Evidence map›Paper›PMID 37988381›Full record

ArticlePLoS biology2023

Key processes required for the different stages of fungal carnivory by a nematode-trapping fungus.

Hung-Che Lin, Guillermo Vidal-Diez de Ulzurrun, Sheng-An Chen, Ching-Ting Yang, Rebecca J Tay, Tomoyo Iizuka, Tsung-Yu Huang, Chih-Yen Kuo, A Pedro Gonçalves, Siou-Ying Lin and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

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  9. Proteomic insights into nematode-trapping fungiJournal of veterinary research · 2025
    Article
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  12. International journal of molecular sciences · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Hung-Che LinInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
Guillermo Vidal-Diez de UlzurrunInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
Sheng-An ChenInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
Ching-Ting YangInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
Rebecca J TayInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
Tomoyo IizukaInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
Tsung-Yu HuangInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
Chih-Yen KuoInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
A Pedro GonçalvesInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
Siou-Ying LinInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.
Yu-Chu ChangDepartment of Biochemistry and Molecular Cell Biology, School of Medicine, Taipei Medical University, Taipei, Taiwan.
Jason E StajichDepartment of Microbiology and Plant Pathology, University of California, Riverside, California, United States of America.
Erich M SchwarzDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
Yen-Ping HsuehInstitute of Molecular Biology, Academia Sinica, Nankang, Taipei, Taiwan.ORCID 0000-0002-9052-5411
Institute of Molecular Biology, Academia Sinica · TWCornell University · USTaipei Medical University · TWUniversity of California, Riverside · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nutritional deprivation triggers a switch from a saprotrophic to predatory lifestyle in soil-dwelling nematode-trapping fungi (NTF). In particular, the NTF Arthrobotrys oligospora secretes food and sex cues to lure nematodes to its mycelium and is triggered to develop specialized trapping devices. Captured nematodes are then invaded and digested by the fungus, thus serving as a food source. In this study, we examined the transcriptomic response of A. oligospora across the stages of sensing, trap development, and digestion upon exposure to the model nematode Caenorhabditis elegans. A. oligospora enacts a dynamic transcriptomic response, especially of protein secretion-related genes, in the presence of prey. Two-thirds of the predicted secretome of A. oligospora was up-regulated in the presence of C. elegans at all time points examined, and among these secreted proteins, 38.5% are predicted to be effector proteins. Furthermore, functional studies disrupting the t-SNARE protein Sso2 resulted in impaired ability to capture nematodes. Additionally, genes of the DUF3129 family, which are expanded in the genomes of several NTF, were highly up-regulated upon nematode exposure. We observed the accumulation of highly expressed DUF3129 proteins in trap cells, leading us to name members of this gene family as Trap Enriched Proteins (TEPs). Gene deletion of the most highly expressed TEP gene, TEP1, impairs the function of traps and prevents the fungus from capturing prey efficiently. In late stages of predation, we observed up-regulation of a variety of proteases, including metalloproteases. Following penetration of nematodes, these metalloproteases facilitate hyphal growth required for colonization of prey. These findings provide insights into the biology of the predatory lifestyle switch in a carnivorous fungus and provide frameworks for other fungal-nematode predator-prey systems.

Indexed as

Caenorhabditis elegansNematodaAnimalsCarnivoryGene Expression ProfilingMetalloproteasesMetalloproteases

Identifiers

PMID37988381
PMCPMC10662756
OpenAlexW4388857736

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.