Evidence map›Paper›PMID 39453964›Full record

ArticlePLoS neglected tropical diseases2024

Bacillus thuringiensis Cry14A family proteins as novel anthelmintics against gastrointestinal nematode parasites.

Duy Hoang, Kelly Flanagan, Qian Ding, Nicholas R Cazeault, Hanchen Li, Stefani Díaz-Valerio, Florentina Rus, Esther A Darfour, Elizabeth Kass, Katherine H Petersson and 4 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

14 authors.

Duy HoangProgram in Molecular Medicine, UMASS Chan Medical School, Worcester, Massachusetts, United States of America.
Kelly FlanaganProgram in Molecular Medicine, UMASS Chan Medical School, Worcester, Massachusetts, United States of America.
Qian DingProgram in Molecular Medicine, UMASS Chan Medical School, Worcester, Massachusetts, United States of America.
Nicholas R CazeaultProgram in Molecular Medicine, UMASS Chan Medical School, Worcester, Massachusetts, United States of America.
Hanchen LiProgram in Molecular Medicine, UMASS Chan Medical School, Worcester, Massachusetts, United States of America.
Stefani Díaz-ValerioDepartment of Genomic and Applied Microbiology & Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August University of Göttingen, Göttingen, Germany.
Florentina RusProgram in Molecular Medicine, UMASS Chan Medical School, Worcester, Massachusetts, United States of America.
Esther A DarfourProgram in Molecular Medicine, UMASS Chan Medical School, Worcester, Massachusetts, United States of America.
Elizabeth KassDepartment of Fisheries, Animal, and Veterinary Sciences, University of Rhode Island, Kingston, Rhode Island, United States of America.
Katherine H PeterssonDepartment of Fisheries, Animal, and Veterinary Sciences, University of Rhode Island, Kingston, Rhode Island, United States of America.
Martin K NielsenM.H. Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, Kentucky, United States of America.
Heiko LiesegangDepartment of Genomic and Applied Microbiology & Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August University of Göttingen, Göttingen, Germany.
Gary R OstroffProgram in Molecular Medicine, UMASS Chan Medical School, Worcester, Massachusetts, United States of America.
Raffi V AroianProgram in Molecular Medicine, UMASS Chan Medical School, Worcester, Massachusetts, United States of America.ORCID 0000-0002-9741-3834

Funding

Function/optimization of a nematicidal Cry toxin arsenalR01AI056189 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI RAFFI V AROIAN · 2005 to 2026
$11.0M
NIAID NIH HHS R01 AI056189
6 · The paper itself

Abstract

Bacillus thuringiensis crystal (Cry) proteins have been expressed in commercial transgenic crops for nearly 30 years, providing safe and effective control of insect pests and significantly reducing the application of hazardous chemical pesticides. B. thuringiensis crystal proteins have also been shown to target parasitic nematodes, including plant parasitic nematodes. Recently, transgenic soybean crops expressing Cry14Ab have been shown to provide control against the soybean cyst nematode Heterodera glycines, marking the first time a crystal protein is being commercialized in transgenic crops for control of a nematode pest. However, apart from H. glycines and the free-living nematode, Caenorhabditis elegans, the breadth of nematode activity of Cry14Ab, e.g., against gastrointestinal parasitic nematodes (GINs), has not been reported. Here we study the efficacy of Cry14Ab against a wide range of gastrointestinal nematode parasites (GINs) in vitro and in vivo. We find that Cry14Ab is effective in vitro against the barber's pole worm Haemonchus contortus larvae, small strongyles cyathostomin larvae, the hookworm Ancylostoma ceylanicum adults, the roundworm Ascaris suum L4 larvae, and the whipworm Trichuris muris adults. In rodents infected with GIN parasites, Cry14Ab is effective as an in vivo anthelmintic against the hookworms A. ceylanicum and N. americanus, against the mouse parasite Heligmosomoides polygyrus bakeri, and against the roundworm A. suum. Cry14Ab also variably reduces the reproduction of the whipworm T. muris in vivo. Using optimized profile Markov Models, we looked for other putative anthelmintic Cry proteins and, within this list, identified a Bt crystal protein, GenBank accession no. MF893203, that we produced and demonstrated intoxicated GINs. This protein, with 90% amino acid identity to Cry14Ab, is active against C. elegans, A. ceylanicum adults, and A. suum L4 larvae in vitro. MF893203 was given the official designation of Cry14Ac. Cry14Ac is also an effective in vivo anthelmintic against A. ceylanicum hookworms in hamsters and intestinal A. suum in mice. Taken together, our results demonstrate that Cry14Ab and Cry14Ac have wide therapeutic utility against GINs.

Indexed as

Bacillus thuringiensis ToxinsBacterial ProteinsEndotoxinsHemolysin ProteinsAnimalsAnthelminticsBacillus thuringiensisCaenorhabditis elegansFemaleMiceNematodaNematode InfectionsAnthelminticsBacillus thuringiensis ToxinsBacterial ProteinsEndotoxinsHemolysin Proteinsinsecticidal crystal protein, Bacillus Thuringiensis

Identifiers

PMID39453964
PMCPMC11540219

What OpenQuestion holds

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LicenceCC BY
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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.