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Toxicity of a Brevibacillus laterosporus strain lacking parasporal crystals against Musca domestica and Aedes aegypti
The pathogenicity potential of Brevibacillus laterosporus against insects of various orders has been demonstrated and the results of recent research raise the possibility that novel strains and toxins against new insect targets may be isolated. This study investigates the toxicity of different fract...
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Published in: | Biological control 2007-10, Vol.43 (1), p.136-143 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The pathogenicity potential of
Brevibacillus laterosporus against insects of various orders has been demonstrated and the results of recent research raise the possibility that novel strains and toxins against new insect targets may be isolated. This study investigates the toxicity of different fractions of an acrystalliferous
B. laterosporus strain already known to be toxic to the housefly, against both
Musca domestica and
Aedes aegypti.
Bacterial cultures become toxic in the stationary phase and toxicity increases and is maintained after sporulation. In our strain the spore and the canoe-shaped parasporal body (CSPB) structure seems to be the main location of toxins active against
M. domestica and
A. aegypti. The loss of most of the spore toxicity by heat treatment, suggests that the toxic factors are likely to be proteins. Major proteins, with a molecular weight of about 14
kDa, contained in these fractions, are probably responsible for the observed toxicity. LC
50 values were 63.77 and 12.81
μg/g of diet for housefly larvae and adults, respectively, and 3.14
μg/ml for
A. aegypti larvae. Based on our results, we suggest that the pathogenic activity of this
B. laterosporus strain for
M. domestica and
A. aegypti is a toxin-mediated process reminiscent of the mechanism of action of
B. thuringiensis δ-endotoxins. However, more work is needed to identify genes encoding for these proteins and to verify if toxicity is maintained when these genes are expressed by a different microrganism. |
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ISSN: | 1049-9644 1090-2112 |
DOI: | 10.1016/j.biocontrol.2007.07.002 |