有机磷杀虫剂T-751对四种害虫的杀虫活性

测定了T-751（O-甲基-O-苯基-S-正丙基硫代磷酸酯）对4种害虫的杀虫活性。结果表明,T-751对东方家蝇、豆蚜和二斑叶螨的LD50分别为0．42、70．5、4．20mg／L。T-751对东方家蝇的杀虫活性要比杀螟硫磷高11倍。在剂量分别为2．95,7．37mg／m2时,该药对东方家蝇和美洲大蠊的KT50分别为13．57和30．83分钟。     

Synthesis of Robinal,a Highly Conjugated Monoterpenoid from the Mite,Rhizoglyphus robini

4-Acetoxy-2-alkenylquinolines, the analogs of quinolinol antibiotic SF2420B (1), were synthesized and their insecticidal activities were evaluated.     

鳞翅目昆虫中肠Bt杀虫蛋白受体研究进展

杀虫晶体蛋白(insecticidal crystal proteins,ICPs;含有Cry和Cyt 2大家族)和营养期杀虫蛋白(vegetative insecticidal proteins,Vips)等Bt杀虫蛋白可有效防治鳞翅目害虫,其中Cry应用最广泛。然而,一些地区的鳞翅目害虫已对Bt杀虫蛋白产生了抗性。目前,普遍认为鳞翅目昆虫中肠受体与Bt杀虫蛋白结合能力的改变是导致其对Bt杀虫蛋白产生抗性的最主要因素。在鳞翅目昆虫中,Cry受体是研究得最为透彻的Bt受体,已经被证实的有氨肽酶N、钙黏蛋白、碱性磷酸酶和ABC转运蛋白等。Vips杀虫蛋白类与鳞翅目昆虫中肠受体的结合方式与Cry杀虫蛋白相似,但结合位点与Cry杀虫蛋白不同。本文从结构特点、作用机制及不同鳞翅目昆虫间的表达差异等角度对以上4种鳞翅目昆虫中肠Bt受体进行了综述,并提出如下展望:(1)以棉铃虫或小菜蛾等鳞翅目昆虫为农业害虫模式生物进行深入研究,阐明其对Bt杀虫蛋白产生抗性的机制,为研究其他鳞翅目农业害虫对Bt杀虫蛋白产生抗性的机制提供理论借鉴;(2)鉴于在不同鳞翅目昆虫间,中肠Bt受体与Bt杀虫蛋白结合存在差异,且同一Bt杀虫蛋白与鳞翅目昆虫Bt受体并不专一性结合,Bt杀虫蛋白多基因组合策略是较为有效的田间鳞翅目昆虫防治策略,是今后一段时间内Bt杀虫蛋白应用的发展方向。     

Field‐level effects of preventative management tactics on soybean aphids (Aphis glycines Matsumura) and their predators

A 2‐year field experiment was conducted in northern Illinois to evaluate the effects of host plant resistance and an insecticidal seed treatment (thiamethoxam) on soybean aphids, Aphis glycines Matsumura and their predators. Densities of soybean aphids varied between the 2 years of the experiment. During both years, resistant plants experienced fewer cumulative aphid days than susceptible plants. Populations of soybean aphids on resistant plants rarely exceeded the economic injury level of 250 soybean aphids per plant. The use of thiamethoxam reduced cumulative aphid days in 2007, but not in 2008. Although soybean aphids reached densities that were sufficient to cause yield‐loss for untreated and susceptible plants, no yield‐benefit was associated with using the two management tactics in either year. This latter finding suggests that densities of soybean aphids need to be greater and sustained for a longer period of time than what we observed if the two management tactics are expected to provide a yield‐benefit. Monitoring natural enemies revealed that densities of key aphidophagous predators were relatively unaffected by host plant resistance or thiamethoxam; the effect of these management tactics on densities of predators, as well as the effectiveness of the method used to sample predators, is discussed.     

植物性杀虫剂及其混剂对螺旋粉虱的毒力测定

【背景】螺旋粉虱是新人侵海南省的严重为害经济作物及园林苗木的害虫。目前,植物源杀虫剂因具有高效和环境友好等特性而被广泛用于害虫防治中。【方法】采用喷雾法和药膜接触法分别测定了9种植物性杀虫剂对螺旋粉虱的毒力。【结果】在供试的9种植物性杀虫剂中,除虫菊素和鱼藤酮对螺旋粉虱成虫的毒力最强,24h的￡c,。分别为2．56和34．15mg· L^-1;印楝素和苦瓜叶提取物的毒力次之,LC50分别为158．36和311．02mg· L^-1。除虫菊素对螺旋粉虱若虫和卵也有一定的触杀作用,LC50分别为61．42和77139mg· L^-1。将印楝素和鱼藤酮分别与除虫菊素以1：1的比例混合,对螺旋粉虱成虫的毒力表现出明显的增效作用,其共毒系数（CTC）分别为193．11和224．35。【结论与意义】除虫菊素、鱼藤酮、印楝素和苦瓜叶提取物对螺旋粉虱均具有较强的毒性;印楝素或鱼藤酮与除虫菊素（1：1）的混合物不仅能增强触杀效果,而且能延缓害虫抗药性的产生。     

Vegetative insecticidal protein enhancing the toxicity of Bacillus thuringiensis subsp kurstaki against Spodoptera exigua

AIMS: The objective of this work was to enhance the insecticidal activity or widen the pesticidal spectrum of a commercial Bacillus thuringiensis strain YBT1520. METHODS AND RESULTS: A vegetative insecticidal protein gene vip3Aa7, under the control of its native promoter and cry3A promoter, was subcloned into B. thuringiensis acrystalliferous BMB171 to generate BMB8901 and BMBvip respectively. It was found that the amount of Vip3Aa7 protein produced by BMBvip was 3.2-fold more than that produced by BMB8901. Therefore, the vip3Aa7 gene under the control of cry3A promoter was transformed into strain YBT1520. The toxicity of the resulting strain BMB218V against Spodoptera exigua was 10-fold more than that of YBT1520, and that the toxicity of BMB218V against Helicoverpa armigera retained the same level as that of strain YBT1520. CONCLUSIONS: Strain YBT1520 obtained high toxicity against S. exigua after it was transformed and expressed the foreign vip3Aa7 gene. SIGNIFICANCE AND IMPACT OF THE STUDY: Commercial B. thuringiensis strain YBT1520 has high toxicity against H. armigera and Plutella xylostella, but almost no activity against S. exigua, which is a major crop pest in China. This work provides a new strategy for widening the activity spectrum of B. thuringiensis against agriculture pests.     

从华蟹甲草中分离的两种活性成分对家蝇的杀虫活性

研究了从我国特有植物华蟹甲草Sinacalia tangutica (Maxim.) B. Nord中经生物活性跟踪实验得出的杀虫活性成分Z,Z,Z-9,12,15-十八碳三烯酸和Z,Z-9,12-十八碳二烯酸对家蝇Musca domestica vicina的生物活性及对其生理生化指标的影响。结果表明,家蝇经该2种化合物1 mg/mL处理后表现出类似神经毒剂中毒的兴奋症状。这2种化合物对家蝇表现出毒杀作用,24 h时,Z,Z,Z-9,12,15-十八碳三烯酸和Z,Z-9,12-十八碳二烯酸对家蝇的LC₅₀值分别为0.26 mg/mL和0.43 mg/mL; 对家蝇触杀作用极低,以1 mg/mL分别点滴处理家蝇后48 h,死亡率分别为21.54%和4.08%。这2种化合物对家蝇的AChE影响不明显,但可引起家蝇的过氧化物酶的活性发生紊乱,对家蝇总糖含量也有一定的影响。Z,Z-9,12-十八碳二烯酸可引起家蝇的Mg-ATPase的比活力降低,而Z,Z,Z-9,12,15-十八碳三烯酸引起家蝇的Na-K-Mg-ATPase和Ca-ATPase的比活力较对照上升。     

In vivo and in vitro activity of venom from the endoparasitic wasp Pimpla turionellae (L.) (Hymenoptera: Ichneumonidae)

The biological activity of venom from Pimpla turionellae L. (Hymenoptera: Ichneumonidae) was examined in vivo toward larvae and pupae of Galleriae mellonella L. (Lepidoptera: Pyralidae), and in vitro toward bacterial and fungal cultures, as well as cultured insect cells. Pupae of G. mellonella were far more susceptible to the venom than larvae. At low doses of venom [0.1 venom reservoir equivalents (VRE)], pupal abdominal mobility was inhibited within 30 min, and by 24 h, all pupae injected with venom concentrations >0.5 VRE were completely paralyzed. These same doses of venom resulted in an inhibition of adult emergence. Host larvae were far less sensitive to wasp venom as evidenced by all venom injected larvae remaining responsive to mechanical stimulation by 1 h post injection, even at concentrations equivalent to 1 venom reservoir. Eventually (>2 h at 25 degrees C), venom-injected larvae became immobile, then flaccid, and all died within 24 h post-injection. At lower concentrations of wasp venom, the onset of paralysis was delayed by comparison to that evoked by 1 VRE, and few host larvae were able to pupate. Development of host larvae to adult emergence was also reduced in a dose-dependent manner, with eclosion completely prevented at high concentrations (>0.5 VRE) of venom. Venom doses <0.5 VRE did not appear to induce paralysis or alter larval development. When venom was incubated with bacterial or fungal cultures, no antimicrobial activity was detected. However, wasp venom was found to be cytotoxic and cytolytic to cultured cells derived from the cabbage looper Trichoplusia ni Hubner (Lepidoptera: Noctuidae) and the yellow fever mosquito, Aedes aegypti (L.) (Diptera: Culcidae). Though both cell types displayed similar susceptibility in terms of LC50s, the lepidopteran cells responded much more rapidly with regard to the onset of morphological changes and the timing of cell death. A possible mode of action for the venom is discussed.     

Solution structure of the plant defensin VrD1 from mung bean and its possible role in insecticidal activity against bruchids

Vigna radiata plant defensin 1 (VrD1) is the first reported plant defensin exhibiting insecticidal activity. We report herein the nuclear magnetic resonance solution structure of VrD1 and the implication on its insecticidal activity. The root-mean-square deviation values are 0.51 +/- 0.35 and 1.23 +/- 0.29 A for backbone and all heavy atoms, respectively. The VrD1 structure comprises a triple-stranded antiparallel beta-sheet, an alpha-helix, and a 3(10) helix stabilized by four disulfide bonds, forming a typical cysteine-stabilized alphabeta motif. Among plant defensins of known structure, VrD1 is the first to contain a 3(10) helix. Glu26 is highly conserved among defensins; VrD1 contains an arginine at this position, which may induce a shift in the orientation of Trp10, thereby promoting the formation of this 3(10) helix. Moreover, VrD1 inhibits Tenebrio molitor alpha-amylase. Alpha-amylase has an essential role in the digestion of plant starch in the insect gut, and expression of the common bean alpha-amylase inhibitor 1 in transgenic pea imparts complete resistance against bruchids. These results imply that VrD1 insecticidal activity has its basis in the inhibition of a polysaccharide hydrolase. Sequence and structural comparisons between two groups of plant defensins having different specificity toward insect alpha-amylase reveal that the loop between beta2 and beta3 is the probable binding site for the alpha-amylase. Computational docking experiments were used to study VrD1-alpha-amylase interactions, and these results provide information that may be used to improve the insecticidal activity of VrD1.