Evidence map›Paper›PMID 33138327›Full record

ArticleMicroorganisms2020

Expanding the Geographic Characterisation of Epstein-Barr Virus Variation through Gene-Based Approaches.

Marco Telford, David A Hughes, David Juan, Mark Stoneking, Arcadi Navarro, Gabriel Santpere

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Microorganisms, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Human herpesvirus diversity is altered in HLA class I binding peptides.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 3 countries.

Marco TelfordInstitute of Evolutionary Biology (CSIC-Universitat Pompeu Fabra), Department of Experimental and Health Sciences (DCEXS), Barcelona Biomedical Research Park, 08003 Barcelona, Spain.
David A HughesBristol Population Health Science Institute, University of Bristol, Bristol BS8 2BN, UK.ORCID 0000-0002-9644-8998
David JuanInstitute of Evolutionary Biology (CSIC-Universitat Pompeu Fabra), Department of Experimental and Health Sciences (DCEXS), Barcelona Biomedical Research Park, 08003 Barcelona, Spain.ORCID 0000-0003-1912-9667
Mark StonekingDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103 Leipzig, Germany.
Arcadi NavarroInstitute of Evolutionary Biology (CSIC-Universitat Pompeu Fabra), Department of Experimental and Health Sciences (DCEXS), Barcelona Biomedical Research Park, 08003 Barcelona, Spain.
Gabriel SantpereNeurogenomics Group, Research Programme on Biomedical Informatics (GRIB), Hospital del Mar Medical Research Institute (IMIM), Department of Experimental and Health Sciences (DXECS), Universitat Pompeu Fabra, 08003 Barcelona, Spain.ORCID 0000-0001-5909-8637
Universitat Pompeu Fabra · ESInstitució Catalana de Recerca i Estudis Avançats · ESMax Planck Institute for Evolutionary Anthropology · DEUniversity of Bristol · GB

Funding

Instituto de Salud Carlos III PT17/0009/0020La Caixa Foundation LCF/BQ/PI19/11690010Ministerio de Ciencia e Innovación PID2019-104700GA-I00
6 · The paper itself

Abstract

The Epstein-Barr Virus (EBV) infects the vast majority of human individuals worldwide (~90%) and is associated with several diseases, including different types of cancer and multiple sclerosis, which show wide variation in incidence among global geographical regions. Genetic variants in EBV genomic sequences have been used to determine the geographical structure of EBV isolates, but our understanding of EBV diversity remains highly incomplete. We generated sequences for 13 pivotal EBV genes derived from 103 healthy individuals, expanding current EBV diversity datasets with respect to both geographic coverage and number of isolates per region. These newly generated sequences were integrated with the more than 250 published EBV genomes, generating the most geographically comprehensive data set of EBV strains to date. We report remarkable variation in single-gene phylogenies that, when analysed together, show robust signals of population structure. Our results not only confirm known major global patterns of geographic variation, such as the clear separation of Asian isolates from the rest, and the intermixed relationships among African, European and Australian isolates, but yield novel phylogenetic relationships with previously unreported populations. We provide a better understanding of EBV's population structure in South America, Africa and, by the inclusion of Turkey and Georgia, we also gain insight into EBV diversity in Western Asia, a crossroads connecting Europe, Africa and Asia. In summary, our results provide a detailed world-wide characterisation of EBV genetic clusters, their enrichment in specific geographic regions, novel inter-population relationships, and a catalogue of geographically informative EBV genetic variants.

Indexed as

Esptein–Barr virusgenegenetic diversitygenomicshuman herpes virus 4phylogenyphylogeography

Identifiers

PMID33138327
PMCPMC7692309
OpenAlexW3095211228

What OpenQuestion holds

Textmetadata
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.