Evidence map›Paper›PMID 28957419›Full record

ArticlePLoS pathogens2017

Interference with the production of infectious viral particles and bimodal inhibition of replication are broadly conserved antiviral properties of IFITMs.

Kevin Tartour, Xuan-Nhi Nguyen, Romain Appourchaux, Sonia Assil, Véronique Barateau, Louis-Marie Bloyet, Julien Burlaud Gaillard, Marie-Pierre Confort, Beatriz Escudero-Perez, Henri Gruffat and 16 more

Abstract read
In one paragraph

Article in PLoS pathogens, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing 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

53 citing papers in PubMed.

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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

26 authors.

Kevin TartourCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Xuan-Nhi NguyenCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Romain AppourchauxCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Sonia AssilCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Véronique BarateauCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Louis-Marie BloyetCIRI, Centre International de Recherche en Infectiologie, Lyon, France.ORCID 0000-0002-5648-3190
Julien Burlaud GaillardPlateforme IBiSA de Microscopie Electronique, Université F. Rabelais et CHRU de Tours, Tours, France.
Marie-Pierre ConfortIVPC UMR754, INRA, Univ Lyon, Université Claude Bernard Lyon1, EPHE, Lyon, France.ORCID 0000-0002-4892-1082
Beatriz Escudero-PerezCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Henri GruffatCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Saw See HongIVPC UMR754, INRA, Univ Lyon, Université Claude Bernard Lyon1, EPHE, Lyon, France.ORCID 0000-0001-8871-0901
Marie MorosoCIRI, Centre International de Recherche en Infectiologie, Lyon, France.ORCID 0000-0002-7132-6329
Olivier ReynardCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Stéphanie ReynardCIRI, Centre International de Recherche en Infectiologie, Lyon, France.ORCID 0000-0002-8508-5167
Elodie DecembreCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Najate FtaichIVPC UMR754, INRA, Univ Lyon, Université Claude Bernard Lyon1, EPHE, Lyon, France.
Axel RossiCIRI, Centre International de Recherche en Infectiologie, Lyon, France.ORCID 0000-0003-0312-3965
Nannan WuCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Frédérick ArnaudIVPC UMR754, INRA, Univ Lyon, Université Claude Bernard Lyon1, EPHE, Lyon, France.ORCID 0000-0001-6893-9848
Sylvain BaizeCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Marlène DreuxCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Denis GerlierCIRI, Centre International de Recherche en Infectiologie, Lyon, France.ORCID 0000-0001-5539-456X
Glaucia Paranhos-BaccalaCIRI, Centre International de Recherche en Infectiologie, Lyon, France.ORCID 0000-0002-6369-5837
Viktor VolchkovCIRI, Centre International de Recherche en Infectiologie, Lyon, France.
Philippe RoingeardPlateforme IBiSA de Microscopie Electronique, Université F. Rabelais et CHRU de Tours, Tours, France.
Andrea CimarelliCIRI, Centre International de Recherche en Infectiologie, Lyon, France.ORCID 0000-0003-0892-0488

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IFITMs are broad antiviral factors that block incoming virions in endosomal vesicles, protecting target cells from infection. In the case of HIV-1, we and others reported the existence of an additional antiviral mechanism through which IFITMs lead to the production of virions of reduced infectivity. However, whether this second mechanism of inhibition is unique to HIV or extends to other viruses is currently unknown. To address this question, we have analyzed the susceptibility of a broad spectrum of viruses to the negative imprinting of the virion particles infectivity by IFITMs. The results we have gathered indicate that this second antiviral property of IFITMs extends well beyond HIV and we were able to identify viruses susceptible to the three IFITMs altogether (HIV-1, SIV, MLV, MPMV, VSV, MeV, EBOV, WNV), as well as viruses that displayed a member-specific susceptibility (EBV, DUGV), or were resistant to all IFITMs (HCV, RVFV, MOPV, AAV). The swapping of genetic elements between resistant and susceptible viruses allowed us to point to specificities in the viral mode of assembly, rather than glycoproteins as dominant factors of susceptibility. However, we also show that, contrarily to X4-, R5-tropic HIV-1 envelopes confer resistance against IFITM3, suggesting that viral receptors add an additional layer of complexity in the IFITMs-HIV interplay. Lastly, we show that the overall antiviral effects ascribed to IFITMs during spreading infections, are the result of a bimodal inhibition in which IFITMs act both by protecting target cells from incoming viruses and in driving the production of virions of reduced infectivity. Overall, our study reports for the first time that the negative imprinting of the virion particles infectivity is a conserved antiviral property of IFITMs and establishes IFITMs as a paradigm of restriction factor capable of interfering with two distinct phases of a virus life cycle.

Indexed as

VirionVirus ReplicationAntigens, DifferentiationCell LineHIV-1Host-Pathogen InteractionsHumansVirus InternalizationAntigens, DifferentiationIFITM

Identifiers

PMID28957419
PMCPMC5619827

What OpenQuestion holds

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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.