Evidence map›Paper›PMID 30249206›Full record

ArticleBMC genomics2018

Genome-wide diversity in temporal and regional populations of the betabaculovirus Erinnyis ello granulovirus (ErelGV).

A F Brito, F L Melo, D M P Ardisson-Araújo, W Sihler, M L Souza, B M Ribeiro

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 23 citations in OpenAlex.

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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 at 4 institutions in 2 countries.

A F BritoCentre for Integrative Systems Biology and Bioinformatics, Department of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
F L MeloLaboratory of Baculovirus, Cell Biology Department, University of Brasilia, Brasília, DF, 70910-970, Brazil.
D M P Ardisson-AraújoLaboratory of Insect Virology, Department of Biochemistry and Molecular Biology, Federal University of Santa Maria, Santa Maria, RS, 97105-900, Brazil.
W SihlerEmbrapa Genetic Resources and Biotechnology, Biological Station Park, Brasília, DF, 70770-917, Brazil.
M L SouzaEmbrapa Genetic Resources and Biotechnology, Biological Station Park, Brasília, DF, 70770-917, Brazil.
B M RibeiroLaboratory of Baculovirus, Cell Biology Department, University of Brasilia, Brasília, DF, 70910-970, Brazil. bergmann@unb.br.ORCID http://orcid.org/0000-0002-1061-196X
Brazilian Agricultural Research Corporation · BRUniversidade de Brasília · BRImperial College London · GBUniversidade Federal de Santa Maria · BR

Funding

SUBTHRESHOLD MUSCLE AFFERENT INPUT TO DORSAL HORNF06TW002012 · FIC · UNIVERSITY OF CALIFORNIA DAVIS · PI KAUFMAN, MARC PETER · 1995 to 1995
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Conselho Nacional de Desenvolvimento Científico e Tecnológico 407908/2013-7Conselho Nacional de Desenvolvimento Científico e Tecnológico 483677/2012-4Fundação de Apoio à Pesquisa do Distrito Federal 193.001.532/2016
6 · The paper itself

Abstract

backgroundErinnyis ello granulovirus (ErelGV) is a betabaculovirus infecting caterpillars of the sphingid moth E. ello ello (cassava hornworm), an important pest of cassava crops (Manihot esculenta). In this study, the genome of seven field isolates of the virus ErelGV were deep sequenced and their inter- and intrapopulational sequence diversity were analyzed.

resultsNo events of gene gain/loss or translocations were observed, and indels were mainly found within highly repetitive regions (direct repeats, drs). A naturally occurring isolate from Northern Brazil (Acre State, an Amazonian region) has shown to be the most diverse population, with a unique pattern of polymorphisms. Overall, non-synonymous substitutions were found all over the seven genomes, with no specific gathering of mutations on hotspot regions. Independently of their sizes, some ORFs have shown higher levels of non-synonymous changes than others. Non-core genes of known functions and structural genes were among the most diverse ones; and as expected, core genes were the least variable genes. We observed remarkable differences on diversity of paralogous genes, as in multiple copies of p10, fgf, and pep. Another important contrast on sequence diversity was found on genes encoding complex subunits and/or involved in the same biological processes, as late expression factors (lefs) and per os infectivity factors (pifs). Interestingly, several polymorphisms in coding regions lie on sequences encoding specific protein domains.

conclusionsBy comparing and integrating information about inter- and intrapopulational diversity of viral isolates, we provide a detailed description on how evolution operates on field isolates of a betabaculovirus. Our results revealed that 35-41% of the SNPs of ErelGV lead to amino acid changes (non-synonymous substitutions). Some genes, especially non-core genes of unknown functions, tend to accumulate more mutations, while core genes evolve slowly and are more conserved. Additional studies would be necessary to understand the actual effects of such gene variations on viral infection and fitness.

Indexed as

Genome, ViralPolymorphism, GeneticBaculoviridaePhylogenyViral ProteinsViral ProteinsBaculovirusBetabaculovirusCassava hornwormParalogous genesSNPsViral evolutionWhole genome sequencing

Identifiers

PMID30249206
PMCPMC6154946
OpenAlexW2952324732

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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.