Cross resistance to juvenile hormone analogues in insecticide-resistant strains of Musca domestica L

Five juvenile hormone analogues (JHAs) were tested by topical application to prepupae of a susceptible (S) and 8 insecticide-resistant (R) strains of the housefly. Activity was measured by the inability to completely emerge from the puparium. Aitosid (isopropyl 11-methoxy-3,7,1l-trimethyldodeca-2,4-dienoate) was the most active compound against the S strain (ED₅₀ 0.0033 μg/prepupa) followed by Ro 7-9767 [6,7-epoxy-3,7-diethyl-(3,4-(methylenedioxy)phenoxy)-2-cis/trans-octene], R-20458 [trans l-(4-ethylphenoxy)-6,7-epoxy-3,7-dimethyl-2-octene], sesamex, and NIA 23509 (10,11 -epoxy-N-ethyl-3,7,11-trimethyI-2,6-dodecadienamide). The R strains, designated by the name of the selecting insecticide, have been under pressure for over 10 years and are considered maximally resistant. The dimethoate-R and OMS-15-R (carbamate-resistant) strains exhibited high levels of cross resistance to all JHAs often exceeding 100x at the ED₉₅ The fenthion-R strain showed high cross resistance toward all JHAs except Altosid, toward which it manifested an intermediate level (17.5x). The DDT/lindane-R demonstrated only negligible tolerance to Aitosid but an intermediate response to all the other JHAs. The OMS-12-R strain (phosphoramidothioate-R) exhibited intermediate to high levels of cross resistance toward all JHAs, whereas the parathion-R, Chlorthion-R and a multi-resistant field-collected strain showed only low to intermediate levels of cross resistance. On the basis of known degradative mechanisms of the OMS-15-R strain, mixed function oxidases apparently play an important role in deactivating JHAs.     

The metabolism of R-20458 [(E)-6,7-epoxy-1-(4-ethylphenoxy)-3,7-dimethyl-2-octene] in rat hepatocyte suspensions

The metabolism of R-20458 [(E)-6,7-epoxy-1-(4-ethylphenoxy)-3,7-dimethyl-2-octene] by rat hepatocytes has been analyzed and compared with that of juvenile hormone I [methyl-(E,E)-cis-10,11-epoxy-7-ethyl-3,11-dimethyl-2,6-tridecadienoate] under identical conditions. The metabolism of R-20458 is characterized by the predominance of NADPH-dependent cytochrome P-450 and epoxide hydrolase reactions; whereas, JH I is metabolized mainly by carboxylesterase, epoxide hydrolase, and glutathione S-transferases. The metabolites of R-20458 have been shown to correspond to (E)-6,7-epoxy-1-(4-hydroxyethylphenoxy)-3,7-dimethyl-2-octene; (E)-6,7-epoxy-1-(4-acetylphenoxy)-3,7-dimethyl-2-octene; (E)-6,7-dihydroxy-1-(4-ethylphenoxy)-3,7-dimethyl-2-octene; and, (E)-6,7-dihydroxy-1-(4-acetylphenoxy)-3,7-dimethyl-2-octene. The production of the α-hydroxyethyl, p-acetylphenoxy, and acetylphenoxy-6,7-diol metabolites is markedly inhibited by SKF 525-A. No dramatic effects are produced by diethylmaleate and 1,2-epoxy-3,3,3-trichloropropane.     

Pyridyl terpenoid ethers with high juvenile hormone activity

Pyridyl terpenoid ethers have outstanding juvenile hormone activity in Tenebrio molitor compared with their phenyl analogues (6,7-epoxy-3,7-dimethyloct-2-enyl 6-ethyl-3-pyridyl ether and 7-ethoxy-3,7-dimethyloct-2-enyl 6-ethyl-3-pyridyl ether are active at 100 pg/larva). The compounds were also active in Galteria mellonella and Culex pipiens.     

Effects of some insect development inhibitors on mosquito larvae

The compounds tested were isopropyl (±)-(E,E)-11 -methoxy-3,7,11-trimethyl-dodeca-2,4-dienoate (ZR 515) and 6,7-epoxy-3-ethyl-7-methylnonyl 4-ethylphenyl ether (R 20458) (two juvenile hormone mimics); 2,6-di-tert-butyl-4-(αα-dimethyl-benzyl)phenol (MON 0585) (which inhibits melanisation during pupation); diflubenzuron and 1-(4-chlorophenyl)-3-(2,6-dichlorobenzoyl)urea (PH 60:38) (which affect chitinisation during moulting); and (E)-oct-2-enoic acid and (E)-non-2-enoic acid (all of which are claimed to have “teratogenic” effects on insects). The relative potencies of these chemicals were assessed on eggs, larvae and pupae of several mosquito species. Their characteristic delayed harmful effects are described and related to various stages of metamorphosis.     

Albumin and cytochrome P450 binding characteristics of juvenile hormone and its analogs

Binding data were gathered for the cecropia juvenile hormone (methyl(E, E cis)-10,11-epoxy-7-ethyl-3,11-dimethyl-2,6-tridecadienoate) and two of its analogs {isopropyl(2E, 4E)-11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate; (E)-4-[(6,7-epoxy-3,7-dimethyl-2-nonenyl)-oxyl]-1,2-(methylenedioxy)benzene} with bovine serum albumin and rat hepatic microsomal cytochrome P₄₅₀. The proteins were found to bind the juvenile hormone and juvenile hormone analogs with affinity constants ranging from 10⁵ to 10⁶M^?1. Thermodynamic calculations suggest that the binding of all three compounds is electrostatic in nature and that the size of the ether and ester substituents can greatly influence the binding to proteins. The juvenile hormone and its analogs all formed spectrally apparent Type I complexes with oxidized cytochrome P₄₅₀; one of the juvenile hormone analogs formed a spectrally observable product adduct with reduced cytochrome P₄₅₀. The product complex may contribute many of the hormonal effects observed for this compound.     

Insect juvenile hormones: Induction of detoxifying enzymes in the housefly and detoxication by housefly enzymes

The cecropia juvenile hormone and three of its analogs were compared as inducers of microsomal epoxidase, O-demethylase, and DDT dehydrochlorinase in the housefly, Musca domestica L. The compounds were the cecropia juvenile hormone, methoprene, hydroprene, 6,7-epoxy-3,7-diethyl-1-[3,4-(methylenedioxy)phenoxy]-2-octene, and piperonyl butoxide, a well known insecticide synergist. The compounds were administered by feeding at levels up to 1% in the diet for 3 days to 1-day-old female adults. Enzymes were then prepared and assayed for their activity using heptachlor, p-nitroanisole, and DDT as substrates.There was approximately a twofold increase in the microsomal oxidases and a 50% increase in DDT dehydrochlorinase after the treatment with the cecropia juvenile hormone, while methoprene had some activity as an inducer of the epoxidase (30% increase) but no activity in the case of the O-demethylase or the dehydrochlorinase. Hydroprene had no effect on any of the enzyme systems, while 6,7-epoxy-3,7-diethyl-1-[3,4-(methylenedioxy)phenoxy]-2-octene was an inhibitor of the two microsomal oxidases. The latter compound and piperonyl butoxide were strong inducers of DDT dehydrochlorinase, causing approximately twofold increases in the activity of this enzyme.There was evidence that the microsomal preparations were able to metabolize and inactivate methoprene and hydroprene, the action being oxidative in the case of methoprene and both oxidative and hydrolytic in the case of hydroprene. The oxidative metabolism of the two juvenile hormone analogs by the microsomal preparations was inducible by the cecropia juvenile hormone and by phenobarbital and dieldrin.     

Bimodal effect of methylenedioxyphenyl compounds on detoxifying enzymes in the housefly

Thirteen methylenedioxyphenyl (MDP) compounds, including commercial insecticide synergists and juvenile hormone analogs, were compared in their effect on detoxifying enzymes in the housefly (Musca domestica). Flies were fed a diet containing 1% of the compounds for 3 days. Enzymes were then assayed in vitro for their activity using aldrin and DDT as substrates. Piperonyl butoxide (PB), sesamex, propyl isome, sulfoxide, safrole, isosafrole, 6,7-epoxy-3,7-diethyl-1-[3-4(methylenedioxy) phenoxy]-2-octene (MDP-JH I) and 6,7-epoxy-3-methyl-7-ethyl-1-[3,4-(methylenedioxy) phenoxy]-2-octene (MDP-JH II) all caused a bimodal effect, inhibiting microsomal epoxidase and inducing DDT-dehydrochlorinase in the resistant Isolan-B strain. Two of these, PB and MDP-JH I, gave similar results with the susceptible strain, stw;w⁵ and two resistant strains, Fc-B and Orlando-DDT. However, o-safrole, piperonylic acid, piperonal, 3,4-methylenedioxybenzyl acetate and methyl-(3,4-methylenedioxy) benzoate had little or no effect on the enzyme systems studied. The standard susceptible strain (WHO-SRS) responded to these compounds very differently. Among those tested, piperonyl butoxide, sesamex, safrole, and isosafrole were inducers of microsomal epoxidase, a 4-fold increase occurring after treatment with sesamex. Only MDP-JH II showed a marked inhibition of the epoxidase. These treatments did not effect DDT-dehydrochlorinase activity in this strain.The enhancement of DDT-dehydrochlorinase activity by the MDP compounds is associated with an increased rate of DDT dehydrochlorination in vivo. The stimulatory effect could be blocked by treatment with actinomycin D or cycloheximide.     

6,7-亚甲二氧基硫代苯并二氢吡喃-4-酮衍生物的合成及抑菌活性

以亚甲二氧基苯为起始原料,经过溴化、硫化、环化等反应合成了19个未见文献报道的6,7-亚甲二氧基硫代苯并二氢吡喃-4-酮衍生物,其结构均经核磁共振氢谱和质谱确认。初步抑菌活性测试结果表明,在50 mg/L下,目标化合物对供试7种植物病原菌均有不同程度的抑制作用,其中化合物5b、5i、5k和5l对马铃薯干腐病菌 Fusarium solani的抑制率均达75%以上,5h和5i对番茄灰霉病菌Botrytis cinerea的抑制率分别是67.7%和70.4%。     

香豆素类化合物对朱砂叶螨的触杀活性及定量构效关系研究

采用玻片浸渍法,测定并筛选了25种具有代表性的香豆素类化合物对朱砂叶螨Tetranychus cinnabarinus雌成螨的触杀活性,并构建了一个预测能力较强的定量构效关系(QSAR)模型。结果表明:所有供试化合物对朱砂叶螨均具有触杀活性,且随着处理时间的延长活性升高。处理48 h后,LC50值低于1000 mg/L的化合物有8个,分别是3-(2-苯并咪唑)-7-(二乙氨基)香豆素(1)、3-(2-苯并噻唑)-7-(二乙氨基)香豆素(2)、3-氨基香豆素(3)、3-乙酰基香豆素(4)、4-甲氧基香豆素(5)、6-硝基香豆素(8)、6,7-二甲氧基香豆素(13)和7,8-二羟基香豆素(21),其中化合物1、2、3、5和13的杀螨活性优于药剂对照螺螨酯或与其活性相当;活性最好的化合物为13,处理48 h和72 h后LC50值分别为284.8和122.2 mg/L,其毒力约为螺螨酯的2倍。通过计算得到25种香豆素类化合物的34种物化参数,以此为描述子,经过SPSS相关性剔除、逐步回归分析和校正,得到一个以扭转力、取向力、总能量和分子半径为自变量的QSAR模型,该模型复相关系数R达到0.987,复判定系数R2也达到0.967,通过F检验证明上述模型具有较高的预测能力。     

Lethal doses of ozone for control of all stages of internal and external feeders in stored products

BACKGROUND: Gaseous ozone (O₃) has potential for control of insects in stored grain. Previous studies have focused on freely exposed insects. Immatures of internal pests (e.g. Sitophilus spp. and most stages of Rhyzopertha dominica F.) are protected within kernels and probably require higher doses and/or longer treatment times for full control. A laboratory study determined the doses of ozone necessary for full control of freely exposed and internal stages of eleven stored‐product pest species. Test insects were three species of Sitophilus, R. dominica, Tribolium confusum Jacquelin du Val, T. castaneum Herbst, Plodia interpunctella Hübner, Sitotroga cerealella Olivier, Oryzaephilus surinamensis L., Ephestia kuehniella Zeller and Stegobium paniceum L. Insects were exposed to continuous flows of ozone in doses of 10–135 ppm and exposure times of 5–8 days. Dose‐mortality bioassays were conducted on three species of Sitophilus and P. interpunctella. RESULTS: Freely exposed stages (with a few exceptions) were controlled with 35 ppm of ozone for 6 days. Full mortality of internal stages within kernels required exposure to 135 ppm for 8 days. CONCLUSION: This study confirms that higher doses and/or longer treatment times are necessary for control of internal stages of stored‐product pests. Copyright © 2012 Society of Chemical Industry     

Large-area field application confirms the effectiveness of toxicant-infused bait for managing Helicoverpa armigera (Hübner) in maize fields

The cover image is based on the Research Article Large-area field application confirms the effectiveness of toxicant-infused bait for managing Helicoverpa armigera (Hübner) in maize fields by Liying Wang et al., https://doi.org/10.1002/ps.7756 .

     

新化合物天维菌素的杀虫杀螨活性

为明确天维菌素(tenvermectin)的杀虫杀螨活性,分别测定了其对小菜蛾Plutellaxylostella (药膜法)、粘虫Mythimna separate Walker (小叶碟添加法)、棉铃虫Helicoverpaarmigera Hübner (饲料混药法)、松材线虫Bursaphelenchus xylophilus (浸渍法)和朱砂叶螨Tetranychus cinnabarinus (叶片浸渍法和玻片浸渍法)的室内毒力,并采用叶碟喷雾法测定了其对朱砂叶螨的盆栽药效。结果表明:天维菌素对鳞翅目害虫小菜蛾、粘虫和棉铃虫的LC50值分别为22.21、19.66和22.09 mg/L,对松材线虫的LC50值为1.94 mg/L,毒力显著高于米尔贝霉素(P50值分别为0.0051和0.0089 mg/L。盆栽试验结果表明:0.2 mg/L的天维菌素药后5 d对朱砂叶螨的防效最高,达97.42%;药后7 d,尽管天维菌素与阿维菌素的防治效果均有所下降,但天维菌素不同浓度(0.0125~0.2 mg/L)处理防效仍保持在80.23%~91.96%之间。研究表明,天维菌素对供试的有害生物均具有较高活性,具有研究开发潜力。     

N-(3,5-二甲氧基-4-烷氧基苯乙基)扁桃酰胺类杀菌剂的设计合成及杀菌活性

以第一个扁桃酰胺类杀菌剂双炔酰菌胺为模板,在炔丙氧基的邻位引入第二个甲氧基,设计合成了15个未见文献报道的 N-(3,5-二甲氧基-4-烷氧基苯乙基)扁桃酰胺类化合物(8a～8o),其结构通过核磁共振氢谱和高分辨质谱确认。初步的离体和活体杀菌试验结果表明,化合物 8e、8h和8o 对辣椒疫霉 Phytophthora capsici 具有较好的杀菌活性,其中 8h和8o 在62.5 mg/L下对辣椒疫霉活体抑制率达100%。     

The effect of some furochromene and benzochromene analogues of 2,2-dimethyl-7-methoxychromene (precocene I) and benzofuran precursors on Oncopeltus fasciatus (dallas) and Locusta migratoria migratorioides (R&F)

As part of an extensive study on insect antijuvenile hormones (AJH) structurally related to 2,2-dimethyl-7-methoxychromene and 6,7-dimeth-oxy-2,2-dimethylchromene (precocenes I and II, respectively), four furophenols, six furochromenes, three benzofuran derivatives and two benzochromenes were tested for biological effects on Oncopeltus fasciatus and Locusta migratoria. Exposure to ajar deposit of the chemical was used for O. fasciatus and topical application in acetone for L. migratoria, with precocenes I and II as standards for comparison. All compounds were toxic to O. fasciatus and in some cases, this may have concealed any potential AJH activity, which was not observed for any compound tested. Toxicity to L. migratoria was less evident and three of the furochromene derivatives, allprecocene-I (PI) analogues, showed AJH activity seven to ten-fold lower than that of PI. Neither of the benzochromenes tested showed any AJH activity. The results are discussed in terms of the known structure-activity relationships for precocene-like AJH activity.     

Synthesis and structure–activity relationships for anticipated molluscicidal activity of some 2-amino-5-substituted pyridine derivatives

A series of 2-amino-5-substituted pyridine derivatives was synthesized and their molluscicidal activity against white garden, Theba pisana (Müller), and brown garden, Helix aspersa (Müller), snails was investigated by two methods of application. Some of these compounds showed strong activity under laboratory conditions against the two types of snail. T pisana was more sensitive to the tested compounds than H aspersa. The most effective compounds were 2-amino-5-(benzotriazole-1-ylmethyl)-3-methylpyridine, 2-amino-5-[1-(benzotriazole-1-yl)nonyl]-3-methylpyridine and 2-[(1,2,4-triazole-1-ylmethyl)amino]-3-methylpyridine which exhibited high molluscicidal activity. The toxicity results are discussed in relation to the chemical structures. © 1999 Society of Chemical Industry     

Development of Fusarium Wilt-resistant Genotypes in Safflower (Carthamus tinctorius)

Screening of 51 promising safflower germplasm lines in Fusarium wilt-infested plots resulted in identification of highly wilt-resistant selections viz., 86-93-36A, 237550, VI-92-4-2 and II-13-2A, with some moderate resistance in HUS-305. Progenies from crosses made using these resistant lines were tested for their reaction to wilt. F₁ progenies from 86-93-36A × 237550 and 86-93-36A × II-13-2A recorded zero wilt incidence, while 237550 × 86-93-36A was highly resistant to the Rajendranagar geographical isolate. The reaction for the three progenies showed stability for wilt resistance with no segregation until the F₇ generation. Geographical isolates of Fusarium oxysporum f. sp. carthami (Foc) were collected from different safflower growing regions and tested for their pathogenic variability on six host differentials under glasshouse conditions. Based on the reaction of the differentials, the Foc isolates were grouped into four biotypes. The three resistant progenies were tested for their reaction to the four biotypes. The progeny of cross 86-93-36A × 237550 showed an immune reaction to all the biotypes, except for a highly resistant reaction to biotype 3. The progenies of the two other crosses (86-93-36A × II-13-2A and 237550 × 86-93-36A) exhibited immune reactions to biotypes 2,3 and 1,3, respectively, and were highly to moderately resistant to biotypes 1,4 and 2,4, respectively.     

Antifeedant activity of a novel 6-(4,7-hydroxy-heptyl) quinone? from the leaves of the milkweed Pergularia daemia on the cotton bollworm Helicoverpa armigera (Hub.) and the tobacco armyworm Spodoptera litura (Fab.)

The effects of crude extracts and an isolated compound from the leaves of milkweed, Pergularia daemia (Forssk) Choiv., on the antifeedant activity against two important lepidopteran pests, Helicoverpa armigera (Hub.) and Spodoptera litura (F.), were studied. Maximum antifeedant activity was recorded in ethyl acetate crude extract against H. armigera (70.3%) and S. litura (71.82%) at 1% concentration. Ethyl acetate crude extract was further subjected to column chromatography, which was performed using hexane as initial solvent and then by increasing the polar strength using ethyl acetate. Fractions collected at hexane and ethyl acetate (80:20) yielded 6-(4,7-hydroxy-heptyl) quinone, a novel compound which showed significant antifeedant activity against H. armigera (80.22% at 2000 ppm) and S. litura (68.31% at 2000 ppm).     

Response of Cucurbita spp. to tomato leaf curl New Delhi virus inoculation and identification of a dominant source of resistance in Cucurbita moschata

Tomato leaf curl New Delhi virus is an emerging whitefly-borne species of begomovirus in Mediterranean regions that poses a severe threat to cucurbit crops of the genus Cucurbita. Until now, only two sources of resistance have been identified in Cucurbita spp., these being PI604506 (cv. Large Cheese) and PI381814 (Indian landrace), both of C. moschata. The resistance of cv. Large Cheese is conferred by a single recessive gene located on chromosome 8. The objective of the present investigation was to screen for tomato leaf curl New Delhi virus (ToLCNDV) resistance among 105 accessions drawn from five species of Cucurbita and, if high resistance was found in any of them, determine the mode of inheritance. Screening was conducted using whitefly-mediated inoculation on all 105 accessions. The accessions showing some resistance were further screened by mechanical inoculation as well as by quantitative PCR-based diagnostics. The results showed that, overall, the accessions of C. pepo and C. maxima were the most susceptible, those of C. argyrosperma and C. ecuadorensis intermediate, and those of C. moschata most resistant to ToLCNDV. Only one accession of C. moschata, BSUAL-252, originating from Japan, was highly resistant to ToLCNDV, showing no symptoms after either method of inoculation, and absence of virus accumulation. Upon crossing BSUAL-252 with a susceptible accession of C. moschata, BSUAL-265, the resistance was observed to be conferred by a single dominant gene. This gene is not linked to the genomic region on chromosome 8 where the locus of the previously identified recessive gene for ToLCNDV resistance resides.     

Rodent tissue residue and secondary hazard studies with bromadiolone1

A series of toxicological, residue, secondary hazard, and environmental fate studies were completed with bromadiolone. The compound was eliminated rapidly after ingestion by Rattus norvegicus and Mus domesticus. In R. norvegicus, 75% of the bromadiolone was eliminated within 4 days. Dead rodents collected from field trials using bromadiolone had residue levels of 1.92 in R. rattus, 1.17 in M. domesticus, and 0.49 ppm in Spermophilus beecheyi. The LD50 for bromadiolone in beagle dogs was calculated at 8.1 mg kg^-1 (10.7 for males and 6.3 mg kg^-1 in females). The approximate LD50 in Canis latrans was 10 mg kg^-1. Dietary LC50 determination compound in Putorius putorius furo was 9.8 ppm. Secondary hazard studies showed the rodenticide to have little potential to snakes and birds of prey if used properly. Field tests with grain and pelleted baits over 21 days demonstrated that the active ingredient degraded by 78 and 45%, respectively.