Next-generation sequencing for cytomegalovirus antiviral resistance genotyping in a clinical virology laboratory.


Journal

Antiviral research
ISSN: 1872-9096
Titre abrégé: Antiviral Res
Pays: Netherlands
ID NLM: 8109699

Informations de publication

Date de publication:
08 2021
Historique:
received: 16 02 2021
revised: 16 06 2021
accepted: 22 06 2021
pubmed: 27 6 2021
medline: 15 12 2021
entrez: 26 6 2021
Statut: ppublish

Résumé

The identification of CMV antiviral drug resistance (AVDR) is a critical diagnostic test for immunocompromised patients with CMV infection and a failure of virologic response on optimal antiviral treatment. We developed a next-generation sequencing (NGS) assay for CMV AVDR testing and compared the AVDR mutations identified by NGS to Sanger sequencing. Retrospective review of CMV AVDR testing requests for UL97 and UL54 at our laboratory from 2014 to 2019 was conducted. NGS was performed on the MinION and compared to Sanger sequencing performed at the national reference laboratory. Analysis of the sequences was completed with a novel cloud bioinformatics platform (BugSeq). Twenty patient samples previously characterized were included for study on the MinION. NGS captured all of the CMV AVDR mutations identified by Sanger, and identified additional mutations in UL97 and/or UL54 in 8/13 (62%) of the samples. An analysis of the depth of coverage at which we no longer detected minority single nucleotide variants (SNVs) detected in the original data was conducted, estimating a recall of 95% at 1800 fold coverage. NGS utilizing MinION technology for the detection of CMV AVDR mutations identified additional minority variants in UL97 and UL54 as compared with Sanger sequencing. Through the application of a bioinformatics pipeline available online, our NGS process eliminates barriers associated with the use of the MinION and NGS in clinical laboratories.

Identifiants

pubmed: 34174249
pii: S0166-3542(21)00113-3
doi: 10.1016/j.antiviral.2021.105123
pii:
doi:

Substances chimiques

Antiviral Agents 0
DNA, Viral 0
UL54 protein, Human herpesvirus 5 0
Viral Proteins 0
Phosphotransferases (Alcohol Group Acceptor) EC 2.7.1.-
ganciclovir kinase EC 2.7.1.-
DNA-Directed DNA Polymerase EC 2.7.7.7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105123

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Samuel D Chorlton (SD)

Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.

Gordon Ritchie (G)

Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada; Division of Medical Microbiology and Virology, St. Paul's Hospital, Vancouver, BC, Canada.

Tanya Lawson (T)

Division of Medical Microbiology and Virology, St. Paul's Hospital, Vancouver, BC, Canada.

Elizabeth McLachlan (E)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.

Marc G Romney (MG)

Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada; Division of Medical Microbiology and Virology, St. Paul's Hospital, Vancouver, BC, Canada.

Nancy Matic (N)

Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada; Division of Medical Microbiology and Virology, St. Paul's Hospital, Vancouver, BC, Canada.

Christopher F Lowe (CF)

Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada; Division of Medical Microbiology and Virology, St. Paul's Hospital, Vancouver, BC, Canada. Electronic address: clowe@providencehealth.bc.ca.

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Classifications MeSH