Santos, Felice Deminco Alves; https://orcid.org/0000-0002-6132-192X; http://lattes.cnpq.br/4554426514301831
Resumo:
Introduction: COVID-19 is a new disease caused by a human coronavirus, whose
etiological agent is SARS-CoV-2. Two years have passed and SARS-CoV-2 has a
great genetic diversity, which favored the emergence of emergency variants during
different periods of the pandemic. Due to the importance employed in viral
surveillance and the limitations found in new generation sequencing platforms, the
objective of this work was to identify the variability in the Spike region of SARS-CoV2, from a Sanger sequencing platform, in patients with COVID-19 treated at the
University Hospital Professor Edgard Santos in Salvador-BA. Methods: This is a
cross-sectional observational study with preserved samples, positive for SARS-CoV2, of individuals over 18 years of age, employees, or patients, treated at the
Professor Edgard Santos University Hospital (HUPES). All samples from the enrolled
participants were confirmed for COVID-19 by an RT-qPCR assay. The extracted viral
genetic material was used for a NESTED-PCR assay on the SARS-CoV-2 S gene
and the results revealed on a 1.5% agarose gel. The sequencing reaction using the
BigDye Terminator V3.1 Cycle Senquencing kit was performed in a region of 1,120
base pairs and the result of this reaction was read by the SeqStudio capillary
electrophoresis machine. The files of sequences generated by the machine were
analyzed for the construction of the consensus sequence from the reference
sequence and identification of mutations throughout the genome. Results: Of all 103
sequenced samples, 69 contained relevant variants represented by 20 BA.1, 13
delta, 22 gamma and 14 zeta, identified between June 2020 and February 2022. All
sequences found were aligned with sequences representative of the variants.
Conclusions: The protocol developed by this work was able to identify and monitor
the variability of the SARS-CoV-2 S gene and, consequently, identify the most
relevant variants for the pandemic, which could be an alternative methodology for
viral molecular surveillance.