Evidence map›Paper›PMID 25123114›Full record

ArticleGenome biology and evolution2014

The transcriptome of Nacobbus aberrans reveals insights into the evolution of sedentary endoparasitism in plant-parasitic nematodes.

Sebastian Eves-van den Akker, Catherine J Lilley, Etienne G J Danchin, Corinne Rancurel, Peter J A Cock, Peter E Urwin, John T Jones

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
12.6field-weighted citation impact, top 1% 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

21 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Nematicidal Activity of the EndophytePlants (Basel, Switzerland) · 2021
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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

7 authors at 5 institutions in 4 countries.

Sebastian Eves-van den AkkerCentre for Plant Sciences, University of Leeds, United Kingdom Cell and Molecular Sciences Group, Dundee Effector Consortium, James Hutton Institute, Dundee, United Kingdom.
Catherine J LilleyCentre for Plant Sciences, University of Leeds, United Kingdom.
Etienne G J DanchinCentre National de la Recherche Scientifique, INRA Institut National de la Recherche Agronomique, UMR 1355, Université de Nice-Sophia Antipolis, Sophia-Antipolis, France.
Corinne RancurelCentre National de la Recherche Scientifique, INRA Institut National de la Recherche Agronomique, UMR 1355, Université de Nice-Sophia Antipolis, Sophia-Antipolis, France.
Peter J A CockInformation and Computational Sciences Group, Dundee Effector Consortium, James Hutton Institute, Dundee, United Kingdom.
Peter E UrwinCentre for Plant Sciences, University of Leeds, United Kingdom p.e.urwin@leeds.ac.uk john.jones@hutton.ac.uk.
John T JonesCell and Molecular Sciences Group, Dundee Effector Consortium, James Hutton Institute, Dundee, United Kingdom p.e.urwin@leeds.ac.uk john.jones@hutton.ac.uk.
Institut Sophia Agrobiotech · FRMolecular Biology Consortium · USJames Hutton Institute · GBPlanta · RUUniversity of Leeds · GB

Funding

Biotechnology and Biological Sciences Research Council BB/F000642/1Biotechnology and Biological Sciences Research Council BB/H000801/1
6 · The paper itself

Abstract

Within the phylum Nematoda, plant-parasitism is hypothesized to have arisen independently on at least four occasions. The most economically damaging plant-parasitic nematode species, and consequently the most widely studied, are those that feed as they migrate destructively through host roots causing necrotic lesions (migratory endoparasites) and those that modify host root tissue to create a nutrient sink from which they feed (sedentary endoparasites). The false root-knot nematode Nacobbus aberrans is the only known species to have both migratory endoparasitic and sedentary endoparasitic stages within its life cycle. Moreover, its sedentary stage appears to have characteristics of both the root-knot and the cyst nematodes. We present the first large-scale genetic resource of any false-root knot nematode species. We use RNAseq to describe relative abundance changes in all expressed genes across the life cycle to provide interesting insights into the biology of this nematode as it transitions between modes of parasitism. A multigene phylogenetic analysis of N. aberrans with respect to plant-parasitic nematodes of all groups confirms its proximity to both cyst and root-knot nematodes. We present a transcriptome-wide analysis of both lateral gene transfer events and the effector complement. Comparing parasitism genes of typical root-knot and cyst nematodes to those of N. aberrans has revealed interesting similarities. Importantly, genes that were believed to be either cyst nematode, or root-knot nematode, "specific" have both been identified in N. aberrans. Our results provide insights into the characteristics of a common ancestor and the evolution of sedentary endoparasitism of plants by nematodes.

Indexed as

Biological EvolutionHost-Parasite InteractionsTranscriptomeAnimalsFemaleHelminth ProteinsHost SpecificityMolecular Sequence DataNicotianaPhylogenyPlant DiseasesSequence AlignmentTylenchoideaHelminth Proteinseffectorshost mimicslateral gene transferphylogeneticsplant-parasitic nematodeRNAseq

Identifiers

PMID25123114
PMCPMC4202313
OpenAlexW2151553925

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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.