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Sequence Evaluation and Comparative Analysis of Novel Assays for Intact Proviral HIV-1 DNA
The HIV proviral reservoir is the major barrier to cure. The predominantly replication-defective proviral landscape makes the measurement of virus that is likely to cause rebound upon antiretroviral therapy (ART)-cessation challenging. To address this issue, novel assays to measure intact HIV provir...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094944/ https://www.ncbi.nlm.nih.gov/pubmed/33361426 http://dx.doi.org/10.1128/JVI.01986-20 |
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author | Gaebler, Christian Falcinelli, Shane D. Stoffel, Elina Read, Jenna Murtagh, Ross Oliveira, Thiago Y. Ramos, Victor Lorenzi, Julio C. C. Kirchherr, Jennifer James, Katherine S. Allard, Brigitte Baker, Caroline Kuruc, JoAnn D. Caskey, Marina Archin, Nancie M. Siliciano, Robert F. Margolis, David M. Nussenzweig, Michel C. |
author_facet | Gaebler, Christian Falcinelli, Shane D. Stoffel, Elina Read, Jenna Murtagh, Ross Oliveira, Thiago Y. Ramos, Victor Lorenzi, Julio C. C. Kirchherr, Jennifer James, Katherine S. Allard, Brigitte Baker, Caroline Kuruc, JoAnn D. Caskey, Marina Archin, Nancie M. Siliciano, Robert F. Margolis, David M. Nussenzweig, Michel C. |
author_sort | Gaebler, Christian |
collection | PubMed |
description | The HIV proviral reservoir is the major barrier to cure. The predominantly replication-defective proviral landscape makes the measurement of virus that is likely to cause rebound upon antiretroviral therapy (ART)-cessation challenging. To address this issue, novel assays to measure intact HIV proviruses have been developed. The intact proviral DNA assay (IPDA) is a high-throughput assay that uses two probes to exclude the majority of defective proviruses and determine the frequency of intact proviruses, albeit without sequence confirmation. Quadruplex PCR with four probes (Q4PCR) is a lower-throughput assay that uses limiting dilution long-distance PCR amplification followed by quantitative PCR (qPCR) and near-full-length genome sequencing (nFGS) to estimate the frequency of sequence-confirmed intact proviruses and provide insight into their clonal composition. To explore the advantages and limitations of these assays, we compared IPDA and Q4PCR measurements from 39 ART-suppressed people living with HIV. We found that IPDA and Q4PCR measurements correlated with one another, but frequencies of intact proviral DNA differed by approximately 19-fold. This difference may be in part due to inefficiencies in long-distance PCR amplification of proviruses in Q4PCR, leading to underestimates of intact proviral frequencies. In addition, nFGS analysis within Q4PCR explained that some of this difference is explained by proviruses that are classified as intact by IPDA but carry defects elsewhere in the genome. Taken together, this head-to-head comparison of novel intact proviral DNA assays provides important context for their interpretation in studies to deplete the HIV reservoir and shows that together the assays bracket true reservoir size. IMPORTANCE The intact proviral DNA assay (IPDA) and quadruplex PCR (Q4PCR) represent major advances in accurately quantifying and characterizing the replication-competent HIV reservoir. This study compares the two novel approaches for measuring intact HIV proviral DNA in samples from 39 antiretroviral therapy (ART)-suppressed people living with HIV, thereby informing ongoing efforts to deplete the HIV reservoir in cure-related trials. |
format | Online Article Text |
id | pubmed-8094944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-80949442021-05-07 Sequence Evaluation and Comparative Analysis of Novel Assays for Intact Proviral HIV-1 DNA Gaebler, Christian Falcinelli, Shane D. Stoffel, Elina Read, Jenna Murtagh, Ross Oliveira, Thiago Y. Ramos, Victor Lorenzi, Julio C. C. Kirchherr, Jennifer James, Katherine S. Allard, Brigitte Baker, Caroline Kuruc, JoAnn D. Caskey, Marina Archin, Nancie M. Siliciano, Robert F. Margolis, David M. Nussenzweig, Michel C. J Virol Pathogenesis and Immunity The HIV proviral reservoir is the major barrier to cure. The predominantly replication-defective proviral landscape makes the measurement of virus that is likely to cause rebound upon antiretroviral therapy (ART)-cessation challenging. To address this issue, novel assays to measure intact HIV proviruses have been developed. The intact proviral DNA assay (IPDA) is a high-throughput assay that uses two probes to exclude the majority of defective proviruses and determine the frequency of intact proviruses, albeit without sequence confirmation. Quadruplex PCR with four probes (Q4PCR) is a lower-throughput assay that uses limiting dilution long-distance PCR amplification followed by quantitative PCR (qPCR) and near-full-length genome sequencing (nFGS) to estimate the frequency of sequence-confirmed intact proviruses and provide insight into their clonal composition. To explore the advantages and limitations of these assays, we compared IPDA and Q4PCR measurements from 39 ART-suppressed people living with HIV. We found that IPDA and Q4PCR measurements correlated with one another, but frequencies of intact proviral DNA differed by approximately 19-fold. This difference may be in part due to inefficiencies in long-distance PCR amplification of proviruses in Q4PCR, leading to underestimates of intact proviral frequencies. In addition, nFGS analysis within Q4PCR explained that some of this difference is explained by proviruses that are classified as intact by IPDA but carry defects elsewhere in the genome. Taken together, this head-to-head comparison of novel intact proviral DNA assays provides important context for their interpretation in studies to deplete the HIV reservoir and shows that together the assays bracket true reservoir size. IMPORTANCE The intact proviral DNA assay (IPDA) and quadruplex PCR (Q4PCR) represent major advances in accurately quantifying and characterizing the replication-competent HIV reservoir. This study compares the two novel approaches for measuring intact HIV proviral DNA in samples from 39 antiretroviral therapy (ART)-suppressed people living with HIV, thereby informing ongoing efforts to deplete the HIV reservoir in cure-related trials. American Society for Microbiology 2021-02-24 /pmc/articles/PMC8094944/ /pubmed/33361426 http://dx.doi.org/10.1128/JVI.01986-20 Text en Copyright © 2021 Gaebler et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Pathogenesis and Immunity Gaebler, Christian Falcinelli, Shane D. Stoffel, Elina Read, Jenna Murtagh, Ross Oliveira, Thiago Y. Ramos, Victor Lorenzi, Julio C. C. Kirchherr, Jennifer James, Katherine S. Allard, Brigitte Baker, Caroline Kuruc, JoAnn D. Caskey, Marina Archin, Nancie M. Siliciano, Robert F. Margolis, David M. Nussenzweig, Michel C. Sequence Evaluation and Comparative Analysis of Novel Assays for Intact Proviral HIV-1 DNA |
title | Sequence Evaluation and Comparative Analysis of Novel Assays for Intact Proviral HIV-1 DNA |
title_full | Sequence Evaluation and Comparative Analysis of Novel Assays for Intact Proviral HIV-1 DNA |
title_fullStr | Sequence Evaluation and Comparative Analysis of Novel Assays for Intact Proviral HIV-1 DNA |
title_full_unstemmed | Sequence Evaluation and Comparative Analysis of Novel Assays for Intact Proviral HIV-1 DNA |
title_short | Sequence Evaluation and Comparative Analysis of Novel Assays for Intact Proviral HIV-1 DNA |
title_sort | sequence evaluation and comparative analysis of novel assays for intact proviral hiv-1 dna |
topic | Pathogenesis and Immunity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094944/ https://www.ncbi.nlm.nih.gov/pubmed/33361426 http://dx.doi.org/10.1128/JVI.01986-20 |
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