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AIDS:
doi: 10.1097/QAD.0000000000000168
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Targeting host nucleotide biosynthesis with resveratrol inhibits emtricitabine-resistant HIV-1.

Heredia, Alonso; Davis, Charles; Amin, Mohammed N.; Le, Nhut M.; Wainberg, Mark A.; Oliveira, Maureen; Deeks, Steven G.; Wang, Lai-Xi; Redfield, Robert R.

Published Ahead-of-Print
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Abstract

Objective: The M184V mutation in the HIV-1 reverse transcriptase gene is frequent (>50%) in patients, both in resource-rich and resource-limited countries, conferring high-level resistance (>100-fold) to the cytosine analog reverse transcriptase inhibitors lamivudine and emtricitabine. The reverse transcriptase enzyme of M184V HIV-1 mutants has reduced processivity, resulting in reduced viral replication, particularly at low-nucleotide (dNTP) levels. We hypothesized that lowering intracellular dNTPs with resveratrol, a dietary supplement, could interfere with replication of M184V HIV-1 mutants.

Design and methods: Evaluation of the activity of resveratrol on infection of primary peripheral blood lymphocytes by wild-type and M184V mutant HIV-1. We assayed both molecular clones and primary isolates of HIV-1, containing M184V alone and in combination with other reverse transcriptase mutations. Viral infection was quantified by p24 ELISA and by quantitative real-time PCR analysis. Cell viability was measured by MTT assays.

Results: In virus-infectivity assays, resveratrol did not inhibit replication of wild-type NL4-3 (resveratrol EC50 > 10 [mu]mol/l), but it inhibited NL4-3 184V mutant (resveratrol EC50 = 5.8 [mu]mol/l). These results were confirmed by real-time PCR analysis of early and late products of reverse transcription. Resveratrol inhibited molecular clones and primary isolates carrying M184V, alone or in combination with other reverse transcriptase mutations (resveratrol EC50 values ranging from 2.5 to 7.7 [mu]mol/l).

Conclusions: Resveratrol inhibits HIV-1 strains carrying the M184V mutation in reverse transcriptase. We propose resveratrol as a potential adjuvant in HIV-1 therapy, particularly in resource-limited settings, to help control emtricitabine-resistant M184V HIV-1mutants.

(C) 2014 Lippincott Williams & Wilkins, Inc.

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