Evidence map›Paper›PMID 33096989›Full record

ArticleBMC genomics2020

A new esophageal gland transcriptome reveals signatures of large scale de novo effector birth in the root lesion nematode Pratylenchus penetrans.

Paulo Vieira, Jonathan Shao, Paramasivan Vijayapalani, Thomas R Maier, Clement Pellegrin, Sebastian Eves-van den Akker, Thomas J Baum, Lev G Nemchinov

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.2field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

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  12. Frontiers in cell and developmental biology · 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

8 authors at 4 institutions in 2 countries.

Paulo VieiraUSDA-ARS, Molecular Plant Pathology Laboratory, Beltsville, MD, 20705-2350, USA. pvieira@vt.edu.ORCID http://orcid.org/0000-0001-5627-2628
Jonathan ShaoUSDA-ARS, Molecular Plant Pathology Laboratory, Beltsville, MD, 20705-2350, USA.
Paramasivan VijayapalaniDepartment of Plant Pathology and Microbiology, Iowa State University, Ames, IA, 50011, USA.
Thomas R MaierDepartment of Plant Pathology and Microbiology, Iowa State University, Ames, IA, 50011, USA.
Clement PellegrinDepartment of Plant Sciences, University of Cambridge, Cambridge, UK.
Sebastian Eves-van den AkkerDepartment of Plant Sciences, University of Cambridge, Cambridge, UK.
Thomas J BaumDepartment of Plant Pathology and Microbiology, Iowa State University, Ames, IA, 50011, USA.
Lev G NemchinovUSDA-ARS, Molecular Plant Pathology Laboratory, Beltsville, MD, 20705-2350, USA.
Iowa State University · USBeltsville Agricultural Research Center · USUniversity of Cambridge · GBAgricultural Research Service · US

Funding

Agricultural Research Service 8042-21000-300-00DBiotechnology and Biological Sciences Research Council BB/R011311/1Biotechnology and Biological Sciences Research Council BB/S006397/1Department for Environment, Food and Rural Affairs 125034/359149/3H2020 Marie Skłodowska-Curie Actions MSCA-IF-EF-ST-882941-NEMABOX
6 · The paper itself

Abstract

backgroundThe root lesion nematode Pratylenchus penetrans is a migratory plant-parasitic nematode responsible for economically important losses in a wide number of crops. Despite the importance of P. penetrans, the molecular mechanisms employed by this nematode to promote virulence remain largely unknown.

resultsHere we generated a new and comprehensive esophageal glands-specific transcriptome library for P. penetrans. In-depth analysis of this transcriptome enabled a robust identification of a catalogue of 30 new candidate effector genes, which were experimentally validated in the esophageal glands by in situ hybridization. We further validated the expression of a multifaceted network of candidate effectors during the interaction with different plants. To advance our understanding of the "effectorome" of P. penetrans, we adopted a phylogenetic approach and compared the expanded effector repertoire of P. penetrans to the genome/transcriptome of other nematode species with similar or contrasting parasitism strategies. Our data allowed us to infer plausible evolutionary histories that shaped the effector repertoire of P. penetrans, as well as other close and distant plant-parasitic nematodes. Two remarkable trends were apparent: 1) large scale effector birth in the Pratylenchidae in general and P. penetrans in particular, and 2) large scale effector death in sedentary (endo) plant-parasitic nematodes.

conclusionsOur study doubles the number of validated Pratylenchus penetrans effectors reported in the literature. The dramatic effector gene gain in P. penetrans could be related to the remarkable ability of this nematode to parasitize a large number of plants. Our data provide valuable insights into nematode parasitism and contribute towards basic understating of the adaptation of P. penetrans and other root lesion nematodes to specific host plants.

Indexed as

TranscriptomeTylenchoideaAnimalsHelminth ProteinsPhylogenyPlant DiseasesHelminth ProteinsEsophageal gland cellsHost-pathogen interactionPioneer effectorsRoot lesion nematodesSecretome

Identifiers

PMID33096989
PMCPMC7585316
OpenAlexW3093647871

What OpenQuestion holds

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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.