: The long-term objectives of the proposed research are to develop more effective and environmentally safe recombinant bacteria for controlling the mosquito vectors of major human diseases including malaria, filariasis, dengue, and the viral encephalitides. These bacteria will be significantly more cost-effective than Bacillus thuringiensis. subsp israelensis (Bti) and Bacillussphaericus (Bs), the two species currently used in operational vector control programs. In addition, they will be much less prone to induce mosquito resistance, which has already developed to B. sphaericus in field populations of Culex mosquitoes in Brazil, China, and India. To support the sustainable use of these new bacteria in vector control programs, novel combinations of insecticidal proteins will used to be evaluate efficacy and resistance management strategies aimed at controlling mosquito species belonging to the most important vector genera, namely, Anopheles, Aedes, and Culex. The development and use of these new recombinants will be enhanced by studies focusing on improving our knowledge of mechanisms underlying the synergism responsible for the high toxicity and capacity of the CytlA protein to delay, avoid, or overcome resistance in vector populations to other bacterial endotoxins. These objectives will be achieved through a comprehensive research program consisting of the following three specific aims: (1)Construction of improved bacterial insecticides based on novel combinations of mosquitocidal endotoxins; (2) Determination of the target spectrum and toxicity of the bacterial recombinants; and (3) Determination of the general mechanism by which CytlA synergizes endotoxins and overcomes resistance. Bacterial insecticides developed through this research should result in improved vector control and disease reduction, with concomitant health benefits accruing from reductions in the use of broad-spectrum synthetic chemical insecticides. Moreover, the insecticidal protein combinations identified to optimize efficacy and resistance management will provide models for engineering field populations of bacteria and algae for vector control, and for resistance management programs for Bt transgenic crops.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI045817-04
Application #
6749046
Study Section
Special Emphasis Panel (ZRG1-TMP (01))
Program Officer
Costero, Adriana
Project Start
2001-07-01
Project End
2005-05-31
Budget Start
2004-06-01
Budget End
2005-05-31
Support Year
4
Fiscal Year
2004
Total Cost
$326,549
Indirect Cost
Name
University of California Riverside
Department
Zoology
Type
Schools of Earth Sciences/Natur
DUNS #
627797426
City
Riverside
State
CA
Country
United States
Zip Code
92521
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Park, Hyun-Woo; Hice, Robert H; Federici, Brian A (2016) Effect of Promoters and Plasmid Copy Number on Cyt1A Synthesis and Crystal Assembly in Bacillus thuringiensis. Curr Microbiol 72:33-40
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Bideshi, Dennis K; Waldrop, Greer; Fernandez-Luna, Maria Teresa et al. (2013) Intermolecular interaction between Cry2Aa and Cyt1Aa and its effect on larvicidal activity against Culex quinquefasciatus. J Microbiol Biotechnol 23:1107-15
Park, Hyun-Woo; Pino, Brent C; Kozervanich-Chong, Switzerlyna et al. (2013) Cyt1Aa from Bacillus thuringiensis subsp. israelensis enhances mosquitocidal activity of B. thuringiensis subsp. kurstaki HD-1 against Aedes aegypti but not Culex quinquefasciatus. J Microbiol Biotechnol 23:88-91
Diaz-Mendoza, Mercedes; Bideshi, Dennis K; Federici, Brian A (2012) A 54-kilodalton protein encoded by pBtoxis is required for parasporal body structural integrity in Bacillus thuringiensis subsp. israelensis. J Bacteriol 194:1562-71

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