HIV Promoters Isolated from Brain and Peripheral Tissue of Virally Suppressed PWH Are Phylogenetically and Functionally Similar

= 5). Following single-genome amplification, sequences were phylogenetically analyzed and transcriptional activity was assessed. In contrast to non-virally suppressed PWH, LTR sequences failed to compartmentalize between the brain and peripheral compartments. Identical LTR sequences were observed across brain and peripheral tissues in 2/5 PWH. While the LTRs remain transcriptionally active, mutations, insertions and deletions predicted to reduce transcription factor binding affinity at key binding sites, including C/EBP, NF-κB, and Sp1 sites, were observed and found to result in reduced basal transcriptional activity. The role of these mutations in latency and viral persistence remains unclear.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2026-03-31
DOI
https://doi.org/10.3390/ijms27073185
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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HIV Promoters Isolated from Brain and Peripheral Tissue of Virally Suppressed PWH Are Phylogenetically and Functionally Similar

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HIV Promoters Isolated from Brain and Peripheral Tissue of Virally Suppressed PWH Are Phylogenetically and Functionally Similar

Anna C. Hearps, Narin Osman, Janna Jamal Eddine, Jingling Zhou, Sarah J. Byrnes, Thomas A. Angelovich, Trisha A. Jenkins, Melissa J. Churchill, Emily Chalmers, Michael Roche
article en

Abstract

= 5). Following single-genome amplification, sequences were phylogenetically analyzed and transcriptional activity was assessed. In contrast to non-virally suppressed PWH, LTR sequences failed to compartmentalize between the brain and peripheral compartments. Identical LTR sequences were observed across brain and peripheral tissues in 2/5 PWH. While the LTRs remain transcriptionally active, mutations, insertions and deletions predicted to reduce transcription factor binding affinity at key binding sites, including C/EBP, NF-κB, and Sp1 sites, were observed and found to result in reduced basal transcriptional activity. The role of these mutations in latency and viral persistence remains unclear.

International Journal of Molecular SciencesVol. 27(7)
Burnet Institute (AU), Peter Doherty Institute (AU), Monash University (AU), RMIT University (AU)
National Health and Medical Research Council, National Institute on Drug Abuse
Good health and well-being
Openalex Percentile: Top 32%
HIV Research and Treatment
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