Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis

Héctor Díaz‐García(Hospital Infantil de México Federico Gómez), Ana Laura Guzmán-Ortiz(Hospital Infantil de México Federico Gómez), Tania Ángeles-Floriano(Hospital Infantil de México Federico Gómez), Israel Parra‐Ortega(Hospital Infantil de México Federico Gómez), Briceida López-Martı́nez(Hospital Infantil de México Federico Gómez), Mirna Martínez‐Saucedo(Hospital Infantil de México Federico Gómez), Guillermo Aquino‐Jarquín(Hospital Infantil de México Federico Gómez), Rocío Sánchez‐Urbina(Hospital Infantil de México Federico Gómez), Héctor Quezada(Hospital Infantil de México Federico Gómez), Javier T. Granados-Riverón(Hospital Infantil de México Federico Gómez)
Genes
April 5, 2021
Cited by 21Open Access
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Abstract

The genome of the SARS-CoV-2 virus, the causal agent of the COVID-19 pandemic, has diverged due to multiple mutations since its emergence as a human pathogen in December 2019. Some mutations have defined several SARS-CoV-2 clades that seem to behave differently in terms of regional distribution and other biological features. Next-generation sequencing (NGS) approaches are used to classify the sequence variants in viruses from individual human patients. However, the cost and relative scarcity of NGS equipment and expertise in developing countries prevent studies aimed to associate specific clades and variants to clinical features and outcomes in such territories. As of March 2021, the GR clade and its derivatives, including the B.1.1.7 and B.1.1.28 variants, predominate worldwide. We implemented the post-PCR small-amplicon high-resolution melting analysis to genotype SARS-CoV-2 viruses isolated from the saliva of individual patients. This procedure was able to clearly distinguish two groups of samples of SARS-CoV-2-positive samples predicted, according to their melting profiles, to contain GR and non-GR viruses. This grouping of the samples was validated by means of amplification-refractory mutation system (ARMS) assay as well as Sanger sequencing.


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