Longitudinal sequencing of HIV-1 infected patients with low-level viremia for years while on ART shows no indications for genetic evolution of the virus

HIV-infected patients on antiretroviral therapy (ART) may present low-level viremia (LLV) above the detection level of current viral load assays. In many cases LLV is persistent but does not result in overt treatment failure or selection of drug resistant viral variants. To elucidate whether LLV ref...

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Veröffentlicht in:Virology (New York, N.Y.) N.Y.), 2017-10, Vol.510, p.185-193
Hauptverfasser: Vancoillie, Leen, Hebberecht, Laura, Dauwe, Kenny, Demecheleer, Els, Dinakis, Sylvie, Vaneechoutte, Dries, Mortier, Virginie, Verhofstede, Chris
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Sprache:eng
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Zusammenfassung:HIV-infected patients on antiretroviral therapy (ART) may present low-level viremia (LLV) above the detection level of current viral load assays. In many cases LLV is persistent but does not result in overt treatment failure or selection of drug resistant viral variants. To elucidate whether LLV reflects active virus replication, we extensively sequenced pol and env genes of the viral populations present before and during LLV in 18 patients and searched for indications of genetic evolution. Maximum likelihood phylogenetic trees were inspected for temporal structure both visually and by linear regression analysis of root-to-tip and pairwise distances. Viral coreceptor tropism was assessed at different time points before and during LLV. In none of the patients consistent indications for genetic evolution were found over a median period of 4.8 years of LLV. As such these findings could not provide evidence that active virus replication is the main driver of LLV. •Viral replication was assessed in 18 patients with persisting low-level viremia.•Blood and plasma samples were analyzed over a long period of time.•Extensive longitudinal pol and env sequencing was performed before and during LLV.•Phylogenetic analysis could not provide proof of virus evolution and replication.
ISSN:0042-6822
1096-0341
DOI:10.1016/j.virol.2017.07.010