Evidence map›Paper›PMID 26629703›Full record

ArticlePLoS pathogens2015

Human Metapneumovirus Is Capable of Entering Cells by Fusion with Endosomal Membranes.

Reagan G Cox, Bernardo A Mainou, Monika Johnson, Andrew K Hastings, Jennifer E Schuster, Terence S Dermody, John V Williams

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.8field-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

38 citing papers in PubMed, 57 citations in OpenAlex.

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  12. Receptors and host factors: key players in human metapneumovirus infection.Frontiers in cellular and infection microbiology · 2025
    Review
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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

7 authors at 4 institutions in 1 country.

Reagan G CoxDepartment of Pathology, Microbiology, & Immunology, Division of Infectious Diseases, Vanderbilt University School of Medicine; Nashville, Tennessee, United States of America.
Bernardo A MainouDepartment of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Monika JohnsonDepartment of Pediatrics, University of Pittsburgh School of Medicine, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States of America.
Andrew K HastingsDepartment of Pathology, Microbiology, & Immunology, Division of Infectious Diseases, Vanderbilt University School of Medicine; Nashville, Tennessee, United States of America.
Jennifer E SchusterDepartment of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, United States of America.
Terence S DermodyDepartment of Pathology, Microbiology, & Immunology, Division of Infectious Diseases, Vanderbilt University School of Medicine; Nashville, Tennessee, United States of America.
John V WilliamsDepartment of Pediatrics, University of Pittsburgh School of Medicine, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States of America.
Vanderbilt University · USChildren's Hospital of Pittsburgh · USChildren's Mercy Hospital · USEmory University · US

Funding

CELL ENTRY OF REOVIRUSR01AI032539 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI TERENCE S. DERMODY · 1998 to 2026
$12.3M
Host Determinants of Human Metapneumovirus Immunity and PathogenesisR01AI085062 · NIAID · VANDERBILT UNIVERSITY · PI John V. Williams · 2010 to 2026
$5.6M
CELLULAR AND MOLECULAR MICROBIOLOGY TRAINING PROGRAMT32AI007611 · NIAID · VANDERBILT UNIVERSITY · PI HAWIGER, JACK J · 1999 to 2010
$1.6M
Cell Entry of Human MetapneumovirusR21AI073697 · NIAID · VANDERBILT UNIVERSITY · PI WILLIAMS, JOHN V. · 2008 to 2009
$422k
NIAID NIH HHS F32 AI801082NIAID NIH HHS R01 AI032539NIAID NIH HHS R01 AI085062NIAID NIH HHS R01 AI08562NIAID NIH HHS R01 AI32539NIAID NIH HHS R21 AI073697NIAID NIH HHS T32 AI007611NIAID NIH HHS T32 AI7611
6 · The paper itself

Abstract

Human metapneumovirus (HMPV), a member of the Paramyxoviridae family, is a leading cause of lower respiratory illness. Although receptor binding is thought to initiate fusion at the plasma membrane for paramyxoviruses, the entry mechanism for HMPV is largely uncharacterized. Here we sought to determine whether HMPV initiates fusion at the plasma membrane or following internalization. To study the HMPV entry process in human bronchial epithelial (BEAS-2B) cells, we used fluorescence microscopy, an R18-dequenching fusion assay, and developed a quantitative, fluorescence microscopy assay to follow virus binding, internalization, membrane fusion, and visualize the cellular site of HMPV fusion. We found that HMPV particles are internalized into human bronchial epithelial cells before fusing with endosomes. Using chemical inhibitors and RNA interference, we determined that HMPV particles are internalized via clathrin-mediated endocytosis in a dynamin-dependent manner. HMPV fusion and productive infection are promoted by RGD-binding integrin engagement, internalization, actin polymerization, and dynamin. Further, HMPV fusion is pH-independent, although infection with rare strains is modestly inhibited by RNA interference or chemical inhibition of endosomal acidification. Thus, HMPV can enter via endocytosis, but the viral fusion machinery is not triggered by low pH. Together, our results indicate that HMPV is capable of entering host cells by multiple pathways, including membrane fusion from endosomal compartments.

Indexed as

Virus InternalizationBronchiCell LineEndosomesFlow CytometryHumansMetapneumovirusMicroscopy, ConfocalParamyxoviridae InfectionsRespiratory MucosaRNA, Small InterferingTransfectionViral Fusion ProteinsRNA, Small InterferingViral Fusion Proteins

Identifiers

PMID26629703
PMCPMC4667933
OpenAlexW2188386475

What OpenQuestion holds

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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.