Evidence map›Paper›PMID 37894953›Full record

ArticleInternational journal of molecular sciences2023

Zinc Uptake by HIV-1 Viral Particles: An Isotopic Study.

Olivia Guillin, Emmanuelle Albalat, Caroline Vindry, Elisabeth Errazuriz-Cerda, Théophile Ohlmann, Vincent Balter, Laurent Chavatte

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 1 institution in 1 country.

Olivia GuillinCentre International de Recherche en Infectiologie (CIRI), 69007 Lyon, France.
Emmanuelle AlbalatEcole Normale Supérieure de Lyon, 69007 Lyon, France.ORCID 0000-0003-0864-5199
Caroline VindryCentre International de Recherche en Infectiologie (CIRI), 69007 Lyon, France.
Elisabeth Errazuriz-CerdaCenter of Quantitative Imagery Lyon Est (CIQLE), Université Claude Bernard Lyon 1, 69008 Lyon, France.
Théophile OhlmannCentre International de Recherche en Infectiologie (CIRI), 69007 Lyon, France.ORCID 0000-0002-2001-8916
Vincent BalterEcole Normale Supérieure de Lyon, 69007 Lyon, France.
Laurent ChavatteCentre International de Recherche en Infectiologie (CIRI), 69007 Lyon, France.ORCID 0000-0001-7696-2431
Université Claude Bernard Lyon 1 · FR

Funding

Agence Nationale de Recherches sur le Sida et les Hépatites Virales ANRSÉcole Normale Supérieure de Lyon Emerging ProjectFrench National Centre for Scientific Research CNRSFrench National Centre for Scientific Research MITI programs "Isotop" and "Metallo-Mix"Inserm INSERM
6 · The paper itself

Abstract

Zinc, an essential trace element that serves as a cofactor for numerous cellular and viral proteins, plays a central role in the dynamics of HIV-1 infection. Among the viral proteins, the nucleocapsid NCp7, which contains two zinc finger motifs, is abundantly present viral particles and plays a crucial role in coating HIV-1 genomic RNA, thus concentrating zinc within virions. In this study, we investigated whether HIV-1 virus production impacts cellular zinc homeostasis and whether isotopic fractionation occurs between the growth medium, the producing cells, and the viral particles. We found that HIV-1 captures a significant proportion of cellular zinc in the neo-produced particles. Furthermore, as cells grow, they accumulate lighter zinc isotopes from the medium, resulting in a concentration of heavier isotopes in the media, and the viruses exhibit a similar isotopic fractionation to the producing cells. Moreover, we generated HIV-1 particles in HEK293T cells enriched with each of the five zinc isotopes to assess the potential effects on the structure and infectivity of the viruses. As no strong difference was observed between the HIV-1 particles produced in the various conditions, we have demonstrated that enriched isotopes can be accurately used in future studies to trace the fate of zinc in cells infected by HIV-1 particles. Comprehending the mechanisms underlying zinc absorption by HIV-1 viral particles offers the potential to provide insights for developing future treatments aimed at addressing this specific facet of the virus's life cycle.

Indexed as

HIV-1Amino Acid SequenceHEK293 CellsHumansIsotopesRNAViral ProteinsVirionZincZinc FingersZinc IsotopesIsotopesRNAViral ProteinsZincZinc IsotopesHIV-1isotope fractionationisotope labelingMC-ICP-MSviral particleszinc

Identifiers

PMID37894953
PMCPMC10607083
OpenAlexW4387694125

What OpenQuestion holds

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LicenceCC BY
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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.