Evidence map›Paper›PMID 36042397›Full record

ArticleBMC genomics2022

Whole genome sequence analysis of equid gammaherpesvirus -2 field isolates reveals high levels of genomic diversity and recombination.

Adepeju E Onasanya, Charles El-Hage, Andrés Diaz-Méndez, Paola K Vaz, Alistair R Legione, Glenn F Browning, Joanne M Devlin, Carol A Hartley

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. 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

8 authors at 1 institution in 1 country.

Adepeju E OnasanyaMelbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The Asia-Pacific Centre for Animal Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
Charles El-HageMelbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The Asia-Pacific Centre for Animal Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
Andrés Diaz-MéndezMelbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The Asia-Pacific Centre for Animal Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
Paola K VazMelbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The Asia-Pacific Centre for Animal Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
Alistair R LegioneMelbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The Asia-Pacific Centre for Animal Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
Glenn F BrowningMelbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The Asia-Pacific Centre for Animal Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
Joanne M Devlin *Melbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The Asia-Pacific Centre for Animal Health, The University of Melbourne, Parkville, VIC, 3010, Australia. devlinj@unimelb.edu.au.
Carol A Hartley *Melbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The Asia-Pacific Centre for Animal Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEquid gammaherpesvirus 2 (EHV2) is a gammaherpesvirus with a widespread distribution in horse populations globally. Although its pathogenic significance can be unclear in most cases of infection, EHV2 infection can cause upper respiratory tract disease in foals. Co-infection of different strains of EHV2 in an individual horse is common. Small regions of the EHV2 genome have shown considerable genetic heterogeneity. This could suggest genomic recombination between different strains of EHV2, similar to the extensive recombination networks that have been demonstrated for some alphaherpesviruses. This study examined natural recombination and genome diversity of EHV2 field isolates.

resultsWhole genome sequencing analysis of 18 EHV2 isolates, along with analysis of two publicly available EHV2 genomes, revealed variation in genomes sizes (from 173.7 to 184.8 kbp), guanine plus cytosine content (from 56.7 to 57.8%) and the size of the terminal repeat regions (from 17,196 to 17,551 bp). The nucleotide sequence identity between the genomes ranged from 86.2 to 99.7%. The estimated average inter-strain nucleotide diversity between the 20 EHV2 genomes was 2.9%. Individual gene sequences showed varying levels of nucleotide diversity and ranged between 0 and 38.1%. The ratio of nonsynonymous substitutions, Ka, to synonymous substitutions, Ks, (Ka/Ks) suggests that over 50% of EHV2 genes are undergoing diversifying selection. Recombination analyses of the 20 EHV2 genome sequences using the recombination detection program (RDP4) and SplitsTree revealed evidence of viral recombination.

conclusionsAnalysis of the 18 new EHV2 genomes alongside the 2 previously sequenced genomes revealed a high degree of genetic diversity and extensive recombination networks. Herpesvirus genome diversification and virus evolution can be driven by recombination, and our findings are consistent with recombination being a key mechanism by which EHV2 genomes may vary and evolve.

Indexed as

Genome, ViralGenomicsAnimalsGenetic VariationHorsesNucleotidesPhylogenyRecombination, GeneticSequence AnalysisNucleotidesDiversityEHV2Equid gammaherpesvirus 2Genome sequenceRecombination

Identifiers

PMID36042397
PMCPMC9426266
OpenAlexW4293547930

What OpenQuestion holds

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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.