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1.
多杀菌素亚致死浓度对小菜蛾解毒酶系活力的影响 总被引：10，自引：3，他引：7
采用多杀菌素亚致死浓度,以浸叶法分别处理小菜蛾Plutella xylostella (L.)敏感种群(SS)和亚致死选育种群 的3龄幼虫,分别测定饲喂处理6、12、24、48和72 h后小菜蛾体内羧酸酯酶(CarE)、谷胱甘肽S-转移酶(GST) 和多功能氧化酶(MFOs)的活性,分析了酶活性的变化动态。结果表明,SS种群小菜蛾CarE的活性在不同时间段波动较大,经多杀菌素处理后,开始时段比活力增加,随着处理时间的延长,比活力逐渐被抑制,Sub-SS种群的GarE活力高于SS种群;多杀菌素对GST具有明显的诱导作用,亚致死浓度处理后GSTs比活力呈上升趋势,且具有一定的时间效应;对细胞色素P450酶系的O-脱甲基酶活性具有明显的抑制作用,多杀菌素亚致死浓度连续处理5代后,该酶活性更低。 相似文献
2.
低剂量乙基多杀菌素对小菜蛾解毒酶的影响 总被引：2，自引：0，他引：2
为探讨低剂量乙基多杀菌素对小菜蛾Plutella xylostella（L.）解毒酶的影响,采用叶片浸渍法,测定了乙基多杀菌素和多杀菌素对小菜蛾敏感种群的毒力,并比较了低剂量（LC25和LC50）处理6、12、24、48和72 h时小菜蛾体内羧酸酯酶（CarE）、谷胱甘肽S-转移酶（GST）和多功能氧化酶系（MFOs）活性的变化动态。结果表明:乙基多杀菌素对小菜蛾的杀虫活性优于多杀菌素,处理48 h后其LC25和LC50浓度分别为0.018和0.048 mg/L,经此低剂量浓度处理后,小菜蛾CarE活性波动较大,6~24 h,处理组CarE活性高于对照组,且均呈先升后降趋势,24~72 h,处理组CarE活性均低于对照组,并且具有一定的时间效应;对GST具有明显的诱导作用,GST活性均高于对照组;对MFOs具有明显的抑制作用,除在48 h时相差不大外,其他时间MFOs活性均显著低于对照组。结果表明,GST可能参与了乙基多杀菌素在小菜蛾体内的代谢。 相似文献
3.
亚致死浓度多杀菌素对西花蓟马解毒酶系活力的影响 总被引：3，自引：1，他引：2
采用亚致死浓度(LC25)多杀菌素对西花蓟马Frankliniella occidentalis相对敏感(SS)种群进行连续选育,获得亚致死(Sub)种群。处理36代后,Sub种群对多杀菌素的敏感性下降到SS种群的5.2倍。用SS和Sub种群各自的LC10和LC25浓度多杀菌素分别处理两种群的2龄若虫,1、6 、12、24和48 h后测定羧酸酯酶(CarE)、谷胱甘肽S-转移酶(GSTs) 和多功能氧化酶(MFOs)的比活力。结果表明,Sub种群对照组CarE和GSTs比活力在除第48 h外的其他时间段都高于SS种群对照组,且6 h时两者CarE比活力差异显著,Sub种群是SS种群的1.37倍;Sub种群对照组MFOs比活力在各时间段都高于SS种群对照组,在1 和6 h时差异显著,前者分别是后者的1.62和1.36倍。再经各自的LC10和LC25浓度多杀菌素处理后,在各时间段Sub种群的CarE比活力均高于SS种群;LC25浓度处理后,Sub种群的GSTs和MFOs比活力虽在短时间内低于SS种群,但随处理时间的延长其比活力均高于SS种群。说明SS种群经亚致死浓度多杀菌素选育36代后,其体内CarE、GSTs和MFOs比活力有上升趋势;继续用亚致死浓度多杀菌素处理,则Sub种群体内解毒酶活力的动态调节能力要强于SS种群。 相似文献
4.
采用叶片药膜法,使用亚致死浓度(LC10、LC25)的氯虫苯甲酰胺对小菜蛾Plutella xylostella(L.)3龄幼虫连续处理5代后,试虫对氯虫苯甲酰胺的敏感度分别比敏感品系下降了57.3% 和67.7%,同时对多杀菌素的敏感度也分别下降了60.2% 和51.5%,但对毒死蜱和高效氯氰菊酯的敏感度变化不明显。采用该浓度的氯虫苯甲酰胺分别处理小菜蛾3龄幼虫24、48和72 h,可诱导其羧酸酯酶(CarE)比活力上升,但对细胞色素P450 O-脱乙基酶(ECOD)、谷胱甘肽S-转移酶(GSTs)和芳基酰胺酶(AA)有明显的抑制作用;连续处理5代后,小菜蛾CarE和ECOD的比活力显著高于对照组,分别为对照组的1.16、1.40倍和1.65、1.56倍,但GSTs和AA的比活力则分别比对照下降了11.0%、27.5%和43.6%、52.5%。结果表明,小菜蛾对氯虫苯甲酰胺产生抗性的风险较高;羧酸酯酶和多功能氧化酶可能与小菜蛾对氯虫苯甲酰胺的敏感度下降有关。 相似文献
5.
亚致死剂量氯虫苯甲酰胺对小菜蛾体内活性酶的影响 总被引：2，自引：0，他引：2
为探讨亚致死剂量氯虫苯甲酰胺对小菜蛾 ［Plutella xylostella (L.)］ 体内活性酶的影响,采用叶片药膜法,用氯虫苯甲酰胺LC50和LC25剂量处理小菜蛾3龄幼虫24、48 h后,测定了幼虫体内羧酸酯酶、多功能氧化酶、谷胱甘肽S-转移酶、乙酰胆碱酯酶等4种酶的活性变化。结果表明,亚致死浓度氯虫苯甲酰胺处理除对羧酸酯酶活性影响不显著外,对另3种酶活性均存在一定的抑制作用。谷胱甘肽S-转移酶活性下降最明显,LC25和LC50处理小菜蛾24 h后,与对照相比分别下降92.57%和98.01%。 相似文献
6.
桃蚜对噻虫嗪代谢抗性机制研究 总被引：1，自引：0，他引：1
对桃蚜进行室内噻虫嗪抗性品系筛选,选育至15代后抗性倍数达到75.6倍。对噻虫嗪敏感品系(THI-S)和抗性品系(THI-R)桃蚜的谷胱甘肽S-转移酶(GSTs)、酸性磷酸酯酶(ACP)、碱性磷酸酯酶(ALP)、羧酸酯酶(CarE)、多功能氧化酶(MFO)O-脱甲基活性进行了比较,结果显示:敏感品系(THI-S)和抗性品系(THI-R)的谷胱甘肽S-转移酶比活力分别为3.127 5和3.215 9,差异不显著,桃蚜抗性品系体内酸性磷酸酯酶、碱性磷酸酯酶、羧酸酯酶和多功能氧化酶O-脱甲基活性均显著高于敏感品系,分别达到了1.57、2.10、6.12、2.03倍。表明桃蚜对噻虫嗪抗性的产生与酸性磷酸酯酶、碱性磷酸酯酶、羧酸酯酶和多功能氧化酶O-脱甲基的活性相关。 相似文献
7.
报道了多杀菌素对甜菜夜蛾Spodopetera exigua(Hübner)多酚氧化酶(PPO)和羧酸酯酶(CarE)的影响, 多杀菌素对甜菜夜蛾表现了很高的毒力,对三龄幼虫的LC50值为0.80 mg/L。离体条件下,1.0×10-3~0.5 mg/L多杀菌素对甜菜夜蛾多酚氧化酶的抑制率超过50％,且表现为随药剂浓度的增加抑制能力增强的趋势。活体条件下,0.1~0.8 mg/L多杀菌素在处理的早期诱导虫体内多酚氧化酶的活性增加,但12 h后却显著抑制多酚氧化酶的活性。1.0×10-3~1.0 mg/L多杀菌素在离体条件下对羧酸酯酶不表现任何抑制作用,但活体条件下同样能诱导虫体内羧酸酯酶活性增强。 相似文献
8.
为明确喜树碱对小菜蛾Plutella xylostella生长发育的抑制作用及其机制,设置0.5、1.0、2.0mg/m L剂量处理其3龄幼虫,采用浸叶饲喂法和高效液相色谱法测定了喜树碱对小菜蛾体内蜕皮激素和保幼激素滴度的影响。结果显示,喜树碱各剂量处理均显著抑制了小菜蛾幼虫的生长发育,抑制率最高达到28.42%;各处理小菜蛾化蛹时间均延迟,异常蛹增多,羽化率降低;其中2.0 mg/m L处理后4 d其化蛹率为6.67%,对照组化蛹率为86.60%。0.5、1.0 mg/m L处理下,小菜蛾体内蜕皮激素滴度显著低于对照组,仅为对照组的0.06倍;而保幼激素滴度增加,分别可达到28.74mg/m L和36.29 mg/m L,是对照组的9倍左右。表明喜树碱可影响小菜蛾体内蜕皮激素和保幼激素的平衡,延迟和影响了小菜蛾的正常发育进程,可实现对小菜蛾种群的控制作用。 相似文献
9.
解毒酶系在小菜蛾对阿维菌素抗性中的作用 总被引：16，自引：1，他引：16
对阿维菌素敏感 (ABM- S)和抗性 (ABM- R)种群小菜蛾的羧酸酯酶 (Car E)、谷胱甘肽 S-转移酶 (GST)和多功能氧化酶 (MFO) O-脱甲基活力进行了比较。结果显示 ,除 1～ 2龄外 ,ABM- R种群的 Car E活力显著高于 ABM- S种群 ,显著性随幼虫龄期的增长而增大 ,ABM- R种群 4龄末期幼虫的 Car E比活力为 ABM- S种群的 2.25倍。动力学研究表明 ,可能是低龄幼虫中酶分子的变构起主要作用 ,而随着虫龄增长 ,酶分子数量的增加对抗性的作用逐渐增大。从酯酶同工酶等电聚焦电泳得出 ,ABM- R种群的 E7、E13和 E15同工酶活力显著提高是导致 ABM- R种群酯酶活力提高的主要原因。ABM- S和 ABM- R种群 GST的活力差异在1～ 2龄期最大 ,为 2.09倍 ,随幼虫龄期的增大而降低 ,4龄幼虫期的 GST无种群差异。未检测到多功能氧化酶的 O-脱甲基活力的种群差异。 相似文献
10.
甲氧虫酰肼对棉铃虫解毒酶活力的亚致死效应研究 总被引：1，自引：0，他引：1
采用亚致死剂量(LC40浓度)的甲氧虫酰肼处理棉铃虫抗甲氧虫酰肼种群(R)和同源敏感种群(S)3龄初幼虫48 h,测定了3～6龄期幼虫体内多功能氧化酶(MFO)、酯酶(EST)和谷胱甘肽S-转移酶(GSTs)的比活力变化。结果发现:经亚致死剂量甲氧虫酰肼处理后,S种群EST比活力除4龄幼虫外均有所升高,且仅在3龄期升高明显;GSTs比活力在5龄幼虫体内显著升高,其他龄期无明显变化;MFO比活力在6龄幼虫体内表现为降低,其他龄期无显著变化。对于R种群,3龄和6龄幼虫体内EST比活力显著降低,各龄期的GSTs和MFO比活力均显著降低。空白对照R种群3～6龄期幼虫的GSTs比活力均高于S种群;EST比活力仅3龄幼虫显著高于S种群;MFO的比活力仅5龄幼虫显著高于S种群。研究表明:棉铃虫对甲氧虫酰肼的抗性与GSTs比活力增大关系较为密切;LC40浓度的甲氧虫酰肼可诱导敏感种群EST和GSTs活力升高,而使抗性种群3种酶的活力受到抑制。 相似文献
11.
William S. Bowers Gopalan C. Unnithan Jun-Ichi Fukushima Jun Toda Takeyoshi Sugiyama 《Pest management science》1995,43(1):1-11
Twenty-one synthetic compounds, containing one or more furan rings, were demonstrated to possess anti-juvenile hormone (AJH) activity as evidenced by their induction of premature metamorphosis in the milkweed bug, Oncopeltus fasciatus (Dallas) by contact, topical application or fumigation. The ED50 of the four most active analogs required to induce precocious metamorphosis from 3rd-instar nymphs by residue contact in a Petri dish compared favorably with that of precocene II (6,7-dimethoxy-2,2-dimethyl 2H-chromene) a naturally occurring phytochemical AJH. Precocious metamorphosis was fully reversible by co-treatment with juvenile hormone (JH III) or JH analogs, demonstrating that the observed AJH activity resulted from an induced deficiency of juvenile hormone. 相似文献
12.
BACKGROUND: One of the most studied actions of juvenile hormone (JH) is its ability to modulate ecdysteroid signaling during insect development and metamorphosis. Previous studies in mosquitoes showed that 20‐hydroxyecdysone (20E) regulates vitellogenin synthesis. However, the action of JH and its mimics, e.g. methoprene, on female reproduction of mosquitoes remains unknown. RESULTS: Here, a major malaria vector, Anopheles gambiae Giles, was used as a model insect to study the action of methoprene on female reproduction. Ecdysteroid titers and expression profiles of ecdysone‐regulated genes were determined before and after a blood meal. An ecdysteroid peak was detected at 12 h post blood meal (PBM). The maximum expression of ecdysone‐regulated genes, such as ecdysone receptor (EcR), hormone receptor 3 (HR3) and vitellogenin (Vg) gene, coincided with the ecdysteroid peak. Interestingly, topical application of methoprene at 6 h PBM delayed ovarian development and egg maturation by suppressing the expression of ecdysone‐regulated genes in female mosquitoes. CONCLUSION: The data suggest that ecdysteroid titers are correlated with Vg synthesis, and methoprene affects vitellogenesis by modulating ecdysteroid action in A. gambiae. Copyright © 2010 Society of Chemical Industry 相似文献
13.
Gopalan C. Unnithan John F. Andersen Tomomi Hisano Eiichi Kuwano Ren Feyereisen 《Pest management science》1995,43(1):13-19
Seventeen substituted imidazoles were tested as inhibitors of juvenile hormone (JH) III synthesis by cockroach corpora allata in an in-vitro radio-chemical assay. Most of these 1,5-disubstituted imidazoles were highly potent, with IC50 values of less than 100nM. The compounds differed in their ability to cause an accumulation of the precursor methyl farnesoate in the glands. Four of the imidazoles were tested by topical application to previtellogenic adult females, and all caused a significant inhibition of JH synthesis and an accumulation of intraglandular methyl farnesoate for at least three days after treatment. Methyl farnesoate epoxidase activity of homogenates of corpora allata was inhibited by the compounds TH -14 and TH -27. This P450-dependent epoxidase activity was inhibited at less than 10 nM. The results show that the 1,5-disubstituted imidazoles are powerful inhibitors of the last step of juvenile synthesis in this cockroach. 相似文献
14.
Pesticide-induced hormesis may be an alternative mechanism for pest resurgence which is a serious problem in agriculture. Confirmation of the general phenomenon of hormesis may have significant implications for the design of pest control strategies and pest resistance management practices, although this has proved difficult due to the lack of appropriate methodology and the absence of well-defined mechanisms to support the experimental observations. In this study, a model-based approach to describe a dose-response relationship incorporating the hormetic effect was applied to the detection and estimation of imidacloprid-induced hormesis in the green peach aphid, Myzus persicae (Sulzer). The results indicated that imidacloprid at low concentrations induced stimulation of fecundity, however, high concentrations inhibition. This was reflected in an inverted U-shaped curve and related to the change of juvenile hormone III (JH III) levels in M. persicae. Fitting the data with quadratic and Weibull functions, which included a parameter for hormesis, showed that the magnitude of the hormetic effect was 31.31% for fecundity and 32.21% for JH III levels. The presence of hormesis in fecundity induced by imidacloprid may be related to the change in JH III levels in M. persicae. 相似文献
15.
The efficacy of juvenile hormone III (JH III) and two JH-mimicking compounds was compared in laboratory experiments with Reticulitermes lucifugus (Rossi), R. santonensis Feytaud and R. virginicus (Banks). Induction of presoldier, soldier and/or soldier-worker intercaste differentiation was taken as positive response to the treatment. The novel juvenogen, a fatty acid ester of a juvenoid alcohol, induced greatest soldier differentiation in all species tested, followed by hydroprene. JH III was less effective. Representatives of three Reticulitermes species showed similar trends in soldier induction rates. Differences in mortality in treatments of termites of the same species from different colonies with the same compound were observed and evidently were caused by differences in the conditions of respective colonies. 相似文献
16.
Reynardt Erasmus Johnnie van den Berg Peet Jansen van Rensburg Hannalene du Plessis 《Pest management science》2023,79(5):1860-1867
BACKGROUND
Tuta absoluta (Lepidoptera: Gelechiidae) is difficult to control by means of foliar insecticides, partly because of the endophytic feeding behavior of its larvae. The biopesticide spinosad is applied as a foliar spray for control of T. absoluta and has systemic properties when applied as a soil drench to the growing medium of tomato plants. The aims of this study were to determine the: (i) instar-dependent tolerance of larvae to spinosad; (ii) efficacy of spinosad drench application for the control of larvae; (iii) residual period of systemic activity of spinosad in leaves and fruit after drenching; and (iv) effect of spinosad drenching on tomato plant growth parameters.RESULTS
The estimated LC50 value (Lethal Concentration at which 50% of the larvae died) differed between instars. The LC50 for second-instar larvae (0.41 ppm) to spinosad was significantly lower than that for third- (0.64 ppm) and fourth-instar (0.63 ppm) larvae. The LC80 value (Concentration at which 80% of the larvae died) for fourth-instar larvae (2.48 ppm) was 2.6- and 1.7-fold higher than that for the second- and third-instar larvae, respectively. The spinosad concentration recorded in leaves at 25 days after treatment (DAT; 0.26 μg g−1) was significantly lower than that in leaves sampled at 3, 10 and 15 DAT. High larval mortalities were, however, recorded for the duration of the experiment, which lasted 25 days (equivalent to one T. absoluta generation).CONCLUSION
Systemic spinosad effectively controlled T. absoluta larvae over a prolonged period. However, drenching this insecticide violates the recommendation of the Insecticide Resistance Action Committee to avoid treating consecutive insect generations with the same mode of action and can therefore result in the evolution of insecticide resistance. © 2023 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. 相似文献17.
Bruce D. Hammock Thomas C. Sparks Susanne M. Mumby 《Pesticide biochemistry and physiology》1977,7(6):517-530
Juvenile hormone III was tritium labeled on the methyl ester and utilized with other substrates in an investigation of inhibition and substrate specificity of hemolymph esterases from the cockroach, Blaberus giganteus. The structure of labeled juvenile hormone III was supported both chemically and biochemically. Forty-two potential inhibitors were examined, and the best inhibitors included phosphoramidothiolates and S-phenylphosphates. One of these inhibitors was found useful in hormone biosynthesis studies dealing with the enzymatic conversion of methyl farnesoate to juvenile hormone in corpora allata homogenates. Several commonly used inhibitors of carboxyesterases caused only weak inhibition of JH esterases. Gel filtration elution patterns, inhibitor relationships, and specific activities of the hemolymph esterases indicate that juvenile hormones I and III are degraded by similar if not identical enzymes. In some cases, α-naphthyl acetate and juvenile hormone esterase activity could be differentially inhibited. Hemolymph esterases were not capable of degrading ethyl or isopropyl conjugated esters of two juvenoids or three model substrates. 相似文献
18.
多杀菌素对菜蛾绒茧蜂的致死和亚致死效应 总被引：5，自引：0，他引：5
以对多杀菌素高抗的小菜蛾纯合子品系作寄主饲养菜蛾绒茧蜂,用多杀菌素田间推荐使用浓度(25 mg/L)分别处理处于卵期、幼虫期和蛹期的绒茧蜂,其中卵期和幼虫期通过处理寄主幼虫间接处理,并测定该药剂对成虫的毒力,系统观察该杀虫剂对绒茧蜂各虫期的致死和亚致死作用。与对照相比,绒茧蜂卵期或幼虫期其寄主受药后,可导致蜂幼虫死于寄主体内或啮出寄主的过程中,使结茧化蛹率下降43% ~56%,成虫羽化率下降19% ~33%,成蜂雌性比下降11% ~25%,而成虫大小、寿命和寄生力未受显著影响;在蛹期受药使成虫羽化率下降10%,成蜂寿命缩短,但对成虫寄生力无显著影响;对成虫24 h的LC99为4.31 mg/L。结果表明,多杀菌素可进入寄主作用于其体内的蜂卵和幼虫,或直接作用于蜂蛹和成虫,从而对绒茧蜂各个虫态产生显著的致死和亚致死效应,尤以对成虫高毒。 相似文献