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      Reduced Membrane-Bound Alkaline Phosphatase Does Not Affect Binding of Vip3Aa in a Heliothis virescens Resistant Colony

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          Abstract

          The Vip3Aa insecticidal protein from Bacillus thuringiensis (Bt) is produced by specific transgenic corn and cotton varieties for efficient control of target lepidopteran pests. The main threat to this technology is the evolution of resistance in targeted insect pests and understanding the mechanistic basis of resistance is crucial to deploy the most appropriate strategies for resistance management. In this work, we tested whether alteration of membrane receptors in the insect midgut might explain the >2000-fold Vip3Aa resistance phenotype in a laboratory-selected colony of Heliothis virescens (Vip-Sel). Binding of 125I-labeled Vip3Aa to brush border membrane vesicles (BBMV) from 3rd instar larvae from Vip-Sel was not significantly different from binding in the reference susceptible colony. Interestingly, BBMV from Vip-Sel larvae showed dramatically reduced levels of membrane-bound alkaline phosphatase (mALP) activity, which was further confirmed by a strong downregulation of the membrane-bound alkaline phosphatase 1 ( HvmALP1) gene. However, the involvement of HvmALP1 as a receptor for the Vip3Aa protein was not supported by results from ligand blotting and viability assays with insect cells expressing HvmALP1.

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          Ligand: a versatile computerized approach for characterization of ligand-binding systems.

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            Biochemistry and genetics of insect resistance to Bacillus thuringiensis.

            Bacillus thuringiensis (Bt) is a valuable source of insecticidal proteins for use in conventional sprayable formulations and in transgenic crops, and it is the most promising alternative to synthetic insecticides. However, evolution of resistance in insect populations is a serious threat to this technology. So far, only one insect species has evolved significant levels of resistance in the field, but laboratory selection experiments have shown the high potential of other species to evolve resistance against Bt. We have reviewed the current knowledge on the biochemical mechanisms and genetics of resistance to Bt products and insecticidal crystal proteins. The understanding of the biochemical and genetic basis of resistance to Bt can help design appropriate management tactics to delay or reduce the evolution of resistance in insect populations.
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              Role of receptors in Bacillus thuringiensis crystal toxin activity.

              Bacillus thuringiensis produces crystalline protein inclusions with insecticidal or nematocidal properties. These crystal (Cry) proteins determine a particular strain's toxicity profile. Transgenic crops expressing one or more recombinant Cry toxins have become agriculturally important. Individual Cry toxins are usually toxic to only a few species within an order, and receptors on midgut epithelial cells have been shown to be critical determinants of Cry specificity. The best characterized of these receptors have been identified for lepidopterans, and two major receptor classes have emerged: the aminopeptidase N (APN) receptors and the cadherin-like receptors. Currently, 38 different APNs have been reported for 12 different lepidopterans. Each APN belongs to one of five groups that have unique structural features and Cry-binding properties. While 17 different APNs have been reported to bind to Cry toxins, only 2 have been shown to mediate toxin susceptibly in vivo. In contrast, several cadherin-like proteins bind to Cry toxins and confer toxin susceptibility in vitro, and disruption of the cadherin gene has been associated with toxin resistance. Nonetheless, only a small subset of the lepidopteran-specific Cry toxins has been shown to interact with cadherin-like proteins. This review analyzes the interactions between Cry toxins and their receptors, focusing on the identification and validation of receptors, the molecular basis for receptor recognition, the role of the receptor in resistant insects, and proposed models to explain the sequence of events at the cell surface by which receptor binding leads to cell death.
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                Author and article information

                Journal
                Toxins (Basel)
                Toxins (Basel)
                toxins
                Toxins
                MDPI
                2072-6651
                19 June 2020
                June 2020
                : 12
                : 6
                : 409
                Affiliations
                [1 ]Department of Genetics, Instituto de Biotecnología y Biomedicina (BIOTECMED), Universitat de València, 46100 Burjassot, Spain; daniel.pinos@ 123456uv.es (D.P.); chakrounmaissa7@ 123456gmail.com (M.C.); anabel.millan@ 123456uv.es (A.M.-L.); patricia.hernandez@ 123456uv.es (P.H.-M.)
                [2 ]Department of Entomology and Plant Pathology, University of Tennessee, Knoxville, TN 37996, USA; jurat@ 123456utk.edu
                [3 ]Department of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, Berks SL5 7PY, UK; d.wright@ 123456imperial.ac.uk
                Author notes
                [* ]Correspondence: juan.ferre@ 123456uv.es
                [†]

                Current address: Centre de Biotechnologie de Sfax, Sfax, Tunisia.

                Author information
                https://orcid.org/0000-0002-3694-8309
                https://orcid.org/0000-0002-8945-1814
                https://orcid.org/0000-0002-3263-5786
                https://orcid.org/0000-0001-5535-0612
                Article
                toxins-12-00409
                10.3390/toxins12060409
                7354626
                32575644
                b802f3db-d34d-49a4-ac65-cac25f6dce72
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 07 May 2020
                : 17 June 2020
                Categories
                Article

                Molecular medicine
                bacillus thuringiensis,insecticidal proteins,insect resistance,tobacco budworm

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