多功能氧化酶系与甜菜夜蛾对氯氟氰菊酯抗药性的关系

比较了甜菜夜蛾Spodoptera exigua (Hübner)抗氯氟氰菊酯品系和敏感品系5龄幼虫中肠、脂肪体及体壁微粒体细胞色素P450的含量,结果表明,抗性和敏感品系不同组织细胞色素P450的含量均为中肠＞脂肪体＞体壁,抗性品系中肠、脂肪体及体壁细胞色素P450的含量分别是敏感品系的1.78、1.54及1.37倍。中肠微粒体甲氧试卤灵-O-脱甲基酶、乙氧试卤灵-O-脱乙基酶、乙氧香豆素-O-脱乙基酶、芳香基羟基化酶及艾氏剂环氧化酶的活性测定结果表明,抗性品系中肠5种酶的活性分别比敏感品系的酶活性提高1.33、1.73、1.40、1.51及1.30倍,说明甜菜夜蛾对氯氟氰菊酯的抗药性与微粒体多功能氧化酶活性的提高密切相关。     

苹果绵蚜田间种群的抗性监测

为了掌握果园重要害虫苹果绵蚜Eriosoma lanigerum的抗药性水平及动态变化,于2012–2015年间利用浸叶法监测了中国新疆察布查尔、山东济南、陕西乾县、河北昌黎和江苏丰县苹果绵蚜对常用药剂吡虫啉、毒死蜱和高效氯氟氰菊酯的敏感性,同时测定了不同苹果绵蚜种群的酯酶和谷胱甘肽S-转移酶活力。以2012年察布查尔苹果绵蚜为相对敏感品系,结果发现:所有种群在不同年度均对吡虫啉产生了低到高水平抗性（最大抗性倍数 >2000倍）;对于高效氯氟氰菊酯,昌黎、乾县及察布查尔2014种群均为敏感,济南、丰县和察布查尔2015种群均产生了中到高水平抗性;对于毒死蜱,乾县种群保持敏感,察布查尔、昌黎、丰县和济南种群产生了低到高水平抗性。酶活力测定结果显示:谷胱甘肽S-转移酶活力与苹果绵蚜对吡虫啉和高效氯氟氰菊酯的抗性水平呈正相关性,而酯酶活力与苹果绵蚜抗药性水平无明显相关性。本研究表明,新疆察布查尔、山东济南、陕西乾县、河北昌黎和江苏丰县的苹果绵蚜对吡虫啉、毒死蜱和高效氯氟氰菊酯的抗性水平均呈逐年提高趋势,其中对吡虫啉的抗性程度最严重,防治中应注意合理轮换用药。     

高效氯氟氰菊酯不同抗性基因型甜菜夜蛾相对适合度研究

在室内相同条件下 ,构建了甜菜夜蛾高效氯氟氰菊酯抗性种群 (R)、敏感种群(S)、正交 F1代 (RS)、反交 F1代 (SR)和对照种群 (CK)的生命表 ,研究了各种群的产卵量、卵孵化率、幼虫和成虫发育历期和蛹重等主要生物学特性。抗高效氯氟氰菊酯基因型甜菜夜蛾在生活力和繁殖力上与其它基因型比较均存在一定程度的不利性 ,杂合子的大部分生物学特性与敏感基因型比较差异不显著。在经过一个完整世代后 ,R、S、RS、SR和 CK种群的净增殖率(R0 )分别为 117.8、624.7、589.1、642 .3、218.8。以敏感种群为参比 ,S、RS、SR、R和 CK种群的相对适合度分别为 1、0 .934、1.028、0.188和 0 .368。与敏感品系 S相比 ,SR和 RS品系的相对适合度无变化 ,抗高效氯氟氰菊酯种群适合度明显降低。     

甜菜夜蛾对三种拟除虫菊酯杀虫剂的抗性稳定性研究

在室内脱离药剂选择的条件下,分别研究了甜菜夜蛾Spodoptera exigua Hübner 对氯氟氰菊酯、氰戊菊酯和顺式氯氰菊酯3种拟除虫菊酯杀虫剂的抗性稳定性及抗性衰退规律。结果表明,即使甜菜夜蛾对氯氟氰菊酯、氰戊 菊酯、顺式氯氰菊酯的抗性分别达522.9倍、669.7倍和2 737.2倍,抗性仍不稳定,分别经10代、8代和9代饲养后抗性下降为60.8倍、90.8倍和180.5倍;对田间抗性种群的抗性衰退研究发现,甜菜夜蛾对这3种拟除虫菊酯的抗性也表现为不稳定性,在无杀虫剂选择的情况下,开始几代抗性下降较快,当下降至一定水平(6~10倍)后,抗性趋于基本稳定,但很难完全恢复对拟除虫菊酯的敏感性。     

单对汰选方法在加速抗高效氯氟氰菊酯棉铃虫品系汰选中的应用

通过设计杂合种群单对杂交方式,研究了加速获得抗性品系的方法。以高效氯氟氰菊酯群体汰选后抗性倍数为4.9倍的棉铃虫种群及其同源对照种群为材料,同时设置常规群体汰选方法与单对汰选方法,研究单对汰选方法在加速抗高效氯氟氰菊酯棉铃虫品系汰选中的作用。结果表明,群体汰选两代后抗性倍数由4.9倍提高到7.4倍, 而单对汰选两代后抗性倍数由4.9倍提高到27.3倍。表明在常规群体汰选中穿插几代单对汰选方法可明显加快棉铃虫种群对高效氯氟氰菊酯的抗性汰选进程。     

阿维·高效氯氟氰菊酯3.5%微乳剂田间药效试验

田间药效试验结果表明阿维·高效氯氟氰菊酯3.5%微乳剂在15～25mL/667m2的剂量下对甘蓝甜菜夜蛾具有良好的防效.药后10d 20～25mL/667m2剂量杀虫效果达97%以上.     

杀虫剂对斜纹夜蛾幼虫的毒力研究

测定了11种杀虫剂对江苏省南京市马群和山东泰安市郊区斜纹夜蛾田间种群的毒力。用点滴法测定结果表明:6种杀虫剂对南京斜纹夜蛾3龄幼虫的毒力(LD50)大小顺序为:高效氯氰菊酯>氯氟氰菊酯>辛硫磷>马拉硫磷>毒死蜱>灭多威;对泰安斜纹夜蛾幼虫的毒力大小顺序为:高效氯氰菊酯>氯氟氰菊酯>马拉硫磷>辛硫磷>毒死蜱>灭多威。高效氯氰菊酯对两种群的毒力最大,灭多威的毒力最小。山东泰安种群较南京种群对杀虫剂略敏感。用浸叶法测定结果表明:9种杀虫剂对南京斜纹夜蛾3龄幼虫的毒力(LC50)大小顺序为:除尽>菜喜>高效氯氰菊酯>米螨>抑太保>氯氟氰菊酯>辛硫磷>毒死蜱>抑食肼。对山东泰安斜纹夜蛾3龄幼虫的毒力大小顺序为:除尽>菜喜>抑太保>高效氯氰菊酯>毒死蜱>辛硫磷>米螨>氯氟氰菊酯>抑食肼。除尽和菜喜对两种群的毒力最高,抑食肼的毒力最低。山东泰安斜纹夜蛾种群除对氯氟氰菊酯和米螨的敏感性略低于南京种群外,对其他药剂均比南京种群敏感。     

北京地区粘虫对5种杀虫剂的抗药性

采用浸叶法测定了北京地区6个粘虫Mythimna separata(Walker)田间种群对5种不同类型杀虫剂的抗药性。结果表明:与相对敏感品系相比,6个田间种群对5种杀虫剂均表现出不同程度的抗性水平。其中,对氯虫苯甲酰胺(抗性倍数为1.314~4.213)、甲氨基阿维菌素苯甲酸盐(抗性倍数为1.000~4.385)和毒死蜱(抗性倍数为1.083~5.936)表现为敏感至低水平抗性;对虫螨腈(抗性倍数为1.355~20.80)和氯氟氰菊酯(抗性倍数为1.748~13.98)表现为敏感至中等水平抗性。因此,北京地区的粘虫防治应注重将氯虫苯甲酰胺、甲氨基阿维菌素苯甲酸盐和毒死蜱与虫螨腈或氯氟氰菊酯交替或轮换使用,以延缓抗药性的产生与发展。     

四种拟除虫菊酯类杀虫剂对枸杞蚜虫的毒力及对三磷酸腺苷酶和谷胱甘肽S-转移酶活性的影响

为寻找防治枸杞蚜虫的适用药剂,采用玻璃管药膜法,测定了4种拟除虫菊酯类杀虫剂对枸杞蚜虫的毒力及对其三磷酸腺苷酶(ATPase)和谷胱甘肽S-转移酶(GSTs)活性的影响。结果表明:枸杞蚜虫对联苯菊酯最敏感,LC50值为4.34 mg/L;氯菊酯、高效氯氰菊酯和甲氰菊酯的LC50值分别为17.08、40.50和184.84 mg/L。4种杀虫剂对枸杞蚜虫两种ATPase活性均有抑制作用,药剂浓度为1×10-4mol/L时,4种药剂对Na+-K+-ATPase活性的抑制率均高于对Ca2+-M g2+-ATPase的抑制率,其中对Na+-K+-ATPase活性的抑制率从高到低依次为:联苯菊酯高效氯氰菊酯氯菊酯甲氰菊酯,而对Ca2+-M g2+-ATPase的抑制率则是联苯菊酯最高(46.41%),高效氯氰菊酯最低(33.04%)。4种药剂对枸杞蚜虫GSTs活性的影响差异较大:联苯菊酯在低浓度时对GSTs具有诱导作用,高浓度时则表现为一定的抑制作用;不同浓度高效氯氰菊酯和氯菊酯对GSTs活性均表现为抑制作用,抑制率最高达85.02%;而甲氰菊酯处理后GSTs的活性则升高了193.07%~249.96%。     

4种杀虫剂对甜菜龟叶甲幼虫毒杀效果初探

采用棉棒涂抹药液法对甜菜龟叶甲幼虫进行了室内触杀试验,调查了吡虫啉、高效氯氟氰菊酯、啶虫脒和虱螨脲4种杀虫剂对甜菜龟叶甲幼虫的毒杀效果。结果表明,高效氯氟氰菊酯的毒杀效果最好,致死中浓度LC_(50)为5.87μL/mL,吡虫啉、啶虫脒、虱螨脲的LC_(50)分别为5.93、23.55、57.94μL/mL。防治藜麦田甜菜龟叶甲幼虫可考虑选用高效氯氟氰菊酯。     

防治棉铃虫的高毒农药替代品种研究

采用室内浸卵、浸叶和点滴法以及田间小区试验,对19种杀虫剂防治棉铃虫的作用特点和效果进行了系统研究。室内生物测定结果表明:多杀菌素对棉铃虫卵孵化有较好的抑制作用,90.40 mg/L多杀菌素处理后棉铃虫卵的孵化率仅为42.86%;多杀菌素、甲氨基阿维菌素、高效氯氟氰菊酯、辛硫磷、丙溴磷、毒死蜱和高效氯氰菊酯对棉铃虫初孵幼虫的毒杀作用明显,原药稀释1.0×104~2.0×104倍时可使初孵幼虫死亡率达100%;昆虫生长调节剂——氟啶脲、氟铃脲、甲氧虫酰肼原药稀释1 000倍对棉铃虫初孵幼虫的致死率大于70％,且幼虫的生长受到明显抑制;甲氨基阿维菌素、高效氯氟氰菊酯、多杀菌素、毒死蜱、高效氯氰菊酯、丙溴磷、辛硫磷对低、高龄棉铃虫幼虫均具有较好的毒杀效果。田间小区试验结果表明,甲氨基阿维菌素、高效氯氟氰菊酯、丙溴磷、高效氯氰菊酯作用效果快且防治效果好,尤其是4 000倍甲氨基阿维菌素和5 000倍高效氯氟氰菊酯处理后第三天,其对棉铃虫的致死率达100％;多杀菌素和甲氧虫酰肼作用效果稍差。若在棉铃虫卵高峰期适时施药,供试的6种药剂均可作为防治棉铃虫的高毒农药替代品种。     

氯虫苯甲酰胺和高效氯氟氰菊酯在豇豆和土壤中的残留行为

建立了采用分散固相萃取法进行样品前处理,分别用液相色谱-质谱联用和气相色谱检测14%氯虫苯甲酰胺·高效氯氟氰菊酯微囊悬浮剂中2种有效成分在豇豆和土壤中的残留量及消解动态的方法。结果表明:豇豆和土壤中分别添加0.005～1 mg/kg 4个水平的氯虫苯甲酰胺和高效氯氟氰菊酯,其平均回收率为80%～105%,相对标准偏差为0.70%～9.5%。北京和海南2地氯虫苯甲酰胺和高效氯氟氰菊酯在豇豆中的半衰期为4～6 d,土壤中的为10～24 d。成熟时采收,豇豆中氯虫苯甲酰胺和高效氯氟氰菊酯的残留量均低于0.2 mg/kg。推荐14%氯虫苯甲酰胺·高效氯氟氰菊酯微囊悬浮剂在豇豆上的使用剂量为有效成分45 g/hm2,使用方式为喷雾,施药次数不超过3次,施药间隔期为7 d,安全间隔期为5 d。     

玫烟色棒束孢的生物学特性与其对小菜蛾致病力的相关性

测定了玫烟色棒束孢原始亲本菌株PFCF-O、退化亲本菌株PFCF-D和单孢分离子菌株PF-CF-D58、PFCF-D20、PFCF-D50的菌落生长速率、产孢量、孢子萌发率和胞外蛋白酶水平等生物学指标以及各菌株对小菜蛾2龄幼虫的校正死亡率。结果表明,菌株PFCF-O的生长速率呈先快后慢的趋势,产孢量为2.7×107个/mL,孢子萌发率为62.59%,胞外蛋白酶水平为1.16,对小菜蛾2龄幼虫校正死亡率达97.74%。而菌株PFCF-D、PFCF-D20、PFCF-D50和PFCF-D58间平均生长速率和孢子萌发率无显著差异,产孢量变化范围为1.05×107~2.34×107个/mL,胞外蛋白酶水平变化范围为1.02~1.07,各生物学指标及其对小菜蛾2龄幼虫的校正死亡率(19.86%~51.44%)都显著低于菌株PFCF-O。相关性分析结果显示,玫烟色棒束孢对小菜蛾的致病力与菌株生长初期的生长速率、产孢量、孢子萌发率和胞外蛋白酶水平呈极显著的正相关关系,与菌株生长后期的生长速率呈极显著负相关关系。     

Oxidative cleavage of a carboxyester bond as a mechanism of resistance to malaoxon in houseflies

The synergistic effect of triphenyl phosphate (a carboxyesterase inhibitor), sesamex (inhibitor of microsomal oxidation) and O,O-diethyl O-phenyl phosphorothioate on the toxicity of malathion and malaoxon for one susceptible and two resistant strains of housefly was studies. It was found that in the resistant strain G (characterized by high carboxyesterase activity) both malathion and malaoxon were synergized by triphenyl phosphate, but only malaoxon (and not malathion) by sesamex. The other resistant strain E 1, moderately tolerant for malathion but highly resistant to malaoxon, differed from strain G in that triphenyl phosphate had no effect; its response to sesamex was similar to that of strain G. The third synergist, O,O-diethyl O-phenyl phosphorothioate, combined the properties of triphenyl phosphate and sesamex. It was found to be the best of the three compounds used.Biochemical in vitro studies showed that both resistant strains could degrade malaoxon oxidatively at a rate at least 10 × higher than that of the susceptible strain. This oxidation could be inhibited by very low concentrations of the thiono analogue; a malaoxon to malathion ratio of 10:1 gave an inhibition of about 70% at a malaoxon concentration of 5 × 10^?6M. The product of this oxidation is malaoxon β-monocarboxylic acid. This metabolite was also found 1 hr after application of malaoxon in vivo.The results mentioned in this paper indicate that houseflies may become resistant to malaoxon by an increased rate of oxidative carboxyester bond cleavage.     

Pyrethroid synergists suppress esterase-mediated resistance in Indian strains of the cotton bollworm, Helicoverpa armigera (Hübner)

The role of esterase in pyrethroid resistance was studied in the final larval instar of different strains of the cotton bollworm, Helicoverpa armigera. The resistant strains viz., Nagpur strain and the Delhi strain were found to have elevated midgut esterase activity in comparison to the susceptible strain. Nagpur strain and Delhi strain have 2.24 and 1.73-fold higher esterase activity, respectively, than that of the susceptible strain. The Native PAGE displayed important differences in the midgut esterase isozyme pattern between the susceptible and the pyrethroid-resistant strains. Out of the 10 esterase isozyme observed, susceptible strain lacked three bands, E2, E6 and E10 that were found in the resistant strains. The potency of the synergists piperonyl butoxide (PBO) and dihydrodillapiole (DDA) as esterase inhibitor were also studied both in vitro and in vivo. The in vitro results clearly show that both PBO and DDA inhibited esterase activity in the two resistant strains, while there was almost no esterase inhibition in the homogenate of the susceptible strain. The in vivo inhibition studies (topical application of PBO and DDA followed by biochemical analysis) illustrated that PBO- and DDA-esterase binding is rather slow and non permanent process. Esterase inhibition did not occur immediately after the synergist treatment but at 4 and 8 h post treatment in case of PBO and DDA, respectively. Native PAGE revealed that the in vivo esterase inhibition caused by both PBO and DDA was due to the binding of the synergist with the E6 isozyme which was not present in the susceptible strain.     

Pyrethroid resistance and esterase activity in three strains of the cotton bollworm, Helicoverpa armigera (Hübner)

Microplate assay technique for estimation of esterase activity in a single insect was used in combination with dose mortality bioassays to detect pyrethroid resistance in three strains of Helicoverpa armigera and to study the frequency of pyrethroid resistant individuals within the population of the same strain at two larval stages, third and fifth instar. The third and fifth instar larvae of the field strains i.e., Nagpur strain and Delhi strain that displayed high degree of resistance towards deltamethrin, had higher esterase activity compared to a susceptible laboratory strain. The frequency distribution of individuals with elevated esterase activity above 1.00 absorbance unit was correlated with the resistance level of the strains. The frequency of resistant individuals in the third instar larvae of Nagpur strain and Delhi strain were 29% and 23%, respectively compared to 4% in the susceptible strain. The resistant individuals in the resistant strains have markedly increased in the fifth instar larvae with a frequency distribution of 63% and 90% in Delhi strain and Nagpur strain, respectively, while only 14% of individuals was found to have elevated esterase activity in the susceptible strain. The results demonstrated the role of esterase in pyrethroid resistance in H. armigera. Microplate assay proved to be a rapid and reliable biochemical technique for monitoring of pyrethroid resistance in H. armigera.     

in vitro metabolism of azinphosmethyl in susceptible and resistant houseflies

The in vitro metabolism of [¹⁴C-methoxy] or [³²P]azinphosmethyl by subcellular fractions of abdomens from a resistant and a susceptible strain of houseflies was studied. The degradative activity in both strains was associated with the microsomal and soluble fractions and required NADPH and glutathione, respectively. The resistant strain possessed higher activity for both the mixed-function oxidases and the glutathione transferase than the susceptible strain, and both systems appear to be important in the resistance mechanism. The mixed-function oxidases were involved in the oxidative desulfuration as well as the dearylation of azinphosmethyl. A glutathione transferase located in the soluble fraction catalyzed the formation of desmethyl azinphosmethyl and methyl glutathione. This enzyme also demethylated azinphosmethyl oxygen analog. Although the soluble fraction exhibited both glutathione S-alkyltransferase and S-aryltransferase activity against noninsecticidal substrates, no evidence of the transfer of the benzazimide moiety from azinphosmethyl to glutathione was obtained. Sephadex G-100 chromatography of the soluble enzymes revealed a common eluting fraction responsible for both types of transferase activity.     

The in vitro degradation of [14C]malathion by enzymatic extracts from resistant and susceptible strains of Drosophila melanogaster

Enzyme preparations from Drosophila melanogaster flies degraded [¹⁴C]malathion to α- and β-malathion monoacids and, hence, were considered to contain malathion carboxylesterase (ME) activity. Although ME- activity was stable during preincubation in the absence of malathion, it decreased dramatically during the course of the reaction, and could not be completely recovered by Sephadex G-25 chromatography. Furthermore, the protein fraction after chromatography still contained ¹⁴C, suggesting that the enzyme had become inhibited by a bound, ¹⁴C-labeled derivative. Extracts from a resistant (malathion-selected), an intermediate control, and the susceptible Canton S strains of D. melanogaster differed in the lability of ME activity during the reaction. This difference was partly attributed to the production of small amounts of malaoxon (2–8%) by the extracts from the more resistant strains. No consistent strain differences were found when the rate of malathion degradation was measured during the first minute of reaction, either with or without a microsomal oxidase inhibitor (metyrapone) present. These results, together with the cross-resistance of the malathion-selected strain to other insecticides and the lack of a synergistic effect of two carboxylesterase inhibitors (triphenyl phosphate and S,S,S-tributylphosphorotrithioate) suggested that malathion carboxylesterase does not contribute significantly to the observed differences in malathion resistance between strains.