Long lasting persistence of Bacillus thuringiensis Subsp. israelensis (Bti) in mosquito natural habitats.

BACKGROUND: The detrimental effects of chemical insecticides on the environment and human health have lead to the call for biological alternatives. Today, one of the most promising solutions is the use of spray formulations based on Bacillus thuringiensis subsp. israelensis (Bti) in insect control programs. As a result, the amounts of Bti spread in the environment are expected to increase worldwide, whilst the common belief that commercial Bti is easily cleared from the ecosystem has not yet been clearly established. METHODOLOGY/MAIN FINDINGS: In this study, we aimed to determine the nature and origin of the high toxicity toward mosquito larvae found in decaying leaf litter collected in several natural mosquito breeding sites in the Rhône-Alpes region. From the toxic fraction of the leaf litter, we isolated B. cereus-like bacteria that were further characterized as B. thuringiensis subsp. israelensis using PCR amplification of specific toxin genes. Immunological analysis of these Bti strains showed that they belong to the H14 group. We finally used amplified length polymorphism (AFLP) markers to show that the strains isolated from the leaf litter were closely related to those present in the commercial insecticide used for field application, and differed from natural worldwide genotypes. CONCLUSIONS/SIGNIFICANCE: Our results raise the issue of the persistence, potential proliferation and environmental accumulation of human-spread Bti in natural mosquito habitats. Such Bti environmental persistence may lengthen the exposure time of insects to this bio-insecticide, thereby increasing the risk of resistance acquisition in target insects, and of a negative impact on non-target insects.

Differential sensitivity to Bacillus thuringiensis var. israelensis and temephos in field mosquito populations of Ochlerotatus cataphylla (Diptera: Culicidae): toward resistance?

In the present study, four populations of the same field mosquito species, Ochlerotatus cataphylla, were sampled over the Rh6ne-Alpes region (France), and their respective sensitivity to the organophosphate temephos and the bacterio-insecticide Bacillus thuringiensis var. israelensis (Bti) was measured. The results obtained in toxicological tests showed significant differences in the larval sensitivities of the four populations for both insecticides. These differences appeared to be related to the activity of the three main families of detoxifying enzymes: Cytochrome P450 monooxygenases, glutathione-S-transferases (GSTs), and esterases. All three enzyme families were significantly overexpressed in the less susceptible larval population, and after multiple regressions, GSTs and esterases came out as the most explicative variables of the larval sensitivity. Considering these results and the chemical history of the sites in terms of insecticide treatments, the hypothesis of cross-effects of insecticides leading to resistance acquisition to Bti in field organisms emerges.

Comparative capability to detoxify vegetable allelochemicals by larval mosquitoes.

In order to confirm the phytotoxicological basis for the ecological specialization of larval culicine fauna among different subalpine mosquito breeding sites, we compared the capability of six different Aedes larval taxa or populations of different ecological origin to detoxify dietary leaf litter originating from the environmental vegetation. Detoxification experiments were performed through in vitro digestion of a toxic leaf litter fraction using larval extracts as the enzymatic sources. Comparison of toxicological and detoxifying properties among the different larval samples indicates an association between their tolerance to leaf litter toxicants and their detoxification capability, which vary according to ecological origin. The fact that the detoxifying factor within the larval extracts appears to be a protein-like compound with a molecular weight bigger than 30 kDa suggests the possible involvement of detoxifying enzymes in larval tolerance to leaf litter toxicants. This is congruent with previous biochemical data that suggests the involvement of cytochrome P450 monooxygenase and esterase activities in the detoxification process.

Hot extraction and characterization of a ligninlike fraction involved in larvicidal effects of decomposed leaf litter against mosquito.

Hot water-extraction was performed on decomposed leaf litter in order to solubilize the toxic fraction involved in the dietary interaction against mosquito larvae in subalpine breeding sites. The toxic fraction was partially extracted by water with an optimum temperature of 60 degrees C and recovered in an insoluble form. Phytochemical characterization was achieved through differential enzymatic hydrolyses, using the laccase mediator delignifying system, and aluminum chloride chelation monitored by standard bioassays; comparative spectrophotometric analyses in ultraviolet light after solubilization in acetyl bromide; and comparative reversed-phase high-performance liquid chromatography of the phenolic aldehydes after alkaline nitrobenzene oxidation. The results suggested the involvement of ligninlike compounds in the toxicity of the isolated fraction. Toxicity of this fraction appeared far stronger than that of the crude leaf litter. The involvement of this ligninlike fraction in the dietary toxicity of leaf litter against larval mosquito was then investigated.

Dietary toxicity of decomposed arborescent leaf litter against larval mosquito: involvement of a lignin-polypeptidic complex.

To characterize the toxic compounds involved in the dietary toxicity of decomposed arborescent leaf litter against larval mosquito, a toxic fraction was extracted from crude leaf litter by using hot water. Preliminary characterization of this fraction, called the insoluble fraction (IF) because it progressively precipitates after extraction, has suggested the involvement of lignin-like compounds in the toxicity. Further analyzes are currently being performed by using additional phytotoxicity-based methods. The involvement of lignin-like compounds in the toxicity was indicated by both the comparative effects of different enzymatic oxidative treatments and reversed-phase high-performance liquid chromatography analysis of the phenolic aldehydes and acids obtained after alkaline nitrobenzene oxidation. However, these lignin-like compounds may not be involved alone in the toxicity, as no specific feature of those components was associated with the toxicity. Among the possible compounds associated with lignin-like compounds in the toxicity, peptidic compounds were suggested by comparative determination of the C/N ratio and then revealed by denaturation experiments, use of specific binding protein molecules, and thin-layer chromatography analysis. A possible role of these peptidic compounds associated with lignin-like compounds in the dietary toxicity of the leaf litter against the larval mosquito midgut is discussed.