Quantitation of Integrated HIV Provirus by Pulsed-Field Gel Electrophoresis and Droplet Digital PCR
We utilized pulsed-field gel electrophoresis (PFGE) to purify high-molecular-weight DNA from HIV-infected cells. This purification, in combination with our previously described droplet digital PCR (ddPCR) assay, was used to develop a method to quantify proviral integrated HIV DNA free of lower-molec...
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Published in | Journal of clinical microbiology Vol. 56; no. 12 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
01.12.2018
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Subjects | |
Online Access | Get full text |
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Summary: | We utilized pulsed-field gel electrophoresis (PFGE) to purify high-molecular-weight DNA from HIV-infected cells. This purification, in combination with our previously described droplet digital PCR (ddPCR) assay, was used to develop a method to quantify proviral integrated HIV DNA free of lower-molecular-weight species of HIV DNA.
We utilized pulsed-field gel electrophoresis (PFGE) to purify high-molecular-weight DNA from HIV-infected cells. This purification, in combination with our previously described droplet digital PCR (ddPCR) assay, was used to develop a method to quantify proviral integrated HIV DNA free of lower-molecular-weight species of HIV DNA. Episomal 2-long-terminal-repeat (2-LTR) circles were completely cleared from HIV DNA samples. Technical replicates of the complete assay, starting with the same specimens, resulted in no statistical differences in quantification of integrated HIV
gag
sequences in cellular DNA from cells from HIV-infected subjects after prolonged treatment with antiretroviral therapy (ART). The PFGE ddPCR assay was compared to the
Alu-gag
quantitative PCR (qPCR) assay, the most widely used assay to measure proviral integrated HIV DNA. Spearman's rho nonparametric correlation determined PFGE ddPCR results to be positively correlated with
Alu-gag
qPCR results (
r
= 0.7052;
P
= 0.0273). In summary, PFGE ddPCR is a sensitive, reproducible, and robust method to measure proviral integrated HIV DNA and is theoretically more accurate than previously described assays, because it is a direct measure of integrated HIV DNA. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Undefined-3 Present address: Steven M. Lada, University of Colorado Denver School of Medicine, Aurora, Colorado, USA; Karissa Huang, University of California, Irvine, Irvine, California, USA; D. Jake VanBelzen, Department of Molecular Biosciences, Northwestern University, Evanston, Illinois, USA. Citation Lada SM, Huang K, VanBelzen DJ, Montaner LJ, O'Doherty U, Richman DD. 2018. Quantitation of integrated HIV provirus by pulsed-field gel electrophoresis and droplet digital PCR. J Clin Microbiol 56:e01158-18. https://doi.org/10.1128/JCM.01158-18. |
ISSN: | 0095-1137 1098-660X 1098-660X |
DOI: | 10.1128/JCM.01158-18 |