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Potential use of high-resolution melting analyses for SARS-CoV-2 genomic surveillance

The pandemic caused by COVID-19 and the emergence of new variants of SARS-CoV-2 have generated clinical and epidemiological impacts on a global scale. The use of strategies for monitoring viral circulation and identifying mutations in genomic regions involved in host interaction are important measur...

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Detalles Bibliográficos
Autores principales: de Souza Andrade, Adriana, Freitas, Eduarda Fernandes, de Castro Barbosa, Emerson, Guimarães, Natália Rocha, de Melo Iani, Felipe Campos, da Costa, Alana Vitor Barbosa, Bernardes, André Felipe Leal, Adelino, Talita Emile Ribeiro, Ataide, Ana Caroline Zampiroli, Gregianini, Tatiana Schäffer, Nunes, Jônathas Dias, Stringari, Lorenzzo Lyrio, Riediger, Irina Nastassja, Fernandes, Sandra Bianchini, de Jesus, Ronaldo, Fonseca, Vagner, Caldas, Sérgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pan American Health Organization. Published by B.V. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10132831/
https://www.ncbi.nlm.nih.gov/pubmed/37116586
http://dx.doi.org/10.1016/j.jviromet.2023.114742
Descripción
Sumario:The pandemic caused by COVID-19 and the emergence of new variants of SARS-CoV-2 have generated clinical and epidemiological impacts on a global scale. The use of strategies for monitoring viral circulation and identifying mutations in genomic regions involved in host interaction are important measures to mitigate viral dissemination and reduce its likely complications on population health. In this context, the objective of this work was to explore the potential of high-resolution melting (HRM) analysis combined with one-step real-time reverse transcription PCR in a closed-tube system, as a fast and convenient method of screening for SARS-CoV-2 mutations with possible implications on host-pathogen interactions. The HRM analyses allowed the distinction of the Gamma, Zeta, Alpha, Delta, and Omicron variants against the predecessors (B.1.1.28, B.1.1.33) of occurrence in Brazil. It is concluded that the molecular tool standardized here has the potential to optimize the genomic surveillance of SARS-CoV-2, and could be adapted for genomic surveillance of other pathogens, due to its ability to detect, prior to sequencing, samples suggestive of new variants, selecting them more assertively and earlier for whole genome sequencing when compared to random screening.