MétaCan
Menu
Back to cohort

Latent HIV-1 can be reactivated by superinfection in a Tat-dependent manner, which can lead to the emergence of recombinant viruses

2013· article· en· W22827969 on OpenAlexaff
Daniel A. Donahue, Sophie M. Bastarache, Richard D. Sloan, Mark A. Wainberg

Bibliographic record

VenueRetrovirology · 2013
Typearticle
Languageen
FieldImmunology and Microbiology
TopicHIV Research and Treatment
Canadian institutionsMcGill University Health Centre
Fundersnot available
KeywordsJurkat cellsSuperinfectionVirologyRecombinant DNABiologyLatent VirusVirusGeneGeneticsT cellImmune system

Abstract

fetched live from OpenAlex

The HIV-1 latent reservoir represents an important source of genetic diversity that could contribute to viral evolution and drug resistance. Latent virus reactivation might occur by superinfection of latently infected cells. Previous studies have suggested that latent viruses contribute to recombination in vivo , but this has not been experimentally studied. We used both Jurkat and primary cell latency models. In Jurkat cells, wt and drug-resistant latent populations were superinfected with wt or drug-resistant viruses, including nef or tat mutants, and treated with various inhibitors. Viral reporter gene expression was measured by FACS. Sequence tags on each resistant virus permitted identification of recombinants. We also performed superinfection experiments in primary cells. Latent viruses were reactivated by superinfection in both latency models. In Jurkat cells, the extent of latent virus reactivation was strongly correlated (r = 0.98) with the extent of superinfection across a wide range of viral inocula. Latent virus reactivation required gene expression of the superinfecting virus, since latent viruses were reactivated in the presence of a protease inhibitor, but not a reverse transcriptase (RT) or integrase inhibitor. Latent virus reactivation occurred following superinfection with nef-deleted or tat-attenuated, but not tat-inactivated, viruses. These results suggest that neither gp120-induced CD4/CXCR4 signalling nor Nef-induced NFkB/NFAT modulation were required for latent virus reactivation, but that superinfecting virus Tat was required. Drug-resistant latent viruses (RT K103N) were reactivated following superinfection with additional drug resistant viruses (RT M184V). The resulting supernatants (containing heterozygous virions) were used to infect new cells, to which the RT inhibitors FTC and EFV were added. Sequencing and restriction digestion confirmed that recombination frequently occurred, leading to FTC/EFV-resistant virions encoding unique sequence tags derived from both parental viruses. We also established latency in unstimulated primary CD4T-cells and subjected them to superinfection. Results from nine individual donors indicate that latent viruses were reactivated by superinfection; these results were statistically significant (p=0.001). Our results suggest that superinfection of latently infected cells can reactivate latent viruses, which can then recombine with the superinfecting virus. Since all viral quasispecies including drug-resistant viruses can be latently archived, reactivation of latent viruses by superinfection or other means could contribute to the emergence of replicatively fit viruses in the face of strong selective pressures.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.274
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.017
GPT teacher head0.252
Teacher spread0.235 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations2
Published2013
Admission routes1
Has abstractyes

Explore more

Same venueRetrovirologySame topicHIV Research and TreatmentFrench-language works237,207