Evidence map›Paper›PMID 38928103›Full record

ArticleInternational journal of molecular sciences2024

Evaluating HIV-1 Infectivity and Virion Maturation across Varied Producer Cells with a Novel FRET-Based Detection and Quantification Assay.

Aidan McGraw, Grace Hillmer, Jeongpill Choi, Kedhar Narayan, Stefania M Mehedincu, Dacia Marquez, Hasset Tibebe, Kathleen L DeCicco-Skinner, Taisuke Izumi

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Aidan McGrawDepartment of Biology, College of Arts and Sciences, American University, Washington, DC 20016, USA.ORCID 0009-0003-9272-0805
Grace HillmerDepartment of Biology, College of Arts and Sciences, American University, Washington, DC 20016, USA.
Jeongpill ChoiDepartment of Biology, College of Arts and Sciences, American University, Washington, DC 20016, USA.
Kedhar NarayanDepartment of Biology, College of Arts and Sciences, American University, Washington, DC 20016, USA.
Stefania M MehedincuDepartment of Biology, College of Arts and Sciences, American University, Washington, DC 20016, USA.
Dacia MarquezDepartment of Biology, College of Arts and Sciences, American University, Washington, DC 20016, USA.
Hasset TibebeDepartment of Biology, College of Arts and Sciences, American University, Washington, DC 20016, USA.
Kathleen L DeCicco-SkinnerDepartment of Biology, College of Arts and Sciences, American University, Washington, DC 20016, USA.ORCID 0000-0002-0256-5609
Taisuke IzumiDepartment of Biology, College of Arts and Sciences, American University, Washington, DC 20016, USA.ORCID 0000-0001-8193-0813

Funding

Role of canonical and non-canonical beta-catenin signaling in HIV-1 latencyR15AI172610 · NIAID · SAINT JOSEPH'S UNIVERSITY · PI Taisuke Izumi · 2022 to 2026
$885k
NIAID NIH HHS R15 AI172610NIH HHS 7R15AI172610-02A1
6 · The paper itself

Abstract

The maturation of HIV-1 virions is a crucial process in viral replication. Although T-cells are a primary source of virus production, much of our understanding of virion maturation comes from studies using the HEK293T human embryonic kidney cell line. Notably, there is a lack of comparative analyses between T-cells and HEK293T cells in terms of virion maturation efficiency in existing literature. We previously developed an advanced virion visualization system based on the FRET principle, enabling the effective distinction between immature and mature virions via fluorescence microscopy. In this study, we utilized pseudotyped, single-round infectious viruses tagged with FRET labels (HIV-1 Gag-iFRET∆Env) derived from Jurkat (a human T-lymphocyte cell line) and HEK293T cells to evaluate their virion maturation rates. HEK293T-derived virions demonstrated a maturity rate of 81.79%, consistent with other studies and our previous findings. However, virions originating from Jurkat cells demonstrated a significantly reduced maturation rate of 68.67% (

Indexed as

Fluorescence Resonance Energy TransferHIV-1VirionHEK293 CellsHIV InfectionsHumansJurkat CellsVirus AssemblyVirus Replicationcomparative viral analysisfluorescent microscopic imagingforster resonance energy transfer (FRET)human immunodeficiency virus type I (HIV-1)virion maturation

Identifiers

PMID38928103
PMCPMC11204348

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.