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Performance of an In-House Human Immunodeficiency Virus Type 1 Genotyping System for Assessment of Drug Resistance in Cuba
As commercial human immunodeficiency virus type 1 drug resistance assays are expensive, they are not commonly used in resource-limited settings. Hence, a more affordable in-house procedure was set up taking into account the specific epidemiological and economic circumstances of Cuba. The performance...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324769/ https://www.ncbi.nlm.nih.gov/pubmed/25671421 http://dx.doi.org/10.1371/journal.pone.0117176 |
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author | Alemán, Yoan Vinken, Lore Kourí, Vivian Pérez, Lissette Álvarez, Alina Abrahantes, Yeissel Fonseca, Carlos Pérez, Jorge Correa, Consuelo Soto, Yudira Schrooten, Yoeri Vandamme, Anne-Mieke Van Laethem, Kristel |
author_facet | Alemán, Yoan Vinken, Lore Kourí, Vivian Pérez, Lissette Álvarez, Alina Abrahantes, Yeissel Fonseca, Carlos Pérez, Jorge Correa, Consuelo Soto, Yudira Schrooten, Yoeri Vandamme, Anne-Mieke Van Laethem, Kristel |
author_sort | Alemán, Yoan |
collection | PubMed |
description | As commercial human immunodeficiency virus type 1 drug resistance assays are expensive, they are not commonly used in resource-limited settings. Hence, a more affordable in-house procedure was set up taking into account the specific epidemiological and economic circumstances of Cuba. The performance characteristics of the in-house assay were evaluated using clinical samples with various subtypes and resistance patterns. The lower limit of amplification was determined on dilutions series of 20 clinical isolates and ranged from 84 to 529 RNA copies/mL. For the assessment of trueness, 14 clinical samples were analyzed and the ViroSeq HIV-1 Genotyping System v2.0 was used as the reference standard. The mean nucleotide sequence identity between the two assays was 98.7% ± 1.0. Additionally, 99.0% of the amino acids at drug resistance positions were identical. The sensitivity and specificity in detecting drug resistance mutations was respectively 94.1% and 99.5%. Only few discordances in drug resistance interpretation patterns were observed. The repeatability and reproducibility were evaluated using 10 clinical samples with 3 replicates per sample. The in-house test was very precise as nucleotide sequence identity among paired nucleotide sequences ranged from 98.7% to 99.9%. The acceptance criteria were met by the in-house test for all performance characteristics, demonstrating a high degree of accuracy. Subsequently, the applicability in routine clinical practice was evaluated on 380 plasma samples. The amplification success rate was 91% and good quality consensus sequences encoding the entire protease and the first 335 codons in reverse transcriptase could be obtained for 99% of the successful amplicons. The reagent cost per sample using the in-house procedure was around € 80 per genotyping attempt. Overall, the in-house assay provided good results, was feasible with equipment and reagents available in Cuba and was half as expensive as commercial assays. |
format | Online Article Text |
id | pubmed-4324769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43247692015-02-18 Performance of an In-House Human Immunodeficiency Virus Type 1 Genotyping System for Assessment of Drug Resistance in Cuba Alemán, Yoan Vinken, Lore Kourí, Vivian Pérez, Lissette Álvarez, Alina Abrahantes, Yeissel Fonseca, Carlos Pérez, Jorge Correa, Consuelo Soto, Yudira Schrooten, Yoeri Vandamme, Anne-Mieke Van Laethem, Kristel PLoS One Research Article As commercial human immunodeficiency virus type 1 drug resistance assays are expensive, they are not commonly used in resource-limited settings. Hence, a more affordable in-house procedure was set up taking into account the specific epidemiological and economic circumstances of Cuba. The performance characteristics of the in-house assay were evaluated using clinical samples with various subtypes and resistance patterns. The lower limit of amplification was determined on dilutions series of 20 clinical isolates and ranged from 84 to 529 RNA copies/mL. For the assessment of trueness, 14 clinical samples were analyzed and the ViroSeq HIV-1 Genotyping System v2.0 was used as the reference standard. The mean nucleotide sequence identity between the two assays was 98.7% ± 1.0. Additionally, 99.0% of the amino acids at drug resistance positions were identical. The sensitivity and specificity in detecting drug resistance mutations was respectively 94.1% and 99.5%. Only few discordances in drug resistance interpretation patterns were observed. The repeatability and reproducibility were evaluated using 10 clinical samples with 3 replicates per sample. The in-house test was very precise as nucleotide sequence identity among paired nucleotide sequences ranged from 98.7% to 99.9%. The acceptance criteria were met by the in-house test for all performance characteristics, demonstrating a high degree of accuracy. Subsequently, the applicability in routine clinical practice was evaluated on 380 plasma samples. The amplification success rate was 91% and good quality consensus sequences encoding the entire protease and the first 335 codons in reverse transcriptase could be obtained for 99% of the successful amplicons. The reagent cost per sample using the in-house procedure was around € 80 per genotyping attempt. Overall, the in-house assay provided good results, was feasible with equipment and reagents available in Cuba and was half as expensive as commercial assays. Public Library of Science 2015-02-11 /pmc/articles/PMC4324769/ /pubmed/25671421 http://dx.doi.org/10.1371/journal.pone.0117176 Text en © 2015 Alemán et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Alemán, Yoan Vinken, Lore Kourí, Vivian Pérez, Lissette Álvarez, Alina Abrahantes, Yeissel Fonseca, Carlos Pérez, Jorge Correa, Consuelo Soto, Yudira Schrooten, Yoeri Vandamme, Anne-Mieke Van Laethem, Kristel Performance of an In-House Human Immunodeficiency Virus Type 1 Genotyping System for Assessment of Drug Resistance in Cuba |
title | Performance of an In-House Human Immunodeficiency Virus Type 1 Genotyping System for Assessment of Drug Resistance in Cuba |
title_full | Performance of an In-House Human Immunodeficiency Virus Type 1 Genotyping System for Assessment of Drug Resistance in Cuba |
title_fullStr | Performance of an In-House Human Immunodeficiency Virus Type 1 Genotyping System for Assessment of Drug Resistance in Cuba |
title_full_unstemmed | Performance of an In-House Human Immunodeficiency Virus Type 1 Genotyping System for Assessment of Drug Resistance in Cuba |
title_short | Performance of an In-House Human Immunodeficiency Virus Type 1 Genotyping System for Assessment of Drug Resistance in Cuba |
title_sort | performance of an in-house human immunodeficiency virus type 1 genotyping system for assessment of drug resistance in cuba |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324769/ https://www.ncbi.nlm.nih.gov/pubmed/25671421 http://dx.doi.org/10.1371/journal.pone.0117176 |
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