(Retrovirology[TA])
1,729 results
  • Metabolic reprogramming of CD4[+] T cells by Zaprinast induces HIV-1 latency reversal ex vivo. [Journal Article]
    Retrovirology. 2026 Jun 13; 23(1).De Masson d'Autume V, LeDouce V, … Gautier WVR
  • CONCLUSIONS: These results highlight that selective targeting of the quiescent metabolic state in resting CD4[+] T cells can facilitate HIV-1 reactivation without compromising cellular integrity. This study identifies host metabolic reprogramming as a promising strategy to enhance latency reversal and complement existing cure strategies. Our work provides new insights into the importance of host metabolic states in governing viral persistence and underscores the translational potential of metabolic interventions in HIV-1 eradication research.
  • Non-integrase mechanisms for dolutegravir resistance. [Review]
    Retrovirology. 2026 Jun 05; 23(1).Engelman ANR
  • CONCLUSIONS: The unexpected observation that multiple non-integrase pathways can contribute to the generation of dolutegravir resistance highlights the remarkable plasticity of HIV-1 to circumvent challenge with a highly efficacious small molecule inhibitor. Given its current global use as a frontline anti-HIV inhibitor, this research informs regions of sequence surveillance for the continued safe and efficacious use of dolutegravir-based antiretroviral therapies.
  • Functional dissection of the prototype foamy virus glycoprotein heparan sulfate binding site. [Journal Article]
    Retrovirology. 2026 Mar 21; 23(1).Büttrich M, Stanke-Scheffler N, … Lindemann DR
  • CONCLUSIONS: The minimal HSBS of the PFV GPC is defined by four central, evolutionarily conserved positively charged residues. Substituting these with negatively charged amino acids abolishes HS-dependent attachment and severely reduces specific infectivity. The minor impact of the peripheral residue mutation K356E, combined with the lack of evolutionary conservation among most peripheral positively charged residues in primate FV species, suggests these residues play only a secondary role in HS interaction. Furthermore, the residual infectivity of PCSP mutants in HS-deficient cells confirms that HS is an important attachment factor but not an essential entry receptor. The functional homology between PFV and SFVggo GPCs strongly suggests that this conserved PCSP constitutes a universal HS-binding site across all FV species.
  • Strand-specific detection of cell-associated sense and antisense HIV-1 RNAs in splenocytes and PBMC from PLWH. [Journal Article]
    Retrovirology. 2025 Dec 24; 23(1):2.Waast L, Geronimi A, … Pique CR
  • CONCLUSIONS: This study demonstrates that HIV-1 antisense RNAs are expressed in spleen and blood of untreated HIV-1-infected individuals, of at least B and CRF02 subtypes, and that the level of antisense transcription can be significant and even predominant, as compared to sense transcription. These data, along with the protocols we described, will enable a more thorough analysis of HIV-1 sense and antisense expression dynamics in vivo, which could pave the way for novel strategies to control HIV-1 infection.
  • Transcriptome mining reveals diversity and evolution of circulating and endogenous amphibian retroviruses. [Journal Article]
    Retrovirology. 2025 Dec 10; 22(1):13.Harding EF, Webster B, … White PAR
  • CONCLUSIONS: Through the characterisation of metatranscriptomic and genomic data from retroviruses in this study, we provide insights into their evolution in amphibians and exemplify the diversity of Retroviridae in vertebrate genomes. The identification of novel retroviral clades, widespread transcription of endogenous retroviruses in amphibians and abundance of ERV copies suggests that Retroviridae have played a significant role in amphibian evolution.
  • t-RNA mediates provirus deletion in HIV-infected cells. [Journal Article]
    Retrovirology. 2025 Jul 01; 22(1):11.Gurgo C, Franchini GR
  • CONCLUSIONS: Large deletions of proviral DNA have been reported in PLWH on ART and attributed to errors that occurred in the synthesis of the minus strand during the reverse transcription of the viral genome. Our results support an additional mechanism for proviral deletions, mediated by tRNA[Gly], in the inactivation of the provirus.