Abstract
In third-world countries, dried blood samples (DBS) are a convenient alternative to plasma for monitoring viral load during HIV-1 therapy. In this study, we evaluated the feasibility of using DBS to perform HIV-1 drug resistance genotyping in a ViroSeq assay in which the protease and reverse transcriptase regions of the pol gene are analyzed. Fifty-seven antiretroviral genotypes from plasma samples were tested, and drug resistance genotypes were determined. Only 38.6% paired DBS samples were sequenced. Failure to amplify DNA from DBS samples generally correlated with plasma viral loads below log10 5.1. The majority of the mutations identified in plasma pol sequences were also found in their DBS counterpart, with a concordance in genotype interpretation of 96.4%. Several factors were identified that could potentially improve both the sensitivity and the quality of genotype data, such as sample storage conditions and sequence analysis. Therefore, DBS sampling is useful to determine viral load and drug resistance genotypes in HIV patients.
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Abbreviations
- DBS:
-
Dried blood sample
- P:
-
Plasma
- HAART:
-
Highly active antiretroviral therapy
- FDA:
-
Federal Drug Administration
- PR:
-
Protease
- RT:
-
Reverse transcriptase
- NRTI:
-
Nucleoside/nucleotide RT inhibitor
- NNRTI:
-
Non-nucleoside RT inhibitor
- PI:
-
Protease inhibitor
- VL:
-
Viral load
- IMSS:
-
Instituto Mexicano del Seguro Social
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Acknowledgments
This work was supported by Consejo Nacional de Ciencia y Tecnologia (CONACYT-SALUD 2004-01-008). We thank Dr. Ana Ma. Cevallos for valuable comments and reviewing the manuscript, and Dr. Margarita Dehesa for inclusion of patients.
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The authors declare that they have no conflict of interest.
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This work was supported by Consejo Nacional de Ciencia y Tecnología SALUD/CONACYT grant 2004-01-008.
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Lira, R., Valdez-Salazar, H., Vazquez-Rosales, G. et al. Genotypic testing for HIV-1 drug resistance using dried blood samples. Arch Virol 155, 1117–1125 (2010). https://doi.org/10.1007/s00705-010-0696-y
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DOI: https://doi.org/10.1007/s00705-010-0696-y