Evidence map›Paper›PMID 32522858›Full record

ArticleJournal of virology2020

Human Cytomegalovirus Utilizes Extracellular Vesicles To Enhance Virus Spread.

Nicholas T Streck, Yuanjun Zhao, Jeffrey M Sundstrom, Nicholas J Buchkovich

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. A viral glycoprotein targets IgGEMBO molecular medicine · 2026
    Article
  3. Frontiers in microbiology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Neutral sphingomyelinase 2: A promising drug target for CNS disease.Advances in pharmacology (San Diego, Calif.) · 2025
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Nicholas T StreckDepartment of Microbiology & Immunology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA.
Yuanjun ZhaoDepartment of Ophthalmology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA.
Jeffrey M SundstromDepartment of Ophthalmology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA.
Nicholas J BuchkovichDepartment of Microbiology & Immunology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA nbuchkovich@pennstatehealth.psu.edu.ORCID 0000-0001-7275-8134
Pennsylvania State University · US

Funding

Molecular Functions and Mechanisms of UL16, A Conserved Tegument Protein of HSVR01AI071286 · NIAID · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI WILLS, JOHN W. · 2007 to 2016
$5.1M
INSTITUTIONAL NATIONAL RESEARCH SERVICE AWARDT32CA060396 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI BRISTOW, ROBERT EDWARD · 1994 to 2020
$4.6M
Analysis of the mechanism of HCMV cytoplasmic envelopmentR01AI130156 · NIAID · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI Christopher C Norbury · 2017 to 2026
$3.8M
NCI NIH HHS T32 CA060396NIAID NIH HHS R01 AI071286NIAID NIH HHS R01 AI130156
6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) manipulates cellular processes associated with secretory pathways within an infected cell to facilitate efficient viral replication. However, little is known about how HCMV infection alters the surrounding cellular environment to promote virus spread to uninfected cells. Extracellular vesicles (EVs) are key signaling molecules that are commonly altered in numerous disease states. Previous reports have shown that viruses commonly alter EVs, which can significantly impact infection. This study finds that HCMV modulates EV biogenesis machinery through upregulation of the endosomal sorting complex required for transport (ESCRT) proteins. This regulation appears to increase the activity of EV biogenesis, since HCMV-infected fibroblasts have increased vesicle release and altered vesicle size compared to EVs from uninfected cells. EVs generated through ESCRT-independent pathways are also beneficial to virus spread in fibroblasts, as treatment with the EV inhibitor GW4869 slowed the efficiency of HCMV spread. Importantly, the transfer of EVs purified from HCMV-infected cells enhanced virus spread. This suggests that HCMV modulates the EV pathway to transfer proviral signals to uninfected cells that prime the cellular environment for incoming infection and enhance the efficiency of virus spread.

Indexed as

Cell MovementCytomegalovirusCytomegalovirus InfectionsExtracellular VesiclesFibroblastsHEK293 CellsHumansProtein TransportSignal TransductionVirus ReplicationCD63ESCRTsextracellular vesiclesGW4869HCMVspread

Identifiers

PMID32522858
PMCPMC7394901
OpenAlexW3033665744

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.