Evidence map›Paper›PMID 26268989›Full record

ArticleRetrovirology2015

Evidence that the endosomal sorting complex required for transport-II (ESCRT-II) is required for efficient human immunodeficiency virus-1 (HIV-1) production.

Bo Meng, Natasha C Y Ip, Liam J Prestwood, Truus E M Abbink, Andrew M L Lever

Open access · goldAbstract read
In one paragraph

Article in Retrovirology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.6field-weighted citation impact, top 6% of its field
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

41 citing papers in PubMed, 65 citations in OpenAlex.

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  13. The Role of Exosome and the ESCRT Pathway on Enveloped Virus Infection.International journal of molecular sciences · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Bo MengDepartment of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK. bm432@cam.ac.uk.
Natasha C Y IpDepartment of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK. natasha.ip@cantab.net.
Liam J PrestwoodDepartment of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK. l.j.p21@hotmail.com.
Truus E M AbbinkDepartment of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK. g.abbink@vumc.nl.
Andrew M L LeverDepartment of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK. amll1@medschl.cam.ac.uk.
Addenbrooke's Hospital · GBUniversity of Cambridge · GBVrije Universiteit Amsterdam · NL

Funding

Medical Research Council G0800142
6 · The paper itself

Abstract

backgroundEgress of a number of different virus species from infected cells depends on proteins of the endosomal sorting complexes required for transport (ESCRT) pathway. HIV has also hijacked this system to bud viruses outward from the cell surface. How ESCRT-I activates ESCRT-III in this process remains unclear with conflicting published evidence for the requirement of ESCRT-II which fulfils this role in other systems. We investigated the role of ESCRT-II using knockdown mediated by siRNA and shRNA, mutants which prevent ESCRT-I/ESCRT-II interaction and a CRISPR/Cas9 EAP45 knockout cell line.

resultsDepletion or elimination of ESCRT-II components from an HIV infected cell produces two distinct effects. The overall production of HIV-1 Gag is reduced leading to a diminished amount of intracellular virion protein. In addition depletion of ESCRT-II produces an effect similar to that seen when ESCRT-I and -III components are depleted, that of a delayed Gag p26 to p24 +p2 cleavage associated with a reduction in export of virion particles and a visible reduction in budding efficiency in virus producing cells. Mutants that interfere with ESCRT-I interacting with ESCRT-II similarly reduce virus export. The export defect is independent of the decrease in overall Gag production. Using a mutant virus which cannot use the ALIX mediated export pathway exacerbates the decrease in virus export seen when ESCRT-II is depleted. ESCRT-II knockdown does not lead to complete elimination of virus release suggesting that the late domain role of ESCRT-II is required for optimal efficiency of viral budding but that there are additional pathways that the virus can employ to facilitate this.

conclusionESCRT-II contributes to efficient HIV virion production and export by more than one pathway; both by a transcriptional or post transcriptional mechanism and also by facilitating efficient virus export from the cell through interactions with other ESCRT components.

Indexed as

Biological TransportCell LineCRISPR-Cas SystemsEndosomal Sorting Complexes Required for Transportgag Gene Products, Human Immunodeficiency VirusGene Knockout TechniquesHIV-1HumansMutationProtein BindingProtein Structure, TertiaryRNA, Small InterferingVirionVirus ReleaseEndosomal Sorting Complexes Required for Transportgag Gene Products, Human Immunodeficiency VirusRNA, Small Interfering

Identifiers

PMID26268989
PMCPMC4535389
OpenAlexW2147257015

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.