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Applied and Environmental Microbiology, November 2006, p. 7029-7035, Vol. 72, No. 11
0099-2240/06/$08.00+0 doi:10.1128/AEM.01454-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
EMBRAPARecursos Genéticos e Biotecnologia, W5 Norte Final, CP 02372, CEP-70.770.970 Brasília, Federal District, Brasil,1 Corporación para Investigaciones Biológicas, Carrera 72-A, No. 78B-141, A.A. 7378, and Escuela de Biociencias, Facultad de Ciencias, Universidad Nacional de Colombia, Medellín,2 Instituto de Biotecnología, Universidad Nacional de Colombia, Cd. Universitaria, AA14490, Bogotá, Colombia,5 Instituto de Microbiología y Zoología Agrícola INTA CC No. 25 (1712) Castelar, Buenos Aires, Argentina,3 Departamento de Genética, Universidad de Valencia, Dr. Moliner 50, Burjassot 46100, Valencia, Spain,4 CINVESTAV IPN, Ap. Postal 629, Irapuato 36500, Guanajuato,6 Instituto de Biotecnología UNAM, Ap. Postal 510-3, Cuernavaca, 62250 Morelos, México,9 Centro de Investigación en Biología Celular y Molecular, Universidad de Costa Rica, Cd. de la Investigación San Pedro, San José, Costa Rica,7 Instituto de Biologia Vegetal y Biotecnologia, Universidad de Talca, Casilla 747, Talca, Chile8
Received 23 June 2006/ Accepted 21 August 2006
Bacillus thuringiensis strains isolated from Latin American soil samples that showed toxicity against three Spodoptera frugiperda populations from different geographical areas (Mexico, Colombia, and Brazil) were characterized on the basis of their insecticidal activity, crystal morphology, sodium dodecyl sulfate-polyacrylamide gel electrophoresis of parasporal crystals, plasmid profiles, and cry gene content. We found that the different S. frugiperda populations display different susceptibilities to the selected B. thuringiensis strains and also to pure preparations of Cry1B, Cry1C, and Cry1D toxins. Binding assays performed with pure toxin demonstrated that the differences in the toxin binding capacities of these insect populations correlated with the observed differences in susceptibility to the three Cry toxins analyzed. Finally, the genetic variability of the three insect populations was analyzed by random amplification of polymorphic DNA-PCR, which showed significant genetic diversity among the three S. frugiperda populations analyzed. The data presented here show that the genetic variability of S. frugiperda populations should be carefully considered in the development of insect pest control strategies, including the deployment of genetically modified maize in different geographical regions.
Published ahead of print on 25 August 2006.
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