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

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          Abstract

          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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          Most cited references51

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          Agrobacterium tumefaciens-mediated transformation of filamentous fungi.

          Agrobacterium tumefaciens transfers part of its Ti plasmid, the T-DNA, to plant cells during tumorigenesis. It is routinely used for the genetic modification of a wide range of plant species. We report that A. tumefaciens can also transfer its T-DNA efficiently to the filamentous fungus Aspergillus awamori, demonstrating DNA transfer between a prokaryote and a filamentous fungus. We transformed both protoplasts and conidia with frequencies that were improved up to 600-fold as compared with conventional techniques for transformation of A. awamori protoplasts. The majority of the A. awamori transformants contained a single T-DNA copy randomly integrated at a chromosomal locus. The T-DNA integrated into the A. awamori genome in a manner similar to that described for plants. We also transformed a variety of other filamentous fungi, including Aspergillus niger, Fusarium venenatum, Trichoderma reesei, Colletotrichum gloeosporioides, Neurospora crassa, and the mushroom Agaricus bisporus, demonstrating that transformation using A. tumefaciens is generally applicable to filamentous fungi.
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            Fighting malaria with engineered symbiotic bacteria from vector mosquitoes

            The most vulnerable stages of Plasmodium development occur in the lumen of the mosquito midgut, a compartment shared with symbiotic bacteria. Here, we describe a strategy that uses symbiotic bacteria to deliver antimalaria effector molecules to the midgut lumen, thus rendering host mosquitoes refractory to malaria infection. The Escherichia coli hemolysin A secretion system was used to promote the secretion of a variety of anti-Plasmodium effector proteins by Pantoea agglomerans, a common mosquito symbiotic bacterium. These engineered P. agglomerans strains inhibited development of the human malaria parasite Plasmodium falciparum and rodent malaria parasite Plasmodium berghei by up to 98%. Significantly, the proportion of mosquitoes carrying parasites (prevalence) decreased by up to 84% for two of the effector molecules, scorpine, a potent antiplasmodial peptide and (EPIP)(4), four copies of Plasmodium enolase-plasminogen interaction peptide that prevents plasminogen binding to the ookinete surface. We demonstrate the use of an engineered symbiotic bacterium to interfere with the development of P. falciparum in the mosquito. These findings provide the foundation for the use of genetically modified symbiotic bacteria as a powerful tool to combat malaria.
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              Driving mosquito refractoriness toPlasmodium falciparumwith engineered symbiotic bacteria

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                Author and article information

                Contributors
                wangyj@zafu.edu.cn
                zlqwz@zjhu.edu.cn
                Journal
                Microb Cell Fact
                Microb. Cell Fact
                Microbial Cell Factories
                BioMed Central (London )
                1475-2859
                23 July 2018
                23 July 2018
                2018
                : 17
                : 116
                Affiliations
                [1 ]ISNI 0000 0000 9152 7385, GRID grid.443483.c, Collaborative Innovation Center of Zhejiang Green Pesticide, School of Forestry and Biotechnology, , Zhejiang A&F University, ; Hangzhou, 311300 China
                [2 ]ISNI 0000 0001 0238 8414, GRID grid.411440.4, School of Life Sciences, , Huzhou University, ; Huzhou, 313000 China
                [3 ]ISNI 0000 0000 9152 7385, GRID grid.443483.c, State Key Laboratory of Subtropical Silviculture, School of Forestry and Biotechnology, , Zhejiang A&F University, ; Hangzhou, 311300 China
                [4 ]Guangdong Eco-Engineering Polytechnic, Guangdong, 510520 China
                Article
                960
                10.1186/s12934-018-0960-5
                6055344
                30037328
                f99885b7-787b-4edf-a4bb-a1b085223312
                © 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.

                History
                : 15 April 2018
                : 9 July 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 31702018
                Award ID: 31550004
                Award Recipient :
                Funded by: Huzhou Municipal Natural Science Foundation
                Award ID: 2017YZ07
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Biotechnology
                bacillus thuringiensis,bursaphelenchus xylophilus,atmt,fungus,crystal protein,nematicide
                Biotechnology
                bacillus thuringiensis, bursaphelenchus xylophilus, atmt, fungus, crystal protein, nematicide

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