Utility of SARS-CoV-2 Genomic Sequencing for Understanding Transmission and School Outbreaks.


Journal

The Pediatric infectious disease journal
ISSN: 1532-0987
Titre abrégé: Pediatr Infect Dis J
Pays: United States
ID NLM: 8701858

Informations de publication

Date de publication:
01 04 2023
Historique:
pubmed: 17 2 2023
medline: 14 3 2023
entrez: 16 2 2023
Statut: ppublish

Résumé

An understanding of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) transmission in schools is important. It is often difficult, using epidemiological information alone, to determine whether cases associated with schools represent multiple introductions from the community or transmission within the school. We describe the use of whole genome sequencing (WGS) in multiple schools to investigate outbreaks of SARS-CoV-2 in the pre-Omicron period. School outbreaks were identified for sequencing by local public health units based on multiple cases without known epidemiological links. Cases of SARS-CoV-2 from students and staff from 4 school outbreaks in Ontario underwent WGS and phylogenetic analysis. The epidemiological clinical cohort data and genomic cluster data are described to help further characterize these outbreaks. A total of 132 positive SARS-CoV-2 cases among students and staff from 4 school outbreaks were identified with 65 (49%) of cases able to be sequenced with high-quality genomic data. The 4 school outbreaks consisted of 53, 37, 21 and 21 positive cases; within each outbreak there were between 8 and 28 different clinical cohorts identified. Among the sequenced cases, between 3 and 7 genetic clusters, defined as different strains, were identified in each outbreak. We found genetically different viruses within several clinical cohorts. WGS, together with public health investigation, is a useful tool to investigate SARS-CoV-2 transmission within schools. Its early use has the potential to better understand when transmission may have occurred, can aid in evaluating how well mitigation interventions are working and has the potential to reduce unnecessary school closures when multiple genetic clusters are identified.

Identifiants

pubmed: 36795555
doi: 10.1097/INF.0000000000003834
pii: 00006454-202304000-00017
pmc: PMC9990487
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

324-331

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to disclose.

Références

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Auteurs

Aaron Campigotto (A)

From the Division of Microbiology, Department of Paediatric Laboratory Medicine, The Hospital for Sick Children.
Department of Laboratory Medicine and Pathobiology, University of Toronto.

Allison Chris (A)

Toronto Public Health.

Julia Orkin (J)

Department of Paediatrics.

Lynette Lau (L)

Division of Genome Diagnostics, Department of Paediatric Laboratory Medicine.

Christian Marshall (C)

Department of Laboratory Medicine and Pathobiology, University of Toronto.
Division of Genome Diagnostics, Department of Paediatric Laboratory Medicine.

Ari Bitnun (A)

Department of Paediatrics.
Division of Infectious Diseases, The Hospital for Sick Children.

Sarah A Buchan (SA)

Public Health Ontario.
Dalla Lana School of Public Health, University of Toronto.

Liane MacDonald (L)

Public Health Ontario.

Nisha Thampi (N)

Department of Paediatrics, Children's Hospital of Eastern Ontario.

Janine McCready (J)

Division of Infectious Diseases, Department of Medicine, Michael Garron Hospital.

Peter Juni (P)

St. Michael's Hospital, Applied Health Research Centre, Li Ka Shing Knowledge Institute, University of Toronto.

Rulan S Parekh (RS)

Department of Medicine, Women's College Hospital, Toronto, ON, Canada.

Michelle Science (M)

Division of Infectious Diseases, The Hospital for Sick Children.
Public Health Ontario.

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