Evidence map›Paper›PMID 41116599›Full record

ArticleProteomics2025

Isolation and Characterization of Extracellular Vesicles From Ascochyta rabiei, a Necrotrophic Fungal Chickpea Pathogen.

Matin Ghaheri, Chamindie Punyadeera, Ido Bar, Prabhakaran T Sambasivam, Abolfazl Jangholi, Donovan Garcia-Ceron, Muhammad J A Shiddiky, Rebecca Ford

Abstract read
In one paragraph

Article in Proteomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Functional and proteomic characterization ofFrontiers in plant science · 2026
    Article
  2. Article
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.

Matin GhaheriSchool of Environment and Science, Griffith University, Queensland, Australia.ORCID 0000-0002-6096-2688
Chamindie PunyadeeraInstitute For Biomedicine and Glycomics (IBG), Griffith University, Queensland, Australia.ORCID 0000-0001-9039-8259
Ido BarSchool of Environment and Science, Griffith University, Queensland, Australia.ORCID 0000-0002-2004-4233
Prabhakaran T SambasivamSchool of Environment and Science, Griffith University, Queensland, Australia.ORCID 0000-0002-9169-5252
Abolfazl JangholiInstitute For Biomedicine and Glycomics (IBG), Griffith University, Queensland, Australia.ORCID 0000-0001-7385-6123
Donovan Garcia-CeronDepartment of Ecological, Plant and Animal Science, La Trobe Institute of Sustainable Agriculture and Food, La Trobe University, Bundoora, Victoria, Australia.ORCID 0000-0003-4718-4233
Muhammad J A ShiddikyRural Health Research Institute, Charles Sturt University, Orange, New South Wales, Australia.ORCID 0000-0003-4526-4109
Rebecca FordSchool of Environment and Science, Griffith University, Queensland, Australia.ORCID 0000-0002-4192-0706

Funding

Grains Research and Development Corporation GRI2007-001RTXInternational Postgraduate Research Scholarships
6 · The paper itself

Abstract

Extracellular vesicles produced by pathogenic organisms play a role in host recognition and invasion across kingdoms, including fungi interacting with their plant hosts. Little is known about EVs from phytopathogenic fungi compared to human fungal pathogens. Ascochyta rabiei is an endemic and widespread necrotrophic ascomycete fungus that causes a significant impact on chickpea production. The presence of EVs generated by A. rabiei during the invasion of chickpea has not previously been reported. Here, A. rabiei EVs were identified and isolated from liquid fungal broth cultures, both with and without host, using optimized ultracentrifugation and filtration techniques. Nanoparticle tracking analysis, transmission electron microscopy, and mass spectrometry revealed 40-200 nm cup-shaped, double-membraned structures. Protein cargo analysis showed significant variations depending on host presence, affecting EV production, size, and composition. The cargo included proteins involved in vesicle transport, basic cellular and oxidation/reduction-related processes, as well as pathogenesis. Some were upregulated in the presence of the host, likely facilitating immune modulation, plant defence alteration, or pathogen establishment. These findings highlight the presence and functional importance of A. rabiei EVs in the interaction with and invasion of chickpea. Future research should concentrate on characterizing EVs under various growth circumstances and confirming fungal-specific EV markers. SUMMARY: This study presents the first characterization of extracellular vesicles (EVs) produced by Ascochyta rabiei, a major phytopathogenic fungus affecting chickpea. An optimized ultracentrifugation and filtration-based isolation method enabled efficient EV recovery without reliance on specialized equipment. Comprehensive proteomic analysis revealed that EV production, size distribution, and protein composition were modulated by the presence of the host. Identified EV-associated proteins were linked to virulence, oxidative stress response, cell wall modification, and effector functions, suggesting a role in host-pathogen interactions. These findings advance the current understanding of fungal EVs in plant infection processes and establish a foundation for future studies investigating their functional significance in pathogenesis.

Indexed as

AscomycotaCicerExtracellular VesiclesFungal ProteinsPlant DiseasesHost-Pathogen InteractionsProteomicsFungal ProteinsAscochyta rabieichickpeaextracellular vesicle (EV)fungiplant‐pathogen interactionproteomics

Identifiers

PMID41116599
PMCPMC12704033

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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.