Evidence map›Paper›PMID 31775619›Full record

ArticleBMC plant biology2019

A metabolomics characterisation of natural variation in the resistance of cassava to whitefly.

Laura Perez-Fons, Adriana Bohorquez-Chaux, Maria L Irigoyen, Danielle C Garceau, Kris Morreel, Wout Boerjan, Linda L Walling, Luis Augusto Becerra Lopez-Lavalle, Paul D Fraser

Abstract read
In one paragraph

Article in BMC plant biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Review
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  4. Genetic mapping and validation of QTL for whitefly resistance in cassava (Manihot esculenta Crantz).TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
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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.

Laura Perez-FonsSchool of Biological Sciences, Royal Holloway University of London, Egham, UK.
Adriana Bohorquez-ChauxInternational Center of Tropical Agriculture (CIAT), Cali, Colombia.
Maria L IrigoyenDepartment of Botany and Plant Sciences, University of California, Riverside, California, USA.
Danielle C GarceauDepartment of Botany and Plant Sciences, University of California, Riverside, California, USA.
Kris MorreelGhent University, Department of Plant Biotechnology and Bioinformatics, Technologiepark 71, 9052, Ghent, Belgium.
Wout BoerjanGhent University, Department of Plant Biotechnology and Bioinformatics, Technologiepark 71, 9052, Ghent, Belgium.
Linda L WallingDepartment of Botany and Plant Sciences, University of California, Riverside, California, USA.
Luis Augusto Becerra Lopez-LavalleInternational Center of Tropical Agriculture (CIAT), Cali, Colombia.
Paul D FraserSchool of Biological Sciences, Royal Holloway University of London, Egham, UK. p.fraser@rhul.ac.uk.

Funding

Bill and Melinda Gates Foundation OPP1058938
6 · The paper itself

Abstract

backgroundCassava whitefly outbreaks were initially reported in East and Central Africa cassava (Manihot esculenta Crantz) growing regions in the 1990's and have now spread to other geographical locations, becoming a global pest severely affecting farmers and smallholder income. Whiteflies impact plant yield via feeding and vectoring cassava mosaic and brown streak viruses, making roots unsuitable for food or trading. Deployment of virus resistant varieties has had little impact on whitefly populations and therefore development of whitefly resistant varieties is also necessary as part of integrated pest management strategies. Suitable sources of whitefly resistance exist in germplasm collections that require further characterization to facilitate and assist breeding programs.

resultsIn the present work, a hierarchical metabolomics approach has been employed to investigate the underlying biochemical mechanisms associated with whitefly resistance by comparing two naturally occurring accessions of cassava, one susceptible and one resistant to whitefly. Quantitative differences between genotypes detected at pre-infestation stages were consistently observed at each time point throughout the course of the whitefly infestation. This prevalent differential feature suggests that inherent genotypic differences override the response induced by the presence of whitefly and that they are directly linked with the phenotype observed. The most significant quantitative changes relating to whitefly susceptibility were linked to the phenylpropanoid super-pathway and its linked sub-pathways: monolignol, flavonoid and lignan biosynthesis. These findings suggest that the lignification process in the susceptible variety is less active, as the susceptible accession deposits less lignin and accumulates monolignol intermediates and derivatives thereof, differences that are maintained during the time-course of the infestation.

conclusionsResistance mechanism associated to the cassava whitefly-resistant accession ECU72 is an antixenosis strategy based on reinforcement of cell walls. Both resistant and susceptible accessions respond differently to whitefly attack at biochemical level, but the inherent metabolic differences are directly linked to the resistance phenotype rather than an induced response in the plant.

Indexed as

HemipteraAnimalsDisease ResistanceGenetic VariationManihotMetabolomicsPhenylpropionatesPlant DiseasesPropanols1-phenylpropanolPhenylpropionatesPropanolsCassavaLC-MSLigninMetabolomicsPhenylpropanoidsResistanceWhitefly

Identifiers

PMID31775619
PMCPMC6882011

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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.