scholarly journals Co-production of parasporal crystal toxins and antimicrobial substances by Bacillus thuringiensis BAR 3

2017 ◽  
Vol 32 (1) ◽  
pp. 41
Author(s):  
D. Chuka-Ogwude ◽  
C.O. Nwuche ◽  
J.C. Ogbonna
Author(s):  
Carmen Sieiro ◽  
Ángeles Pichardo-Gallardo ◽  
Lara Areal-Hermida ◽  
Raquel Almuiña-González ◽  
Tomás G. Villa

2009 ◽  
Vol 75 (14) ◽  
pp. 4661-4667 ◽  
Author(s):  
Alejandro Hernández-Soto ◽  
M. Cristina Del Rincón-Castro ◽  
Ana M. Espinoza ◽  
Jorge E. Ibarra

ABSTRACT Bacillus thuringiensis subsp. israelensis is the most widely used microbial control agent against mosquitoes and blackflies. Its insecticidal success is based on an arsenal of toxins, such as Cry4A, Cry4B, Cry11A, and Cyt1A, harbored in the parasporal crystal of the bacterium. A fifth toxin, Cry10Aa, is synthesized at very low levels; previous attempts to clone and express Cry10Aa were limited, and no parasporal body was formed. By using a new strategy, the whole Cry10A operon was cloned in the pSTAB vector, where both open reading frames ORF1 and ORF2 (and the gap between the two) were located, under the control of the cyt1A operon and the STAB-SD stabilizer sequence characteristic of this vector. Once the acrystalliferous mutant 4Q7 of B. thuringiensis subsp. israelensis was transformed with this construct, parasporal bodies were observed by phase-contrast microscopy and transmission electron microscopy. Discrete, ca. 0.9-μm amorphous parasporal bodies were observed in the mature sporangia, which were readily purified by gradient centrifugation once autolysis had occurred. Pure parasporal bodies showed two major bands of ca. 68 and 56 kDa on sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis. These bands were further characterized by N-terminal sequencing of tryptic fragments using matrix-assisted laser desorption ionization-time of flight mass spectrometry analysis, which identified both bands as the products of ORF1 and ORF2, respectively. Bioassays against fourth-instar larvae of Aedes aegypti of spore-crystal complex and pure crystals of Cry10Aa gave estimated 50% lethal concentrations of 2,061 ng/ml and 239 ng/ml, respectively. Additionally, synergism was clearly detected between Cry10A and Cyt1A, as the synergistic levels (potentiation rates) were estimated at 13.3 for the mixture of Cyt1A crystals and Cry10Aa spore-crystal complex and 12.6 for the combination of Cyt1A and Cry10Aa pure crystals.


2020 ◽  
Vol 29 (3) ◽  
pp. 301-308
Author(s):  
H. Zhou ◽  
W. Hu ◽  
Q. Huang ◽  
M. Abouzaid ◽  
H. Jin ◽  
...  

Insects ◽  
2019 ◽  
Vol 10 (5) ◽  
pp. 129 ◽  
Author(s):  
Christophe Buisson ◽  
Michel Gohar ◽  
Eugénie Huillet ◽  
Christina Nielsen-LeRoux

Bacillus thuringiensis is an invertebrate pathogen that produces insecticidal crystal toxins acting on the intestinal barrier. In the Galleria mellonella larvae infection model, toxins from the PlcR virulence regulon contribute to pathogenicity by the oral route. While B. thuringiensis is principally an oral pathogen, bacteria may also reach the insect haemocoel following injury of the cuticle. Here, we address the question of spore virulence as compared to vegetative cells when the wild-type Bt407cry- strain and its isogenic ∆plcR mutant are inoculated directly into G. mellonella haemocoel. Mortality dose-response curves were constructed at 25 and 37 °C using spores or vegetative cell inocula, and the 50% lethal dose (LD50) in all infection conditions was determined after 48 h of infection. Our findings show that (i) the LD50 is lower for spores than for vegetative cells for both strains, while the temperature has no significant influence, and (ii) the ∆plcR mutant is four to six times less virulent than the wild-type strain in all infection conditions. Our results suggest that the environmental resistant spores are the most infecting form in haemocoel and that the PlcR virulence regulon plays an important role in toxicity when reaching the haemocoel from the cuticle and not only following ingestion.


2013 ◽  
Vol 641-642 ◽  
pp. 781-784
Author(s):  
Yi Lin ◽  
Li Min Liao ◽  
Shu Fang Lin

The growth of Bacillus subtilis was highly inhibited by crystal proteins of Bacillus thuringiensis ly36 strain with or without the treatment of proteinase K. And human hepatoma cell lines SMMC-7721 and Bel-7402 were killed by the proteinase K-treated crystal proteins of B. thuringiensis ly36 strain.


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