Explore the vast range of titles available.

The evolution of insect resistance to pesticides poses a continuing threat to agriculture and human health. While much is known about the proximate molecular and biochemical mechanisms that confer resistance, far less is known about the regulation of the specific genes/gene families involved, particularly by trans-acting factors such as signal-regulated transcription factors. Here we resolve in fine detail the trans-regulation of CYP6CM1, a cytochrome P450 that confers resistance to neonicotinoid insecticides in the whitefly Bemisia tabaci, by the mitogen-activated protein kinase (MAPK)-directed activation of the transcription factor cAMP-response element binding protein (CREB). Reporter gene assays were used to identify the putative promoter of CYP6CM1, but no consistent polymorphisms were observed in the promoter of a resistant strain of B. tabaci (imidacloprid-resistant, IMR), which overexpresses this gene, compared to a susceptible strain (imidaclopridsusceptible, IMS). Investigation of potential trans-acting factors using in vitro and in vivo assays demonstrated that the bZIP transcription factor CREB directly regulates CYP6CM1 expression by binding to a cAMP-response element (CRE)-like site in the promoter of this gene. CREB is overexpressed in the IMR strain, and inhibitor, luciferase, and RNA interference assays revealed that a signaling pathway of MAPKs mediates the activation of CREB, and thus the increased expression of CYP6CM1, by phosphorylation-mediated signal transduction. Collectively, these results provide mechanistic insights into the regulation of xenobiotic responses in insects and implicate both the MAPK-signaling pathway and a transcription factor in the development of pesticide resistance.

Bumblebees are essential pollinators of crops and wild plants, but are in decline across the globe. Neonicotinoid pesticides have been implicated as a potential driver of these declines, but most of our evidence base comes from studies of a single species. There is an urgent need to understand whether such results can be generalized across a range of species. Here, we present results of a laboratory experiment testing the impacts of field-relevant doses (1.87–5.32 ppb) of the neonicotinoid thiamethoxam on spring-caught wild queens of four bumblebee species: Bombus terrestris, B. lucorum, B. pratorum and B. pascuorum. Two weeks of exposure to the higher concentration of thiamethoxam caused a reduction in feeding in two out of four species, suggesting species-specific anti-feedant, repellency or toxicity effects. The higher level of thiamethoxam exposure resulted in a reduction in the average length of terminal oocytes in queens of all four species. In addition to providing the first evidence for general effects of neonicotinoids on ovary development in multiple species of wild bumblebee queens, the discovery of species-specific effects on feeding has significant implications for current practices and policy for pesticide risk assessment and use.

A sensitive and rapid method named dispersive solid–liquid microextraction combining in situ acid–base reaction-based effervescence and solidification of a floating organic droplet was developed for the simultaneous determination of eight neonicotinoid insecticides and two metabolites in rice by ultra-performance liquid chromatography-tandem mass spectrometry. The samples were extracted with sodium citrate monobasic-modified acetonitrile by vortexing and purified by primary secondary amine, and then a mixture of 1-undecanol and sodium carbonate aqueous solution was rapidly injected. An acid–base reaction and carbon dioxide bubbles were generated in situ, which promoted the dispersion of 1-undecanol droplets and subsequent transfer of the analytes from the acidified acetonitrile extract to 1-undecanol. The 1-undecanol phase was easily retrieved by centrifugation and solidification in an ice bath. This novel dispersive solid–liquid microextraction fully utilized the advantages of the effervescent reaction and floating droplet solidification, which was carried out in a tube and did not require stepwise analysis for a solid matrix. Under the optimized conditions, the average recoveries of the analytes ranged from 77.8 to 97.1% with relative standard deviations less than 7.3. The limits of detection varied between 0.01 and 0.1 μg kg−1, and enrichment factors were 42–55. The proposed method provides a quantitative, sensitive, and convenient analytical tool applicable for routine monitoring of neonicotinoids in rice.

Background Dinotefuran (CAS No. 165252–70-0), a neonicotinoid insecticide, has been used to protect various crops against invertebrate pests and has been associated with numerous negative sublethal effects on honey bees. Long noncoding RNAs (lncRNAs) play important roles in mediating various biological and pathological processes, involving transcriptional and gene regulation. The effects of dinotefuran on lncRNA expression and lncRNA function in the honey bee brain are still obscure. Results Through RNA sequencing, a comprehensive analysis of lncRNAs and mRNAs was performed following exposure to 0.01 mg/L dinotefuran for 1, 5, and 10 d. In total, 312 lncRNAs and 1341 mRNAs, 347 lncRNAs and 1458 mRNAs, and 345 lncRNAs and 1155 mRNAs were found to be differentially expressed (DE) on days 1, 5 and 10, respectively. Gene set enrichment analysis (GSEA) indicated that the dinotefuran-treated group showed enrichment in carbohydrate and protein metabolism and immune-inflammatory responses such as glycine, serine and threonine metabolism, pentose and glucuronate interconversion, and Hippo and transforming growth factor-β (TGF-β) signaling pathways. Moreover, the DE lncRNA TCONS_00086519 was shown by fluorescence in situ hybridization (FISH) to be distributed mainly in the cytoplasm, suggesting that it may serve as a competing endogenous RNA and a regulatory factor in the immune response to dinotefuran. Conclusion This study characterized the expression profile of lncRNAs upon exposure to neonicotinoid insecticides in young adult honey bees and provided a framework for further study of the role of lncRNAs in honey bee growth and the immune response.

A neonicotinoid insecticide, imidacloprid (IMI), has been widely used by seed treatment to control the sucking and biting insects since the nineties. Although it has been regarded as a highly recalcitrant pesticide, with reports of half-lives in the soil of 174 days and its use was banned in several countries for use on several crops, there is a limited number of reports on its mycoremediation. Considering also the difficulties in the control of its illegal use in some countries, seventeen fungal strains were isolated and tested for their IMI removal capacity in the current study, and Acremonium sclerotigenum was selected for further experiments. This is the first report indicating the usability of this biomass material cultivated in the molasses medium for IMI removal. Effect of some parameters on bioremoval rate, such as pH (4, 5, 6, 7), pesticide concentration (2.6, 6.7, 18.3, 33.9 and 44.0 mg/L), incubation time (48, 96 and 144 h), and amount of inoculum were tested. The maximum specific IMI uptake was obtained as 15.4 mg/g at 33.9 mg/L IMI concentration. The highest bioremoval rates observed for 2.6 and 6.7 mg/L pesticide levels were 100% at the end of 48 h at pH 6. The fungus could also remove 8.9% of 44.0 mg/L IMI at 96 h. This study suggests that A. sclerotigenum holds the potential for effective removal of IMI from the affected environment.

Acetamiprid and imidacloprid are two important neonicotinoid insecticides that are widely utilized under field conditions for the management of sucking insect pests, including the solenopsis mealybug Phenacoccus solenopsis Tinsley (Hemiptera: Pseudococcidae). Although some information is available regarding their lethal effects, nothing is currently known about the sublethal effects of these insecticides. We, therefore, performed a series of experiments to test the lethal and sublethal effects of these chemicals on oviposition duration and fecundity. We also assessed sublethal effects on feeding behavior using the electrical penetration graph (EPG) technique. The results of this study reveal that acetamiprid toxicity is higher than imidacloprid and that both insecticides have negative effects on the oviposition, fecundity, and feeding behavior of P. solenopsis when applied at sublethal dosages. These chemicals also significantly reduce oviposition duration and fecundity and significantly prolong nonprobing duration, increase penetration problems, and reduce phloem and xylem feeding activities when compared with adults exposed to just water. No significant differences were detected in all waveform durations and events when adults previously exposed to foliage treated with each of these two insecticides were compared. The results of this study, therefore, suggest that both insecticides are capable of protecting crops from mealybug damage by not only killing these pests directly but also reducing their fecundity and inhibiting feeding behaviors when applied at sublethal dosages.

Pesticide loads and associated toxicity can be significantly reduced using integrated vegetated treatment systems, which remove moderately soluble and hydrophobic pesticides, but need a sorbent material to remove more soluble pesticides. Neonicotinoids such as imidacloprid are widely used insecticides, acutely toxic, and have been linked to a range of ecological effects. Laboratory experiments were conducted to test the sorptive capacity of granulated activated carbon and biochar for removing imidacloprid and the organophosphate insecticide chlorpyrifos in a scaled-down treatment system. Simulated irrigation water spiked with individual pesticides was treated with a bench-top system designed to mimic a 600 L carbon installation receiving 108,000 L of flow per day for sixteen days. Biochar reduced insecticides to less than detectable and non-toxic levels. Granulated activated carbon similarly reduced chlorpyrifos, but allowed increasing concentrations of imidacloprid to break through. Both media treated environmentally relevant concentrations, and would be effective if used under conditions with reduced particle loads.

Neonicotinoid insecticides (NEOs) are commonly used to prevent unwanted insects in urban fields. Degradation processes have been one of the important environmental behaviors of NEOs in an aquatic environment. In this research, hydrolysis, biodegradation, and photolysis processes of four typical NEOs (i.e., thiacloprid (THA), clothianidin (CLO), acetamiprid (ACE), and imidacloprid (IMI)) were examined through the adoption of response surface methodology–central composite design (RSM-CCD) for an urban tidal stream in South China. The influences of multiple environmental parameters and concentration levels on the three degradation processes of these NEOs were then evaluated. The results indicated that the three degradation processes of the typical NEOs followed a pseudo-first-order reaction kinetics model. The primary degradation process of the NEOs were hydrolysis and photolysis processes in the urban stream. The hydrolysis degradation rate of THA was the highest (1.97 × 10−5 s−1), and that of CLO was the lowest (1.28 × 10−5 s−1). The temperature of water samples was the main environmental factor influencing the degradation processes of these NEOs in the urban tidal stream. Salinity and humic acids could inhibit the degradation processes of the NEOs. Under the influence of extreme climate events, the biodegradation processes of these typical NEOs could be suppressed, and other degradation processes could be further accelerated. In addition, extreme climate events could pose severe challenges to the migration and degradation process simulation of NEOs.

Microbial degradation is acknowledged as a viable and eco-friendly approach for diminishing residues of neonicotinoid insecticides. This study reports the dominant strain of Md2 that degrades acetamiprid was screened from soil and identified as Aspergillus heterochromaticus, and the optimal degradation conditions were determined. Research indicated that the degradation of Md2 to 100 mg/L acetamiprid was 55.30%. Toxicological analyses of acetamiprid and its metabolites subsequently revealed that acetamiprid and its metabolites inhibited the germination of cabbage seed, inhibited the growth of Escherichia coli, and induced the production of micronuclei in the root tip cells of faba beans. Based on the analysis of metabolic pathways, it has been determined that the primary metabolic routes of acetamiprid include N-demethylation to form IM-2-1 and oxidative cleavage of the cyanoimino group to produce IM-1-3. Using 16S rRNA high-throughput sequencing, the results showed that acetamiprid and Md2 elevated the relative abundance of Acidithiobacillus, Ascomycetes, and Stramenobacteria, with increases of 10~12%, 6%, and 9%, respectively, while reducing the relative abundance of Acidobacteria, Chlorobacteria, Ascomycetes, and Sporobacteria, with decreases of 15%, 8%, 32%, and 6%, respectively. The findings will facilitate the safety evaluation of the toxicological properties of neonicotinoid insecticides, their biodegradable metabolites, and associated research on their degradation capabilities.