Evidence map›Paper›PMID 40534215›Full record

ArticlePest management science2025

Proteolytic stabilization of a spider venom peptide results in an orally active bioinsecticide.

Breck R Davis, Alexandra M Haase, Joseph S Tourtois, Daniel L Hulbert, Rachel E Cornell, Brian T DeVree, Cadence J Flohrschutz, Lucille M Bell, Daniel C Peck, Trang T Nguyen and 3 more

Abstract read
In one paragraph

Article in Pest management science, 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. 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

13 authors.

Breck R DavisVestaron Crop Protection, Kalamazoo, Michigan, USA.
Alexandra M HaaseVestaron Crop Protection, Kalamazoo, Michigan, USA.
Joseph S TourtoisVestaron Crop Protection, Kalamazoo, Michigan, USA.
Daniel L HulbertVestaron Crop Protection, Kalamazoo, Michigan, USA.ORCID https://orcid.org/0000-0002-0188-443X
Rachel E CornellVestaron Crop Protection, Kalamazoo, Michigan, USA.
Brian T DeVreeVestaron Crop Protection, Kalamazoo, Michigan, USA.
Cadence J FlohrschutzVestaron Crop Protection, Kalamazoo, Michigan, USA.
Lucille M BellVestaron Crop Protection, Kalamazoo, Michigan, USA.
Daniel C PeckVestaron Crop Protection, Kalamazoo, Michigan, USA.
Trang T NguyenVestaron Crop Protection, Kalamazoo, Michigan, USA.
Lin BaoVestaron Crop Protection, Kalamazoo, Michigan, USA.
Robert M KennedyVestaron Crop Protection, Kalamazoo, Michigan, USA.
Kyle D SchneiderVestaron Crop Protection, Kalamazoo, Michigan, USA.ORCID https://orcid.org/0009-0000-4070-0202

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe toxin peptide U1-AGTX-Ta1b from the Hobo spider, Eratigena agrestis (Walckenaer, 1802), was studied to determine its potential to serve as a bioinsecticide.

resultsU1-AGTX-Ta1b has insecticidal potencies similar to commercial insecticides when injected directly into insect hemolymph but lacks activity when ingested by lepidopterans due to trypsin-like gut proteases. Alanine scanning identified an arginine and lysine rich patch on the peptide's surface that is critical for bioactivity. Targeted stability studies on these basic residues identified a single site, R9, to be the rate limiting site in U1-AGTX-Ta1b proteolysis. Mutation of position R9 to glutamine was sufficient to stabilize the peptide and render the toxin orally active with the additional benefit of enhanced temperature stability. Further refinement of the peptide to remove an O-linked glycosylation site and prevent exoprotease activity during expression in yeast led to a final peptide sequence suitable for commercialization as a bioinsecticide. This peptide displayed activity comparable to commercial insecticides in a range of crop/pest combinations.

conclusionA novel, peptide-based bioinsecticide derived from spider venom was developed to be stable and active by ingestion by lepidopteran pests. The peptide, U1-AGTX-Ta1b-QA, can replace or reduce the use of chemical insecticides and has been approved by the United States Environmental Protection Agency. © 2025 The Author(s). Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Indexed as

InsecticidesPeptidesSpidersSpider VenomsAdministration, OralAmino Acid SequenceAnimalsMothsProtein StabilityProteolysisInsecticidesPeptidesSpider Venomscrop protectioninsecticidepeptidessustainable agriculture

Identifiers

PMID40534215
PMCPMC12441774

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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.