Bacillus thuringiensis isolates from the Philippines: habitat distribution, delta-endotoxin diversity, and toxicity to rice stem borers (Lepidoptera: Pyralidae)

Bacillus thuringiensisBerliner isolates were detected in 57% of 801 samples of rice grain dust, soil, rice field arthropods, and miscellaneous habitats (rice straw compost and mammal faeces) collected at 100 sites in the Philippines. The collection yielded 3950 isolates ofB. thuringiensis(8.7 isolat...

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Detalles Bibliográficos
Autores principales: Theunis, W., Aguda, R.M., Cruz, W.T., Decock, C., Peferoen, M., Lambert, B., Bottrell, D.G., Gould, F.L., Litsinger, J.A., Cohen, M.B.
Formato: Journal Article
Lenguaje:Inglés
Publicado: Cambridge University Press 1998
Materias:
Acceso en línea:https://hdl.handle.net/10568/166156
Descripción
Sumario:Bacillus thuringiensisBerliner isolates were detected in 57% of 801 samples of rice grain dust, soil, rice field arthropods, and miscellaneous habitats (rice straw compost and mammal faeces) collected at 100 sites in the Philippines. The collection yielded 3950 isolates ofB. thuringiensis(8.7 isolates/positive sample). Grain dust from rice mills was the richest source (63% of the samples were positive, with 10.2 isolates/positive sample), followed by rice field arthropods, soil, and miscellaneous habitats. Polyclonal antibodies to six δ-endotoxin groups (Cry1A, Cry1B, Cry1C, Cry1D, Cry1E, and Cry3A) were used in enzyme-linked immunosorbent assays (ELISA) to characterize the toxins produced by each isolate. Subsamples of isolates representing the diversity of isolate sources and δ-endotoxin profiles were bioassayed against the yellow stem borer,Scirpophaga incertulas(Walker) and striped stem borer,Chilo suppressalis(Walker). Eighteen isolates highly toxic to both species were selected for characterization of δ-endotoxin genes by polymerase chain reaction (PCR) with primers specific to 14 genes or gene subfamilies, and Western blotting with Cry2A antibodies. At least two novel δ-endotoxin genes, related tocry1Bandcry1F, were detected by DNA sequencing of PCR products.