Systemic nematicidal activity of fluensulfone against the root-knot nematode Meloidogyne incognita on pepper

BACKGROUND: Fluensulfone, a new nematicide of the fluoroalkenyl group, has proved to be very effective in controlling root‐knot nematodes, Meloidogyne spp., by soil application. The systemic activity of this compound against M. incognita on peppers via soil drenching and foliar spray was evaluated. RESULTS: Root application of fluensulfone via soil drenching showed slight and no nematode control activity when applied 4 and 10 days, respectively, after inoculation. A single foliar spray of peppers with a fluensulfone solution at 3.0 g L^?1 prior to inoculation reduced the galling index by 80% and the number of nematode eggs by 73–82% of controls. The reduction in these parameters by fluensulfone was much higher than that obtained with oxamyl or fenamiphos at the same concentration. This activity was also observed when the plants were sprayed 21 days before inoculation. A series of experiments suggested that foliar spray with fluensulfone prior to inoculation reduces nematode invasion. However, foliar spray after inoculation did not inhibit nematode development inside roots. CONCLUSION: Fluensulfone showed relatively high nematode control activity when sprayed on the foliage before inoculation. Fluensulfone may be used as a foliar application, in addition to soil application, for root‐knot nematode control. Copyright © 2011 Society of Chemical Industry     

酸黄瓜南方根结线虫病抗性的解剖学及其细胞学研究

为探明酸黄瓜南方根结线虫病抗性的内在机理,以抗病材料酸黄瓜与感病材料北京截头为试材,对南方根结线虫侵入与幼虫发育、根的解剖学及线虫侵入诱导形成的取食位点的细胞学结构进行了比较研究。结果表明,抗病材料酸黄瓜根系中线虫侵入率极显著低于感病材料北京截头(P0.01),酸黄瓜能够有效抵抗南方根结线虫的侵入;抗、感材料根系中雌雄虫个体比例分别为1∶12和1∶5(P0.01),抗性反应能够抑制线虫取食和幼虫发育;酸黄瓜根的解剖结构与普通栽培黄瓜相似,酸黄瓜的根不具有结构抗性;抗病反应中细胞发生过敏性坏死,感病反应中无此类现象发生。抗侵入、抑制取食和坏死反应是抗病材料酸黄瓜抗性反应的主要特征。     

八角根围土壤真菌种类鉴定及其对南方根结线虫的活性评价

采用平板稀释法分离广西八角根围土壤真菌13个属1 329株, 利用贝氏皿浸渍法对其发酵液进行了杀线虫活性筛选, 计算其对南方根结线虫卵孵化抑制率及对2龄幼虫(J2)致死率的影响。菌株Gisf326、Gisf495和Gisf415发酵液原液对南方根结线虫卵孵化的相对抑制率分别为96.67%、83.33%和73.33%, 发酵液20倍稀释液对J2校正死亡率分别为93.13%、87.81%和93.38%; 经形态学鉴定和ITS序列分析, 3种真菌分别为淡紫拟青霉( Paecilomyces lilacinus )、黑曲霉( Aspergillus niger ) 和日本曲霉( A. japonicus )。本研究为植物线虫病害的防治提供了新的生防真菌资源。     

In vitro and in planta nematicidal activity of Fumaria parviflora (Fumariaceae) against the southern root‐knot nematode Meloidogyne incognita

Root and stem extracts of Fumaria parviflora showed strong nematicidal activity against Meloidogyne incognita in in vitro and in planta experiments. Phytochemical screening of F. parviflora revealed the presence of seven classes of bioactive compounds (alkaloids, flavonoids, glycosides, tannins, saponins, steroids and phenols). Quantitative determination of the plant extracts showed the highest percentages of alkaloids (0·9 ± 0·04) and saponins (1·3 ± 0·07) in the roots and total phenolic contents in the stem (16·75 ± 0·07 μg dry g^?1). The n‐hexane, chloroform, ethyl acetate and methanol extracts of roots and stems at concentrations of 3·12, 6·24, 12·5, 25·0 and 50·0 mg mL^?1, significantly inhibited hatching and increased mortality of second‐stage juveniles (J2s) compared with water controls. Percentage J2 mortality and hatch inhibition were directly related to exposure time. In pot trials with tomato cv. Rio Grande, root and stem extracts at concentrations of 1000, 2000 and 3000 ppm, applied as soil drenches, significantly reduced the number of galls, galling index, eggs masses, eggs and reproduction factor compared with the water control. Regardless of concentration, all the extracts significantly increased the host plant growth parameters studied. The n‐hexane extracts from the roots and stem were the most active, followed by the methanol ones, at all concentrations. The in vitro and in planta results suggest that extracts from the roots and stem of F. parviflora may be potential novel nematicides.     

内生菌荧光假单胞菌DLJ1和蜡状芽胞杆菌SZ5对南方根结线虫胁迫下辣椒植株抗性与产量品质的影响

为了检验内生菌荧光假单胞菌DLJ1和蜡状芽胞杆菌SZ5的促生与提高植株对南方根结线虫的防治效果, 确定合适的菌剂接种方式, 并分析其机制, 本文以杀线剂阿维菌素为对照, 比较了不同接菌方式下DLJ1 和SZ5对辣椒植株在南方根结线虫胁迫下的抗性以及对产量品质的影响?结果证实DLJ1在种子萌发期的一次接菌与萌发期与田间的5次接菌处理均可使根系根结数减少70%以上, 使植株对南方根结线虫的抗性升至高抗级别, 辣椒产量提高超过150%; DLJ1一次接菌处理组的果型最大?Vc与可溶性蛋白含量最高?SZ5萌发期一次处理根结数降低40%, 植株对南方根结线虫表现为中抗, 产量提高60%以上; SZ5多次接菌处理根结数只能降低27%, 产量仅提高6%左右?阿维菌素处理的效果介于DLJ1和SZ5之间, 可降低植株根结数45%, 提高产量49%左右?分析其机理发现, 两菌剂处理均可通过提高植株的POD酶活性和总酚含量, 降低O2-产生速率和MDA积累, 提高光合色素含量等来促进植物生长, 通过提高几丁质酶活性来提高植株对线虫的抗性?总之, 只需要在辣椒种子萌发期进行一次DLJ1接菌处理, 即可使植株获得稳定而显著的促生和防治南方根结线虫双重效果, 提示DLJ1菌在农业生产上的应用前景广阔?     

Insecticidal properties of essential plant oils against the mosquito Culex pipiens molestus (Diptera: Culicidae)

The insecticidal activities of essential oil extracts from leaves and flowers of aromatic plants against fourth-instar larvae of the mosquito Culex pipiens molestus Forskal were determined. Extracts of Myrtus communis L were found to be the most toxic, followed by those of Origanum syriacum L, Mentha microcorphylla Koch, Pistacia lentiscus L and Lavandula stoechas L with LC50 values of 16, 36, 39, 70 and 89 mg litre-1, respectively. Over 20 major components were identified in extracts from each plant species. Eight pure components (1,8-cineole, menthone, linalool, terpineol, carvacrol, thymol, (1S)-(-)-alpha-pinene and (1R)-(+)-alpha-pinene) were tested against the larvae. Thymol, carvacrol, (1R)-(+)-alpha-pinene and (1S)-(-)-alpha-pinene were the most toxic (LC50 = 36-49 mg litre-1), while menthone, 1,8-cineole, linalool and terpineol (LC50 = 156-194 mg litre-1) were less toxic.     

Nematicidal activity of essential oils and organic amendments from Asteraceae against root-knot nematodes

The essential oil of Chrysanthemum coronarium flowerheads showed strong nematicidal activity in vitro and in growth-chamber experiments. Essential oil concentrations of 2, 4, 8 and 16  µ L mL⁻¹, significantly reduced hatch, J ₂ survival (determined by final value and area under curves of cumulative percentage hatch or mortality) and reproduction rate of Meloidogyne artiellia in vitro , with the lowest values occurring at 16  µ L mL⁻¹. In pot trials with chickpea cv. PV 61, essential oil concentrations of 10–40  µ L per 500 cm³ soil, applied on sterile cotton pellets, also significantly reduced the nematode's reproduction rate. The biological processes of mortality and hatching/reproduction were adequately described by the monomolecular and expanded negative exponential models, respectively. Effectiveness of soil amendment with either flowers, leaves, roots or seeds of C. coronarium , and flowers from several species of Asteraceae ( Chrysanthemum segetum , Calendula maritima , Calendula officinalis and Calendula suffruticosa ) at 5 g per 500 cm³ soil was tested for suppression of M. artiellia and growth of chickpea cv. PV 61 under growth-chamber conditions. In these tests, flowers of all five Asteraceae species and various parts of C. coronarium significantly reduced reproduction rates of M. artiellia , by 83·0–95·9%, with the minimum rates occurring in infected chickpea plants amended with flowers of C. officinalis and C. suffruticosa . The in vitro and in planta results suggest that the essential oil of C. coronarium and organic amendments from Asteraceae species may serve as nematicides.     

Larvicidal activity against Plutella xylostella of cordycepin from the fruiting body of Cordyceps militaris

The insecticidal activities of methanol extracts of Cordyceps militaris Link (Ascomycotina: Clavicipitaceae) cultured on fresh pupae of Bombyx mori L against 3rd-instar larvae of Plutella xylostella L were examined using direct contact application. The larvicidal activity was more pronounced in an extract of C militaris fruiting body than in an extract of the pupae separated from the culture. The biologically active constituent of the Cordyceps fruiting body was characterized as cordycepin (3'-deoxyadenosine) by spectroscopic analysis. Responses varied according to dose, exposure time and application method. In a leaf-dipping test, cordycepin at 500 mg litre-1 caused no mortality at 1 DAT (day after treatment) but 78 and 100% mortality at 2 and 4 DAT, respectively, whereas 34 and 88% mortality at 3 and 5 DAT, respectively was observed at 300 mg litre-1. Cordycepin caused body colour change from pale green to dark brown and eventually body lysis. These results suggested that the larvicidal action may be attributable to a direct effect rather than an inhibitory action on chitin synthesis. There was a significant difference in insecticidal activity of cordycepin between leaf dipping (500 mg litre-1) with 100% mortality and topical application (10 micrograms per larva) with 0% mortality, suggesting that cordycepin has stomach action. Cordycepin merits further study as a potential P xylostella control agent or as a lead compound.     

Nicotinic acetylcholine receptor binding of imidacloprid-related diaza compounds with various ring sizes and their insecticidal activity against Musca domestica

Fifteen 5-substituted 1-(6-chloro-3-pyridylmethyl)-2-nitromethylene-1,3- diazacyclohexanes and three other related compounds having a five- or seven-membered ring were synthesized and their biological activities were measured in vivo and in vitro. The insecticidal (in vivo) activity was evaluated against houseflies Musca domestica L under synergistic conditions with propargyl propyl phenyl phosphonate and piperonyl butoxide. The binding activity of each compound to nicotinic acetylcholine receptor in vitro was measured using [125I] alpha-bungarotoxin. The insecticidal activities of the unsubstituted diazacyclohexane analogues were slightly higher than those of the imidazolidine analogues, but the enlargement of ring size to diazacycloheptane lowered the activity. Substitution of 1,3-diazacyclohexane or imidazolidine rings was not generally favourable for the activity, but the unsubstituted 1,3-diazacyclohexane analogue showed the highest binding activity. Ring substitutions and ring enlargement decreased the activity 100-30,000-fold.     

Insecticidal and binding activities of N3-substituted imidacloprid derivatives against the housefly Musca domestica and the alpha-bungarotoxin binding sites of nicotinic acetylcholine receptors

N3-substituted imidacloprid congeners containing C1-C6 alkyl groups or various analogous groups, and their corresponding nitromethylene analogues, were used in this study. Their insecticidal activity against the housefly, Musca domestica, and their binding activity toward the nicotinic acetylcholine receptor were determined. The insecticidal test was conducted using the synergists piperonyl butoxide and propargyl propyl phenylphosphonate. The binding assay was performed with housefly head membrane preparations using radio-labelled alpha-bungarotoxin. Both insecticidal and binding activities were drastically lowered by the introduction of alkyl/allyl groups at the imidazolidine NH sites of both nitroimino and nitromethylene compounds. The binding activity of N3-substituted nitromethylene analogues was much higher than that of the corresponding nitroimino analogues. However, the insecticidal activity of both series of compounds with a given substituent was nearly identical. The insecticidal activity correlated positively with the binding activity after taking into account the structural difference of the nitroimino and nitromethylene moieties and a structural feature of the N3-substituents.     

Binding activity of substituted benzyl derivatives of chloronicotinyl insecticides to housefly‐head membranes,and its relationship to insecticidal activity against the housefly Musca domestica

Variously substituted benzyl derivatives of chloronicotinyl insecticides were synthesized with a wide range of substituents including halogens, NO₂, CN, CF₃ and small alkyl and alkoxy groups at the ortho, meta and para positions, as well as multiple‐substituted benzyl analogues. Their binding activity to the α‐bungarotoxin binding site in housefly (Musca domestica) head membrane preparations was measured. Among the compounds tested, the activity of the meta‐CN derivative was the highest, being 20–100 times higher than those of imidacloprid, acetamiprid and nitenpyram. The synergized insecticidal activity against houseflies was also measured for selected compounds with the metabolic inhibitor, NIA16388 (propargyl propyl phenylphosphonate). For the nitromethylene analogues, including both benzyl and pyridylmethyl analogues, higher binding activity usually resulted in higher insecticidal activity. © 2000 Society of Chemical Industry