Evidence map›Paper›PMID 25299706›Full record

ArticlePloS one2014

Permeability changes of integrin-containing multivesicular structures triggered by picornavirus entry.

Pan Soonsawad, Lassi Paavolainen, Paula Upla, Wattana Weerachatyanukul, Nina Rintanen, Juan Espinoza, Gregory McNerney, Varpu Marjomäki, R Holland Cheng

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

9 authors at 2 institutions in 3 countries.

Pan SoonsawadDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America; Department of Anatomy, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Lassi PaavolainenDepartment of Biological and Environmental Science/Nanoscience Center, University of Jyväskylä, Jyväskylä, Finland.
Paula UplaDepartment of Biological and Environmental Science/Nanoscience Center, University of Jyväskylä, Jyväskylä, Finland.
Wattana WeerachatyanukulDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America; Department of Anatomy, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Nina RintanenDepartment of Biological and Environmental Science/Nanoscience Center, University of Jyväskylä, Jyväskylä, Finland.
Juan EspinozaDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America.
Gregory McNerneyDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America; Department of Biological and Environmental Science/Nanoscience Center, University of Jyväskylä, Jyväskylä, Finland.
Varpu MarjomäkiDepartment of Biological and Environmental Science/Nanoscience Center, University of Jyväskylä, Jyväskylä, Finland.
R Holland ChengDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America.
University of California, Davis · USUniversity of Jyväskylä · FI

Funding

Present Homologous and Heterologous Antigen with Hepatitis E VirusR56AI095382 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHENG, R.HOLLAND · 2012 to 2012
$385k
NIAID NIH HHS AI095382NIAID NIH HHS R56 AI095382
6 · The paper itself

Abstract

Cellular uptake of clustered α2β1-integrin induces the formation of membrane compartments that subsequently mature into a multivesicular body (MVB). Enhanced internalization mediated by clustered integrins was observed upon infection by the picornavirus echovirus 1 (EVI). We elucidated the structural features of virus-induced MVBs (vMVBs) in comparison to antibody-induced control MVBs (mock infection) by means of high-pressure cryo fixation of cells followed by immuno electron tomography during early entry of the virus. Three-dimensional tomograms revealed a marked increase in the size and complexity of these vMVBs and the intraluminal vesicles (ILVs) at 2 and 3.5 hours post infection (p.i.), in contrast to the control MVBs without virus. Breakages in the membranes of vMVBs were detected from tomograms after 2 and especially after 3.5 h suggesting that these breakages could facilitate the genome release to the cytoplasm. The in situ neutral-red labeling of viral genome showed that virus uncoating starts as early as 30 min p.i., while an increase of permeability was detected in the vMVBs between 1 and 3 hours p.i., based on a confocal microscopy assay. Altogether, the data show marked morphological changes in size and permeability of the endosomes in the infectious entry pathway of this non-enveloped enterovirus and suggest that the formed breakages facilitate the transfer of the genome to the cytoplasm for replication.

Indexed as

Cell Line, TumorCell MembraneCytoplasmElectron Microscope TomographyEndosomesHumansIntegrin alpha2beta1Microscopy, ConfocalMultivesicular BodiesPermeabilityPicornaviridaePicornaviridae InfectionsIntegrin alpha2beta1

Identifiers

PMID25299706
PMCPMC4191987
OpenAlexW1995319311

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.