4.5 Article

Invertebrate pathogenicity and toxin-producing potential of strains of Bacillus thuringiensis endemic to Antarctica

Journal

JOURNAL OF INVERTEBRATE PATHOLOGY
Volume 107, Issue 2, Pages 132-138

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jip.2011.03.008

Keywords

Bacillus thuringiensis; delta-Endotoxin; Springtails; Pathogenicity; Antarctica

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Several strains of Bacillus thuringiensis were previously isolated from soil in Antarctica and appeared to have physiological adaptations to this cold, nutrient-poor environment. In spite of this they could produce abnormally large, parasporal crystals under laboratory conditions. Here, they have been further characterised for toxin genes and invertebrate pathogenicity. All of the strains were positive in PCR assays for the cry1Aa and cry2 genes. This was confirmed by sequence analysis and the parasporal crystals of all strains contained polypeptides of about 130 kDa. This potential for lepidopteran toxicity was borne out in bioassays of purified delta-endotoxins against larvae of Pieris brassicae: the LD50 values of B2408 (288 mu g) were comparable to that of the reference strain, HD-12 (201 mu g). There was no activity against the nematode Caenorhabditis elegans in spite of the fact that all strains appeared to possess the cry6 gene. PCR screening for genes encoding other nematode-toxic classes of toxins (Cry5, 4 and 21) was negative. B. thuringiensis has never previously been shown to be toxic to Collembola (springtails) but the purified delta-endotoxins of one of the Antarctic strains showed some activity against Folsomia candida and Seira domestica (224 mu g and 238 mu g, respectively). It seems unlikely that the level of toxicity demonstrated against springtails would support a pathogenic life-style in nature. All of the strains were positive for genes encoding Bacillus cereus-type enterotoxins. In the absence of higher insects and mammals the ecological value of retaining the toxic capability demonstrated here is uncertain. (C) 2011 Elsevier Inc. All rights reserved.

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