Literature DB >> 11166987

Why Bacillus thuringiensis insecticidal toxins are so effective: unique features of their mode of action.

A I Aronson1, Y Shai.   

Abstract

The spore-forming bacterium Bacillus thuringiensis produces intracellular inclusions comprised of protoxins active on several orders of insects. These highly effective and specific toxins have great potential in agriculture and for the control of disease-related insect vectors. Inclusions ingested by larvae are solubilized and converted to active toxins in the midgut. There are two major classes, the cytolytic toxins and the delta-endotoxins. The former are produced by B. thuringiensis subspecies active on Diptera. The latter, which will be the focus of this review, are more prevalent and active on at least three orders of insects. They have a three-domain structure with extensive functional interactions among the domains. The initial reversible binding to receptors on larval midgut cells is largely dependent upon domains II and III. Subsequent steps involve toxin insertion into the membrane and aggregation, leading to the formation of gated, cation-selective channels. The channels are comprised of certain amphipathic helices in domain I, but the three processes of insertion, aggregation and the formation of functional channels are probably dependent upon all three domains. Lethality is believed to be due to destruction of the transmembrane potential, with the subsequent osmotic lysis of cells lining the midgut. In this review, the mode of action of these delta-endotoxins will be discussed with emphasis on unique features.

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Year:  2001        PMID: 11166987     DOI: 10.1111/j.1574-6968.2001.tb10489.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  41 in total

1.  Helix 4 mutants of the Bacillus thuringiensis insecticidal toxin Cry1Aa display altered pore-forming abilities.

Authors:  Vincent Vachon; Gabrielle Préfontaine; Cécile Rang; Florence Coux; Marc Juteau; Jean-Louis Schwartz; Roland Brousseau; Roger Frutos; Raynald Laprade; Luke Masson
Journal:  Appl Environ Microbiol       Date:  2004-10       Impact factor: 4.792

2.  Single molecule fluorescence study of the Bacillus thuringiensis toxin Cry1Aa reveals tetramerization.

Authors:  Nicolas Groulx; Hugo McGuire; Raynald Laprade; Jean-Louis Schwartz; Rikard Blunck
Journal:  J Biol Chem       Date:  2011-10-17       Impact factor: 5.157

3.  Hemolytic and nonhemolytic enterotoxin genes are broadly distributed among Bacillus thuringiensis isolated from wild mammals.

Authors:  Izabela Swiecicka; Géraldine A Van der Auwera; Jacques Mahillon
Journal:  Microb Ecol       Date:  2006-08-31       Impact factor: 4.552

Review 4.  Mode of action of Bacillus thuringiensis Cry and Cyt toxins and their potential for insect control.

Authors:  Alejandra Bravo; Sarjeet S Gill; Mario Soberón
Journal:  Toxicon       Date:  2006-11-30       Impact factor: 3.033

5.  Helix alpha 4 of the Bacillus thuringiensis Cry1Aa toxin plays a critical role in the postbinding steps of pore formation.

Authors:  Frédéric Girard; Vincent Vachon; Gabrielle Préfontaine; Lucie Marceau; Jean-Louis Schwartz; Luke Masson; Raynald Laprade
Journal:  Appl Environ Microbiol       Date:  2008-11-14       Impact factor: 4.792

6.  Aminopeptidase N5 (APN5) as a Putative Functional Receptor of Cry1Ac Toxin in the Larvae of Athetis lepigone.

Authors:  Li-Yu Wang; Shao-Hua Gu; Zi-Yan Nangong; Ping Song; Qin-Ying Wang
Journal:  Curr Microbiol       Date:  2017-02-21       Impact factor: 2.188

7.  Cry6Aa1, a Bacillus thuringiensis nematocidal and insecticidal toxin, forms pores in planar lipid bilayers at extremely low concentrations and without the need of proteolytic processing.

Authors:  Eva Fortea; Vincent Lemieux; Léna Potvin; Vimbai Chikwana; Samantha Griffin; Timothy Hey; David McCaskill; Kenneth Narva; Sek Yee Tan; Xiaoping Xu; Vincent Vachon; Jean-Louis Schwartz
Journal:  J Biol Chem       Date:  2017-06-16       Impact factor: 5.157

8.  Characterisation of the binding properties of Bacillus thuringiensis 18 toxin on leukaemic cells.

Authors:  Rebecca S Y Wong; Shar M Mohamed; Vishna D Nadarajah; Ibrahim Azmi T Tengku
Journal:  J Exp Clin Cancer Res       Date:  2010-06-30

9.  Mutations in domain I interhelical loops affect the rate of pore formation by the Bacillus thuringiensis Cry1Aa toxin in insect midgut brush border membrane vesicles.

Authors:  Geneviève Lebel; Vincent Vachon; Gabrielle Préfontaine; Frédéric Girard; Luke Masson; Marc Juteau; Aliou Bah; Geneviève Larouche; Charles Vincent; Raynald Laprade; Jean-Louis Schwartz
Journal:  Appl Environ Microbiol       Date:  2009-04-17       Impact factor: 4.792

10.  Specific binding of Bacillus thuringiensis Cry2A insecticidal proteins to a common site in the midgut of Helicoverpa species.

Authors:  Carmen Sara Hernández-Rodríguez; Adri Van Vliet; Nadine Bautsoens; Jeroen Van Rie; Juan Ferré
Journal:  Appl Environ Microbiol       Date:  2008-10-17       Impact factor: 4.792

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