取食不同寄主植物小菜蛾对氯虫苯甲酰胺敏感性及体内解毒酶活性的变化

为探明寄主植物影响小菜蛾Plutella xylostella L.抗药性的内在因素,本研究以小菜蛾嗜好性不同的菜心(Brassica parachinensis)、芥菜(B.juncea)、白菜(B.chinensis)和芥蓝(B.alboglabra)4种寄主植物为材料,利用生物测定和解毒酶活力测定的方法,研究了取食不同寄主植物的小菜蛾幼虫对氯虫苯甲酰胺敏感性及体内解毒酶活力变化情况。结果表明,4种寄主植物饲养小菜蛾5代后,其敏感性分别为菜心>芥菜>白菜>芥蓝,且其体内活性酶谷胱甘肽S-转移酶(GSTs)、羧酸酯酶(CarE)比活力差异显著(P<0.05),活性的强弱与其敏感性相一致。以取食芥蓝的小菜蛾体内2种解毒酶活性最强。说明寄主植物能影响小菜蛾药剂敏感性及解毒酶活性。试验结果对小菜蛾的综合防控及抗氯虫苯甲酰胺机理研究具有重要的参考价值。     

取食不同寄主植物对棉蚜后代抗药性的影响

测定了5种药剂对棉蚜Aphis gossypii抗氰戊菊酯、吡虫啉品系和敏感品系取食棉花、黄瓜和石榴的后代的毒力,并对它们的后代体内乙酰胆碱酯酶和羧酸酯酶的比活力做了初步探索。结果表明,氰戊菊酯抗性品系取食棉花比取食黄瓜的后代对氰戊菊酯的抗性大76.4倍,对灭多威、氧乐果、硫丹和吡虫啉的抗性也大0.5～4.6倍;取食石榴的后代对5种药剂的抗性介于取食棉花和黄瓜的之间。吡虫啉抗性品系的测定结果与氰戊菊酯抗性品系基本一致。敏感品系取食黄瓜比取食棉花的后代对5种药剂的敏感性更高。3个品系取食不同植物的后代相比,其体内乙酰胆碱酯酶的比活力,取食棉花的为取食黄瓜的2.4～2.8倍;羧酸酯酶的比活力,取食棉花的为取食黄瓜的1.8～2.4倍。证明棉蚜的抗性和敏感品系取食的寄主植物不同,可引起对药剂敏感性的变化。乙酰胆碱酯酶和羧酸酯酶活力的变化均是引起这种变化的重要因素。     

敏感和抗性棉铃虫对溴氰菊酯毒力反应的机理研究

通过生物测定和生物化学方法比较了棉铃虫玎Helicoverpa armigera敏感和抗性种群对溴氰菊酯毒力反应及其3种解毒酶的差异。结果表明,田间抗性种群和室内药剂汰选的抗性种群对溴氰菊酯均有较高的抗性,其抗性倍数分别达到195.8和37 375倍。水解酯酶和多功能氧化酶是导致棉铃虫对溴氰菊酯产生高抗性的重要酶系。特异性抑制剂活体内外抑制作用测试发现,敏感种群和抗性种群均含有较高量的乙酰胆碱酯酶,但两个种群对抑制剂的亲和力反应不同,表明乙酰胆碱酯酶在敏感种群和抗性种群中发生了不同的变化,这种变化可能与棉铃虫对溴氰菊酯的抗性有关。由此推断,棉铃虫对拟除虫菊酯这类中枢神经系统神经毒剂产生抗性,乙酰胆碱酯酶发生变化可能也是一个重要因子。     

白纹伊蚊溴氰菊酯抗性和敏感品系羧酸酯酶性质比较

本文对白纹伊蚊Aedes albopictus溴氰菊酯抗性品系和敏感品系羧酸酯酶的生物化学性质进行了比较。白纹伊蚊抗性品系和敏感品系羧酸酯酶随底物浓度(α-乙酸萘酯或β-乙酸萘酯)的变化比活力变化趋势一致,但抗性品系对这2种底物的比活力均高于敏感品系,抗性品系羧酸酯酶的米氏常数和最大反应速度与敏感品系有显著差异。胆碱酯酶抑制剂测定结果表明,抗性品系羧酸酯酶对敌敌畏和磷酸三苯酯的敏感性高于敏感品系,对残杀威的敏感性低于敏感品系。2个品系羧酸酯酶对脱叶磷的敏感性差异不大。说明羧酸酯酶可能与白纹伊蚊对溴氰菊酯抗性有关。     

茄无网蚜几种酶对溴氰菊酯与高温胁迫的应答

[目的]通过研究茄无网蚜Acyrthosiphon solani(Kaltenbach)在溴氰菊酯和高温2种胁迫方式下其单位虫体质量解毒酶、保护酶和代谢酶活力的变化情况,为茄无网蚜耐药性研究、发生期预测等提供相应的理论依据.[方法]本文用LC50溴氰菊酯和32℃高温分别胁迫3龄茄无网蚜6、12、24、48和72 h,分析并比较其单位虫体质量谷胱甘肽-S-转移酶、过氧化物酶、羧酸酯酶和海藻糖酶的活力变化.[结果]过氧化物酶和羧酸酯酶对2种胁迫方式的响应剧烈,单位虫体质量的过氧化物酶活力在茄无网蚜被溴氰菊酯胁迫6、24和48 h后被显著抑制(P＜0.05),在温度胁迫处理组中均高于对照组,且在6、12和24 h处理组差异显著(P＜0.05);羧酸酯酶活力在溴氰菊酯胁迫时有较大波动,在6、24、48和72 h处理组与对照差异显著(P＜0.05).海藻糖酶对2种胁迫方式的响应较剧烈,海藻糖酶活力在溴氰菊酯胁迫6、24、48和72 h处理组显著高于对照(P＜0.05),在温度胁迫6、12和72 h处理组与对照组差异显著(P＜0.05).谷胱甘肽-S-转移酶对2种胁迫方式的响应相对较弱,谷胱甘肽-S-转移酶活力仅在溴氰菊酯胁迫6h和24 h处理组与温度胁迫24 h处理组显著高于对照(P＜0.05).[结论]LC50溴氰菊酯胁迫比温度胁迫对茄无网蚜体内4种酶活力的影响更大;2种胁迫方式对茄元网蚜体内4种酶活性均产生影响,过氧化物酶与羧酸酯酶参与度更高.     

棉蚜对有机磷杀虫剂抗性的生化机理

本文对有机磷抗性和感性棉蚜Aphis gossypii三个种群抗性生化机制进行了讲究.首先用解毒酶的抑制剂测定药剂的解毒途径.进一步测定乙酰胆碱酯酶活力及其敏感性和多功能氧化酶、谷胱甘肽s-转移酶、α-乙酸萘酯酶和α-乙酸萘酯羧酸酯酶等解毒酶的活力.结果表明,体内条件下,多功能氧化酶与抗性有关,但在离体条件下,在棉蚜匀浆液中有内源抑制剂存在.α-乙酸萘酯酶和α-乙酸萘酯羧酸酯酶活力的增加,乙酰胆碱酯酶对杀虫剂敏感性的降低也是造成棉蚜对有机磷产生抗性的原因.     

棉铃虫对拟除虫菊酯杀虫剂敏感性的修复及其乙酰胆碱酯酶的变化

利用生物测定和生物化学方法研究了抗药性棉铃虫Helicoverpa armigera(Hubner)对拟除虫菊酯敏感性修复及其体内乙酰胆碱酯酶的变化,结果表明：当去除药剂选择压后,棉铃虫对拟除虫菊酯的抗性为不稳定。随着停止用药的时间加长,敏感性增加。从田间收集的棉铃虫在室内饲养后第1代对拟除虫菊酯的抗性下降速度较迅速。特异性酶抑制剂对敏感和抗性棉铃虫种群的乙酰胆碱酯酶亲和力试验结果证实,乙酰胆碱酯酶在抗性棉铃虫对杀虫剂反应发生变化的过程中发生改变,这种酶的改变可能对棉铃虫抗药性的不稳定性有重要影响。     

桃小食心虫幼虫越冬前后对几种杀虫剂敏感性的差异

用药液浸渍法测定了桃小食心虫幼虫越冬前和越冬后对三唑磷、辛硫磷、马拉硫磷、毒死蜱、高效氯氟氰菊酯和阿维菌素等杀虫剂的敏感性差异.结果表明:越冬后幼虫对上述药剂的敏感性分别是越冬前幼虫的34.50、16.71、3.89、3.28、5.90和2.73倍.幼虫越冬后体内能源物质蛋白质、糖元和脂肪含量分别比越冬前降低17.10%、41.76%和30.08%;羧酸酯酶、酸性磷酸酯酶、碱性磷酸酯酶及谷胱甘肽-S-转移酶的活力分别比越冬前降低62.36%、53.47%、76.19%和80.60%;超氧化物歧化酶、过氧化氢酶、过氧化物酶等保护酶活力比越冬前分别降低18.77%、14.16%和64.02%;而幼虫体内多种农药的靶标酶乙酰胆碱酯酶活力的变化则相反,该酶在越冬后幼虫体内的活力是越冬前的1.41倍.表明越冬后幼虫对药剂敏感性的提高与体内能源物质含量、代谢酶、保护酶和靶标酶的活力变化有关.     

寄主对豆野螟的药剂敏感性和体内解毒酶活性的影响

比较取食不同寄主植物的豆野螟MarucatestulalisGeyer幼虫对3种药剂敏感性的差异,及其体内4种解毒酶活性之间的差异。结果表明:取食不同寄主植物的豆野螟对高效顺反氯氰菊酯和灭多威的敏感性差异显著,豇豆>四季豆>扁豆;对茚虫威的敏感性差异不显著。取食不同寄主植物的豆野螟体内4种酶活性都发生了变化,乙酰胆碱酯酶(AChE)羧酸酯酶(CarE)和多功能氧化酶(MFO)活性之间存在显著差异,豇豆>四季豆>扁豆;但谷胱甘肽-S转移酶(GST)活性之间不具有显著差异。推测:取食扁豆的豆野螟体内产生对高效顺反氯氰菊酯和灭多威具有一定解毒作用的物质;而取食豇豆的豆野螟产生的某种物质对茚虫威具有一定的解毒作用,4种酶在其对茚虫威的解毒过程中起一定的作用。     

害虫抗药性的生化机理

害虫的抗药性是与杀虫剂穿透昆虫表皮速率降低,解毒作用增强和靶标部位敏感性降低有关。昆虫体内多功能氧化酶、磷酸酯酶、羧酸酯酶、谷胱甘肽－Ｓ－转酶和脱氯化氢酶活力的增加是害虫抗性的主要生化机理。抗性昆虫体内乙酰胆碱酯酶对杀虫剂敏感性降低,中枢神经组织敏感性降低和“抗击倒基因”（Ｋｄｒ）的存在是拟除虫菊酯类杀虫剂的主要抗性机制。     

Glutathione S-transferase in the defence against pyrethroids in insects

The correlation between the natural levels of GST and the tolerance to the insecticide decamethrin (dMT), as well as the interaction between the molecules of affinity purified enzyme and the insecticide were investigated in order to collect further information on the obscure role of the Glutathione S-transferase system (GST) as a mechanism of defence against pyrethroids. The studies were carried out, comparatively, on the larvae and pupae developmental stages of the coleopteran Tenebrio molitor, which exhibit varying natural levels of GST activity. No stage dependent susceptibility of the insect against pyrethroid insecticides was found during the first 24 h, however 48 h after treatment, the KD50 dose increased significantly due to the recovery of some individuals from the larvae stage. Simultaneous injection of decamethrin with compounds which inhibit GST activity in vitro, resulted in an increased tolerance, which was more pronounced in the pupae stage. Inhibition studies combined with competitive fluorescence spectroscopy and high pressure liquid chromatography (HPLC) showed that the insecticide binds probably to the active site of the enzyme inhibiting its activity towards CDNB in a competitive manner, but is not conjugated with GSH. According to this, GST offers a passive protection towards pyrethroid insecticides by binding to their molecule in a sequestering mechanism.     

Susceptibility of Various Stages of Trichogrammatoidea armigera Nagaraja to Some Pesticides and Effect of Residues on Survival and Parasitizing Ability

The toxicity, persistence and effect on parasitism of 10 insecticides, eight fungicides and one acaricide on Trichogrammatoidea armigera Nagaraja, an egg parasitoid of a Helicoverpa armigera (Hb), were investigated in the laboratory and under field conditions. At field recommended dosages, the fungicides oxycarboxin, copperoxychloride, streptomycin sulphate + tetracycline hydrochloride and 2‐bromo‐2‐nitropropane‐1,3‐diol and the acaricide dicofol were safe, while the insecticide phosalone and fungicide tridemorph were moderately toxic to adults. All other insecticides tested, namely dimethoate, fenitrothion, monocrotophos, phosphamidon, endosulfan, cypermethrin, decamethrin, fenvalerate and fluvalinate, and the fungicides carbendazim, methyl thiophenate and carboxin were toxic to adults. A high level of parasitism was recorded for all fungicide treatments and for dicofol and fluvalinate. The larval stage of the parasitoid was more tolerant than other stages. The residual toxicity of all fungicides, and dicofol, did not affect the ability of the parasitoid to parasitize its host, while the insecticides phosalone and fluvalinate were slightly persistent, favouring 44.7% and 49.3% parasitism after 15 days. Residues of dimethoate, decamethrin, cypermethrin, fenvalerate, monocrotophos and phosphanidon were moderately persistent, while fenitrothion and endosulfan were persistent.     

寄主植物对斜纹夜蛾酯酶和乙酰胆碱酯酶活性的影响

利用生物测定与生物化学的方法,就取食不同寄主植物的2个斜纹夜蛾[Spodoptera litura(Fab.)]品系对丙溴磷和灭多威的敏感性及其体内的酯酶与乙酰胆碱酯酶的活性变化进行了研究。结果表明,取食不同寄主植物的斜纹夜蛾对丙溴磷和灭多威的敏感性不同。在敏感品系中,取食不同食料的斜纹夜蛾后代对灭多威的敏感性顺序为:烟草<棉花<大豆<人工饲料;对丙溴磷而言,敏感性顺序则为:棉花<烟草<大豆<人工饲料。而在田间抗性品系中,对丙溴磷的敏感性顺序为:棉花<烟草<人工饲料<大豆;对灭多威的敏感性顺序为:棉花<烟草<大豆<人工饲料。此外,在田间抗性和敏感品系中,取食不同食料的斜纹夜蛾体内的酯酶活性之间均存在显著差异,对其乙酰胆碱酯酶的活性也有程度不同的诱导效应,但并不会引起乙酰胆碱酯酶的质变。     

寄生蜂抗药性研究进展

植物-植食性昆虫-寄生蜂三级营养结构之间由于长期相互适应和协同进化,产生了一系列独特的相互关系。选择压力将对害虫和寄生蜂的抗药性演化产生影响,但由于寄生蜂具有与植食性昆虫不同的生物学及生态学特性,选择压力对害虫和寄生蜂抗药性演化的影响作用也是不同的。研究结果表明,除体外杀虫剂对寄生蜂的直接汰选因素外,进入寄主昆虫体内的杀虫剂成分、寄主昆虫取食不同植物的特有成分以及气候因子等均会对寄生蜂的抗药性演化产生影响。     

Toxoplasma gondii: the enzymic defect of a mutant resistant to 5-fluorodeoxyuridine.

We have previously described a mutant of Toxoplasma gondii that was 100-fold more resistant to 5-fluorodeoxyuridine, as measured by growth in human fibroblast cultures. Various pyrimidine salvage enzymes were measured in the wild type and the mutant parasites to determine the biochemical basis for resistance to fluorodeoxyuridine. Both the resistant mutant and the wild type parasite had little or no uridine kinase, an enzyme readily detectable in the human fibroblast host cells. Uridine and deoxyuridine phosphorylases were found in both parasites while human fibroblasts had much less of these enzymes. The critical difference between the mutant and the wild type parasites proved to be a 100-fold lower concentration of uracil phosphoribosyltransferase in the fluorodeoxyuridine-resistant mutant. A back mutant of the resistant strain, selected for its ability to use uracil, simultaneously regained uracil phosphoribosyltransferase and sensitivity to fluorodeoxyuridine. This enzymic evidence together with previously published data show that in wild type T. gondii, deoxyuridine is incorporated into nucleic acids through a phosphorolysis to produce uracil which is then converted to uridylic acid by uracil phosphoribosyltransferase.     

棉铃虫抗药性的生理生化机制研究

本文报道了棉铃虫Helicoverpa armigera田间抗性种群对杀虫剂抗药性的生理生化机制。抗性种群(HJ-R)5龄幼虫羧酸酯酶、谷胱甘肽转移酶、多功能氧化酶活力均明显高于相对敏感种群(HD-S)。两种群乙酰胆碱酯酶对杀虫剂敏感性没有显著差异。HJ-R种群的腹神经索对氰戊菊酯表现了2-3倍的神经不敏感性。HJ-R种群对氨基甲酸酯类杀虫剂的抗性主要是由代谢机制引起,其中多功能氧化酶可能起主导作用;对菊酯的抗性是由多功能氧化酶、酯酶、以及神经不敏感性几个因子综合作用的结果。     

The presence of knockdown resistance mutations reduces male mating competitiveness in the major arbovirus vector,Aedes aegypti

BackgroundThe development of insecticide resistance in mosquitoes can have pleiotropic effects on key behaviours such as mating competition and host-location. Documenting these effects is crucial for understanding the dynamics and costs of insecticide resistance and may give researchers an evidence base for promoting vector control programs that aim to restore or conserve insecticide susceptibility.Methods and findingsWe evaluated changes in behaviour in a backcrossed strain of Aedes aegypti, homozygous for two knockdown resistance (kdr) mutations (V1016G and S989P) isolated in an otherwise fully susceptible genetic background. We compared biting activity, host location behaviours, wing beat frequency (WBF) and mating competition between the backcrossed strain, and the fully susceptible and resistant parental strains from which it was derived. The presence of the homozygous kdr mutations did not have significant effects on blood avidity, the time to locate a host, or WBF in females. There was, however, a significant reduction in mean WBF in males and a significant reduction in estimated male mating success (17.3%), associated with the isolated kdr genotype.ConclusionsOur results demonstrate a cost of insecticide resistance associated with an isolated kdr genotype and manifest as a reduction in male mating success. While there was no recorded difference in WBF between the females of our strains, the significant reduction in male WBF recorded in our backcrossed strain might contribute to mate-recognition and mating disruption. These consequences of resistance evolution, especially when combined with other pleiotropic fitness costs that have been previously described, may encourage reversion to susceptibility in the absence of insecticide selection pressures. This offers justification for the implementation of insecticide resistance management strategies based on the rotation or alternation of different insecticide classes in space and time.     

昆虫神经毒素的研究:各种神经毒剂引起毒素的产生

用五类(七种)神经毒性的杀虫药剂,对美洲(虫非)蠊测定了它们能否引起血淋巴中毒素的产生。DDT、溴氰菊酯及六六六均能引起血淋巴中毒素的产生,而E605、西维因、巴丹及杀虫脒均无此效果。纸层析及薄层层析,用标准样品(酪氨酸、酪胺、苯乙胺、L-亮氨酸及异戊胺)作比较,测定了这一产生的血淋巴中的毒素乃是酪胺,或主要是酪胺。增效试验,证明了杀虫脒与DDT或溴氰菊酯合用时,能增加酪胺的产量。讨论了这一毒素产生的条件,以及这一毒素有可能不是单一成分,而是几种单胺及氨基酸的复合物,但酪胺为其主要成分。     

杀虫剂胁迫下褐飞虱迁飞虫和本地虫后代体内粗脂肪、可溶性糖及氨基酸含量的比较

为了解迁飞种群与居留种群后代发生再猖獗的生理生化差异,探讨再猖獗的机制,比较研究了在两个水稻品种（TN1和协优963）上施用杀虫剂后褐飞虱Nilaparvata lugens (Stål)迁飞虫和本地虫后代3龄、5龄若虫和成虫体内可溶性糖和粗脂肪含量以及迁飞成虫与其后代成虫体内游离氨基酸含量的变化。结果表明： 施药以及未施药处理(对照)TN1水稻品种上的迁飞后代3龄、5龄若虫和成虫体内的可溶性糖含量均显著高于本地虫。与可溶性糖含量相比,施药以及对照TN1水稻品种上的迁飞后代3龄、5龄若虫和成虫体内的粗脂肪含量均显著低于本地虫。协优963上3龄、5龄若虫体内可溶性糖含量的变化趋势与TN1上相同。对照水稻上迁飞成虫的粗脂肪含量显著高于本地种群,迁飞与本地3龄、5龄若虫间粗脂肪含量没有显著差异。杀虫剂处理后的水稻上迁飞后代5龄若虫和成虫体内粗脂肪含量显著高于本地虫。方差分析结果也显示,可溶性糖和粗脂肪含量的变化在虫源和杀虫剂,虫源和杀虫剂浓度以及杀虫剂类型和浓度方面有显著交互作用。两种水稻品种上,迁飞当代成虫体内的游离氨基酸含量显著低于其后代成虫。在经3种杀虫剂处理后,TN1上施用三唑磷后成虫体内的氨基酸含量显著高于施用溴氰菊酯和吡虫啉的处理,而协优963上施用溴氰菊酯和吡虫啉显著高于施用三唑磷的处理。本研究结果对深入阐明农药诱导褐飞虱再猖獗的机制具有参考价值。