Evidence map›Paper›PMID 10884436›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Retrograde axonal transport of herpes simplex virus: evidence for a single mechanism and a role for tegument.

E L Bearer, X O Breakefield, D Schuback, T S Reese, J H LaVail

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% 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

79 citing papers in PubMed, 1 synthesis or guideline pooled it, 150 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. HSV-1 as a Potential Driver of Alzheimer's Disease.Pathogens (Basel, Switzerland) · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Superior antiviral activity of IFNβ in genital HSV-1 infection.Frontiers in cellular and infection microbiology · 2022
    Article
  14. The Giant Axon of the Squid: A Simple System for Axonal Transport Studies.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  15. Tissue specific signature of HHV-6 infection in ME/CFS.Frontiers in molecular biosciences · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

19 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

E L BearerDepartment of Pathology and Laboratory Medicine, Brown University, Providence, RI 02912, USA. Elaine_Bearer@Brown.edu
X O Breakefield
D Schuback
T S Reese
J H LaVail
National Institute of Neurological Disorders and Stroke · USMarine Biological Laboratory · US

Funding

TRANSPORT OF HERPES SIMPLEX VIRUS IN OCULAR TISSUESR01EY008773 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LAVAIL, JENNIFER HART · 1990 to 2006
$1.9M
PROTEIN EXPORT BY AN ACCESSORY PROTEIN-SPECIFIED PATHWAYR01GM047638 · NIGMS · GEORGIA STATE UNIVERSITY · PI TAI, PHANG C. · 1991 to 1993
–
NEI NIH HHS EYO8773NIGMS NIH HHS GM47638
6 · The paper itself

Abstract

Herpes simplex virus type I (HSV) typically enters peripheral nerve terminals and then travels back along the nerve to reach the neuronal cell body, where it replicates or enters latency. To monitor axoplasmic transport of HSV, we used the giant axon of the squid, Loligo pealei, a well known system for the study of axoplasmic transport. To deliver HSV into the axoplasm, viral particles stripped of their envelopes by detergent were injected into the giant axon, thereby bypassing the infective process. Labeling the viral tegument protein, VP16, with green fluorescent protein allowed viral particles moving inside the axon to be imaged by confocal microscopy. Viral particles moved 2.2 +/- 0.26 micrometer/sec in the retrograde direction, a rate comparable to that of the transport of endogenous organelles and of virus in mammalian neurons in culture. Electron microscopy confirmed that 96% of motile (stripped) viral particles had lost their envelope but retained tegument, and Western blot analysis revealed that these particles had retained protein from capsid but not envelope. We conclude that (i) HSV recruits the squid retrograde transport machinery; (ii) viral tegument and capsid but not envelope are sufficient for this recruitment; and (iii) the giant axon of the squid provides a unique system to dissect the viral components required for transport and to identify the cellular transport mechanisms they recruit.

Indexed as

Axonal TransportAnimalsAxonsBiological TransportDecapodiformesGreen Fluorescent ProteinsHerpes Simplex Virus Protein Vmw65Herpesvirus 1, HumanLuminescent ProteinsMicroinjectionsMicroscopy, ConfocalMicroscopy, VideoMovementGreen Fluorescent ProteinsHerpes Simplex Virus Protein Vmw65Luminescent Proteins

Identifiers

PMID10884436
PMCPMC16684
OpenAlexW1967437498

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.