: Bacillus thuringiensis is a microbial insecticide that is widely used to control insects, including mosquitoes and black flies. The long-range goal of this project is to investigate the binding and mechanism of action of several mosquitocidal proteins against key pestiferous mosquito species, Anopheles gambiae, Aedes aegypti and Culex quinquefaciatus. The main mosquitocidal toxins of interest are the toxins of B. thuringiensis var. israelensis (Bti), Cry4Aa, Cry4Ab and Cry11Aa. Other mosquitocidal toxins, Cry11Ba, Cry19Aa and Cry2Aa, will also be investigated. The hypothesis to be tested is that these toxins bind to specific receptors on the mosquito midgut as recognized in model insect-toxin studies (the Lepidoptera-toxin paradigm); i.e., an array of mosquito midgut proteins (cadherin-like and aminopeptidases) and glycoproteins bind the toxins; and, that domains II and Ill of the are the interacting binding epitopes. A corollary hypothesis is that the reduced ability of mosquitoes to develop resistance to Bti is due to a combination of toxins (Cry4Aa, Cry4Ab and Cry11Aa) each of which binds to a unique receptor or non-competing binding site.
The specific aims of the proposal are: (1) Test the competition, saturation and irreversible binding of Cry4Aa, 4Ba, 11Aa, 11Ba, 19Aa and 2Aa toxins to mosquito BBMV and purified receptors. New mosquitocidal activity has been introduced into Cry4Ba (Culex activity) and 19Aa (Aedes activity). The mechanistic basis for these new activities will be investigated. (2) Examine the mechanism of action of mosquitocidal of these toxins, in comparison to the Lepidoptera toxins paradigm; specifically, to define the binding epitopes of these toxins to brush border membrane vesicles (BBMV) of the mosquitoes Aedes aegypti, Anopheles gambiae and Culex quinquefasciatus. (3) Examine the nature of mosquito midgut receptors in relation to what has been learned from Lepidoptera receptor paradigm; specifically, to identify the specific binding of these mosquitocidal Cry proteins on aminopeptidases, cadherin-like proteins, glycoproteins and other potential receptors of these mosquitoes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI029092-16
Application #
7188964
Study Section
Special Emphasis Panel (ZRG1-TMP (01))
Program Officer
Costero, Adriana
Project Start
1989-07-01
Project End
2009-02-28
Budget Start
2007-03-01
Budget End
2009-02-28
Support Year
16
Fiscal Year
2007
Total Cost
$435,255
Indirect Cost
Name
Ohio State University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
Nair, Manoj S; Dean, Donald H (2015) Composition of the Putative Prepore Complex of Bacillus thuringiensis Cry1Ab Toxin. Adv Biol Chem 5:179-188
Zhang, Qi; Hua, Gang; Bayyareddy, Krishnareddy et al. (2013) Analyses of ?-amylase and ?-glucosidase in the malaria vector mosquito, Anopheles gambiae, as receptors of Cry11Ba toxin of Bacillus thuringiensis subsp. jegathesan. Insect Biochem Mol Biol 43:907-15
Hua, Gang; Zhang, Qi; Zhang, Rui et al. (2013) AgCad2 cadherin in Anopheles gambiae larvae is a putative receptor of Cry11Ba toxin of Bacillus thuringiensis subsp. jegathesan. Insect Biochem Mol Biol 43:153-61
Bayyareddy, Krishnareddy; Zhu, Xiang; Orlando, Ron et al. (2012) Proteome analysis of Cry4Ba toxin-interacting Aedes aegypti lipid rafts using geLC-MS/MS. J Proteome Res 11:5843-55
McNeil, Betina C; Dean, Donald H (2011) Bacillus thuringiensis Cry2Ab is active on Anopheles mosquitoes: single D block exchanges reveal critical residues involved in activity. FEMS Microbiol Lett 325:16-21
Alzate, Oscar; Osorio, Cristina; Florez, Alvaro M et al. (2010) Participation of valine 171 in alpha-Helix 5 of Bacillus thuringiensis Cry1Ab delta-endotoxin in translocation of toxin into Lymantria dispar midgut membranes. Appl Environ Microbiol 76:7878-80
Zhang, Rui; Hua, Gang; Urbauer, Jeffrey L et al. (2010) Synergistic and inhibitory effects of aminopeptidase peptides on Bacillus thuringiensis Cry11Ba toxicity in the mosquito Anopheles gambiae. Biochemistry 49:8512-9
Hua, Gang; Zhang, Rui; Bayyareddy, Krishnareddy et al. (2009) Anopheles gambiae alkaline phosphatase is a functional receptor of Bacillus thuringiensis jegathesan Cry11Ba toxin. Biochemistry 48:9785-93
Park, Youngjin; Hua, Gang; Abdullah, Mohd Amir F et al. (2009) Cadherin fragments from Anopheles gambiae synergize Bacillus thuringiensis Cry4Ba's toxicity against Aedes aegypti larvae. Appl Environ Microbiol 75:7280-2
Bayyareddy, Krishnareddy; Andacht, Tracy M; Abdullah, Mohd Amir et al. (2009) Proteomic identification of Bacillus thuringiensis subsp. israelensis toxin Cry4Ba binding proteins in midgut membranes from Aedes (Stegomyia) aegypti Linnaeus (Diptera, Culicidae) larvae. Insect Biochem Mol Biol 39:279-86

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