to be optimal samples of choice for SARS-CoV-2 surveillance sequencing studies, both in terms of strain identification and sequencing depth of coverage, with NovaSeq 6000 providing higher coverage than the NextSeq 550. The most frequent variants identified were the B.1.617.2 Delta (India) and P.1 Gamma (Brazil) variants in the samples sequenced between April 2021 and June 2021. At the time of submission, the most common variant > 99% of positives sequenced was Omicron.
CONCLUSION CONCLUSIONS
These initial analyses highlight the importance of sequencing platform, sample collection methods, and RT-PCR Ct values in guiding surveillance efforts. These surveillance studies evaluating genetic changes of SARS-CoV-2 have been identified as critical by the CDC that can affect many aspects of public health including transmission, disease severity, diagnostics, therapeutics, and vaccines.

Identifiants

pubmed: 35468749
doi: 10.1186/s12879-022-07374-7
pii: 10.1186/s12879-022-07374-7
pmc: PMC9035976
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

404

Subventions

Organisme : NCCDPHP CDC HHS
ID : 75D30121C10587
Pays : United States

Informations de copyright

© 2022. The Author(s).

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Auteurs

Chirayu Goswami (C)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Michael Sheldon (M)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Christian Bixby (C)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Mehdi Keddache (M)

Illumina, 5200 Illumina Way, San Diego, CA, 92122, USA.

Alexander Bogdanowicz (A)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Yihe Wang (Y)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Jonathan Schultz (J)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Jessica McDevitt (J)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

James LaPorta (J)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Elaine Kwon (E)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Steven Buyske (S)

Rutgers University, 559 Hill Center, 110 Frelinghuysen Rd, Piscataway, NJ, 08854, USA.

Dana Garbolino (D)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Glenys Biloholowski (G)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Alex Pastuszak (A)

Vault Health, 115 Broadway Suite 1800, 18th Floor, Dobbs Ferry, NY, 10522, USA.

Mary Storella (M)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Amit Bhalla (A)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Florence Charlier-Rodriguez (F)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Russ Hager (R)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Robin Grimwood (R)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA.

Shareef A Nahas (SA)

Infinity-Biologix LLC, 30 Knightsbridge Road, Piscataway, NJ, 08854, USA. shareef.nahas@infinity-biologix.com.

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Classifications MeSH