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Suppressing a plant-parasitic nematode with fungivorous behavior by fungal transformation of a Bt cry gene

BACKGROUND: Pine wilt disease, caused by the pinewood nematode Bursaphelenchus xylophilus (PWN), is an important destructive disease of pine forests worldwide. In addition to behaving as a plant-parasitic nematode that feeds on epithelial cells of pines, this pest relies on fungal associates for com...

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Autores principales: Cheng, Chihang, Qin, Jialing, Wu, Choufei, Lei, Mengying, Wang, Yongjun, Zhang, Liqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055344/
https://www.ncbi.nlm.nih.gov/pubmed/30037328
http://dx.doi.org/10.1186/s12934-018-0960-5
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author Cheng, Chihang
Qin, Jialing
Wu, Choufei
Lei, Mengying
Wang, Yongjun
Zhang, Liqin
author_facet Cheng, Chihang
Qin, Jialing
Wu, Choufei
Lei, Mengying
Wang, Yongjun
Zhang, Liqin
author_sort Cheng, Chihang
collection PubMed
description BACKGROUND: Pine wilt disease, caused by the pinewood nematode Bursaphelenchus xylophilus (PWN), is an important destructive disease of pine forests worldwide. In addition to behaving as a plant-parasitic nematode that feeds on epithelial cells of pines, this pest relies on fungal associates for completing its life cycle inside pine trees. Manipulating microbial symbionts to block pest transmission has exhibited an exciting prospect in recent years; however, transforming the fungal mutualists to toxin delivery agents for suppressing PWN growth has received little attention. RESULTS: In the present study, a nematicidal gene cry5Ba3, originally from a soil Bacillus thuringiensis (Bt) strain, was codon-preferred as cry5Ba3Φ and integrated into the genome of a fungus eaten by PWN, Botrytis cinerea, using Agrobacterium tumefaciens-mediated transformation. Supplementing wild-type B. cinerea extract with that from the cry5Ba3Φ transformant significantly suppressed PWN growth; moreover, the nematodes lost fitness significantly when feeding on the mycelia of the cry5Ba3Φ transformant. N-terminal deletion of Cry5Ba3Φ protein weakened the nematicidal activity more dramatically than did the C-terminal deletion, indicating that domain I (endotoxin-N) plays a more important role in its nematicidal function than domain III (endotoxin-C), which is similar to certain insecticidal Cry proteins. CONCLUSIONS: Transformation of Bt nematicidal cry genes in fungi can alter the fungivorous performance of B. xylophilus and reduce nematode fitness. This finding provides a new prospect of developing strategies for breaking the life cycle of this pest in pines and controlling pine wilt disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0960-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-60553442018-07-30 Suppressing a plant-parasitic nematode with fungivorous behavior by fungal transformation of a Bt cry gene Cheng, Chihang Qin, Jialing Wu, Choufei Lei, Mengying Wang, Yongjun Zhang, Liqin Microb Cell Fact Research BACKGROUND: Pine wilt disease, caused by the pinewood nematode Bursaphelenchus xylophilus (PWN), is an important destructive disease of pine forests worldwide. In addition to behaving as a plant-parasitic nematode that feeds on epithelial cells of pines, this pest relies on fungal associates for completing its life cycle inside pine trees. Manipulating microbial symbionts to block pest transmission has exhibited an exciting prospect in recent years; however, transforming the fungal mutualists to toxin delivery agents for suppressing PWN growth has received little attention. RESULTS: In the present study, a nematicidal gene cry5Ba3, originally from a soil Bacillus thuringiensis (Bt) strain, was codon-preferred as cry5Ba3Φ and integrated into the genome of a fungus eaten by PWN, Botrytis cinerea, using Agrobacterium tumefaciens-mediated transformation. Supplementing wild-type B. cinerea extract with that from the cry5Ba3Φ transformant significantly suppressed PWN growth; moreover, the nematodes lost fitness significantly when feeding on the mycelia of the cry5Ba3Φ transformant. N-terminal deletion of Cry5Ba3Φ protein weakened the nematicidal activity more dramatically than did the C-terminal deletion, indicating that domain I (endotoxin-N) plays a more important role in its nematicidal function than domain III (endotoxin-C), which is similar to certain insecticidal Cry proteins. CONCLUSIONS: Transformation of Bt nematicidal cry genes in fungi can alter the fungivorous performance of B. xylophilus and reduce nematode fitness. This finding provides a new prospect of developing strategies for breaking the life cycle of this pest in pines and controlling pine wilt disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0960-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-23 /pmc/articles/PMC6055344/ /pubmed/30037328 http://dx.doi.org/10.1186/s12934-018-0960-5 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Cheng, Chihang
Qin, Jialing
Wu, Choufei
Lei, Mengying
Wang, Yongjun
Zhang, Liqin
Suppressing a plant-parasitic nematode with fungivorous behavior by fungal transformation of a Bt cry gene
title Suppressing a plant-parasitic nematode with fungivorous behavior by fungal transformation of a Bt cry gene
title_full Suppressing a plant-parasitic nematode with fungivorous behavior by fungal transformation of a Bt cry gene
title_fullStr Suppressing a plant-parasitic nematode with fungivorous behavior by fungal transformation of a Bt cry gene
title_full_unstemmed Suppressing a plant-parasitic nematode with fungivorous behavior by fungal transformation of a Bt cry gene
title_short Suppressing a plant-parasitic nematode with fungivorous behavior by fungal transformation of a Bt cry gene
title_sort suppressing a plant-parasitic nematode with fungivorous behavior by fungal transformation of a bt cry gene
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055344/
https://www.ncbi.nlm.nih.gov/pubmed/30037328
http://dx.doi.org/10.1186/s12934-018-0960-5
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