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Abstract Background Bacillus thuringiensis svar. israelensis (Bti) is an effective and safe biolarvicide to control Aedes aegypti. Its mode of action based on four protoxins disfavors resistance; however, control in endemic areas that display high mosquito infestation throughout the year requires continuous larvicide applications, which imposes a strong selection pressure. Therefore, this study aimed to investigate the effects of an intensive Bti exposure on an Ae. aegypti strain (RecBti), regarding its susceptibility to Bti and two of its protoxins tested individually, to other control agents temephos and diflubenzuron, and its profile of detoxifying enzymes. Methods The RecBti strain was established using a large egg sample (10,000) from Recife city (Brazil) and more than 290,000 larvae were subjected to Bti throughout 30 generations. Larvae susceptibility to larvicides and the activity of detoxifying enzymes were determined by bioassays and catalytic assays, respectively. The Rockefeller strain was the reference used for these evaluations. Results Bti exposure yielded an average of 74% mortality at each generation. Larvae assessed in seven time points throughout the 30 generations were susceptible to Bti crystal (resistance ratio RR ≤ 2.8) and to its individual toxins Cry11Aa and Cry4Ba (RR ≤ 4.1). Early signs of altered susceptibility to Cry11Aa were detected in the last evaluations, suggesting that this toxin was a marker of the selection pressure imposed. RecBti larvae were also susceptible (RR ≤ 1.6) to the other control agents, temephos and diflubenzuron. The activity of the detoxifying enzymes α- and β-esterases, glutathione-S-transferases and mixed-function oxidases was classified as unaltered in larvae from two generations (F19 and F25), except for a β-esterases increase in F25. Conclusions Prolonged exposure of Ae. aegypti larvae to Bti did not evolve into resistance to the crystal, and no cross-resistance with temephos and diflubenzuron were recorded, which supports their sustainable use with Bti for integrated control practices. The unaltered activity of most detoxifying enzymes suggests that they might not play a major role in the metabolism of Bti toxins, therefore resistance by this mechanism is unlikely to occur. This study also highlights the need to establish suitable criteria to classify the status of larval susceptibility/resistance.

The insecticidal Cry4Ba and Cry11Aa crystal proteins from Bacillus thuringiensis subsp. israelensis (Bti) are highly toxic to Ae. aegypti larvae. The glycosylphosphatidylinositol (GPI)-anchored APN was identified as an important membrane-bound receptor for multiple Cry toxins in numerous Lepidoptera, Coleoptera, and Diptera insects. However, there is no direct molecular evidence to link APN of Ae. aegypti to Bti toxicity in vivo. In this study, two Cry4Ba/Cry11Aa-binding Ae. aegypti GPI-APN isoforms (AeAPN1 and AeAPN2) were individually knocked-out using CRISPR/Cas9 mutagenesis, and the AeAPN1/AeAPN2 double-mutant homozygous strain was generated using the reverse genetics approach. ELISA assays showed that the high binding affinity of Cry4Ba and Cry11Aa protoxins to the midgut brush border membrane vesicles (BBMVs) from these APN knockouts was similar to the background from the wild-type (WT) strain. Likewise, the bioassay results showed that neither the single knockout of AeAPN1 or AeAPN2, nor the simultaneous disruption of AeAPN1 and AeAPN2 resulted in significant changes in susceptibility of Ae. aegypti larvae to Cry4Ba and Cry11Aa toxins. Accordingly, our results suggest that AeAPN1 and AeAPN2 may not mediate Bti Cry4Ba and Cry11Aa toxicity in Ae. aegypti larvae as their binding proteins.

Introduction: Bacillus thuringiensis is the most important biological agent and by producing parasporal body it acts as a key role against agricultural pests. Furthermore, it produces Surface layer (S-layer) which is a protein or glycoprotein crystalline structure and has wide applications in nanobiotechnology. Accordingly it is significant to study more about this surface layer and toxin. Materials and methods: In this study, purified parasporal body and mixed crystal/ spore were stained with coomasie blue G250 and were observed with light microscope. With a point mutation in CRY4Ba, protein stabilization was predicted and the location of protein cavities were predicted by Molegro software. Finally, the surface layer was extracted and its molecular weight and morphology were determined. To compare the surface layer and parasporal body, some features of them were estimated by the Protparam server. Results: The results confirm the presence of polyhedral crystal proteins which were accumulated to form larger crystals after releasing spores. Also, it is predicted that in this research replacing the aspartic acid position- 451 with isoleucine, a more stable CRY4Ba pesticide protein is probably produced. This protein with three subunits contains 59 cavities and like the surface layer in this strain, it comprises low percent of methionine, histidine, cysteine and tryptophan. Discussion and conclusion: In sporulation phase, Bacillus thuringiensis produces insecticidal crystals that integrate to form larger crystals. It is predicted that replacing the aspartic­ acid position- 451 with isoleucine would ameliorate the stability of CRY4Ba pesticide protein. This bacterium in vegetative phase produces a surface 100 KD protein which is similar to parasporal body in a shape and the percentage of some of amino acid.

Yellow fever mosquito, Aedes aegypti , is an important medical insect that can transmit vector borne disease to human and animal. Mosquito control is the only way to stop the spread of arboviral diseases since no vaccines and effective drugs are available to vector borne diseases. In this study, Bacillus thuringiensis subsp. israelnsis Cry4Ba has high toxicity to A. aegypti larvae and the calculated 50% lethal concentration of Cry4Ba was 21.28 ng/mL. The gram-negative bacteria Xenorhabdus and Photorhabdus are symbiotically associated with nematode, which is one of biological agents for insect control with high pathogenicity. In here, X. nematophila and P. luminescens showed 52% and 43% of oral toxicity against Aedes aegypti larvae at 72 h after bacterial ingestion. Remarkable, the mortality of larvae was enhanced up to 95% or 87% by X. nematophila or P. luminescens at 48 h, when larvae were exposed to these bacteria with Cry4Ba toxin (5 ng/mL), which has 20% of larval mortality at 48 h after toxin ingestion along. This study reports that entomopthogenic bacteria enhance Cry4Ba's toxicity against A. aegypti larvae. These results may have promising basis for practical application to mosquito control in preventing arboviral diseases transfer and reducing the Bt resistance risk to mosquito. [ABSTRACT FROM AUTHOR]

Introduction: Bacillus thuringiensis is the most important biological agent and by producing parasporal body it acts as a key role against agricultural pests. Furthermore, it produces Surface layer (S-layer) which is a protein or glycoprotein crystalline structure and has wide applications in nanobiotechnology. Accordingly it is significant to study more about this surface layer and toxin. Materials and methods: In this study, purified parasporal body and mixed crystal/ spore were stained with coomasie blue G250 and were observed with light microscope. With a point mutation in CRY4Ba, protein stabilization was predicted and the location of protein cavities were predicted by Molegro software. Finally, the surface layer was extracted and its molecular weight and morphology were determined. To compare the surface layer and parasporal body, some features of them were estimated by the Protparam server. Results: The results confirm the presence of polyhedral crystal proteins which were accumulated to form larger crystals after releasing spores. Also, it is predicted that in this research replacing the aspartic acid position- 451 with isoleucine, a more stable CRY4Ba pesticide protein is probably produced. This protein with three subunits contains 59 cavities and like the surface layer in this strain, it comprises low percent of methionine, histidine, cysteine and tryptophan. Discussion and conclusion: In sporulation phase, Bacillus thuringiensis produces insecticidal crystals that integrate to form larger crystals. It is predicted that replacing the aspartic acid position-451 with isoleucine would ameliorate the stability of CRY4Ba pesticide protein. This bacterium in vegetative phase produces a surface 100 KD protein which is similar to parasporal body in a shape and the percentage of some of amino acid. [ABSTRACT FROM AUTHOR]

Oligomerization has been shown to contribute to the toxicity of Bacillus thuringiensis Cry toxins. Mutations have been made in the Cry4Ba toxin and resulted in toxic to non-toxic mutants toward Aedes aegypti larvae. In this study, Cry4Ba wild type and mutants were analyzed for oligomer formation in vitro , biochemical properties and their relationships with larvicidal activity. In vitro , the Cry4Ba forms two-main types of the oligomers including (1) the 260-kDa and larger oligomers, which assembled in the carbonate buffer, pH 10.0 and completely dissociated by heating at 90 °C and (2) 190-kDa oligomer, which was induced by heat, sodium-salt and detergent addition. Polar and charge residues in the toxin domain I and II may contribute to formation of the 260-kDa oligomers. A single Cys-525 in domain III was replaced with serine resulting in the C525S mutant, which exhibited a 50% reduction in larvicidal activity compared to the Cry4Ba wild-type. The mutant exhibited partial loss in larger oligomer of the 260 kDa and total loss of 190-kDa oligomer. The results revealed an important role of the Cys-525 in intermolecular disulfide formation of larger oligomer as well as the 190-kDa oligomer. Despite of their formations in the receptor free condition, the 260-kDa and larger oligomers were found to strongly correspond to Cry4Ba toxicity suggesting their functional roles in the A. aegypti larvae. Also, possible roles of the 260-kDa and larger oligomers have been proposed in this report. [ABSTRACT FROM AUTHOR]

Abstract: Novel Bacillus thuringiensis subsp. israelensis (Bti) Cry4Ba toxin-binding proteins have been identified in gut brush border membranes of the Aedes (Stegomyia) aegypti mosquito larvae by combining 2-dimensional gel electrophoresis (2DE) and ligand blotting followed by protein identification using mass spectrometry and database searching. Three alkaline phosphatase isoforms and aminopeptidase were identified. Other Cry4Ba binding proteins identified include the putative lipid raft proteins flotillin and prohibitin, V-ATPase B subunit and actin. These identified proteins might play important roles in mediating the toxicity of Cry4Ba due to their location in the gut brush border membrane. Cadherin-type protein was not identified, although previously, we identified a midgut cadherin AgCad1 as a putative Cry4Ba receptor in Anopheles gambiae mosquito larvae [Hua, G., Zhang, R., Abdullah, M.A., Adang, M.J., 2008. Anopheles gambiae cadherin AgCad1 binds the Cry4Ba toxin of Bacillus thuringiensis israelensis and a fragment of AgCad1 synergizes toxicity. Biochemistry 47, 5101–5110]. Other identified proteins in this study that might have lesser roles include mitochondrial proteins such as ATP synthase subunits, mitochondrial processing peptidase and porin; which are likely contaminants from mitochondria and are not brush border membrane components. Trypsin-like serine protease was also identified as a protein that binds Cry4Ba. Identification of these toxin-binding proteins will lead to a better understanding of the mode of action of this toxin in mosquito. [Copyright &y& Elsevier]

This work shows in vitro processing of Bacillus thuringiensis svar. isralensis Cry toxins and the capacity of the active fragments to bind the midgut microvilli of Aedes aegypti larvae. Processing of Cry11Aa, Cry4Aa and Cry4Ba yielded double fragments of 38–30, 45–20 and 45–18 kDa, respectively. Competition assays showed that all active 125I-Cry toxins are able to specifically bind to brush border membrane fractions and they might share a common class of binding sites. The values of IC50 suggested that toxins do not display high affinity for the receptors from brush border membrane fractions, while dissociation assays showed that binding was irreversible, indicating the insertion of toxins in the cell membrane. [ABSTRACT FROM AUTHOR]

Abstract: Response surface optimization of Bacillus thuringiensis subsp. israelensis HD 500 fermentation for the production of its toxin proteins Cry4Ba and Cry11Aa was performed. Since the interaction of the medium components as well as cultivation conditions were expected to influence the production of the toxin proteins, an experimental chart was prepared by accepting the previously reported optimal values for the most important parameters as zero points: [Mn], 10−6 M; [K2HPO4], 50mM; C:N ratio, 20:1 and incubation temperature; 30°C. When the combinations of these variables at different levels were studied at 30 batch cultures and analysed for the optimum toxin protein concentrations: temperature, 28.3°C; [Mn], 3.3×10−7 M; C:N ratio, 22.2 and [K2HPO4], 66.1mM yielded the highest concentrations of both Cry4Ba and Cry11Aa toxin proteins. [Copyright &y& Elsevier]

Simple Summary: The midgut aminopeptidase N (APN) isoforms have been identified as the binding receptor of insecticidal Cry toxins in numerous insects, including the major arbovirus vector Aedes aegypti (Ae. aegypti). However, whether the Cry-binding APN acts as an essential functional receptor to mediate Bacillus thuringiensis subsp. israelensis (Bti) toxicity in Ae. aegypti larvae remains to be determined. In this study, our results provide the direct molecular evidence demonstrating that two Cry-binding APN isoforms (AeAPN1 and AeAPN2) did not play a key role in mediating Bti Cry4Ba and Cry11Aa toxicity in Ae. aegypti larvae. The insecticidal Cry4Ba and Cry11Aa crystal proteins from Bacillus thuringiensis subsp. israelensis (Bti) are highly toxic to Ae. aegypti larvae. The glycosylphosphatidylinositol (GPI)-anchored APN was identified as an important membrane-bound receptor for multiple Cry toxins in numerous Lepidoptera, Coleoptera, and Diptera insects. However, there is no direct molecular evidence to link APN of Ae. aegypti to Bti toxicity in vivo. In this study, two Cry4Ba/Cry11Aa-binding Ae. aegypti GPI-APN isoforms (AeAPN1 and AeAPN2) were individually knocked-out using CRISPR/Cas9 mutagenesis, and the AeAPN1/AeAPN2 double-mutant homozygous strain was generated using the reverse genetics approach. ELISA assays showed that the high binding affinity of Cry4Ba and Cry11Aa protoxins to the midgut brush border membrane vesicles (BBMVs) from these APN knockouts was similar to the background from the wild-type (WT) strain. Likewise, the bioassay results showed that neither the single knockout of AeAPN1 or AeAPN2, nor the simultaneous disruption of AeAPN1 and AeAPN2 resulted in significant changes in susceptibility of Ae. aegypti larvae to Cry4Ba and Cry11Aa toxins. Accordingly, our results suggest that AeAPN1 and AeAPN2 may not mediate Bti Cry4Ba and Cry11Aa toxicity in Ae. aegypti larvae as their binding proteins. [ABSTRACT FROM AUTHOR]

Abstract: Bioassays of insecticidal proteins from Bacillus thuringiensis subsp. israelensis with larvae of the malaria vector mosquito Anopheles albimanus showed that the cytolytic protein Cyt1Aa was not toxic alone, but it increased the toxicity of the crystalline proteins Cry4Ba and Cry11Aa. Synergism also occurred between Cry4Ba and Cry11Aa toxins. Whereas many previous analyses of synergism have been based on a series of toxin concentrations leading to comparisons between expected and observed values for the concentration killing 50% of insects tested (LC50), we describe and apply a method here that enables testing for synergism based on single concentrations of toxins. [Copyright &y& Elsevier]

Background: Bacillus thuringiensis svar. israelensis (Bti) is an effective and safe biolarvicide to control Aedes aegypti. Its mode of action based on four protoxins disfavors resistance; however, control in endemic areas that display high mosquito infestation throughout the year requires continuous larvicide applications, which imposes a strong selection pressure. Therefore, this study aimed to investigate the effects of an intensive Bti exposure on an Ae. aegypti strain (RecBti), regarding its susceptibility to Bti and two of its protoxins tested individually, to other control agents temephos and diflubenzuron, and its profile of detoxifying enzymes. Methods: The RecBti strain was established using a large egg sample (10,000) from Recife city (Brazil) and more than 290,000 larvae were subjected to Bti throughout 30 generations. Larvae susceptibility to larvicides and the activity of detoxifying enzymes were determined by bioassays and catalytic assays, respectively. The Rockefeller strain was the reference used for these evaluations. Results: Bti exposure yielded an average of 74% mortality at each generation. Larvae assessed in seven time points throughout the 30 generations were susceptible to Bti crystal (resistance ratio RR ≤ 2.8) and to its individual toxins Cry11Aa and Cry4Ba (RR ≤ 4.1). Early signs of altered susceptibility to Cry11Aa were detected in the last evaluations, suggesting that this toxin was a marker of the selection pressure imposed. RecBti larvae were also susceptible (RR ≤ 1.6) to the other control agents, temephos and diflubenzuron. The activity of the detoxifying enzymes α- and β-esterases, glutathione-S-transferases and mixed-function oxidases was classified as unaltered in larvae from two generations (F19 and F25), except for a β-esterases increase in F25. Conclusions: Prolonged exposure of Ae. aegypti larvae to Bti did not evolve into resistance to the crystal, and no cross-resistance with temephos and diflubenzuron were recorded, which supports their sustainable use with Bti for integrated control practices. The unaltered activity of most detoxifying enzymes suggests that they might not play a major role in the metabolism of Bti toxins, therefore resistance by this mechanism is unlikely to occur. This study also highlights the need to establish suitable criteria to classify the status of larval susceptibility/resistance. [ABSTRACT FROM AUTHOR]