Evidence map›Paper›PMID 27122580›Full record

ArticleJournal of virology2016

Migration of Nucleocapsids in Vesicular Stomatitis Virus-Infected Cells Is Dependent on both Microtubules and Actin Filaments.

Shalane K Yacovone, Amanda M Smelser, Jed C Macosko, George Holzwarth, David A Ornelles, Douglas S Lyles

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. The prion-like characteristic of ORF3 contributes to virion release and pathogenesis of hepatitis E virus.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  3. Article
  4. Review
  5. Article
  6. Article
  7. A Traditional Chinese Medicine, Maoto, Suppresses Hepatitis B Virus Production.Frontiers in cellular and infection microbiology · 2020
    Article
  8. Article
  9. Article
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

6 authors at 1 institution in 1 country.

Shalane K YacovoneDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Amanda M SmelserDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Jed C MacoskoDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA Department of Physics, Wake Forest University, Winston-Salem, North Carolina, USA.
George HolzwarthDepartment of Physics, Wake Forest University, Winston-Salem, North Carolina, USA.
David A OrnellesDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Douglas S LylesDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA dlyles@wakehealth.edu.
Wake Forest University · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
FUSION OF VIRUS ENVELOPE WITH CELL MEMBRANESR01AI015892 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LYLES, DOUGLAS S. · 1985 to 2013
$4.0M
RNA-Binding Proteins and Host Shut-Off by VSVR01AI105012 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LYLES, DOUGLAS S. · 2014 to 2018
$2.2M
Prenatal adenovirus infection, inhibition of DNA repair, and childhood leukemiaR01CA127621 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ORNELLES, DAVID ARNOLD · 2009 to 2013
$2.1M
Structural and Computational Biophysics Training ProgramT32GM095440 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HOLLIS, THOMAS J, LYLES, DOUGLAS S. · 2011 to 2020
$1.7M
NCI NIH HHS P30 CA012197NCI NIH HHS R01 CA127621NIAID NIH HHS R01 AI015892NIAID NIH HHS R01 AI105012NIGMS NIH HHS T32 GM095440
6 · The paper itself

Abstract

unlabelledThe distribution of vesicular stomatitis virus (VSV) nucleocapsids in the cytoplasm of infected cells was analyzed by scanning confocal fluorescence microscopy using a newly developed quantitative approach called the border-to-border distribution method. Nucleocapsids were located near the cell nucleus at early times postinfection (2 h) but were redistributed during infection toward the edges of the cell. This redistribution was inhibited by treatment with nocodazole, colcemid, or cytochalasin D, indicating it is dependent on both microtubules and actin filaments. The role of actin filaments in nucleocapsid mobility was also confirmed by live-cell imaging of fluorescent nucleocapsids of a virus containing P protein fused to enhanced green fluorescent protein. However, in contrast to the overall redistribution in the cytoplasm, the incorporation of nucleocapsids into virions as determined in pulse-chase experiments was dependent on the activity of actin filaments with little if any effect on inhibition of microtubule function. These results indicate that the mechanisms by which nucleocapsids are transported to the farthest reaches of the cell differ from those required for incorporation into virions. This is likely due to the ability of nucleocapsids to follow shorter paths to the plasma membrane mediated by actin filaments. IMPORTANCE: Nucleocapsids of nonsegmented negative-strand viruses like VSV are assembled in the cytoplasm during genome RNA replication and must migrate to the plasma membrane for assembly into virions. Nucleocapsids are too large to diffuse in the cytoplasm in the time required for virus assembly and must be transported by cytoskeletal elements. Previous results suggested that microtubules were responsible for migration of VSV nucleocapsids to the plasma membrane for virus assembly. Data presented here show that both microtubules and actin filaments are responsible for mobility of nucleocapsids in the cytoplasm, but that actin filaments play a larger role than microtubules in incorporation of nucleocapsids into virions.

Indexed as

Virus AssemblyActin CytoskeletonCell NucleusCytochalasin DCytoplasmDemecolcineGreen Fluorescent ProteinsHeLa CellsHumansMicroscopy, Electron, ScanningMicrotubulesNocodazoleNucleocapsidPhosphoproteinsVesicular stomatitis Indiana virusViral ProteinsCytochalasin DDemecolcineenhanced green fluorescent proteinGreen Fluorescent ProteinsNocodazolePhosphoproteinsP protein, Vesicular stomatitis virusViral ProteinsViral Structural Proteins

Identifiers

PMID27122580
PMCPMC4907246
OpenAlexW2342393818

What OpenQuestion holds

Textmetadata
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.