SAMHD1 Has Differential Impact on the Efficacies of HIV Nucleoside Reverse Transcriptase Inhibitors

Sterile alpha motif- and histidine/aspartic acid domain-containing protein 1 (SAMHD1) limits HIV-1 replication by hydrolyzing deoxynucleoside triphosphates (dNTPs) necessary for reverse transcription. Nucleoside reverse transcriptase inhibitors (NRTIs) are components of anti-HIV therapies. We report...

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Veröffentlicht in:Antimicrobial agents and chemotherapy 2014-08, Vol.58 (8), p.4915-4919
Hauptverfasser: HUBER, Andrew D, MICHAILIDIS, Eleftherios, LANDAU, Nathaniel R, SARAFIANOS, Stefan G, SCHULTZ, Megan L, ONG, Yee T, BLOCH, Nicolin, PURAY-CHAVEZ, Maritza N, LESLIE, Maxwell D, JUAN JI, LUCAS, Anthony D, KIRBY, Karen A
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Sprache:eng
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Zusammenfassung:Sterile alpha motif- and histidine/aspartic acid domain-containing protein 1 (SAMHD1) limits HIV-1 replication by hydrolyzing deoxynucleoside triphosphates (dNTPs) necessary for reverse transcription. Nucleoside reverse transcriptase inhibitors (NRTIs) are components of anti-HIV therapies. We report here that SAMHD1 cleaves NRTI triphosphates (TPs) at significantly lower rates than dNTPs and that SAMHD1 depletion from monocytic cells affects the susceptibility of HIV-1 infections to NRTIs in complex ways that depend not only on the relative changes in dNTP and NRTI-TP concentrations but also on the NRTI activation pathways.
ISSN:0066-4804
1098-6596
DOI:10.1128/AAC.02745-14