Your browser doesn't support javascript.
loading
Evaluation of 5 Polymerase Chain Reaction Assays for the Detection of Mpox Virus.
Fattouh, Ramzi; Boissinot, Karel; Jeong, Esther; Mendlowitz, Andrew B; Sjaarda, Calvin P; Wong, Henry; Kozak, Robert; Sheth, Prameet M; Matukas, Larissa M.
  • Fattouh R; Department of Laboratory Medicine, St Michael's Hospital, Unity Health Toronto, Toronto, Canada.
  • Boissinot K; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
  • Jeong E; Li Ka Shing Knowledge Institute, Unity Health Toronto, Toronto, Canada.
  • Mendlowitz AB; Department of Laboratory Medicine, St Michael's Hospital, Unity Health Toronto, Toronto, Canada.
  • Sjaarda CP; Department of Laboratory Medicine, St Michael's Hospital, Unity Health Toronto, Toronto, Canada.
  • Wong H; Toronto Centre for Liver Disease/Viral Hepatitis Care Network (VIRCAN), University Health Network, Toronto, Canada.
  • Kozak R; Division of Microbiology, Kingston Health Sciences Centre, Kingston, Canada.
  • Sheth PM; Department of Pathology and Molecular Medicine, Queen's University, Kingston, Canada.
  • Matukas LM; Division of Microbiology, Kingston Health Sciences Centre, Kingston, Canada.
J Infect Dis ; 229(Supplement_2): S156-S162, 2024 Mar 26.
Article en En | MEDLINE | ID: mdl-38531075
ABSTRACT

BACKGROUND:

In 2022, the global dissemination of mpox virus (MPXV) outside endemic regions prompted the expansion of diagnostic testing worldwide. This study assesses the performance characteristics of 5 real-time polymerase chain reaction (PCR) assays in detecting MPXV during the 2022 outbreak.

METHODS:

Clinical specimens collected from patients across Ontario, Canada, were tested on the following assays RealStar Orthopoxyvirus PCR and FlexStar Monkeypox virus PCR (Altona Diagnostics), Novaplex MPXV (Seegene), VIASURE Monkeypox virus Real Time PCR Reagents (CerTest Biotec), and a laboratory-developed test. Positive percent agreement (PPA), negative percent agreement (NPA), relative limit of detection (LOD), and precision were evaluated and MPXV lineages were determined using an amplicon-based whole-genome sequencing (WGS) assay.

RESULTS:

Swabs were collected from various anatomic sites (65 positive and 30 negative). All assays demonstrated 100% NPA (95% confidence interval, 88.4%/88.1%-100.0%), with PPA ranging from 92.2% (82.7%-97.4%) to 96.9% (89.3%-99.6%). LOD and precision were comparable across assays, with coefficient of variations <3%. WGS analysis identified 6 lineages, all belonging to subclade IIb.

CONCLUSIONS:

The assays exhibited excellent PPA, NPA, LOD, and precision. Ongoing performance monitoring is essential to detect assay escape mutants and ensure universal detection of evolving MPXV strains.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Bioensayo / Monkeypox virus Límite: Humans País como asunto: America do norte Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Bioensayo / Monkeypox virus Límite: Humans País como asunto: America do norte Idioma: En Año: 2024 Tipo del documento: Article