Evidence map›Paper›PMID 31882903›Full record

ArticleScientific reports2019

ABC transporter genes ABC-C6 and ABC-G33 alter plant-microbe-parasite interactions in the rhizosphere.

Deborah Elizabeth Cox, Steven Dyer, Ryan Weir, Xavier Cheseto, Matthew Sturrock, Danny Coyne, Baldwyn Torto, Aaron G Maule, Johnathan J Dalzell

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. 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
5.5field-weighted citation impact, top 5% 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, 34 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

9 authors at 3 institutions in 2 countries.

Deborah Elizabeth CoxSchool of Biological Sciences, Institute for Global Food Security, Queen's University Belfast, Belfast, UK.
Steven DyerSchool of Biological Sciences, Institute for Global Food Security, Queen's University Belfast, Belfast, UK.
Ryan WeirSchool of Biological Sciences, Institute for Global Food Security, Queen's University Belfast, Belfast, UK.
Xavier ChesetoThe International Center of Insect Physiology and Ecology, Nairobi, Kenya.
Matthew SturrockSchool of Biological Sciences, Institute for Global Food Security, Queen's University Belfast, Belfast, UK.
Danny CoyneThe International Institute for Tropical Agriculture, Nairobi, Kenya.
Baldwyn TortoThe International Center of Insect Physiology and Ecology, Nairobi, Kenya.ORCID http://orcid.org/0000-0002-5080-9903
Aaron G MauleSchool of Biological Sciences, Institute for Global Food Security, Queen's University Belfast, Belfast, UK.
Johnathan J DalzellSchool of Biological Sciences, Institute for Global Food Security, Queen's University Belfast, Belfast, UK. j.dalzell@qub.ac.uk.
Queen's University Belfast · GBInternational Centre of Insect Physiology and Ecology · KEInternational Institute of Tropical Agriculture · KE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plants are master regulators of rhizosphere ecology, secreting a complex mixture of compounds into the soil, collectively termed plant root exudate. Root exudate composition is highly dynamic and functional, mediating economically important interactions between plants and a wide range of soil organisms. Currently we know very little about the molecular basis of root exudate composition, which is a key hurdle to functional exploitation of root exudates for crop improvement. Root expressed transporters modulate exudate composition and could be manipulated to develop beneficial plant root exudate traits. Using Virus Induced Gene silencing (VIGS), we demonstrate that knockdown of two root-expressed ABC transporter genes in tomato cv. Moneymaker, ABC-C6 and ABC-G33, alters the composition of semi-volatile compounds in collected root exudates. Root exudate chemotaxis assays demonstrate that knockdown of each transporter gene triggers the repulsion of economically relevant Meloidogyne and Globodera spp. plant parasitic nematodes, which are attracted to control treatment root exudates. Knockdown of ABC-C6 inhibits egg hatching of Meloidogyne and Globodera spp., relative to controls. Knockdown of ABC-G33 has no impact on egg hatching of Meloidogyne spp. but has a substantial inhibitory impact on egg hatching of G. pallida. ABC-C6 knockdown has no impact on the attraction of the plant pathogen Agrobacterium tumefaciens, or the plant growth promoting Bacillus subtilis, relative to controls. Silencing ABC-G33 induces a statistically significant reduction in attraction of B. subtilis, with no impact on attraction of A. tumefaciens. By inoculating selected differentially exuded compounds into control root exudates, we demonstrate that hexadecaonic acid and pentadecane are biologically relevant parasite repellents. ABC-C6 represents a promising target for breeding or biotechnology intervention strategies as gene knockdown leads to the repulsion of economically important plant parasites and retains attraction of the beneficial rhizobacterium B. subtilis. This study exposes the link between ABC transporters, root exudate composition, and ex planta interactions with agriculturally and economically relevant rhizosphere organisms, paving the way for new approaches to rhizosphere engineering and crop protection.

Indexed as

Agrobacterium tumefaciensAnimalsBacillus subtilisBiotechnologyGene SilencingPlant ExudatesPlant ProteinsPlant RootsRhizosphereSolanum lycopersicumTylenchoideaPlant ExudatesPlant Proteins

Identifiers

PMID31882903
PMCPMC6934816
OpenAlexW2996781230

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.