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Comparative Analysis of Five Multiplex RT-PCR Assays in the Screening of SARS-CoV-2 Variants.
De Pace, Vanessa; Bruzzone, Bianca; Orsi, Andrea; Ricucci, Valentina; Domnich, Alexander; Guarona, Giulia; Randazzo, Nadia; Stefanelli, Federica; Battolla, Enrico; Dusi, Pier Andrea; Lillo, Flavia; Icardi, Giancarlo.
  • De Pace V; Hygiene Unit, Ospedale Policlinico San Martino-IRCCS, 16132 Genoa, Italy.
  • Bruzzone B; Hygiene Unit, Ospedale Policlinico San Martino-IRCCS, 16132 Genoa, Italy.
  • Orsi A; Department of Health Sciences (DISSAL), University of Genoa, 16132 Genoa, Italy.
  • Ricucci V; Hygiene Unit, Ospedale Policlinico San Martino-IRCCS, 16132 Genoa, Italy.
  • Domnich A; Hygiene Unit, Ospedale Policlinico San Martino-IRCCS, 16132 Genoa, Italy.
  • Guarona G; Department of Health Sciences (DISSAL), University of Genoa, 16132 Genoa, Italy.
  • Randazzo N; Hygiene Unit, Ospedale Policlinico San Martino-IRCCS, 16132 Genoa, Italy.
  • Stefanelli F; Hygiene Unit, Ospedale Policlinico San Martino-IRCCS, 16132 Genoa, Italy.
  • Battolla E; Division of Clinical Pathology, Azienda Sanitaria Locale n°5, 19121 La Spezia, Italy.
  • Dusi PA; Microbiology Department, Sanremo Hospital, 18038 Imperia, Italy.
  • Lillo F; Laboratory of Clinical Pathology, ASL2 Savonese, 17100 Savona, Italy.
  • Icardi G; Department of Health Sciences (DISSAL), University of Genoa, 16132 Genoa, Italy.
Microorganisms ; 10(2)2022 Jan 27.
Article in English | MEDLINE | ID: covidwho-1662700
ABSTRACT
The rapid and presumptive detection of SARS-CoV-2 variants may be performed using multiplex RT-PCR assays. The aim of this study was to evaluate the diagnostic performance of five qualitative RT-PCR tests as compared with next-generation sequencing (NGS). We retrospectively examined a multi-variant panel (n = 72) of SARS-CoV-2-positive nasopharyngeal swabs categorized as variants of concern (Alpha, Beta, Gamma and Delta), variants under monitoring (Iota and Kappa) and wild-type strains circulating in Liguria (Italy) from January to August 2021. First, NGS libraries of study samples were prepared and mapped to the reference genome. Then, specimens were screened for the detection of L452R, W152C, K417T, K417N, E484Q, E484K and N501Y mutations using the SARS-CoV-2 Variants II Assay Allplex, UltraGene Assay SARS-CoV-2 452R & 484K & 484Q Mutations V1, COVID-19 Ultra Variant Catcher, SARS-CoV-2 Extended ELITe MGB and Simplexa SARS-CoV-2 Variants Direct. The overall accuracy of these assays ranged from 96.9% to 100%. Specificity and sensitivity were 100% and 96-100%, respectively. We highly recommend the use of these assays as second-level tests in the routine workflow of SARS-CoV-2 laboratory diagnostics, as they are accurate, user friendly, low cost, may identify specific mutations in about 2-3 h and, therefore, optimize the surveillance of SARS-CoV-2 variants.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Qualitative research Topics: Variants Language: English Year: 2022 Document Type: Article Affiliation country: Microorganisms10020306

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Qualitative research Topics: Variants Language: English Year: 2022 Document Type: Article Affiliation country: Microorganisms10020306