Identification of a critical region in the Drosophila ryanodine receptor that confers sensitivity to diamide insecticides

Anthranilic diamides, which include the new commercial insecticide, chlorantraniliprole, are an exciting new class of chemistry that target insect ryanodine receptors. These receptors regulate release of stored intracellular calcium and play a critical role in muscle contraction. As with insects, nematodes express ryanodine receptors and are sensitive to the plant alkaloid, ryanodine. However the plant parasitic nematode, Meloidogyne incognita, is insensitive to anthranilic diamides. Expression of a full-length Drosophila melanogaster ryanodine receptor in an insect cell line confers sensitivity to the receptor agents, caffeine and ryanodine along with nanomolar sensitivity to anthranilic diamides. Replacement of a 46 amino acid segment in a highly divergent region of the Drosophila C-terminus with that from Meloidogyne results in a functional RyR which lack sensitivity to diamide insecticides. These findings indicate that this region is critical to diamide sensitivity in insect ryanodine receptors. Furthermore, this region may contribute to our understanding of the differential selectivity diamides exhibit for insect over mammalian ryanodine receptors.     

Neonicotinoids Show Selective and Diverse Actions on Their Nicotinic Receptor Targets: Electrophysiology,Molecular Biology,and Receptor Modeling Studies

Neonicotinoid insecticides, which act selectively on insect nicotinic acetylcholine receptors (nAChRs), are used worldwide for insect pest management. Studies that span chemistry, biochemistry, molecular biology, and electrophysiology have contributed to our current understanding of the important physicochemical and structural properties essential for neonicotinoid actions as well as key receptor residues contributing to the high affinity of neonicotinoids for insect nAChRs. Research to date suggests that electrostatic interactions and possibly hydrogen bond formation between neonicotinoids and nAChRs contribute to the selectivity of these chemicals. A rich diversity of neonicotinoid-nAChR interactions has been demonstrated using voltage-clamp electrophysiology. Computational modeling of nAChR-imidacloprid interaction has assisted in the interpretation of these results.     

Neonicotinoids show selective and diverse actions on their nicotinic receptor targets: electrophysiology, molecular biology, and receptor modeling studies

Neonicotinoid insecticides, which act selectively on insect nicotinic acetylcholine receptors (nAChRs), are used worldwide for insect pest management. Studies that span chemistry, biochemistry, molecular biology, and electrophysiology have contributed to our current understanding of the important physicochemical and structural properties essential for neonicotinoid actions as well as key receptor residues contributing to the high affinity of neonicotinoids for insect nAChRs. Research to date suggests that electrostatic interactions and possibly hydrogen bond formation between neonicotinoids and nAChRs contribute to the selectivity of these chemicals. A rich diversity of neonicotinoid-nAChR interactions has been demonstrated using voltage-clamp electrophysiology. Computational modeling of nAChR-imidacloprid interaction has assisted in the interpretation of these results.     

新型二酰胺类杀虫剂对鱼尼丁受体作用的分子机理

最近发现了一类新型二酰胺类杀虫剂——氟虫酰胺和氯虫酰胺,其作用靶标是鱼尼丁受体 (ryanodine receptors, RyRs)。本文对RyR的结构与功能、电压门控钙离子通道和鱼尼丁受体钙离子释放通道对细胞质钙离子内环境稳定的调节以及二酰胺类杀虫剂对RyRs作用的分子机理进行综述。二酰胺类杀虫剂使昆虫RyR通道处于持续的开放状态,引发钙离子从肌质网腔内大量释放,破坏了细胞质钙离子内环境的稳定,从而产生不同的药物学特性。这些变化都是由一个不同于鱼尼丁在RyR上的结合部位介导的。该类杀虫剂的作用对昆虫RyR s是高度专一的,结果产生选择毒性。由于二酰胺类杀虫剂的结构独特,作用方式新颖,对鳞翅目害虫效果好、杀虫谱广,对各种益虫和天敌安全,并对现用的杀虫剂无交互抗性,故它们非常适合于抗性治理和IPM。     

Receptors for gamma-aminobutyric acid and voltage-dependent chloride channels as targets for drugs and toxicants

The function of chloride (Cl-) channel proteins is to regulate the transport of Cl- across membranes. There are two major kinds of Cl- channels: 1) those activated by binding of a transmitter such as gamma-aminobutyric acid (GABA), glycine, or glutamate, and thus are receptors; and 2) those activated by membrane depolarization or by calcium. There are two kinds of GABA receptors: GABAA is the major inhibitory receptor of vertebrate brain and the one that operates a Cl- channel, and the GABAB receptor, which is proposed to regulate cAMP production that is stimulated by other receptors. Except for binding of GABA, these two GABA receptors differ completely in their drug specificities. However, there are many similarities among the GABAA receptor, the glycine receptor, and the voltage-dependent Cl- channel. The two receptors and Cl- channels bind avermectin, whereas bicuculline binds only to mammalian GABAA and glycine receptors, not to the insect brain GABAA receptor. Barbiturates bind to GABAA and voltage-dependent Cl- channels, possibly directly activating them. Benzodiazepines potentiate both the glycine and GABAA receptors. Several insecticides act on the GABAA receptor and voltage-dependent Cl- channel. It is suggested that the GABAA receptor is the primary target for the action of toxaphene and cyclodiene insecticides but a secondary target for lindane and type II pyrethroids. On the other hand, the Cl- channel may be a primary target for avermectin and lindane but a secondary one for cyclodienes. The similarity in certain drug specificities and the operation of Cl- channels suggest a degree of homology between the subunits of GABAA and glycine receptors and the voltage-dependent Cl- channels.     

Insect ryanodine receptors: molecular targets for novel pest control chemicals

Ryanodine receptors (RyRs) are a distinct class of ligand-gated calcium channels controlling the release of calcium from intracellular stores. They are located on the sarcoplasmic reticulum of muscle and the endoplasmic reticulum of neurons and many other cell types. Ryanodine, a plant alkaloid and an important ligand used to characterize and purify the receptor, has served as a natural botanical insecticide, but attempts to generate synthetic commercial analogues of ryanodine have proved unsuccessful. Recently two classes of synthetic chemicals have emerged resulting in commercial insecticides that target insect RyRs. The phthalic acid diamide class has yielded flubendiamide, the first synthetic ryanodine receptor insecticide to be commercialized. Shortly after the discovery of the phthalic diamides, the anthranilic diamides were discovered. This class has produced the insecticides Rynaxypyr(R) and Cyazypyrtrade mark. Here we review the structure and functions of insect RyRs and address the modes of action of phthalic acid diamides and anthranilic diamides on insect ryanodine receptors. Particularly intersting is the inherent selectivity both chemical classes exhibit for insect RyRs over their mammalian counterparts. The future prospects for RyRs as a commercially-validated target site for insect control chemicals are also considered.     

Recent progress in understanding the interaction between avermectins and ligand-gated ion channels: putting the pests to sleep

Avermectins and milbemycins are an important family of anthelmintics, insecticides and acaricides. Their mode of action is as positive allosteric modulators of ligand-gated chloride channels, and at higher concentrations, they gate some channels directly. Though it has long been known that the avermectins do not compete for the ligand binding site, the actual site at which they interact with their receptors has been unclear. Recent data demonstrate the importance to drug binding of amino acid residues predicted to line a water-filled pocket in the channel domain. This pocket acts as the binding site for anaesthetics and other modulators of mammalian GABA_A and glycine receptors, suggesting similarities in the mode of action between these drugs and the avermectins/milbemycins.     

Crystal structures of Lymnaea stagnalis AChBP in complex with neonicotinoid insecticides imidacloprid and clothianidin

Neonicotinoid insecticides, which act on nicotinic acetylcholine receptors (nAChRs) in a variety of ways, have extremely low mammalian toxicity, yet the molecular basis of such actions is poorly understood. To elucidate the molecular basis for nAChR-neonicotinoid interactions, a surrogate protein, acetylcholine binding protein from Lymnaea stagnalis (Ls-AChBP) was crystallized in complex with neonicotinoid insecticides imidacloprid (IMI) or clothianidin (CTD). The crystal structures suggested that the guanidine moiety of IMI and CTD stacks with Tyr185, while the nitro group of IMI but not of CTD makes a hydrogen bond with Gln55. IMI showed higher binding affinity for Ls-AChBP than that of CTD, consistent with weaker CH-pi interactions in the Ls-AChBP-CTD complex than in the Ls-AChBP-IMI complex and the lack of the nitro group-Gln55 hydrogen bond in CTD. Yet, the NH at position 1 of CTD makes a hydrogen bond with the backbone carbonyl of Trp143, offering an explanation for the diverse actions of neonicotinoids on nAChRs.     

杀虫药剂的神经毒理学研究进展

大多数杀虫药剂都具有较强的神经毒性,它们对神经系统的作用靶标不同。有机磷类杀虫剂不仅抑制乙酰胆碱酯酶活性和乙酰胆碱受体功能,影响乙酰胆碱的释放,而且还具有非胆碱能毒性,有些有机磷杀虫剂还能引发迟发性神经毒性。新烟碱类杀虫剂作为烟碱型乙酰胆碱受体（nAChR）的激动剂,作用于该类受体的α亚基;它对昆虫的毒性比对哺乳动物的毒性大得多,乃是因为它对昆虫和哺乳动物nAChR的作用位点不同。拟除虫菊酯类杀虫剂主要作用于神经细胞钠通道,引起持续开放,导致传导阻滞;该类杀虫剂也可抑制钙通道。另外,这类杀虫剂还干扰谷氨酸递质和多巴胺神经元递质的释放。拟除虫菊酯类杀虫剂对昆虫的选择毒性很可能是因为昆虫神经元的钠通道结构与哺乳动物的不同。阿维菌素类杀虫剂主要作用于γ-氨基丁酸（GABA）受体,它能促进GABA的释放,增强GABA与GABA受体的结合,使氯离子内流增加,导致突触后膜超级化。由于这类杀虫剂难以穿透脊椎动物的血脑屏障而与中枢神经系统的GABA受体结合,故该类杀虫剂对脊椎动物的毒性远低于对昆虫的毒性。多杀菌素类杀虫剂可与中枢神经系统的nAChR作用,引起Ach长时间释放,此外,这类杀虫剂还可作用于昆虫的GABA受体,改变GABA门控氯通道的功能。     

New measures of insecticidal efficacy and safety obtained with the 39K promoter of a recombinant baculovirus

Baculoviruses are orally infectious to insects and considered to be natural insecticides. To enhance their speed-of-kill these viruses were engineered to express arthropod neurotoxins under the control of various strong promoters. Although this strategy proved to be efficient, it raised recently concerns about safety. We analyzed the speed-of-kill and safety of Autographa californica multiple nucleopolyhedrovirus expressing the insecticidal scorpion neurotoxin AaIT and found that the mortality of Helicoverpa armigera larvae was enhanced significantly when the expression was controlled by the baculovirus delayed-early promoter 39K rather than the very late promoter p10. This improvement was also reflected in better protection of cotton leaves on which these insects were fed. Using lacZ as a sensitive reporter we also found that expression driven by the 39K promoter was detected in insect but not in mammalian cells. These results imply that by selection of an appropriate viral promoter, engineered baculoviruses may comply with the high standard biosafety requirements from a genetically modified organism (GMO). Our results provide further support for the potential use of engineered baculoviruses in insect pest control in a safely manner.     

Prevalence and stability of insecticide resistances in field population of Spodoptera litura (Lepidoptera: Noctuidae) from Huizhou,Guangdong Province,China

The field population of Spodoptera litura from Huizhou, Guangdong Province, China was evaluated for resistance to 21 insecticides, including conventional and new chemistry insecticides. Extreme levels of resistance were observed to metaflumizone and emamectin benzoate with resistance factors of 234.1 and 183.3, respectively. Resistance to abamectin was also high (perhaps extremely high) and over 71.9-fold. The Huizhou population of S. litura possessed high resistance to deltamethrin (96.5-fold) and moderate resistance to beta cyfluthrin and lambda cyhalothrin but remained susceptible to bifenthrin. Moderate resistance to chlorantraniliprole (22.3-fold), endosulfan (22.2-fold), tebufenozide (10.7-fold) and thiodicarb (14.3-fold), and low-level resistance to fipronil, indoxacarb and spinosad were also reported in this population. This field population remained susceptible to acetamiprid, chlorfenapyr, chlorfluazuron, hexaflumuron, chlorpyrifos, pyridalyl and spinetoram. The stabilities of resistance to metaflumizone, emamectin benzoate, deltamethrin, chlorantraniliprole and endosulfan were evaluated, the resistance level decreased when the insecticide stress was removed, suggesting stop of the application of insecticides with high level resistance could be implemented into the resistance management. Because S. litura from Huizhou developed resistance to multiple insecticides, integration of different control practices, especially the rotation of insecticides with biocontrol agents, should be performed in the management of this pest. The results suggested the suspension of the application of insecticide to which S. litura had developed high level of resistance in order to mitigate the resistance status, and the use of the insecticides to which this pest remained sensitive, including spinetoram, pyridalyl, indoxacarb, hexaflumuron, chlorfluazuron, chlorfenapyr and bifenthrin, could be incorporated into the alternating application for resistance management.     

Present and future prospects for entomopathogenic nematode products

Entomopathogenic nematodes in the genera Steinernema and Heterorhabditis have emerged as excellent candidates for biological control of insect pests. Attributes making the nematodes ideal biological insecticides include their broad host range, high virulence, safety for nontarget organisms and high efficacy in favourable habitats. Progress achieved in liquid fermentation, formulation stability and application strategy has allowed nematode‐based products to become competitive with chemical insecticides in medium‐ and high‐value crops on the basis of cost/benefit ratio and ease of application. Further technological advancements are needed to expand and improve the market potential of the nematode‐based products.     

转基因抗虫作物中苏云金芽孢杆菌Cry蛋白的食品安全问题

苏云金芽孢杆菌(Bt)微生物制剂是农业、林业和饮用水等领域用来控制靶标害虫幼虫的有效工具,至今已经有50余年的使用历史。同时其在美国、欧洲和其他一些国家被广泛用于经过认证的有机农业生产之中。目前已获审批的转基因Bt作物中最常使用的是Cry蛋白。Cry蛋白的作用机制、食品安全性以及致敏性已经经过啮齿类动物、农场动物和人体内试验和生物信息学研究的严格检验。Cry蛋白的杀虫作用只在靶标害虫的碱性消化道内,与中肠上皮细胞的特异蛋白受体结合才能起到杀虫作用,而其他非靶标生物体内(人类、猕猴、小鼠、大鼠和牛等)都被证明没有这种特异蛋白质受体。美国、欧洲和其他国家的管理机构都已经证实了转基因Bt作物和Cry蛋白在农作物和饮用水中残留的安全性。食物加工过程能够最大化地减少转基因作物中功能性Cry蛋白的摄入。转基因抗虫作物有利于降低农药杀虫剂的使用的同时,也能够有效防止玉米中伏马菌毒素的污染。     

Combinatorial chemistry in the agrosciences

Combinatorial chemistry and high throughput screening have had a profound effect upon the way in which agrochemical companies conduct their lead discovery research. The article reviews recent applications of combinatorial synthesis in the lead discovery process for new fungicides, herbicides and insecticides. The role and importance of bioavailability guidelines, natural products, privileged structures, virtual screening and X-ray crystallographic protein structures on the design of solid- and solution-phase compound libraries is discussed and illustrated.     

4-Azolylphenyl isoxazoline insecticides acting at the GABA gated chloride channel

Isoxazoline insecticides have been shown to be potent blockers of insect GABA receptors with excellent activity on a broad pest range, including Lepidoptera and Hemiptera. Herein we report on the synthesis, biological activity and mode-of-action for a class of 4-heterocyclic aryl isoxazoline insecticides.     

常见蝽类昆虫的化学成分及药理活性研究进展

本文综述了国内外常见的半翅目蝽类昆虫化学成分以及药理作用的研究。从生物学、化学、医学等方面阐述了此类昆虫的研究价值,为进一步研究开发提供科学依据。     

噻虫胺及其混配制剂对意大利蜜蜂和玉米螟赤眼蜂的急性毒性

【目的】明确新烟碱类杀虫剂噻虫胺及其2种混剂对意大利蜜蜂 Apis mellifera ligustica 和玉米螟赤眼蜂 Trichogramma ostriniae 的毒性。【方法】采用摄入法、接触法和药膜法分别测定3种制剂对意大利蜜蜂成年工蜂和玉米螟赤眼蜂成蜂的急性毒性。【结果】急性毒性测定结果表明,30%噻虫胺悬浮剂、30%吡蚜酮·噻虫胺悬浮剂和20%醚菊酯·噻虫胺悬浮剂对意大利蜜蜂成年工蜂的急性摄入毒性均为剧毒,LC₅₀ 值(48 h)分别为0.0200（0.0143~0.0272）, 0.084（0.0658~0.1157）和0.1594（0.1200~0.2056） mg a.i./L;3种制剂对意大利蜜蜂成年工蜂急性接触毒性均为高毒,LD₅₀ 值(48 h)分别为0.0155（0.0114~0.0197）, 0.0426（0.0335~0.0539）和0.1122（0.0796~0.1385）μg a.i./蜂。药膜法测定3种制剂对玉米螟赤眼蜂成蜂的LD₅₀ 值(24 h)分别为0.0232（0.0180~0.0295）, 0.1050（0.0940~0.1170）和0.0059（0.0054~0.0065） mg a.i./L;安全性评价结果表明,3种制剂对玉米螟赤眼蜂成蜂均存在极高风险性,安全系数分别为5.95×10^-4, 2.69×10^-3和9.50×10^-5。【结论】噻虫胺及其混剂对意大利蜜蜂和玉米螟赤眼蜂均存在较高的毒性风险,在害虫综合治理中应谨慎使用。     

Nicotinic acetylcholine receptors: targets for commercially important insecticides

Nicotinic acetylcholine receptors (nAChRs) are major excitatory neurotransmitter receptors in both vertebrates and invertebrates. In insects, nAChRs are the target site for several naturally occurring and synthetic compounds that exhibit potent insecticidal activity. Several compounds isolated from plants are potent agonists or antagonists of nAChRs, suggesting that these may have evolved as a defence mechanism against insects and other herbivores. Nicotine, isolated from the tobacco plant, has insecticidal activity and has been used extensively as a commercial insecticide. Spinosad, a naturally occurring mixture of two macrocyclic lactones isolated from the microorganism Saccharopolyspora spinosa, acts upon nAChRs and has been developed as a commercial insecticide. Since the early 1990s, one of the most widely used and rapidly growing classes of insecticides has been the neonicotinoids. Neonicotinoid insecticides are potent selective agonists of insect nAChRs and are used extensively in both crop protection and animal health applications. As with other classes of insecticides, there is growing evidence for the evolution of resistance to insecticides that act on nAChRs.     

新烟碱类和大环内酯类杀虫剂对四种赤眼蜂成蜂急性毒性和安全性评价

为了明确新烟碱类和大环内酯类杀虫剂对天敌赤眼蜂Trichogramma spp.的影响, 在室内采用药膜法测定了其对稻螟赤眼蜂Trichogramma japonicum Ashmead、 亚洲玉米螟赤眼蜂Trichogramma ostriniae Pang et Chen、 拟澳洲赤眼蜂Trichogramma confusum Viggiani和广赤眼蜂Trichogramma evanescens Westwood成蜂的急性毒性, 并进行了安全性评价。急性毒性测定结果表明： 在测定的新烟碱类药剂中, 噻虫嗪对拟澳洲赤眼蜂和稻螟赤眼蜂表现出最高的急性毒性, 其LC₅₀分别为0.24 (0.21~0.27) 和0.40 (0.37~0.44) mg a.i./L; 其次为烯啶虫胺, 该药剂对上述两种赤眼蜂的LC₅₀分别为0.83 (0.74~0.96) 和0.72 (0.65~0.80) mg a.i./L; 而吡虫啉对亚洲玉米螟赤眼蜂和拟澳洲赤眼蜂的毒性最低, 其LC₅₀分别为502.13 (459.80~549.62)和752.62 (687.51~828.63) mg a.i./L。在测定的大环内酯类药剂中, 阿维菌素对稻螟赤眼蜂的急性毒性最高, 其LC₅₀为0.49 (0.46~0.65) mg a.i./L, 而甲氨基阿维菌素苯甲酸盐对拟澳洲赤眼蜂表现出最低的急性毒性, 其LC₅₀为21.76 (19.59~24.40) mg a.i./L。安全性评价结果表明, 吡虫啉、 啶虫脒、 氯噻啉和甲氨基阿维菌素苯甲酸盐对4种赤眼蜂为低风险~中等风险性, 安全性系数为0.57~23.54; 噻虫啉和依维菌素对4种赤眼蜂却为中等风险~高风险性, 安全性系数为0.16~3.45; 而烯啶虫胺、 噻虫嗪和阿维菌素对4种赤眼蜂为高风险~极高风险性, 安全性系数为0.01~0.15。本研究测定的大部分杀虫剂对赤眼蜂都有一定的急性毒性风险。因此, 在害虫综合治理中应谨慎使用新烟碱类和大环内酯类杀虫剂尤其是烯啶虫胺、 噻虫嗪和阿维菌素, 以免造成对赤眼蜂的大量杀伤。