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1.
Pestic Biochem Physiol ; 181: 105017, 2022 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-35082040

RESUMO

Broflanilide is a novel insecticide with a unique mode of action on the insect GABA receptor and is registered worldwide for the control of agricultural pests. It shows high efficacy in controlling the fall armyworm (FAW) Spodoptera frugiperda, which is a destructive pest to various crops. FAW was exposed to sublethal concentrations of broflanilide to determine its impact on insect development. Sublethal doses (LD10 and LD30) caused failure of ecdysis, reduced body length of larvae, malformation of pupae, and vestigial wing formation in adults. Also, broflanilide at LD30 significantly reduced the amount of molting hormone (MH). After exposure to LD10 or LD30 broflanilide, expression of five Halloween genes, which participate in MH biosynthesis, were found to be altered. Specifically, the transcript levels of SfrCYP307A1 (Spook), SfrCYP314A1 (Shade) and SfrCYP315A1 (Shadow) in 3rd day larvae were significantly decreased as well as SfrCYP302A1 (Disembodied) and SfrCYP306A1 (Phantom) in 5th day pupae. In contrast, the transcript levels of SfrCYP302A1 in 3rd day larvae, SfrCYP307A1 and SfrCYP314A1 in 5th day pupae, and SfrCYP306A1, SfrCYP307A1 and SfrCYP315A1 in 0.5th day adults were significantly increased. Our results demonstrate that broflanilide caused the failure of ecdysis in FAW possibly by influencing the intake of cholesterol through inhibition of feeding and also via altering expression of genes important for MH biosynthesis.


Assuntos
Ecdisona , Muda , Animais , Benzamidas , Fluorocarbonos , Larva , Spodoptera/genética
2.
Pest Manag Sci ; 78(3): 1081-1089, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-34786809

RESUMO

BACKGROUND: Broflanilide has been registered in China for the control of Lepidoptera and Coleoptera pests, and is widely used to control the target pests at lethal and sublethal levels. The lethal and sublethal effects of broflanilide on the common cutworm (CCW) Spodoptera litura Fabricius, a representative Lepidopteran pest in agricultural crops, were examined to explore its ecological influence on pests. RESULTS: In F0 , broflanilide had little influence on the hatchability of eggs, but significantly reduced the neonate survival rate. The lethal activity of broflanilide towards third-instar larvae and adults was 0.13 mg kg-1 (LD50 ) and 3.59 mg L-1 (LC50 ) respectively at 48 h. After being treated with a sublethal dose (LD10 and LD30 ) of broflanilide, the duration of third- to sixth-instar larvae and the mean fecundity of reproductive females were significantly increased, but pupation rate, weight of pupae and life-cycle rate were significantly decreased. In F1 , the duration of F1 larvae and the doubling time were prolonged, whereas the rates of pupation and the life cycle were decreased by 14.92% and 18.00%, respectively. The intrinsic rate of increase, finite rate of increase and net reproductive rate in the sublethal group were lower than in the control group. The relative fitness of F1 treated by LD10 and LD30 was 0.81 and 0.66, respectively. CONSLUSION: Broflanilide not only has highly lethal activity, but also suppresses the population growth and progeny of CCW, as a critical factor for guidelines of its usage in the field.


Assuntos
Inseticidas , Animais , Benzamidas , Diamida , Feminino , Fluorocarbonos , Humanos , Recém-Nascido , Inseticidas/farmacologia , Larva , Spodoptera
3.
J R Soc Interface ; 18(185): 20210753, 2021 12.
Artigo em Inglês | MEDLINE | ID: mdl-34875876

RESUMO

Monitoring human respiratory patterns is of great importance as it gives essential information for various medical conditions, e.g. sleep apnoea syndrome and chronic obstructive pulmonary disease and asthma, etc. Herein, we have developed a polymeric airflow sensor based on nanocomposites of vertically grown graphene nanosheets (VGNs) with polydimethylsiloxane (PDMS) and explored their applications in monitoring human respiration. The sensing performance of the VGNs/PDMS nanocomposite was characterized by exposing to a range of airflow rates (20-130 l min-1), and a linear performance with high sensitivity and low response time (mostly below 1 s) was observed. To evaluate the experimental results, finite-element simulation models were developed in the COMSOL Multiphysics package. The piezoresistive properties of VGNs/PDMS thin film and fluid-solid interaction were thoroughly studied. Laser Doppler vibrometry measures of sensor tip displacement closely approximated simulated deflection results and validated the dynamic response of the sensor. By comparing the proposed sensor and some other airflow sensors in the literature, it is concluded that the VGNs/PDMS airflow sensor has excellent features in terms of sensor height, detection range and sensitivity. The potential application of the VGNs/PDMS airflow sensor in detecting the respiration pattern of human exercises like walking, jogging and running has been demonstrated.


Assuntos
Grafite , Nanocompostos , Dispositivos Eletrônicos Vestíveis , Humanos , Monitorização Fisiológica
4.
Pestic Biochem Physiol ; 179: 104973, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34802523

RESUMO

The fall armyworm (FAW) Spodoptera frugiperda (Lepidoptera: Noctuidae) is a severe agricultural pest, which has invaded into China in 2019 and caused heavy damage to maize. The γ-aminobutyric acid receptor (GABAR)-targeted insecticides including broflanilide, fluralaner and fipronil exhibit high toxicity towards lepidopteran pests. However, whether they could be used for control of FAW and their possible mode of action in FAW remain unclear. In this study, broflanilide, fluralaner and fipronil exhibited high oral toxicity in FAW larvae with median lethal dose (LD50) values of 0.677, 0.711, and 23.577 mg kg-1 (active ingredient/ artificial food), respectively. In the electrophysiological assay, fluralaner and fipronil could strongly inhibit GABA-induced currents of homomeric FAW resistance to dieldrin 1 (RDL1) receptor with median inhibitory concentration (IC50) values of 5.018 nM (95% confidence interval (CI) 2.864-8.789) and 8.595 nM (95% CI 5.105-14.47), respectively, whereas broflanilide could not. In addition, the cytochrome P450 (P450), glutathione-S-transferase (GST) and carboxylesterase (CarE) activities were positively response to broflanilide, P450 and GST to fluralaner, and GST and CarE to fipronil, respectively, compared with those of control. In conclusion, we firstly reported a notable insecticidal activity of three representative GABAR-targeted insecticides to FAW in vivo, and in vitro using electrophysiological assay. The GST is the primary detoxification enzyme for three tested insecticides. Our results would guide the rotational use of GABAR-targeted insecticides in field.


Assuntos
Inseticidas , Animais , Inseticidas/toxicidade , Larva , Receptores de GABA , Spodoptera , Zea mays
5.
J Agric Food Chem ; 69(39): 11582-11591, 2021 Oct 06.
Artigo em Inglês | MEDLINE | ID: mdl-34555899

RESUMO

The ionotropic γ-aminobutyric acid (iGABA) receptor is commonly considered as a fast inhibitory channel and is an important insecticide target. Since 1990, RDL, LCCH3, and GRD have been successively isolated and found to be potential subunits of the insect iGABA receptor. More recently, one orphan gene named 8916 was found and considered to be another potential iGABA receptor subunit according to its amino acid sequence. However, little information about 8916 has been reported. Here, the 8916 subunit from Chilo suppressalis was studied to determine whether it can form part of a functional iGABA receptor by co-expressing this subunit with CsRDL1 or CsLCCH3 in the Xenopus oocyte system. Cs8916 or CsLCCH3 did not form functional ion channels when expressed alone. However, Cs8916 was able to form heteromeric ion channels when expressed with either CsLCCH3 or CsRDL1. The recombinant heteromeric Cs8916/LCCH3 channel was a cation-selective channel, which was sensitive to GABA or ß-alanine. The current of the Cs8916/LCCH3 channel was inhibited by dieldrin, endosulfan, fipronil, or ethiprole. In contrast, fluralaner, broflanilide, and avermectin showed little effect on the Cs8916/LCCH3 channel (IC50s > 10 000 nM). The Cs8916/RDL1 channel was sensitive to GABA, but was significantly different in EC50 and Imax for GABA to those of homomeric CsRDL1. Fluralaner, fipronil, or dieldrin showed antagonistic actions on Cs8916/RDL1. In conclusion, Cs8916 is a potential iGABA receptor subunit, which can interact with CsLCCH3 to generate a cation-selective channel that is sensitive to several insecticides. Also, as Cs8916/RDL1 has a higher EC50 than homomeric CsRDL1, Cs8916 may affect the physiological functions of CsRDL1 and therefore play a role in fine-tuning GABAergic signaling.


Assuntos
Inseticidas , Mariposas , Sequência de Aminoácidos , Animais , Inseticidas/farmacologia , Mariposas/metabolismo , Receptores de GABA/genética , Receptores de GABA/metabolismo , Receptores de GABA-A , Ácido gama-Aminobutírico
6.
J Econ Entomol ; 114(4): 1789-1795, 2021 08 05.
Artigo em Inglês | MEDLINE | ID: mdl-34137856

RESUMO

Pyrethroid insecticides have been widely utilized for insect pest control. Target-site resistance is one of the major mechanisms explaining pest resistance to pyrethroids. This study quantified pyrethroid resistance and fitness cost conferred by the voltage-gated sodium channel (VGSC) M918L mutation in Rhopalosiphum padi. Six s-kdr-SS and six s-kdr-RS parthenogenetic lineages were established from the same field population and were reared in the laboratory without exposure to pesticides for more than one year. Enzyme activity analysis demonstrated that metabolic resistance had no impact on these lineages. Bioassays showed that the M918L mutation strongly affected pyrethroid efficiency, conferring moderate resistance to bifenthrin (type I) (39.0-fold) and high resistance to lambda-cyhalothrin (type II) (194.7-fold). Compared with the life table of s-kdr-SS lineages, s-kdr-RS lineages exhibited a relative fitness cost with significant decreases in longevity and fecundity. Meanwhile, competitive fitness was measured by blending various ratios of s-kdr-SS and s-kdr-SS aphids. The results indicated that M918L-mediated resistance showed a significant fitness cost in the presence of wild aphids without insecticide pressure. The fitness cost strongly correlated with the initial resistance allele frequency. This work characterized the novel s-kdr M918L mutation in R. padi, defined its function in resistance to different types of pyrethroids, and documented that the M918L-mediated resistance has a significant fitness cost.


Assuntos
Afídeos , Inseticidas , Piretrinas , Animais , Afídeos/genética , Resistência a Inseticidas/genética , Inseticidas/farmacologia , Mutação
7.
Pest Manag Sci ; 77(6): 2964-2970, 2021 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-33624401

RESUMO

BACKGROUND: Two-spotted spider mite (TSSM), Tetranychus urticae Koch, is one of the most serious pests of agricultural crops. Broflanilide exhibits high lethality against various pests and has been marketed worldwide under the Vedira and Tenebenal brands in 2020. Nevertheless, little information has been reported about its effects on agricultural mites. RESULTS: Broflanilide displayed higher toxicity to TSSM eggs (24 h LC50 , 1.015 mg L-1 ) and adult females (24 h LC50 , 2.062 mg L-1 ) than commercial acaricides, including cyflumetofen, bifenazate, and profenofos. In contrast, the adverse effects of broflanilide on the predatory mite, Typhlodromips swirskii Athias-Henriot, was lower than those of fenpyroximate and abamectin. In the sublethal effect study, while adult females were treated with broflanilide, the number of eggs and longevity were reduced in LC10 and LC30 treatments; when eggs were treated with broflanilide, the egg duration and deutonymph duration were prolonged in LC30 treatment. A significant decrease in the total life span and duration and fecundity of adult females was observed in LC10 and LC30 treatments. Furthermore, the number of eggs per adult female was significantly reduced from 103.48 ± 3.69 in the control group to 69.42 ± 2.22 and 48.33 ± 1.75 in LC10 and LC30 treatments, respectively. In the greenhouse bioassay, broflanilide 5% suspension concentrate (MCI-8007) showed excellent acaricidal activity to TSSM, with 99.22% corrected control, compared with the MCI-8007 untreated group. CONCLUSION: Our results indicated that broflanilide has a high acaricidal activity to TSSM and significant inhibition to fecundity of adult female, and could be considered as a potential alternative for TSSM management. © 2021 Society of Chemical Industry.


Assuntos
Acaricidas , Ácaros , Tetranychidae , Acaricidas/farmacologia , Animais , Benzamidas , Feminino , Comportamento Predatório
8.
Insect Sci ; 28(3): 757-768, 2021 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-32293803

RESUMO

The resistance to dieldrin gene (RDL) encodes the primary subunit of the insect ionotropic γ-aminobutyric acid (GABA) receptor (GABAR), which is the target of phenylpyrazole and isoxazoline insecticides. The splice variants in exons 3 and 6 of RDL, which have been widely explored in many insects, modulate the agonist potency of the homomeric RDL GABAR and potentially play an important role in the development of insects. In the present study, four splice variants of exon 9 were identified in RDL of the small brown planthopper, Laodelphax striatellus (LsRDL), resulting in LsRDL-9a, LsRDL-9a', LsRDL-9b, and LsRDL-9c. LsRDL-9a has one more amino acid (E, glutamic acid) compared with LsRDL-9a', and LsRDL-9b lacked two amino acids and had seven different amino acids compared with LsRDL-9c. Two-electrode voltage-clamp recording on LsRDLs expressed in Xenopus oocytes showed that alternative splicing of exon 9 has significant impact on LsRDL sensitivity to the agonists GABA and ß-alanine, whereas no significant difference was observed in the potencies of the non-competitive antagonists (NCAs) ethiprole and fluralaner on the splice variants. Our results suggest that alternative splicing of RDL exon 9 broadens functional capabilities of the GABAR in L. striatellus by influencing the action of GABA.


Assuntos
Hemípteros/metabolismo , Receptores de GABA , Processamento Alternativo , Animais , Resistência a Inseticidas/genética , Inseticidas/farmacologia , Receptores de GABA/efeitos dos fármacos , Receptores de GABA/genética , Receptores de GABA/metabolismo
9.
J Hazard Mater ; 394: 122521, 2020 07 15.
Artigo em Inglês | MEDLINE | ID: mdl-32279005

RESUMO

Broflanilide, a novel meta-diamide insecticide, shows high insecticidal activity against agricultural pests and is scheduled to be launched onto the market in 2020. However, little information about its potential toxicological effects on fish has been reported. In this study, broflanilide showed low toxicity to the zebrafish, Danio rerio, with LC50 > 10 mg L-1 at 96 h and also did not inhibit GABA-induced currents of the heteromeric Drα1ß2Sγ2 GABA receptor. Broflanilide showed medium bioconcentration level with a bioconcentration factor at steady state (BCFss) of 10.02 and 69.40 in D. rerio at 2.00 mg L-1 and 0.20 mg L-1, respectively. In the elimination process, the concentration of broflanilide rapidly decreased within two days and slowly dropped below the limit of quantification after ten days. In the 2.00 mg L-1 broflanilide treatment, CYP450 activity was significantly increased up to 3.11-fold during eight days. Glutathione-S- transferase (GST) activity significantly increased by 91.44 % within four days. In conclusion, the acute toxicity of broflanilide was low, but it might induce chronic toxicity, affecting metabolism. To our knowledge, this is the first report of the toxicological effects of broflanilide on an aquatic organism, which has the potential to guide the use of broflanilide in the field.


Assuntos
Benzamidas/toxicidade , Inseticidas/toxicidade , Poluentes Químicos da Água/toxicidade , Peixe-Zebra/metabolismo , Animais , Benzamidas/metabolismo , Bioacumulação , Sistema Enzimático do Citocromo P-450/metabolismo , Glutationa Transferase/metabolismo , Inseticidas/metabolismo , Oócitos/efeitos dos fármacos , Receptores de GABA/efeitos dos fármacos , Poluentes Químicos da Água/metabolismo , Xenopus laevis
10.
BMC Genomics ; 21(1): 120, 2020 Feb 03.
Artigo em Inglês | MEDLINE | ID: mdl-32013879

RESUMO

BACKGROUND: Fluralaner is a novel isoxazoline insecticide with a unique action site on the γ-aminobutyric acid receptor (GABAR), shows excellent activity on agricultural pests including the common cutworm Spodoptera litura, and significantly influences the development and fecundity of S. litura at either lethal or sublethal doses. Herein, Illumina HiSeq Xten (IHX) platform was used to explore the transcriptome of S. litura and to identify genes responding to fluralaner exposure. RESULTS: A total of 16,572 genes, including 451 newly identified genes, were observed in the S. litura transcriptome and annotated according to the COG, GO, KEGG and NR databases. These genes included 156 detoxification enzyme genes [107 cytochrome P450 enzymes (P450s), 30 glutathione S-transferases (GSTs) and 19 carboxylesterases (CarEs)] and 24 insecticide-targeted genes [5 ionotropic GABARs, 1 glutamate-gated chloride channel (GluCl), 2 voltage-gated sodium channels (VGSCs), 13 nicotinic acetylcholine receptors (nAChRs), 2 acetylcholinesterases (AChEs) and 1 ryanodine receptor (RyR)]. There were 3275 and 2491 differentially expressed genes (DEGs) in S. litura treated with LC30 or LC50 concentrations of fluralaner, respectively. Among the DEGs, 20 related to detoxification [16 P450s, 1 GST and 3 CarEs] and 5 were growth-related genes (1 chitin and 4 juvenile hormone synthesis genes). For 26 randomly selected DEGs, real-time quantitative PCR (RT-qPCR) results showed that the relative expression levels of genes encoding several P450s, GSTs, heat shock protein (HSP) 68, vacuolar protein sorting-associated protein 13 (VPSAP13), sodium-coupled monocarboxylate transporter 1 (SCMT1), pupal cuticle protein (PCP), protein takeout (PT) and low density lipoprotein receptor adapter protein 1-B (LDLRAP1-B) were significantly up-regulated. Conversely, genes encoding esterase, sulfotransferase 1C4, proton-coupled folate transporter, chitinase 10, gelsolin-related protein of 125 kDa (GRP), fibroin heavy chain (FHC), fatty acid synthase and some P450s were significantly down-regulated in response to fluralaner. CONCLUSIONS: The transcriptome in this study provides more effective resources for the further study of S. litura whilst the DEGs identified sheds further light on the molecular response to fluralaner.


Assuntos
Isoxazóis/farmacologia , Spodoptera/efeitos dos fármacos , Spodoptera/genética , Transcriptoma/genética , Animais , Sistema Enzimático do Citocromo P-450/genética , Perfilação da Expressão Gênica/métodos , Inativação Metabólica/efeitos dos fármacos , Inativação Metabólica/genética , Proteínas de Insetos/genética , Inseticidas/farmacologia , Larva/efeitos dos fármacos , Larva/genética , Pupa/efeitos dos fármacos , RNA-Seq/métodos , Regulação para Cima/genética , Sequenciamento do Exoma/métodos
11.
Nanomicro Lett ; 12(1): 109, 2020 May 11.
Artigo em Inglês | MEDLINE | ID: mdl-34138091

RESUMO

This paper suggests development of a flexible, lightweight, and ultra-sensitive piezoresistive flow sensor based on vertical graphene nanosheets (VGNs) with a mazelike structure. The sensor was thoroughly characterized for steady-state and oscillatory water flow monitoring applications. The results demonstrated a high sensitivity (103.91 mV (mm/s)-1) and a very low-velocity detection threshold (1.127 mm s-1) in steady-state flow monitoring. As one of many potential applications, we demonstrated that the proposed VGNs/PDMS flow sensor can closely mimic the vestibular hair cell sensors housed inside the semicircular canals (SCCs). As a proof of concept, magnetic resonance imaging of the human inner ear was conducted to measure the dimensions of the SCCs and to develop a 3D printed lateral semicircular canal (LSCC). The sensor was embedded into the artificial LSCC and tested for various physiological movements. The obtained results indicate that the flow sensor is able to distinguish minute changes in the rotational axis physical geometry, frequency, and amplitude. The success of this study paves the way for extending this technology not only to vestibular organ prosthesis but also to other applications such as blood/urine flow monitoring, intravenous therapy (IV), water leakage monitoring, and unmanned underwater robots through incorporation of the appropriate packaging of devices.

12.
Pest Manag Sci ; 76(3): 888-893, 2020 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-31429178

RESUMO

BACKGROUND: Two-spotted spider mite (TSSM), Tetranychus urticae Koch is a serious agricultural pest and has developed high levels of resistance to many acaricides. Hence, screening new acaricides is important in the control of TSSM. Fluralaner, a novel isoxazoline, has high activity against agricultural and ectoparasitic pests; however, little information is available about its effects on agricultural mites. Lethal and sublethal effects of fluralaner towards TSSM eggs and female adults were therefore evaluated in this study. RESULTS: Fluralaner exhibited higher activity towards TSSM female adults (LC50 , 0.49 mg L-1 ) compared with commercial acaricides including fenpyroximate, pyridaben and hexythiazox, and also excellent activity towards eggs (LC50 , 0.36 mg L-1 ). The results of a sublethal effect study showed a significant reduction in the duration and fecundity of female adults with increases in the tested concentrations. The net reproductive rate (R0 ) decreased to 67.34 ± 3.96 and 50.29 ± 3.40 offspring per individual in LC10 and LC30 treatments compared with control (108.31 ± 7.61 offspring per individual). The intrinsic rate of increase (r) and finite rate of increase (λ) in the controls (0.30 and 1.36 d-1 ) were significantly higher than in the LC30 treatment (0.25 and 1.29 d-1 ); whereas, they were almost identical to values for the LC10 treatment. No change in mean generation time (T) was observed at sublethal concentrations treatments. CONCLUSION: Our results demonstrated that fluralaner has high acaricidal activity and could be considered a potential acaricide for TSSM management. © 2019 Society of Chemical Industry.


Assuntos
Acaricidas , Ácaros , Tetranychidae , Animais , Feminino , Isoxazóis
13.
Pest Manag Sci ; 75(11): 2901-2909, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31081291

RESUMO

BACKGROUND: Fluralaner, a novel pesticide that targets the γ-aminobutyric acid (GABA) receptor (GABAR) subunit of resistant to dieldrin (RDL), exhibits strong potential to be an insecticide to control agricultural insect pests. However, the risk and action of fluralaner to economic insects, e.g., honeybee Apis mellifera Linnaeus, remains unclear. RESULTS: In this study, both oral and contact toxicity of fluralaner to honeybee were found to be 0.13 µg adult-1 . Abamectin, dieldrin, ethiprole, α-endosulfan, fipronil and fluralaner strongly inhibited the GABA-induced current in A. mellifera RDL (AmRDL), expressed in Xenopus laevis oocytes, with median inhibitory concentration (IC50 ) values of 7.99, 868.1, 27.10, 412.0, 11.21 and 13.59 nM, respectively. The binding free energy and electrophysiological response of AmRDL and insecticides were opposite. The correlation values between toxicity (to A. mellifera) and binding free energy/electrophysiological inhibition (to AmRDL) were at a moderate level. CONCLUSION: In conclusion, we report for the first time the notable risk of fluralaner to honeybee in vivo and compared the actions of GABAR-targeted insecticides on the AmRDL receptor. © 2019 Society of Chemical Industry.


Assuntos
Abelhas/efeitos dos fármacos , Inseticidas/toxicidade , Isoxazóis/toxicidade , Neurotoxinas/toxicidade , Animais , Relação Dose-Resposta a Droga , Proteínas de Insetos/genética , Proteínas de Insetos/metabolismo , Receptores de GABA/genética , Receptores de GABA/metabolismo
14.
J Hazard Mater ; 366: 643-650, 2019 03 15.
Artigo em Inglês | MEDLINE | ID: mdl-30580138

RESUMO

The ionotropic GABAA receptor (GABAAR) is the main fast inhibitory post-synaptic receptor and is also an important insecticidal target. Effect of insecticides on fish has attracted intensive attention. However, no systematic study on heteromeric zebrafish GABAAR expressed in oocytes has been reported to date. In this study, the α1 subunit, the ß2S subunit lacking 47 amino acid residues compared with the ß2L subunit, and the γ2 subunit having five transmembrane domains were isolated from zebrafish Danio rerio. The responses of homomeric and heteromeric (α1, ß2S and γ2) channels to agonists and GABAAR-targeted compounds were detected with two-electrode voltage clamp. Dose-dependent responses were observed in heteromeric α1ß2S, ß2Sγ2, and α1ß2Sγ2 GABAR channels with EC50 values at 21.75, 6291, and 33.69 µM for GABA-induced current and 3.28, 155.5, and 3.79 mM for ß-alanine-induced current, respectively. However, no response was induced by benzamidine in all GABAR channels. Abamectin, dieldrin, fluralaner and fipronil could strongly inhibited GABA-induced inward current ≥50% at 10-6 M, while α-endosulfan, flufiprole and ethiprole only inhibited GABA-induced current <50%. This study has clarified the interaction of insecticides with the heteromeric GABAAR channel, which could help us further explore the potential function and toxicological importance of GABAARs from D. rerio.


Assuntos
Canais de Cloreto/metabolismo , Inseticidas/farmacologia , Receptores de GABA/metabolismo , Peixe-Zebra/metabolismo , Animais
15.
Pestic Biochem Physiol ; 152: 8-16, 2018 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-30497715

RESUMO

The increasing occurrence of resistance to chemical insecticides in insect pest populations is a serious threat to the integrity of current pest management strategies, and exploring new alternative chemistries is one important way to overcome this obstacle. Fluralaner, as a novel isoxazoline insecticide, has broad spectrum activity against a variety of insect pests, but little data is available about its effect on Lepidopterans. The effects of fluralaner on Spodoptera litura Fabricius, a widespread and polyphagous pest, were evaluated in the present study. Our results showed younger larvae were more susceptible to fluralaner treatment, but feeding and topical applications were similarly effective in 3rd instar larvae. Synergism assays indicated that piperonyl butoxide (PBO) could increase the toxicity of fluralaner to S. litura to a certain degree and P450 may be involved in the detoxification of fluralaner in vivo. Sublethal developmental effects included reduced larval body weight, decreased pupation and emergence, and notched wings in adults, accompanied by changes in the transcript levels of chitinase 5 (CHT5) and juvenile hormone acid methyltransferase (Jhamt), genes vital for insect development. Above results manifested that fluralaner is highly toxic to S. litura larvae via either topical or oral application and provide an indication of how this insecticide is metabolized in vivo. Further, our results provided a foundation for further development of fluralaner as a new tool in insect pest management.


Assuntos
Inseticidas/toxicidade , Isoxazóis/toxicidade , Spodoptera/efeitos dos fármacos , Animais , Quitinases/genética , Sistema Enzimático do Citocromo P-450/genética , Glutationa Transferase/genética , Proteínas de Insetos/genética , Larva/efeitos dos fármacos , Larva/genética , Larva/crescimento & desenvolvimento , Metiltransferases/genética , Sinergistas de Praguicidas/toxicidade , Butóxido de Piperonila/toxicidade , Spodoptera/genética , Spodoptera/crescimento & desenvolvimento
16.
ACS Appl Mater Interfaces ; 10(42): 36312-36322, 2018 Oct 24.
Artigo em Inglês | MEDLINE | ID: mdl-30256087

RESUMO

Here, we report a new type of strain sensors consisting of vertical graphene nanosheets (VGNs) with mazelike network, sandwiched between poly(dimethylsiloxane) (PDMS) substrates. The new sensors outperform most graphene thin-film-based sensors reported previously and show an outstanding combination of high stretchability of ∼120%, excellent linearity over the entire detection range, and high sensitivity with a gauge factor of ∼32.6. The sensitivity can be tuned by controlling the thickness of VGNs, with sensors consisting of thicker VGNs showing higher sensitivity but slightly lower stretchability (the maximum gauge factor is ∼88.4 with a maximum detection strain of ∼55%). Detailed microscopic examinations reveal that the ultrahigh sensitivity stems from the formation of microcracks initiated in the buffer layer. These microcracks are bridged by strings of graphene/PDMS, enabling the conductive network to continue to function up to a strain level significantly higher than that of previously reported graphene thin-film-based sensors. Furthermore, the present sensors have been found to be insensitive to temperatures and various liquids, including water and 0.1 mol L-1 sodium chloride solution (similar to the sweat on human skin). Demonstrations are presented to highlight the new sensors' potential as wearable devices for human motion detection and pressure distribution measurement.

17.
Pest Manag Sci ; 74(11): 2645-2651, 2018 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-29718557

RESUMO

BACKGROUND: Phenylpyrazole (fiprole) insecticides, including ethiprole, fipronil and flufiprole with excellent activity on rice planthoppers, are very important in Asia but resistance has developed after decades of use. The molecular mechanism of fipronil- but not ethiprole-resistance has been previously studied in rice planthoppers. In our laboratory, a small brown planthopper Laodelphax striatellus strain with ethiprole-resistance was cultured and the molecular mechanisms of ethiprole resistance and of cross-resistance among fiprole insecticides were investigated. RESULTS: Ethiprole-resistant L. striatellus has >5000-fold resistance compared to the susceptible strain, and exhibits around 200-fold cross-resistance with fipronil and flufiprole. RDL genes were isolated from susceptible and ethiprole-resistant L. striatellus and expressed in Xenopus oocytes. Electrophysiological studies showed fiprole insecticides inhibited γ-aminobutyric acid (GABA)-induced current with IC50 = 0.1-1.4 µM to LsRDL-S homomers. In LsRDL-R with A2'N mutation, only 1-13% inhibition was observed on treatment with 10 µM ethiprole, fipronil or flufiprole. Homology models indicate A2'N mutation allows crosslinking hydrogen bonding between Asn sidechains at the 2' position around the channel pore, blocking insecticides from interacting near this position. In contrast, insecticides showed favorable binding near A2' in wild-type L. striatellus. CONCLUSION: Cross-resistance is increasing for fiprole insecticides in L. striatellus and management strategies are necessary to minimize resistance. © 2018 Society of Chemical Industry.


Assuntos
Hemípteros/genética , Proteínas de Insetos/genética , Resistência a Inseticidas/genética , Inseticidas/farmacologia , Pirazóis/farmacologia , Receptores de GABA/genética , Animais , Fenômenos Eletrofisiológicos , Hemípteros/efeitos dos fármacos , Hemípteros/fisiologia , Proteínas de Insetos/metabolismo , Resistência a Inseticidas/fisiologia , Simulação de Acoplamento Molecular , Receptores de GABA/metabolismo
18.
Insect Biochem Mol Biol ; 94: 18-27, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29408355

RESUMO

Insect γ-aminobutyric acid (GABA) receptor (GABAR) is one of the major targets of insecticides. In the present study, cDNAs (CsRDL1A and CsRDL2S) encoding the two isoforms of RDL subunits were cloned from the rice stem borer Chilo suppressalis. Transcripts of both genes demonstrated similar expression patterns in different tissues and developmental stages, although CsRDL2S was ∼2-fold more abundant than CsRDL1A throughout all development stages. To investigate the function of channels formed by CsRDL subunits, both genes were expressed in Xenopus laevis oocytes singly or in combination in different ratios. Electrophysiological results using a two-electrode voltage clamp demonstrated that GABA activated currents in oocytes injected with both cRNAs. The EC50 value of GABA in activating currents was smaller in oocytes co-injected with CsRDL1A and CsRDL2S than in oocytes injected singly. The IC50 value of the insecticide fluralaner in inhibiting GABA responses was smaller in oocytes co-injected with different cRNAs than in oocytes injected singly. Co-injection also changed the potency of the insecticide dieldrin in oocytes injected singly. These findings suggested that heteromeric GABARs were formed by the co-injections of CsRDL1A and CsRDL2S in oocytes. Although the presence of Ser at the 2'-position in the second transmembrane segment was responsible for the insensitivity of GABARs to dieldrin, this amino acid did not affect the potencies of the insecticides fipronil and fluralaner. These results lead us to hypothesize that C. suppressalis may adapt to insecticide pressure by regulating the expression levels of CsRDL1A and CsRDL2S and the composition of both subunits in GABARs.


Assuntos
Regulação da Expressão Gênica/genética , Proteínas de Insetos/genética , Resistência a Inseticidas/genética , Inseticidas/efeitos adversos , Mariposas/genética , Pirazóis/efeitos adversos , Receptores de GABA/genética , Sequência de Aminoácidos , Animais , Perfilação da Expressão Gênica , Proteínas de Insetos/química , Proteínas de Insetos/metabolismo , Larva/efeitos dos fármacos , Larva/genética , Larva/crescimento & desenvolvimento , Larva/metabolismo , Mariposas/efeitos dos fármacos , Mariposas/crescimento & desenvolvimento , Mariposas/metabolismo , Filogenia , Receptores de GABA/química , Receptores de GABA/metabolismo , Alinhamento de Sequência
19.
Nat Commun ; 9(1): 683, 2018 02 14.
Artigo em Inglês | MEDLINE | ID: mdl-29445161

RESUMO

The inability of membranes to handle a wide spectrum of pollutants is an important unsolved problem for water treatment. Here we demonstrate water desalination via a membrane distillation process using a graphene membrane where water permeation is enabled by nanochannels of multilayer, mismatched, partially overlapping graphene grains. Graphene films derived from renewable oil exhibit significantly superior retention of water vapour flux and salt rejection rates, and a superior antifouling capability under a mixture of saline water containing contaminants such as oils and surfactants, compared to commercial distillation membranes. Moreover, real-world applicability of our membrane is demonstrated by processing sea water from Sydney Harbour over 72 h with macroscale membrane size of 4 cm2, processing ~0.5 L per day. Numerical simulations show that the channels between the mismatched grains serve as an effective water permeation route. Our research will pave the way for large-scale graphene-based antifouling membranes for diverse water treatment applications.

20.
Environ Pollut ; 232: 183-190, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-28923341

RESUMO

Fluralaner is a novel isoxazoline insecticide which shows high insecticidal activity against parasitic, sanitary and agricultural pests, but there is little information about the effect of fluralaner on non-target organisms. This study reports the acute toxicity, bioconcentration, elimination and antioxidant response of fluralaner in zebrafish. All LC50 values of fluralaner to zebrafish were higher than 10 mg L-1 at 24, 48, 72 and 96 h. To study the bioconcentration and elimination, the zebrafish were exposed to sub-lethal concentrations of fluralaner (2.00 and 0.20 mg L-1) for 15 d and then held 6 d in clean water. The results showed medium BCF of fluralaner with values of 12.06 (48 h) and 21.34 (144 h) after exposure to 2.00 and 0.20 mg L-1 fluralaner, respectively. In the elimination process, a concentration of only 0.113 mg kg-1 was found in zebrafish on the 6th day after removal to clean water. After exposure in 2.00 mg L-1 fluralaner, the enzyme activities of SOD, CAT, and GST, GSH-PX, CarE and content of MDA were measured. Only CAT and CarE activities were significantly regulated and the others stayed at a stable level compared to the control group. Meanwhile, transcriptional expression of CYP1C2, CYP1D1, CYP11A were significantly down-regulated at 12 h exposed to 2.00 mg L-1 of fluralaner. Except CYP1D1, others CYPs were up-regulated at different time during exposure periods. Fluralaner and its formulated product (BRAVECTO®) are of low toxicity to zebrafish and are rapidly concentrated in zebrafish and eliminated after exposure in clean water. Antioxidant defense and metabolic systems were involved in the fluralaner-induced toxicity. Among them, the activities of CAT and CarE, and most mRNA expression level of CYPs showed fast response to the sub-lethal concentration of fluralaner, which could be used as a biomarker relevant to the toxicity.


Assuntos
Inseticidas/toxicidade , Isoxazóis/toxicidade , Poluentes Químicos da Água/toxicidade , Peixe-Zebra/fisiologia , Animais , Antioxidantes/metabolismo , Biomarcadores/metabolismo , Catalase/metabolismo , Sistema Enzimático do Citocromo P-450/metabolismo , Glutationa Transferase/metabolismo , Superóxido Dismutase/metabolismo , Testes de Toxicidade Aguda , Peixe-Zebra/metabolismo
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