Evidence map›Paper›PMID 29186766›Full record

ReviewViruses2017

Autophagy in Measles Virus Infection.

Aurore Rozières, Christophe Viret, Mathias Faure

Open access · goldAbstract readReview
In one paragraph

Review in Viruses, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  19. Article
  20. Autophagy, EVs, and Infections: A Perfect Question for a Perfect Time.Frontiers in cellular and infection microbiology · 2018
    Review
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

3 authors at 3 institutions in 1 country.

Aurore RozièresInternational Center for Infectiology Research (CIRI), Université de Lyon, 69007 Lyon, France
Christophe ViretInternational Center for Infectiology Research (CIRI), Université de Lyon, 69007 Lyon, France
Mathias FaureInternational Center for Infectiology Research (CIRI), Université de Lyon, 69007 Lyon, France
Centre National de la Recherche Scientifique · FRÉcole Normale Supérieure de Lyon · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a biological process that helps cells to recycle obsolete cellular components and which greatly contributes to maintaining cellular integrity in response to environmental stress factors. Autophagy is also among the first lines of cellular defense against invading microorganisms, including viruses. The autophagic destruction of invading pathogens, a process referred to as xenophagy, involves cytosolic autophagy receptors, such as p62/SQSTM1 (Sequestosome 1) or NDP52/CALCOCO2 (Nuclear Dot 52 KDa Protein/Calcium Binding And Coiled-Coil Domain 2), which bind to microbial components and target them towards growing autophagosomes for degradation. However, most, if not all, infectious viruses have evolved molecular tricks to escape from xenophagy. Many viruses even use autophagy, part of the autophagy pathway or some autophagy-associated proteins, to improve their infectious potential. In this regard, the measles virus, responsible for epidemic measles, has a unique interface with autophagy as the virus can induce multiple rounds of autophagy in the course of infection. These successive waves of autophagy result from distinct molecular pathways and seem associated with anti- and/or pro-measles virus consequences. In this review, we describe what the autophagy-measles virus interplay has taught us about both the biology of the virus and the mechanistic orchestration of autophagy.

Indexed as

AutophagyCell Cycle ProteinsGTP-Binding ProteinsHumansIntracellular Signaling Peptides and ProteinsMeaslesMeasles virusMembrane Cofactor ProteinMembrane Transport ProteinsNeoplasm ProteinsNuclear ProteinsSequestosome-1 ProteinTranscription Factor TFIIIAVirus ReplicationCALCOCO2 protein, humanCD46 protein, humanCell Cycle ProteinsGTP-Binding ProteinsIntracellular Signaling Peptides and ProteinsIRGM protein, humanMembrane Cofactor ProteinMembrane Transport ProteinsNeoplasm ProteinsNuclear ProteinsOPTN protein, humanSequestosome-1 ProteinSQSTM1 protein, humanTAX1BP1 protein, humanTranscription Factor TFIIIAautophagyautophagy receptorsCD46IRGMmeasles virusNDP52OPTNselective autophagyT6BP

Identifiers

PMID29186766
PMCPMC5744134
OpenAlexW2768928645

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.