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Inicio Annals of Hepatology P-14 OPTIMIZATION OF MOLECULAR METHODS FOR SARS-CoV-2 QUALITATIVE DETECTION AND ...
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Vol. 28. Issue S1.
Abstracts of the 2022 Annual Meeting of the ALEH
(March 2023)
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Vol. 28. Issue S1.
Abstracts of the 2022 Annual Meeting of the ALEH
(March 2023)
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P-14 OPTIMIZATION OF MOLECULAR METHODS FOR SARS-CoV-2 QUALITATIVE DETECTION AND GENOTYPING IN RESPIRATORY SPECIMENS FROM PATIENTS WITH LIVER DISEASE
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Vanessa Duarte da Costa1, Alanna Calheiros Santos1, Lucas Limas da Silva1, Wilian Jean Wiggers2, Claudia Alexandra Pontes Ivantes2, Danielle Malta Lima3, Jeová Keny Baima Colares3, Deusilene Souza Vieira Dallacqua4, Ana Rita Coimbra Motta-Castro5, Vanessa Salete de Paula6, Alberto Martín Rivera Dávila7, Priscilla Pollo-Flores8, Lia Laura Lewis-Ximenez1, Livia Melo Villar1
1 Brazilian Reference Laboratory of Viral Hepatitis, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil
2 Service of Gastroenterology, Hepatology and Liver Transplantation, Hospital Nossa Senhora das Graças, Curitiba, Paraná, Brazil
3 Postgraduate Program in Pathology, Federal University of Ceará, Fortaleza, Ceará, Brazil
4 Molecular Virology Laboratory, Oswaldo Cruz Foundation, FIOCRUZ, Porto Velho, Rondônia, Brazil
5 Federal University of Mato Grosso do Sul, Campo Grande, Mato Grosso do Sul, Brazil; Oswaldo Cruz Foundation, Campo Grande, Mato Grosso do Sul, Brazil
6 Molecular Virology Laboratory, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, Brazil
7 Computational and Systems Biology Laboratory, Graduate Program in Biodiversity and Health, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, Brazil
8 Internal Medicine Department, Fluminense Federal University, Niterói, Rio de Janeiro, Brazil
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Vol. 28. Issue S1

Abstracts of the 2022 Annual Meeting of the ALEH

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Introduction and Objectives

SARS-CoV-2 active infection diagnosis is currently performed through RT-qPCR. Despite the fact that PCR-based assays can provide results relatively fast, these techniques require capable professionals, specific equipment and adequate infrastructure. In order to facilitate COVID-19 diagnosis in remote areas, an alternative to RT-qPCR would be loop-mediated isothermal (RT-LAMP) amplification. SARS-CoV-2 variant genotyping through high-throughput sequencing (HTS) allows SARS-CoV-2 genomic surveillance, especially for patients with a higher vulnerability. This study aimed to optimize RT-LAMP and HTS methods for SARS-CoV-2 RNA detection and genotyping, respectively, in respiratory samples from patients with liver disease.

Materials and Methods

A total of 142 respiratory secretions were obtained from individuals with SARS-CoV-2 RNA detectable by RT-qPCR (N1 Ct ≤ 30), divided into groups with (n=18) or without (n=124) liver disease. The study also enrolled 55 individuals who had SARS-CoV-2 RNA undetectable at RT-qPCR. For RT-LAMP methodology, primers were used for ORF1 gene amplification. As for HTS genotyping, the steps of cDNA synthesis, complete SARS-CoV-2 genome PCR amplification, preparation of genomic libraries and sequencing in MinION device were performed for 26 swab samples.

Results

Samples with viral RNA detectable by RT-qPCR had a mean Ct value of 24.3 ± 3.75. Referring to RT-LAMP, it was observed a sensitivity of 71.1% (101/142). When considering RT-qPCR mean Ct value, RT-LAMP sensitivity was 88.9% (16/18), associated with a mean Ct of 23.3 ± 3.5 for patients with COVID and hepatitis. A specificity of 100% (55/55) was observed since all negative swabs tested by RT-qPCR were negative at RT-LAMP. Through sequencing by MinION, SARS-CoV-2 lineages gamma (7/26; 27%), zeta (1/26; 3.9%), delta (6/26; 23%) and omicron (12/26; 46.1%) were genotyped and detected by RT-LAMP.

Conclusions

RT-LAMP demonstrated high sensitivity for molecular detection of SARS-CoV-2 RNA for patients with high viral load. Besides, RT-LAMP was capable of detecting all SARS-CoV-2 lineages genotyped by MinION in both groups.

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