嘧菌酯与三种外源硒对不同生命阶段斑马鱼的联合毒性

分别测定了嘧菌酯、3种外源硒 (亚硒酸钠、硒代蛋氨酸和纳米硒) 对水体模式生物斑马鱼不同生命阶段的单一急性毒性,以及等毒性配比的二元混合体系的联合急性毒性,并分别采用相加指数 (AI) 法、毒性单位 (TU) 法和混合毒性指数 (MTI) 法对其联合效应进行了评价。结果表明:斑马鱼3个生命阶段对亚硒酸钠的敏感性 (以96 h-LC₅₀ (致死中浓度) mg/L表示,其中mg指硒的质量) 顺序为:仔鱼(1.11 mg/L) >胚胎(1.48 mg/L) >成鱼(13.05 mg/L);对硒代蛋氨酸的敏感性:仔鱼(0.80 mg/L) >胚胎(1.03 mg/L) >成鱼(9.36 mg/L);对纳米硒的敏感性:成鱼(0.48 mg/L) >仔鱼(1.67 mg/L) >胚胎(4.32 mg/L)。除MTI法计算嘧菌酯与硒代蛋氨酸对成鱼表现为部分相加作用外,采用AI法、TU法和MTI法计算嘧菌酯与亚硒酸钠、硒代蛋氨酸和纳米硒对斑马鱼成鱼、仔鱼和胚胎的联合作用结果一致,均表现为拮抗作用。     

苯氧威对斑马鱼不同发育阶段急性毒性及胚胎卵黄囊仔鱼阶段慢性毒性作用

为了解苯氧威对斑马鱼的毒性作用,采用半静态方法,研究了苯氧威对斑马鱼不同发育阶段的急性毒性。结果表明:苯氧威对斑马鱼胚胎、孵化12 h和72 h的仔鱼以及成鱼的96 h-LC50值分别为2.35、0.98、1.87和1.67 mg/L,其对斑马鱼成鱼具有中等毒性;苯氧威对斑马鱼胚胎的自主运动、心率、孵化率、仔鱼体长等亚致死效应指标均有影响,并使得胚胎出现了心包囊肿、脊柱弯曲及无黑色素附着等畸形现象。进一步研究了苯氧威对斑马鱼胚胎卵黄囊仔鱼阶段的慢性毒性作用。结果显示:苯氧威对斑马鱼胚胎24 h自主运动、48 h心率、72 h畸形率及11 d孵化仔鱼体长均有不同程度的抑制作用,其最低可观测效应浓度(LOEC)值分别为0.60、0.20、0.60和0.80 mg/L,而与之对应的无可观测效应浓度(NOEC)值分别为0.40、0.10、0.40和0.60 mg/L。试验中还发现:苯氧威对斑马鱼胚胎孵化有明显抑制作用;心率是斑马鱼胚胎卵黄囊仔鱼阶段毒性试验最敏感的观察指标。     

乙草胺对斑马鱼幼鱼早期发育阶段甲状腺相关基因的影响

为评价乙草胺的毒性,以斑马鱼为受试生物,采用静态法和实时荧光定量PCR方法,研究了乙草胺对斑马鱼成鱼和胚胎的急性毒性、对胚胎的致畸作用,以及不同窗口期暴露对幼鱼甲状腺相关基因的影响。结果表明:乙草胺对斑马鱼成鱼96 h-LC50值为3.04 mg/L,属中等毒性,对胚胎的120 h-LC50值为5.32 mg/L;斑马鱼胚胎受精后于0.3 mg/L乙草胺中暴露5 d,幼鱼可出现心包囊水肿、脊索弯曲等致畸现象。窗口期暴露试验表明:斑马鱼胚胎受精后3 h起于0.06 mg/L乙草胺中暴露10和14 d,以及在0.3 mg/L乙草胺中暴露10 d,均会引起幼鱼脱碘酶基因(d1、d2)、甲状腺激素受体基因(trα、trβ)、钠/碘同向转运体基因(s1c5a5)、促甲状腺激素释放激素基因(crh)、促甲状腺激素基因(tsh)等的表达呈现不同程度下调,而在0.3 mg/L乙草胺中暴露14 d,除d1的表达量显著上调外,对其余各相关基因的表达均无明显影响。试验结果表明,乙草胺能够干扰斑马鱼幼鱼早期发育,且在不同暴露浓度和时间下,干扰效应存在较大差异。     

几种农药多元组合对HepG2人肝癌细胞的联合毒性效应

多种农药残留经膳食暴露途径进入人体后,其联合毒性的潜在风险通常超过单一农药。为探明农药多残留的联合暴露毒性,采用经典MTT (噻唑蓝) 比色法,测定了阿维菌素、啶虫脒、多菌灵、百菌清、毒死蜱、高效氯氟氰菊酯、咪酰胺和三唑磷8种农药多种组合方式联合暴露下对HepG2人肝癌细胞增殖的抑制活性。结果表明:联合暴露24 h后,不同种类农药组合对HepG2细胞存活率的影响存在较大差异,随着组合农药质量浓度升高,部分组合对HepG2细胞增殖的抑制效应分别呈现S型变化和线性变化。例如,二元组合 (多菌灵+高效氯氟氰菊酯) 在0~10.00 mg/L、三元组合 (多菌灵+阿维菌素+高效氯氟氰菊酯) 在0~24.12 mg/L、四元组合 (三唑磷+高效氯氟氰菊酯+多菌灵+阿维菌素) 在0~47.46 mg/L以及五元组合 (毒死蜱+阿维菌素+啶虫咪+高效氯氟氰菊酯+三唑磷) 在0~62.80 mg/L暴露条件下其抑制效应表现为S型变化,即随着组合农药质量浓度增大,细胞存活率先迅速降低,之后则缓慢降低;二元组合 (多菌灵+百菌清) 在0~8.46 mg/L、三元组合 (毒死蜱+啶虫脒+多菌灵) 在0~39.97 mg/L、四元组合 (多菌灵+高效氯氟氰菊酯+百菌清+阿维菌素) 在0~25.92 mg/L以及六元组合 (啶虫脒+毒死蜱+三唑磷+多菌灵+高效氯氟氰菊酯+阿维菌素) 在0~57.48 mg/L暴露条件下其抑制效应表现为线性变化,即随着组合农药质量浓度升高,细胞存活率呈线性降低。本研究对农产品中农药多残留的体外细胞毒性进行了评估,明确了不同农药多残留组合对HepG2人肝癌细胞增殖的抑制作用剂量-效应关系,可为进一步探索农药多残留的细胞毒性机制和开展食品安全风险评估提供依据。     

毒死蜱和甲氰菊酯对家蚕毒性与安全评价研究

通过食下毒叶法和接触法测定了毒死蜱和甲氰菊酯对家蚕的毒性。结果表明:食下毒叶法对2龄起蚕的LC50(48h)分别为:毒死蜱2.3322mg/kg桑叶和甲氰菊酯0.1522mg/kg桑叶,其浸渍桑叶的药液浓度分别为4.6622mg/L和0.3044mg/L。接触法中毒死蜱和甲氰菊酯对2龄起蚕的LC50值(24h)分别为:6.32μg/cm2和0.92μg/cm2。毒死蜱和甲氰菊酯的毒性比都<1,对家蚕的毒性为高毒。     

毒死蜱和甲氰菊酯对蜜蜂毒性与安全评价研究

通过接触法和摄入法测定了毒死蜱和甲氰菊酯对蜜蜂的毒性。结果表明，毒死蜱和甲氰菊酯对蜜蜂的接触毒性(24h LD50)分别为0．1634μg／蜂和0．0501μg／蜂，胃毒毒性(24h LE50)分别为0．6406mg／L和7．8261mg／L。根据Atkins毒性等级划分标准，毒死蜱和甲氰菊酯对蜜蜂的毒性均为高毒，应禁止在蜜蜂活动区域使用。     

昆虫病原线虫H06与化学杀虫剂对韭菜迟眼蕈蚊的联合作用

为合理协调生物防治与化学防治,在室内测定了昆虫病原线虫与杀虫剂的联合作用。结果表明,昆虫病原线虫Heterorhabditis bacteriphora H06(150~300条/虫)对韭菜迟眼蕈蚊Bradysina odoriphaga幼虫(韭蛆)的侵染致死率为1.2%~23.8%。4种杀虫剂对韭蛆的LC50值为0.34 ~8.79 mg/L,毒力大小依次为楝素>毒死蜱>辛硫磷>吡虫啉;杀虫剂对H06线虫的LC50值为595 ~4 388 mg/L。将H06线虫(150条/虫)分别与4种杀虫剂混合处理韭蛆,韭蛆死亡率明显高于线虫和杀虫剂单用处理。药后2 d,辛硫磷12.5 ~100 mg/L+H06处理的韭蛆死亡率为73.0% ~82.0%,辛硫磷单用时死亡率为38.0% ~60.0%;楝素0.16 ~1.25 mg/L+H06处理的死亡率为90.0% ~97.5%,楝素单用时的死亡率为13.8% ~37.5%;毒死蜱15 ~120 mg/L和吡虫啉1.56 ~12.54 mg/L单用时韭蛆的死亡率分别为14.0% ~28.0%和0% ~7.5%,与H06线虫混用处理的死亡率分别为50.0% ~65.0%和58.8% ~80.0%。药后5 d,毒死蜱和吡虫啉与H06线虫对韭蛆的联合致死率分别达87.0% ~95.0%和61.3% ~88.8%。结果表明,昆虫病原线虫与上述4种杀虫剂联合防治韭蛆具有更好的效果。     

近两年贵州省白背飞虱的抗药性现状

采用稻茎浸渍法测定了2013年和2014年采自贵州省贵阳、平坝、遵义、黔西、平塘及玉屏6地白背飞虱种群对8种杀虫剂的敏感性。测定结果表明,白背飞虱对噻虫嗪的敏感性最高,LC50值为0.060~0.93 mg/L(平均0.33mg/L);其次为吡虫啉、毒死蜱、环氧虫啶和噻嗪酮,其LC50值分别为0.080~2.84mg/L(平均1.03mg/L)、1.09~3.89 mg/L(平均2.27 mg/L)、0.59~10.07 mg/L(平均2.71 mg/L)和0.28~18.15 mg/L(平均4.96mg/L);白背飞虱对敌敌畏、吡蚜酮和异丙威的敏感性相对较低,LC50值为0.89~57.96mg/L,LC50平均值分别为10.03、12.16和22.44mg/L。两年抗药性检测结果表明,贵州省6地白背飞虱种群对吡蚜酮、噻嗪酮和吡虫啉表现出低至中等水平的抗性,而对其余5种药剂仍较敏感。     

农药和重金属复合污染物对大型溞的毒性效应

农药和重金属作为水环境中两类常见的污染物,其复合污染已经对水体生态和人类生存环境构成严重威胁。作者研究了3种常用农药（毒死蜱、三唑磷、氟虫腈）及2种常见重金属（铅、镉）对大型溞的急性毒性,同时采用五因素五水平二次通用旋转组合设计方案,研究了复合污染物体系对大型溞的联合毒性效应。结果表明:毒死蜱、三唑磷、氟虫腈、铅离子和镉离子对大型溞的48 h-EC50值分别为6.30、7.27、2.17、454.97和1 175.74 μg/L;5种污染物对大型溞的毒性效应贡献值依次为镉离子 > 三唑磷 > 氟虫腈 > 毒死蜱 > 铅离子;复合污染物对大型溞的毒性呈现出一定的相加效应;当水中毒死蜱质量浓度为0.81 μg/L、三唑磷为17.22 μg/L、氟虫腈为5.65 μg/L、铅离子为83.75 μg/L、镉离子为3 793.15 μg/L时,复合污染物毒性的理论协同效应最大。研究结果可为复合污染物风险评估提供参考。     

含酰腙结构的新型吡唑酰胺衍生物对小菜蛾的生物活性

采用浸虫法、夹毒叶片法和叶碟法分别测定了13个含酰腙结构的新型吡唑酰胺衍生物对小菜蛾3龄幼虫的触杀、胃毒和拒食活性。结果表明:该类化合物对小菜蛾3龄幼虫具有较高的胃毒和拒食活性,其中苯环上含有氯原子、且酰腙一端的取代基含有杂原子且体积较小的化合物 H7的胃毒和拒食活性最好,明显高于对照药剂毒死蜱。H7 72 h胃毒作用LC50值为0.6 mg/L(毒死蜱的LC50值为7.4 mg/L);有10个化合物的拒食活性高于毒死蜱,其中 H7 48 h的拒食中浓度(AFC50) 最低,为0.6 mg/L,明显低于毒死蜱(AFC50=6.5 mg/L)。供试化合物对小菜蛾3龄幼虫均无触杀活性。     

三种常用农药对环棱螺、圆田螺和河蚬的急性毒性研究

采用急性毒性试验方法,研究了3种常用农药毒死蜱、丁草胺和三唑酮对3种本地底栖生物环棱螺Bellamya quadrata、圆田螺Cipangopaludina cathayensis和河蚬Corbicula fluminea的毒性效应,同时测定了螺类不同大小个体对供试农药的敏感性。结果显示:毒死蜱、丁草胺和三唑酮对环棱螺的96 h-LC50值分别为4.32、3.62和15.2 mg/L,对圆田螺的96 h-LC50值分别为6.31、4.31和16.9 mg/L,对河蚬的96 h-LC50值分别为8.75、6.83和26.5 mg/L;毒死蜱和丁草胺对3种供试生物均为中等毒性,三唑酮属低毒。环棱螺幼螺对毒死蜱、丁草胺和三唑酮的敏感性分别比大螺高2.52、1.84和1.72倍,圆田螺幼螺对毒死蜱、丁草胺和三唑酮的敏感性分别比大螺高2.26、2.26和2.67倍。因此,在田间使用3种供试农药时需注意对供试底栖生物尤其是其幼体的保护。     

氟铃脲对韭菜迟眼蕈蚊不同虫态的致毒特点及毒力

为明确氟铃脲对韭菜迟眼蕈蚊不同虫态的致毒特点及毒力,采用胃毒触杀联合毒力法、药液定量滴加法及药膜法分别对韭菜迟眼蕈蚊卵、幼虫、蛹、成虫进行了生物测定。结果表明,经氟铃脲处理的0.5~1、1.5~2和2.5~3日龄韭菜迟眼蕈蚊卵至孵化24 h后,LC_(50)依次为2.27、1.60和0.64 mg/L,对1.5~3日龄卵的毒力高于对0.5~1日龄卵;经氟铃脲处理的2日龄卵、2龄幼虫、4龄幼虫、1日龄和3日龄蛹至羽化时LC_(50)分别为0.06、0.30、0.34、24.05和27.42 mg/L,毒力程度随韭菜迟眼蕈蚊发育而逐步下降;对蛹和成虫毒力较低,100 mg/L氟铃脲染毒1、3日龄蛹的羽化率分别高于10%和20%;药膜法100、1 000 mg/L氟铃脲处理成虫24 h,校正死亡率低于20%。研究表明,氟铃脲对韭菜迟眼蕈蚊各虫态的生长发育均有不利影响,抑制卵的孵化并导致初孵幼虫存活率降低;对幼虫毒杀作用较慢,对蛹及成虫阶段毒力较低。     

Toxicity of chlordimeform and amitraz to the egyptian cotton leafworm (Spodoptera littoralis) and the tobacco budworm (Heliothis virescens)

The relative toxicity (μg a.i. g^?1 body wt) of the formamidine insecticide chlordimeform (CDM) and the triazapentadiene insecticide amitraz was examined in two species of noctuid moth Spodoptera littoralis and Heliothis virescens. When applied topically, there was an unexpected and marked difference in the toxicity of CDM base and its hydrochloride to adults of both species, the salt being appreciably more toxic. For H. virescens at least, this difference in toxicity could not be explained by differences in penetration. This trend was reversed for larval instars of S. littoralis; while there was relatively little difference in the toxicity of the base to adult and larval stages, the salt was at least 1000-fold more toxic to adults than to larvae. N¹-Demethylchlordimeform (DCDM) was the only metabolite of CDM to show biological activity against either species, but was much less toxic than the parent compound. Amitraz was far less toxic than either CDM or DCDM; like the CDM salt, it appeared to be more toxic to adult than larval stages of S. littoralis. Application of piperonyl butoxide significantly increased the toxicity of the CDM salt, DCDM and amitraz to adult H. virescens, the synergist being particularly effective with DCDM and amitraz. In contrast, piperonyl butoxide had no significant effect on the toxicity of DCDM, and slightly antagonised the toxicity of DCDM to fourth-instar larvae of S. littoralis.     

毒死蜱微球和乳油在水中的消解动态及其对白纹伊蚊幼虫的毒力

室内条件下,研究了不同浓度毒死蜱微球和毒死蜱乳油在水中的消解动态及其对白纹伊蚊Aedes albopictus 3龄幼虫的持续毒杀作用。结果表明:毒死蜱微球在水中的消解速率比乳油慢,半 衰期比乳油的长,高浓度微球和乳油的消解半衰期均长于低浓度下的消解半衰期。有效成分为1.2、 12和24 mg/L的毒死蜱微球和毒死蜱乳油在水中的消解半衰期分别为(19.4±2.1) d、(27.8±1.6) d、(31.0±1.7) d和(12.8±1.0) d、(16.1±0.9) d、(19.7±1.1) d;毒死蜱微球对白纹伊蚊3龄幼虫的毒杀作用强于乳油且持效期长,1.2 mg/L的毒死蜱微球水解85 d后处理白纹伊蚊3龄幼虫的死亡率高达76.6%,高于相同浓度、相同条件乳油的处理(53.3%),具有良好的持效性。     

亚致死浓度毒死蜱对小麦禾谷缢管蚜生长和繁殖的影响

为探讨毒死蜱对小麦禾谷缢管蚜Rhopalosiphum padi(Linnaeus)的亚致死效应,采用玻璃管药膜法确定了其亚致死浓度(LC10、LC20和LC30),并研究了该浓度下毒死蜱对小麦禾谷缢管蚜生长和繁殖的影响。结果表明:以LC10、LC20和LC30浓度处理后,禾谷缢管蚜成蚜的寿命分别为(8.60±0.22)、(8.03±0.18)和(6.68±0.18)d,均显著短于对照的(10.36±0.31)d;单雌产仔量分别为(21.88±0.63)、(20.41±0.53)和(16.68±0.35)只,也均显著少于对照的(26.40±0.89)只;产仔历期分别为(7.55±0.22)、(6.69±0.17)和(5.64±0.15)d,均显著短于对照的(9.13±0.31)d;试验浓度药剂处理对下一代若蚜期的影响不显著;LC30浓度处理对下一代成蚜繁殖有显著的抑制作用,可减少单雌产仔量3.74只,缩短产仔历期1.39 d。生命表参数分析表明:LC30浓度毒死蜱处理使小麦禾谷缢管蚜的净增殖率(R0)比对照降低了34.71%,使种群加倍时间(t)比对照延长了17.37%;LC20浓度处理使小麦禾谷缢管蚜的平均世代历期(T)延长了12.59%;LC10浓度处理组各项指标与对照间无显著性差异。研究表明,亚致死浓度毒死蜱能够缩短小麦禾谷缢管蚜成蚜的寿命,降低其繁殖力,该结果对小麦禾谷缢管蚜综合防治策略的制定具有积极意义。     

Oxidative stress, steroid hormone concentrations and acetylcholinesterase activity in Oreochromis niloticus exposed to chlorpyrifos

We investigated the endocrine disrupting effects of chlorpyrifos-ethyl which is suspected to be originated from oxidative stress. Initially, the 96 h LC₅₀ values of chlorpyrifos in juvenile and adult of Oreochromis niloticus were determined to be 98.67 μg/L and 154.01 μg/L, respectively. Sub-lethal concentrations of chlorpyrifos-ethyl (5 ppb, 10 ppb, 15 ppb) were administrated to adult fish for 15 and 30 days. Fish were then left to depurate for 15 days in pesticide-free water. Gonadal somatic indices, serum sex steroids as indicators of reproductive function and cortisol level as indicator of stress condition were measured to observe the endocrine disruption effects of chlorpyrifos-ethyl. Gonadal glutathione S-transferase and antioxidant enzyme activities and lipid peroxidation as indicators of oxidative stress were also measured. Acetylcholinesterase activity was measured as a marker of chlorpyrifos toxicity. Results showed that serum estradiol, testosteron and cortisol levels in fish exposed to chlorpyrifos were lower than those of the control fish while gonad somatic indices did not change during the experiments. After 30 days, chlorpyrifos exposure decreased GST activity, and increased SOD enzyme activity by up to 215-446% compared with the control, suggesting there was a oxidative stress. No statistically significant differences between GPx and CAT specific activities, protein contents and lipid peroxidation were determined between control and treatment groups in all exposure concentrations and periods. Acetylcholinesterase activity decreased (45.83-77.28%) in gonad tissues. After recovery serum estradiol and testosteron levels were similar to those of the control levels. An increase in the GST and SOD enzyme activities were determined. Cortisol level and AChE activity in all exposure groups decreased after the depuration period, and fish were unable to overcome the stress of chlorpyrifos. Thus, this study revealed that after chlorpyrifos treatments there exists a protective function of antioxidant enzymes against lipid peroxidation in gonad tissue of O. niloticus. There also exist lower testosteron and estradiol levels in exposed fish than those of the control fish without any alterations in oxidative stress, which is attributed to the capability of chlorpyrifos to impair steroid hormone levels.     

Residual sprays for the control of the crazy ant Anoplolepis longipes (Jerd.) in the seychelles

Attempts to find suitable quick-acting toxic sprays, for the control of Anoplolepis longipes (Jerd.) in buildings, involved investigations of the toxicity and weathering properties of several insecticide formulations. Their mammalian toxicity was also considered and, particularly for indoor applications, their odour and non-staining properties. Bendiocarb, gamma-HCH and chlorpyrifos were particularly effective, killing ants rapidly after minimal contact with spray deposits, but gamma-HCH and chlorpyrifos weathered better than bendiocarb and were therefore more suitable for outdoor applications.     

Toxicity of selected insecticides to the two-spot ladybird <Emphasis Type="Italic">Adalia bipunctata</Emphasis>

The toxicity of pirimicarb, imidacloprid, dimethoate, lambda-cyhalothrin, flonicamid and spinosad to the two-spot ladybird, Adalia bipunctata, was evaluated in a laboratory study. Susceptibility of fourth instars and female adults was assessed by measuring toxicity via residual contact and ingestion through feeding on contaminated green peach aphids (Myzus persicae). Flonicamid and spinosad had no lethal effects on larvae and female adults. Pirimicarb was harmless to the predator by ingestion exposure but showed some residual toxicity at high concentrations to both larval and adult stages. Imidacloprid was highly toxic to the larval stage by residual and ingestion exposure but caused very low adult mortality when ingested through contaminated prey. Dimethoate and lambda-cyhalothrin were highly toxic to both the larval and adult stages of the ladybird. Our findings indicate that pest management programs in agricultural crops using dimethoate, lambda-cyhalothrin and, to a lesser degree, imidacloprid, are detrimental to A. bipunctata, whereas pirimicarb, flonicamid and spinosad are more compatible with the use of this predator.     

Fumigant toxicity of essential oils fromLaurus nobilis andRosmarinus officinalis against all life stages ofTribolium confusum

The essential oils from rosemary (Rosmarinus officinalis L.) and laurel (Laurus nobilis L.) obtained from Mersin Province in Turkey, were tested for their fumigant toxicity against all life stages of confused flour beetle (Tribolium confusum du Val.). GC-MS analysis showed that 1,8-cineole was found to be the major component of both rosemary and laurel essential oils. Vapors of rosemary and laurel essential oils were toxic to all life stages ofT. confusum. Only 65% mortality of the eggs was achieved when exposed to a dose of 172.6 mgl ⁻¹ air of rosemary essential oil at the longest exposure period (144 h); at the same dose, the pupae were the most resistant stage, with LT₉₀ (lethal time) value of 120.2 h. The adults were the most resistant stage to laurel essential oil, with LT₉₀ value of 77.2 h. On the basis of LT₉₀ values, tolerance of the life stages ofT. confusum to rosemary and laurel essential oils was, in descending order: pupa < larva < adult, and larva < adult < egg < pupa, respectively. Based on the concentration × time (Ct) products (g hl ⁻¹), rosemary essential oil was more toxic than laurel to the adults and larvae ofT. confusum. However, laurel essential oil was more toxic than rosemary to the eggs and pupae. Since these essential oils need such high Ct products to obtain complete mortality ofT. confusum compared with the most commonly used commercial fumigants, it would be impossible to use them on their own as a commercial fumigant against stored-product insects.     

甜菜夜蛾细胞色素P450(CYP9A11)与3种杀虫剂的结合机理研究

细胞色素P450(以下简称CYP)与昆虫的抗药性密切相关。本研究运用AutoDock分子对接技术和分子力学泊松-波尔兹曼表面积法(molecular mechanics Poisson-Boltzmann surface area,MM-PBSA)结合自由能计算方法,分析了甜菜夜蛾CYP9A11与3种杀虫剂结合的作用位点、作用力类型和大小。结果表明:CYP9A11与毒死蜱结合形成两个氢键,有8个氨基酸残基参与形成疏水作用力,二者结合自由能为-3659.80 kJ/mol;CYP9A11与灭多威结合形成5个氢键,有3个氨基酸残基形成疏水作用力,结合自由能为-470.92 kJ/mol;CYP9A11中有7个氨基酸残基与氯氰菊酯结合形成疏水作用力,结合自由能为-473.44 kJ/mol。范德华力是CYP9A11与毒死蜱结合的主要驱动力,极性溶剂化能是CYP9A11与氯氰菊酯和灭多威结合的主要驱动力,这些结果为阐明甜菜夜蛾CYP9A11与3种杀虫剂的结合机理提供了参考。