Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-018-20682-w
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dc.titleNo evidence of ongoing evolution in replication competent latent HIV-1 in a patient followed up for two years
dc.contributor.authorMok, H.P
dc.contributor.authorNorton, N.J
dc.contributor.authorHirst, J.C
dc.contributor.authorFun, A
dc.contributor.authorBandara, M
dc.contributor.authorWills, M.R
dc.contributor.authorLever, A.M.L
dc.date.accessioned2020-10-20T03:29:06Z
dc.date.available2020-10-20T03:29:06Z
dc.date.issued2018
dc.identifier.citationMok, H.P, Norton, N.J, Hirst, J.C, Fun, A, Bandara, M, Wills, M.R, Lever, A.M.L (2018). No evidence of ongoing evolution in replication competent latent HIV-1 in a patient followed up for two years. Scientific Reports 8 (1) : 2639. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-018-20682-w
dc.identifier.issn20452322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/177829
dc.description.abstractThe persistence of infected T cells harbouring intact HIV proviruses is the barrier to the eradication of HIV. This reservoir is stable over long periods of time despite antiretroviral therapy. There has been controversy on whether low level viral replication is occurring at sanctuary sites periodically reseeding infected cells into the latent reservoir to account its durability. To study viral evolution in a physiologically relevant population of latent viruses, we repeatedly performed virus outgrowth assays on a stably treated HIV positive patient over two years and sequenced the reactivated latent viruses. We sought evidence of increasing sequence pairwise distances with time as evidence of ongoing viral replication. 64 reactivatable latent viral sequences were obtained over 103 weeks. We did not observe an increase in genetic distance of the sequences with the time elapsed between sampling. No evolution could be discerned in these reactivatable latent viruses. Thus, in this patient, the contribution of low-level replication to the maintenance of the latent reservoir detectable in the blood compartment is limited. © 2018 The Author(s).
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectadult
dc.subjectarticle
dc.subjectblood
dc.subjectgenetic distance
dc.subjecthuman
dc.subjectHuman immunodeficiency virus 1
dc.subjectHuman immunodeficiency virus infected patient
dc.subjectnonhuman
dc.subjectsampling
dc.subjectvirus replication
dc.subjectCD4+ T lymphocyte
dc.subjectHuman immunodeficiency virus 1
dc.subjectHuman immunodeficiency virus infection
dc.subjectmale
dc.subjectmiddle aged
dc.subjectmolecular evolution
dc.subjectphysiology
dc.subjectprocedures
dc.subjectvirology
dc.subjectvirus latency
dc.subjectvirus load
dc.subjectvirus replication
dc.subjectCD4-Positive T-Lymphocytes
dc.subjectEvolution, Molecular
dc.subjectHIV Infections
dc.subjectHIV-1
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectViral Load
dc.subjectVirus Latency
dc.subjectVirus Replication
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.description.doi10.1038/s41598-018-20682-w
dc.description.sourcetitleScientific Reports
dc.description.volume8
dc.description.issue1
dc.description.page2639
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