Evidence map›Paper›PMID 26508717›Full record

ArticleEvolution, medicine, and public health2015

Viral meningitis epidemics and a single, recent, recombinant and anthroponotic origin of swine vesicular disease virus.

Christian A W Bruhn, Sandra C Abel Nielsen, Jose Alfredo Samaniego, Jemma Wadsworth, Nick J Knowles, M Thomas P Gilbert

Abstract read
In one paragraph

Article in Evolution, medicine, and public health, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Journal of virology · 2025
    Review
  4. Review
  5. Article
  6. Zoonotic and reverse zoonotic transmission of viruses between humans and pigs.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2021
    Review
  7. Article
  8. Article
  9. Article
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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

6 authors.

Christian A W BruhnCentre for GeoGenetics, Natural History Museum of Denmark, Soelvgade 83 S, Copenhagen K, DK-1307, Denmark; Present address: Weinberger Lab, Laboratory of Epidemiology and Public Health, Yale School of Medicine, 60 College Street, 06510 New Haven, CT and christianwbruhn@gmail.com.
Sandra C Abel NielsenCentre for GeoGenetics, Natural History Museum of Denmark, Soelvgade 83 S, Copenhagen K, DK-1307, Denmark; Stanford University, School of Medicine, 300 Pasteur Drive, CA 94305, USA.
Jose Alfredo SamaniegoCentre for GeoGenetics, Natural History Museum of Denmark, Soelvgade 83 S, Copenhagen K, DK-1307, Denmark;
Jemma WadsworthThe Pirbright Institute, Ash Road, Pirbright, Woking, Surrey, GU24 0NF, UK;
Nick J KnowlesThe Pirbright Institute, Ash Road, Pirbright, Woking, Surrey, GU24 0NF, UK;
M Thomas P GilbertCentre for GeoGenetics, Natural History Museum of Denmark, Soelvgade 83 S, Copenhagen K, DK-1307, Denmark;

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesSwine vesicular disease virus (SVDV) is a close relative of the human Enterovirus B serotype, coxsackievirus B5. As the etiological agent of a significant emergent veterinary disease, several studies have attempted to explain its origin. However, several key questions remain, including the full biological ancestry of the virus, and its geographical and temporal origin. METHODOLOGY: We sequenced near-complete genomes of 27 SVDV and 13 coxsackievirus B5 samples, all originally isolated between 1966 and 2006, and analysed these in conjunction with existing sequences and historical information.

resultsWhile analyses incorporating 24 additional near-complete SVDV genomic sequences indicate clear signs of within-SVDV recombination, all 51 SVDV isolates remain monophyletic. This supports a hypothesis of a single anthroponotic transfer origin. Analysis of individual coding and non-coding regions supports that SVDV has a recombinant origin between coxsackievirus B5 and another Enterovirus B serotype, most likely coxsackievirus A9. Extensive Bayesian sequence-based analysis of the time of the most recent common ancestor of all analysed sequences places this within a few years around 1961. Epidemiological evidence points to China as an origin, but there are no available samples to test this conclusively. CONCLUSIONS AND IMPLICATIONS: Historical investigation and the clinical aspects of the involved Enterovirus B serotypes, makes the current results consistent with a hypothesis stating that SVDV originated through co-infection, recombination, and a single anthroponotic event, during large viral meningitis epidemics around 1960/1961 involving the ancestral serotypes. The exact geographical origin of SVDV may remain untestable due to historical aspects.

Indexed as

emerging diseasesEnterovirus BPicornaviridaeRNA virusesSVDVviral meningitis

Identifiers

PMID26508717
PMCPMC4661520

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Registered trials

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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.