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Bacillus thuringiensis Cry14A family proteins as novel anthelmintics against gastrointestinal nematode parasites.
- Source :
-
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2024 Oct 25; Vol. 18 (10), pp. e0012611. Date of Electronic Publication: 2024 Oct 25 (Print Publication: 2024). - Publication Year :
- 2024
-
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.<br />Competing Interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: The University of Massachusetts Chan Medical School is pursuing patent protection related to the use of Cry14Ab as anthelmintic via U.S. Provisional Patent Application Serial No. 63/439,759 (K.F. and R.V.A. as inventors) and the University of Massachusetts Chan Medical School and University of Göttingen are pursing patent protection related to the use of Cry14Ac as anthelmintic via U.S. Provisional Patent Application Serial No. 63/649,526 (K.F., S.D.V., H.L., and R.V.A. as inventors).<br /> (Copyright: © 2024 Hoang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
- Subjects :
- Animals
Mice
Anthelmintics pharmacology
Nematoda drug effects
Nematoda genetics
Female
Nematode Infections drug therapy
Nematode Infections parasitology
Bacillus thuringiensis genetics
Bacillus thuringiensis chemistry
Caenorhabditis elegans drug effects
Caenorhabditis elegans genetics
Bacillus thuringiensis Toxins genetics
Hemolysin Proteins genetics
Hemolysin Proteins pharmacology
Bacterial Proteins genetics
Endotoxins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1935-2735
- Volume :
- 18
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- PLoS neglected tropical diseases
- Publication Type :
- Academic Journal
- Accession number :
- 39453964
- Full Text :
- https://doi.org/10.1371/journal.pntd.0012611