| Literature DB >> 33148702 |
Mario Frías1, Pedro López-López1, Ismael Zafra1, Javier Caballero-Gómez1,2, Isabel Machuca1, Ángela Camacho1, María A Risalde3, Antonio Rivero-Juárez4, Antonio Rivero1.
Abstract
The objective of this study was to design a pangenotypic PCR-based assay for the detection and quantification of hepatitis E virus (HEV) RNA from across the entire spectrum of described genotypes belonging to the Orthohepevirus A genus. The optimal conditions and the performance of the assay were determined by testing the WHO standard strain (6219/10) and the WHO HEV panel (8578/13). Similarly, performance comparisons were made with two commercial assays (Real Star HEV RT-PCR 2.0 and ampliCube HEV 2.0 Quant) to detect HEV RNA at concentrations below 1,000 IU/ml with viral strains from the WHO and to test samples from 54 patients with acute hepatitis. The assay presented in this study was able to detect the entire spectrum of described genotypes belonging to the Orthohepevirus A genus, demonstrating better performance than both commercial kits. This procedure may represent a significant improvement in the molecular diagnosis of HEV infection.Entities:
Keywords: HEV RNA; RT-PCR; limit of detection; pangenotypic; performance; primers; probe
Year: 2021 PMID: 33148702 PMCID: PMC8111163 DOI: 10.1128/JCM.02075-20
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948