Evidence map›Paper›PMID 32703219›Full record

ArticleBMC biology2020

Genomic architecture of endogenous ichnoviruses reveals distinct evolutionary pathways leading to virus domestication in parasitic wasps.

Fabrice Legeai, Bernardo F Santos, Stéphanie Robin, Anthony Bretaudeau, Rebecca B Dikow, Claire Lemaitre, Véronique Jouan, Marc Ravallec, Jean-Michel Drezen, Denis Tagu and 7 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
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  4. The genome sequence of an ichneumonid wasp,Wellcome open research · 2024
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  6. Article
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  9. The genome sequence of an ichneumon wasp,Wellcome open research · 2023
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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

17 authors at 9 institutions in 3 countries.

Fabrice LegeaiIGEPP, Agrocampus Ouest, INRAE, Université de Rennes 1, 35650, Le Rheu, France.
Bernardo F SantosDepartment of Entomology, National Museum of Natural History, Smithsonian Institution, 10th and Constitution Avenue NW, Washington, DC, 20560-0165, USA.
Stéphanie RobinIGEPP, Agrocampus Ouest, INRAE, Université de Rennes 1, 35650, Le Rheu, France.
Anthony BretaudeauIGEPP, Agrocampus Ouest, INRAE, Université de Rennes 1, 35650, Le Rheu, France.
Rebecca B DikowDepartment of Entomology, National Museum of Natural History, Smithsonian Institution, 10th and Constitution Avenue NW, Washington, DC, 20560-0165, USA.
Claire LemaitreUniversité Rennes 1, INRIA, CNRS, IRISA, F-35000, Rennes, France.
Véronique JouanDGIMI, INRAE, University of Montpellier, 34095, Montpellier, France.
Marc RavallecDGIMI, INRAE, University of Montpellier, 34095, Montpellier, France.
Jean-Michel DrezenInstitut de Recherche sur la Biologie de l'Insecte, UMR 7261, CNRS - Université de Tours, UFR des Sciences et Techniques, Parc de Grandmont, Tours, France.
Denis TaguIGEPP, Agrocampus Ouest, INRAE, Université de Rennes 1, 35650, Le Rheu, France.
Frédéric BaudatInstitut de Génétique Humaine, CNRS, University of Montpellier, 34396, Montpellier, France.
Gabor GyapayCommissariat à l'Energie Atomique (CEA), Institut de Génomique (IG), Genoscope, 2 rue Gaston Crémieux, BP5706, 91057, Evry, France.
Xin ZhouDepartment of Entomology, China Agricultural University, Beijing, 100193, People's Republic of China.
Shanlin LiuDepartment of Entomology, China Agricultural University, Beijing, 100193, People's Republic of China.
Bruce A WebbDepartment of Entomology, University of Kentucky, Lexington, USA.
Seán G BradyDepartment of Entomology, National Museum of Natural History, Smithsonian Institution, 10th and Constitution Avenue NW, Washington, DC, 20560-0165, USA.
Anne-Nathalie VolkoffDGIMI, INRAE, University of Montpellier, 34095, Montpellier, France. anne-nathalie.volkoff@inrae.fr.ORCID 0000-0002-7211-1370
Centre National de la Recherche Scientifique · FRSmithsonian Institution · USUniversité de Montpellier · FRChina Agricultural University · CNChina National GeneBank · CNCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRInstitut Agro Rennes-Angers · FRUniversité de Tours · FRUniversity of Kentucky · US

Funding

Agence Nationale de la Recherche ANR-12-ADAP-0001
6 · The paper itself

Abstract

backgroundPolydnaviruses (PDVs) are mutualistic endogenous viruses inoculated by some lineages of parasitoid wasps into their hosts, where they facilitate successful wasp development. PDVs include the ichnoviruses and bracoviruses that originate from independent viral acquisitions in ichneumonid and braconid wasps respectively. PDV genomes are fully incorporated into the wasp genomes and consist of (1) genes involved in viral particle production, which derive from the viral ancestor and are not encapsidated, and (2) proviral segments harboring virulence genes, which are packaged into the viral particle. To help elucidating the mechanisms that have facilitated viral domestication in ichneumonid wasps, we analyzed the structure of the viral insertions by sequencing the whole genome of two ichnovirus-carrying wasp species, Hyposoter didymator and Campoletis sonorensis.

resultsAssemblies with long scaffold sizes allowed us to unravel the organization of the endogenous ichnovirus and revealed considerable dispersion of the viral loci within the wasp genomes. Proviral segments contained species-specific sets of genes and occupied distinct genomic locations in the two ichneumonid wasps. In contrast, viral machinery genes were organized in clusters showing highly conserved gene content and order, with some loci located in collinear wasp genomic regions. This genomic architecture clearly differs from the organization of PDVs in braconid wasps, in which proviral segments are clustered and viral machinery elements are more dispersed.

conclusionsThe contrasting structures of the two types of ichnovirus genomic elements are consistent with their different functions: proviral segments are vehicles for virulence proteins expected to adapt according to different host defense systems, whereas the genes involved in virus particle production in the wasp are likely more stable and may reflect ancestral viral architecture. The distinct genomic architectures seen in ichnoviruses versus bracoviruses reveal different evolutionary trajectories that have led to virus domestication in the two wasp lineages.

Indexed as

Evolution, MolecularGenome, ViralHost Microbial InteractionsAnimalsPolydnaviridaeSpecies SpecificityWaspsWhole Genome SequencingCampopleginaeEndogenous virus architectureIVSPERsKoinobiontParasitoid waspPolydnavirus

Identifiers

PMID32703219
PMCPMC7379367
OpenAlexW3044841809

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LicenceCC BY
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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.