灰飞虱体内类酵母共生菌异常毕赤酵母的分离培养及其对杀菌剂的敏感性

【目的】随着杀虫剂等化学农药的大规模使用,灰飞虱Laodelphax striatellus的抗药性不断增强,防治效果下降,因此寻找新的防治方法尤为重要。本研究探索使用杀菌剂来减少灰飞虱体内共生菌的数量,以降低灰飞虱的活力,为"抑菌防虫"提供理论依据。【方法】对灰飞虱体内的类酵母共生菌(yeast-like symbiotes,YLS)进行离体培养并鉴定,测定离体培养YLS对不同浓度不同种类杀菌剂的敏感性,将对其抑制作用明显的杀菌剂喷施于麦苗,待灰飞虱取食后统计灰飞虱死亡率、体重,并通过荧光定量PCR检测体内共生菌的数量变化。【结果】离体培养得到1株YLS,经碳源同化实验和18S r DNA分子鉴定,将该菌株归为异常毕赤酵母Pichia anomala,以变性梯度凝胶电泳(denatured gradient gel electrophoresis,DGGE)技术验证了该菌株在灰飞虱体内的存在。对杀菌剂敏感性的测定结果显示,70%丙森锌和50%戊唑醇+25%肟菌酯对P.anomala抑制效果明显,而氟吡菌胺+霜霉威盐酸盐(687.5 g a.i./L)与40%嘧霉胺对P.anomala的抑制效果较差。用对P.anomala抑制效果明显的两种杀菌剂(70%丙森锌和50%戊唑醇+25%肟菌酯)以800 mg/L浓度喷施麦苗,灰飞虱取食喷施麦苗后的死亡率分别达到46.7%与63.3%,显著高于对照,而体重比对照组显著低。荧光定量检测结果表明,灰飞虱体内3种共生菌(Noda菌、季也蒙毕赤酵母和异常毕赤酵母)的数量在使用了各种杀菌剂后均显著降低。【结论】结果说明,体外喷施杀菌剂对灰飞虱体内共生菌有抑制作用,进而对灰飞虱的生长存活产生影响,这为杀菌剂与杀虫剂的协同使用防治灰飞虱奠定基础。     

Logarithmic Transformation is Essential for Statistical Analysis of Fungicide EC50 Values

Half maximal (50%) effective concentration (EC50) values are widely used to express fungicide potency and sensitivity of plant pathogens. This study explored the necessity of logarithmic transformation for statistical analysis of EC50 values. The results demonstrated that without logarithmic transformation, none of the five sets of epoxiconazole EC50 data (n = 26–33) against Sclerotinia sclerotiorum fitted a normal distribution. But after logarithmic transformation, four of the five datasets became normally distributed. Of the five sets of pyraclostrobin EC50 data (n = 29–32), only one dataset fitted a normal distribution. After logarithmic transformation, four datasets became normally distributed. Logarithmic transformation transformed the heterogeneity of variance across the five sets of epoxiconazole EC50 data to homogeneity but failed to improve the heterogeneity of variance across the five sets of pyraclostrobin EC50 data. For 150 isolates' EC50 values to epoxiconazole and 153 isolates' EC50 values to pyraclostrobin, the intervals of arithmetic means ± standard deviations (SD) covered 85.3% and 90.2% of data points, respectively, whereas the intervals of geometric means (*) multiplied/divided by the multiplicative SD (S*) covered 69.3% and 70.9% of data points, respectively, which approximated the theoretical value of 68.3%. Distribution normality and homogeneity of variance are prerequisites for analysis of variance (anova ) and the two parameters could be improved by logarithmic transformation, therefore, power and efficiency of statistical tests on EC50 data will be greatly enhanced by this kind of transformation.     

Tebuconazole Sorption in Contrasting Soil Types

This study investigates the sorption of tebuconazole in contrasting soil types (Rendzic Leptosol, Haplic Arenosol, and Haplic Cambisol). Tebuconazole was used both as an analytical-grade chemical and as a commercial product. Sorption experiments were performed using the batch equilibrium approach. The sorption of analytical-grade tebuconazole in soils was lower compared to the commercial product, with the exception of the Cambisol. The highest sorption was observed for the Cambisol regardless of the tebuconazole form. In the experiment with the commercial formula containing tebuconazole, a higher sorption was observed for the Leptosol compared to the Arenosol; the experiment with analytical-grade tebuconazole showed an opposite trend. The differences in sorption of the commercially available and analytical-grade tebuconazole can be attributed to the additives present in the commercial product. Based on the obtained results, tebuconazole sorption is mainly influenced by soil organic matter and the mineralogical composition, but fungicide composition plays an important role as well. Additives present in the commercial products support fungicide sorption in soils. These findings confirm that tebuconazole is adsorbed in soils with high contents of organic matter and clay minerals and its application to such soils should not lead to risks associated with fungicide leaching.     

Design,synthesis, and biological properties of triazole derived compounds and their transition metal complexes

Triazole derived Schiff bases and their metal complexes (cobalt(II), copper(II), nickel(II), and zinc(II)) have been prepared and characterized using IR, ¹H and ¹³C NMR, mass spectrometry, magnetic susceptibility and conductivity measurements, and CHN analysis data. The structure of L², N-[(5-methylthiophen-2-yl)methylidene]-1H-1,2,4-triazol-3-amine, has also been determined by the X-ray diffraction method. All the metal(II) complexes showed octahedral geometry except the copper(II) complexes, which showed distorted octahedral geometry. The triazole ligands and their metal complexes have been screened for their in vitro antibacterial, antifungal, and cytotoxic activity. All the synthesized compounds showed moderate to significant antibacterial activity against one or more bacterial strains. It is revealed that all the synthesized complexes showed better activity than the ligands, due to coordination.     

Management of the late blight (Phytophthora infestans) disease of potato in the southern hills of India

Late blight of potato is considered to be the most devastating problem causing severe yield losses in potato worldwide. Among the different management strategies, the use of resistant cultivars is the most viable option, but the non‐availability of enough quantity of quality seed materials of resistant cultivars forces the farmers to grow susceptible cultivars with proper fungicide scheduling. Therefore, in the present study, chemical control using fungicide has been attempted with newer molecules in the susceptible cultivar along with a resistant cultivar as a positive control. All the tested fungicides were found safe, and no phytotoxicity was observed with any chemical at the applied rate. In resistant cultivar, no late blight was appeared in both the years, whereas maximum AUDPC was observed in the untreated control (276.3) and minimum (41.7) in mancozeb‐cymoxanil + mancozeb based scheduling which was found on par with chlorothalonil‐famoxadone + cymoxanil (51.3) and chlorothalonil‐ametoctradin + dimethomorph (53.5) based scheduling. Among the treatments, resistant cultivar, Kufri Girdhari followed by chlorothalonil‐ametoctradin + dimethomorph and mancozeb‐cymoxanil + mancozeb based fungicidal scheduling were proven as the best treatments for both the crop seasons resulting in the highest yield parameters. The disease severity showed a strong negative correlation with the tuber yield of potatoes in both the years. Based on overall observations including BC ratio, it can be concluded that, wherever seed material of resistant cultivar is available farmers should grow the same or else with susceptible cultivars the fungicidal scheduling based on mancozeb‐cymoxanil + mancozeb or chlorothalonil‐ametoctradin + dimethomorph can be followed to obtain the maximum returns with effective management of late blight at the southern hills of India.     

Mycolytic effect of fluorescent Pseudomonas in biocontrolling of fungal phytopathogenic Curvularia lunata,Fusarium oxysporum,Alternaria padwickii and Rhizoctonia solani

About 50 bacterial strains, each of Pseudomonas fluorescens, from different rhizospheric soil of different plants were screened for antagonistic activity against Curvularia lunata, Fusarium oxysporum, Alternaria padwickii, Rhizoctonia solani causing black kernel, kernel spotting, root rots, stackburn and sheath blight diseases of rice (Oryza sativa L.). Out of the 50 isolates, 15 isolates were found to be effective in lysing the cell wall of the above-mentioned putative pathogens tested in vitro. These Pseudomonas isolates produced mycolytic enzymes, viz. β-1,3-glucanases, β-1,4-glucanases and lipases. P. fluorescens PAK1 and PAK12 among the strains were more effective for the production of these enzymes while PAK12 produce good level of β-1,3-glucanases, β-1,4-glucanases and lipases against tested fungal pathogens. These findings demonstrate a mechanism of antagonism by P. fluorescens against different fungal plant pathogens.     

Biotoxic effects of Sumisclex and Carbomar fungicides on four Aspergillus species isolated from the rhizosphere of some Taif plants

Abstract

The antifungal activities of two systemic fungicides (Sumisclex and Carbomar) on four rhizospheric Aspergillus species (A. candidus, A. sydawi, A. niger1 and A. niger2) were studied. Also the phytotoxicity against some saudian seeds was analysed. Results indicated that Sumisclex fungicide was more effective on the growth of A. candidus and A. sydawi under laboratory conditions (the IC₅₀ of 3 and 4 ppm were recorded, respectively) than Carbomar where an IC₅₀ of 11 ppm for A. candidus and 35 ppm for A. sydawi were observed. The growth of the two strains of A. niger was completely inhibited by Carbomar even at the lowest 10 ppm concentration. On the other hand results revealed that phytotoxicity was apparently linked with the type of the fungicide and its concentration. However, the root system was more sensitive to the tested fungicides especially at higher concentrations.     

四种杀菌剂对玉米螟赤眼蜂酚氧化酶活性的影响

为明确杀菌剂对玉米螟赤眼蜂Trichogramma ostriniae Pang et Chen毒性大小及其成蜂体内酚氧化酶（phenoloxidase, PO）活性影响, 本实验通过测定三唑酮（triadimefon）、 肟菌脂（trifloxystrobin）、 咪鲜胺（prochloraz）、 申嗪霉素（phenazino-1-carboxylic acid）4种杀菌剂对玉米螟赤眼蜂的急性毒性, 并分别测定活体和离体条件下各杀菌剂处理后酚氧化酶的比活性。结果表明, 各药剂对赤眼蜂的急性毒性大小为： 三唑酮＞咪鲜胺＞肟菌酯＞申嗪霉素, 其LC₅₀值分别为3.27, 6.46, 4.06和 9.72 mg/L, 其安全系数依次为0.07, 0.10, 0.20和1.47, 其中申嗪霉素为中等风险性, 其余3种药剂为高风险性, 且杀菌剂明显激活了PO的活性。活体条件下亚致死剂量处理得到的PO比活力高于离体处理, 且三唑酮处理组具有明显的剂量效应。本实验为研究杀菌剂对赤眼蜂的毒性及对PO的影响作了初步的探索, 为进一步研究赤眼蜂对杀菌剂的抗性及免疫能力奠定基础。     

Click chemistry based synthesis of dopamine D4 selective receptor ligands for the selection of potential PET tracers

Taking advantage of click chemistry, a library of N-arylpiperazinylmethyl triazoles bearing fluoro substituted appendages was synthesized and the target compounds were investigated for dopamine and serotonin receptor binding. With the aim to bias their hydrophilicity and to optimize their D4 receptor affinity and selectivity, a concise series of triazoles containing fluoroalkyl, fluoroalkoxy, fluoroalkoxyphenyl, and deoxyfluoroglucosyl substituents was studied. The D4 receptor affinity and selectivity could be tuned by altering the chemical moiety attached to the triazole unit. Among the test compounds, the fluoroethoxyphenyl derivative 15b showed weak partial agonism at D4 and a K_i value of 14 nM, while its fluoropropoxyphenyl homologue 16a turned out to act as a neutral D4 antagonist (K_i = 5.1 nM). Both, 15b and 16a revealed an excellent balance between D4 receptor affinity and subtype selectivity, providing lead candidates for the development of ¹⁸F-labeled radioligands for D4 receptor imaging studies by positron emission tomography (PET).     

Chemotherapy of leishmaniasis. Part XII: Design,synthesis and bioevaluation of novel triazole integrated phenyl heteroterpenoids as antileishmanial agents

A novel series of triazole integrated phenyl heteroterpenoids have been synthesized and screened for their in vitro activity against intracellular amastigote form of Leishmania donovani. Among all tested compounds, compound 3a was found to be the most active with IC₅₀ 6.4 μM and better selectivity index (SI) 18 as compared to reference drugs, miltefosine and miconazole. When evaluated in vivo in L. donovani/hamster model, 3a has exhibited 79 ± 11% inhibition of parasite multiplication at 50 mg kg^?1 × 5 days on day 7 post treatment.