Evidence map›Paper›PMID 39528973›Full record

ArticleBMC genomics2024

Multi-omics approaches define novel aphid effector candidates associated with virulence and avirulence phenotypes.

Peter Thorpe, Simone Altmann, Rosa Lopez-Cobollo, Nadine Douglas, Javaid Iqbal, Sadia Kanvil, Jean-Christophe Simon, James C Carolan, Jorunn Bos, Colin Turnbull

Abstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Functional Genomics: From Soybean to Legume.International journal of molecular sciences · 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

10 authors.

Peter ThorpeDivision of Computational Biology, School of Life Sciences, University of Dundee, Dundee, DD5 4EH, UK.
Simone AltmannDivision of Plant Sciences, School of Life Sciences, University of Dundee, Dundee, DD5 4EH, UK.
Rosa Lopez-CobolloDepartment of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
Nadine DouglasSustainable Ecosystems Group, Department of Biology, Maynooth University, Co Kildare, Maynooth, Republic of Ireland.
Javaid IqbalDepartment of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
Sadia KanvilDepartment of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
Jean-Christophe SimonInstitut de Génétique Environnement et Protection des Plantes (IGEPP), INRAE, 35653, Le Rheu, France.
James C CarolanSustainable Ecosystems Group, Department of Biology, Maynooth University, Co Kildare, Maynooth, Republic of Ireland.
Jorunn BosDivision of Plant Sciences, School of Life Sciences, University of Dundee, Dundee, DD5 4EH, UK. j.bos@dundee.ac.uk.
Colin TurnbullDepartment of Life Sciences, Imperial College London, London, SW7 2AZ, UK. c.turnbull@imperial.ac.uk.

Funding

Biotechnology and Biological Sciences Research Council BB/N002660/1Biotechnology and Biological Sciences Research Council BB/N002830/1
6 · The paper itself

Abstract

backgroundCompatibility between plant parasites and their hosts is genetically determined {Citation}both interacting organisms. For example, plants may carry resistance (R) genes or deploy chemical defences. Aphid saliva contains many proteins that are secreted into host tissues. Subsets of these proteins are predicted to act as effectors, either subverting or triggering host immunity. However, associating particular effectors with virulence or avirulence outcomes presents challenges due to the combinatorial complexity. Here we use defined aphid and host genetics to test for co-segregation of expressed aphid transcripts and proteins with virulent or avirulent phenotypes.

resultsWe compared virulent and avirulent pea aphid parental genotypes, and their bulk segregant F1 progeny on Medicago truncatula genotypes carrying or lacking the RAP1 (Resistance to Acyrthosiphon pisum 1) resistance quantitative trait locus. Differential gene expression analysis of whole body and head samples, in combination with proteomics of saliva and salivary glands, enabled us to pinpoint proteins associated with virulence or avirulence phenotypes. There was relatively little impact of host genotype, whereas large numbers of transcripts and proteins were differentially expressed between parental aphids, likely a reflection of their classification as divergent biotypes within the pea aphid species complex. Many fewer transcripts intersected with the equivalent differential expression patterns in the bulked F1 progeny, providing an effective filter for removing genomic background effects. Overall, there were more upregulated genes detected in the F1 avirulent dataset compared with the virulent one. Some genes were differentially expressed both in the transcriptome and in the proteome datasets, with aminopeptidase N proteins being the most frequent differentially expressed family. In addition, a substantial proportion (27%) of salivary proteins lack annotations, suggesting that many novel functions remain to be discovered.

conclusionsEspecially when combined with tightly controlled genetics of both insect and host plant, multi-omics approaches are powerful tools for revealing and filtering candidate lists down to plausible genes for further functional analysis as putative aphid effectors.

Indexed as

AphidsPhenotypeAnimalsGene Expression ProfilingGenomicsGenotypeInsect ProteinsMedicago truncatulaMultiomicsProteomicsQuantitative Trait LociSalivaTranscriptomeVirulenceInsect ProteinsAphidAvirulenceEffectorProteomicsSalivaTranscriptomicsVirulence

Identifiers

PMID39528973
PMCPMC11552303

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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.