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HIV-1 drug resistance genotyping from dried blood spots stored for 1 year at 4°C
BACKGROUND: Dried blood spots (DBSs) are an attractive alternative to plasma for HIV-1 drug resistance testing in resource-limited settings. We recently showed that HIV-1 can be efficiently genotyped from DBSs stored at −20°C for prolonged periods (0.5–4 years). Here, we evaluated the efficiency of...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386080/ https://www.ncbi.nlm.nih.gov/pubmed/18344550 http://dx.doi.org/10.1093/jac/dkn100 |
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author | Youngpairoj, Ae S. Masciotra, Silvina Garrido, Carolina Zahonero, Natalia de Mendoza, Carmen García-Lerma, J. Gerardo |
author_facet | Youngpairoj, Ae S. Masciotra, Silvina Garrido, Carolina Zahonero, Natalia de Mendoza, Carmen García-Lerma, J. Gerardo |
author_sort | Youngpairoj, Ae S. |
collection | PubMed |
description | BACKGROUND: Dried blood spots (DBSs) are an attractive alternative to plasma for HIV-1 drug resistance testing in resource-limited settings. We recently showed that HIV-1 can be efficiently genotyped from DBSs stored at −20°C for prolonged periods (0.5–4 years). Here, we evaluated the efficiency of genotyping from DBSs stored at 4°C for 1 year. METHODS: A total of 40 DBSs were prepared from residual diagnostic specimens collected from HIV subtype B-infected persons and were stored with desiccant at 4°C. Total nucleic acids were extracted after 1 year using a modification of the Nuclisens assay. Resistance testing was performed using the ViroSeq HIV-1 assay and an in-house nested RT–PCR method validated for HIV-1 subtype B that amplifies a smaller (1 kb) pol fragment. RESULTS: Using the ViroSeq assay, only 23 of the 40 (57.5%) DBS specimens were successfully genotyped; 22 of these specimens had plasma viraemia >10 000 RNA copies/mL. When the specimens were tested using the in-house assay, 38 of the 40 DBSs (95%) were successfully genotyped. Overall, resistance genotypes generated from the DBSs and plasma were highly concordant. CONCLUSIONS: We show that drug resistance genotyping from DBSs stored at 4°C with desiccant is highly efficient but requires the amplification of small pol fragments and the use of an in-house nested PCR protocol with quality-controlled reagents. These findings suggest that 4°C may represent a suitable temperature for long-term storage of DBSs. |
format | Text |
id | pubmed-2386080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-23860802009-02-25 HIV-1 drug resistance genotyping from dried blood spots stored for 1 year at 4°C Youngpairoj, Ae S. Masciotra, Silvina Garrido, Carolina Zahonero, Natalia de Mendoza, Carmen García-Lerma, J. Gerardo J Antimicrob Chemother Original Research BACKGROUND: Dried blood spots (DBSs) are an attractive alternative to plasma for HIV-1 drug resistance testing in resource-limited settings. We recently showed that HIV-1 can be efficiently genotyped from DBSs stored at −20°C for prolonged periods (0.5–4 years). Here, we evaluated the efficiency of genotyping from DBSs stored at 4°C for 1 year. METHODS: A total of 40 DBSs were prepared from residual diagnostic specimens collected from HIV subtype B-infected persons and were stored with desiccant at 4°C. Total nucleic acids were extracted after 1 year using a modification of the Nuclisens assay. Resistance testing was performed using the ViroSeq HIV-1 assay and an in-house nested RT–PCR method validated for HIV-1 subtype B that amplifies a smaller (1 kb) pol fragment. RESULTS: Using the ViroSeq assay, only 23 of the 40 (57.5%) DBS specimens were successfully genotyped; 22 of these specimens had plasma viraemia >10 000 RNA copies/mL. When the specimens were tested using the in-house assay, 38 of the 40 DBSs (95%) were successfully genotyped. Overall, resistance genotypes generated from the DBSs and plasma were highly concordant. CONCLUSIONS: We show that drug resistance genotyping from DBSs stored at 4°C with desiccant is highly efficient but requires the amplification of small pol fragments and the use of an in-house nested PCR protocol with quality-controlled reagents. These findings suggest that 4°C may represent a suitable temperature for long-term storage of DBSs. Oxford University Press 2008-06 2008-03-15 /pmc/articles/PMC2386080/ /pubmed/18344550 http://dx.doi.org/10.1093/jac/dkn100 Text en Published by Oxford University Press 2008 |
spellingShingle | Original Research Youngpairoj, Ae S. Masciotra, Silvina Garrido, Carolina Zahonero, Natalia de Mendoza, Carmen García-Lerma, J. Gerardo HIV-1 drug resistance genotyping from dried blood spots stored for 1 year at 4°C |
title | HIV-1 drug resistance genotyping from dried blood spots stored for 1 year at 4°C |
title_full | HIV-1 drug resistance genotyping from dried blood spots stored for 1 year at 4°C |
title_fullStr | HIV-1 drug resistance genotyping from dried blood spots stored for 1 year at 4°C |
title_full_unstemmed | HIV-1 drug resistance genotyping from dried blood spots stored for 1 year at 4°C |
title_short | HIV-1 drug resistance genotyping from dried blood spots stored for 1 year at 4°C |
title_sort | hiv-1 drug resistance genotyping from dried blood spots stored for 1 year at 4°c |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386080/ https://www.ncbi.nlm.nih.gov/pubmed/18344550 http://dx.doi.org/10.1093/jac/dkn100 |
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