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1.
M. A. De Waard J. G. M. Van Nistelrooy 《European journal of plant pathology / European Foundation for Plant Pathology》1980,86(5):251-258
Pyrazophos-resistant strains ofPyricularia oryzae were isolated from sectors in colonies of the fungus on a pyrazophos-containing agar medium. In contrast to the wild-type strain, resistant strains did not metabolize pyrazophos (Afugan, Curamil) into its phosphate analogue and 2-hydroxy-5-methyl-6-ethoxycarbonylpyrazolo(1,5-a)pyrimidine (PP), which is regarded as the fungitoxic principle of pyrazophos. Resistant strains possessed a slightly increased sensitivity to PP. These data indicate that the mechanism of resistance to pyrazophos is not related to a change of the target sites of PP, but rather with inability to convert pyrazophos into PP. The pyrazophos-resistant strains displayed cross-resistance to the organophosphorus fungicides EBP (Kitazin) and edifenphos (Hinosan). The mechanism of cross-resistance involved is not understood.Samenvatting Pyrazofos-resistente stammen vanPyricularia oryzae werden geïsoleerd van sectoren in kolonies op een pyrazofos-houdend medium. In tegenstelling tot de wild-stam zetten deze resistente stammen pyrazofos (Afugan, Curamil) niet om in zijn fosfaat-analoog en 2-hydroxy-5-methyl-6-ethoxycarbonylpyrazolo(1,5-a)pyrimidine (PP), dat als het fungitoxische principe van pyrazofos wordt beschouwd. De gevoeligheid van de resistente stammen voor PP was iets hoger dan die van de wild-stam. Deze gegevens wijzen er op dat het resistantie-mechanisme geen verband houdt met een verandering van de aangrijpingsplaatsen van PP, maar met het overmogen om pyrazofos in PP om te zetten. De pyrazofos-resistente stammen vertoonden kruisresistentie met andere organische fosforfungiciden als EBP (Kitazin) en edifenfos (Hinosan). Een verklaring voor deze kruisresistentie kan nog niet gegeven worden. 相似文献
2.
Action of methyl-2-benzimidazolecarbamate (MBC), a breakdown product of benomyl, was studied in synchronous cultures of Ustilago maydis and Saccharomyces cerevesiae. Cells treated with MBC developed similarly to control cells until the two portions of the doublets (joined mother and daughter “cells”) were morphologically equivalent. At this point development of the treated cells ceased but control doublets separated to form two new cells. The compound did not prevent DNA synthesis during the first cell cycle of synchronized S. cerevesiae cells but did prevent completion of cell division, as it did also in synchronized U. maydis sporidia which already contained the DNA complement needed for completion of the first division. Mitosis did not go to completion in MBC-treated cells so the doublets formed contained only a single compact nucleus. The effect of MBC markedly resembles mitotic arrest caused by colchicine and isopropyl N-phenylcarbamate in higher plants and griseofulvin in the fungus Aspergillus nidulans. Inhibition of DNA synthesis in U. maydis and inhibition of cytokinesis in both organisms studied are secondary effects attributable to mitotic failure.A volatile compound toxic to U. maydis and S. cerevesiae was demonstrated in air over moistened benomyl. Hexane, through which such air samples were passed, or hexane extracts of aqueous suspensions of benomyl contained a substance having the same ir spectrum and retention time in two gas chromatographic systems as butyl isocyanate (BIC).BIC inhibited respiration of U. maydis and S. cerevesiae in a manner similar to benomyl. Benomyl partially inhibited respiration of subcellular particles from both organisms. MBC had essentially no effect on whole cell or subcellular particle respiration of either organism. Toxicity of benomyl preparations is not attributed to “benomyl” as such, but to two breakdown products, MBC and BIC. Therefore, differential effects of benomyl preparations and of MBC on growth and metabolism in fungi should be ascribed to BIC. 相似文献
3.
The relationships between the development of disease symptoms ofPuccinia sorghi, Exserohilum turcicum andHelminthosporium maydis on susceptible sweet corn plants, and the water status of the plants, were studied. At a relative water content (RWC) of 75% the development of sori ofP. sorghi, and the leaf area infected byE. turcicum andH. maydis, were inhibited by 38, 75 and 84%, respectively, as compared with the control plants (RWC = 100%).P. sorghi andH. maydis were not inhibited by a slight decrease in the RWC (96%), but development of leaf area infected byE. turcicum was inhibited by 33%.P. sorghi seemed to be better adapted to relatively high water deficiency in the host plants thanH. maydis orE. turcicum. 相似文献
4.
A variety of thiophene carboxamide compounds have been synthesized and tested on the succinate dehydrogenase complex (SDC) in mitochondria from a wild-type strain and carboxin-resistant strains of Ustilago maydis (corn smut). The site of action of thiophene carboxamides is identical to that of carboxin (5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxanilide) and thenoyltrifluoroacetone, that is, the succinate-ubiquinone reductase (complex II) span in the mitochondrial electron transfer chain. This investigation reveals new molecular structures which are strong inhibitors of wild-type and carboxin-resistant SDCs. The 5-amino analog of the parent anilide, 3-methylthiophene-2-carboxanilide (I), proved to be an especially potent inhibitor of the wild-type SDC (I50, 0.019 μM). Analogs of (I) such as 4′-carboethoxy, 4′-nbutyl, 4′-phenyl, and 4′-benzoyl were negatively correlated in activity to the carboxanilide (I) with respect to resistance level. A number of structures showed considerable selectivity for mutated SDCs from both highly and (particularly) moderately carboxin-resistant SDCs of U. maydis, markedly lowering the resistance level, i.e., the degree of resistance. Thus, in addition to the oxathiins, specific structural groups of thiophene carboxamides can also alleviate or reverse the effect of carboxin-selected mutation with reference to inhibition of the SDC. Of important significance was the finding that molecular selectivity for mutated, carboxin-resistant SDCs can be influenced by replacement of an oxathiin by a thiophene heterocyclic ring as well as by the substitutive group on the amide nitrogen, permitting different categories of mutant types and even mutants within a single category to be distinguished from one another. With all the structural combinations available, it appears quite possible, in terms of inhibition, to overcome any type of mutation in a fungal SDC which arises through selection by carboxin or other carboxamide compounds. A reasonable correlation generally exists between inhibition by thiophene carboxamides of the SDC and sporidial growth of wild-type and carboxin-resistant strains of U. maydis. A permeability barrier to 4′-substituted analogs of (I) was encountered in the wild-type strain but not mutant strains. Excellent protectant activity against bean rust (Uromyces phaseoli) was obtained with the 3′-nhexyl, 3′-nhexyloxy, and 4′-phenoxy analogs of (I). 相似文献
5.
The systemic fungicide carboxin (5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxanilide) and structurally related analogs are powerful inhibitors of succinate oxidation in mitochondria isolated from a variety of sources. The site of action which is, apparently, also that for thenoyltrifluoracetone, is in the complex II (succinate-ubiquinone reductase) region of the mitochondrial electron transfer chain. The succinic dehydrogenase complex (SDC) in mitochondria from carbon-resistant mutant strains of Ustilago maydis and Aspergillus nidulans is resistant to the fungicide in vitro. The current study shows that certain oxathiin carboxamides are selectively active against particular mutated SDCs of U. maydis and A. nidulans. Molecular structures affecting the phenotypic expression of mutation to carboxin resistance in U. maydis do not appear to affect similarly such expression in A. nidulans and vice versa. Of particular interest was the discovery of oxathiin carboxamides, e.g., 4′-phenylcarboxin, which were more inhibitory to the enzyme complex from one category of carboxin-resistant mutants of U. maydis than from the wild-type strain. Although such negative correlation between carboxin and other carboxin analogs has not been observed in studies with other categories of mutants, structures which drastically lower the resistance level were found in all cases. It appears that for any given mutation affecting carboxin sensitivity of the SDC in fungi, a specific structural group of carboxamides (or even a specific carboxamide) may be found which will alleviate or reverse the effect of the mutation in terms of inhibition of the SDC. If the mutations alter a protein receptor site for carboxamides, such mutations might be expected to influence the binding of carboxins of different structure. In essence, then, different molecular structures can “recognize” different alterations in the mutated enzyme complex and inhibit effectively. With few exceptions, the inhibition by carboxamides of cell growth of wild-type and carboxin-resistant strains of U. maydis and A. nidulans closely paralleded the inhibition of their respective SDCs. Although the few analogs tested were found unable to control corn smut systemically in seedlings artificially inoculated with compatible carboxin-resistant strains, control of naturally occurring carboxin-resistant strains of pathogenic fungi may be possible using particular structural analogs of carboxin which selectively inhibit the mutant organisms. 相似文献
6.
The systemic fungicide, carboxin (5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxanilide) and a variety of carboxamide compounds exhibit a marked specificity for Basidiomycete fungi. This unique specificity resides in the mitochondrial succinic dehydrogenase complex (SDC) of sensitive Basidiomycetes such as Ustilago maydis, the corn smut fungus. The present study examines in detail the structure-activity relationships of 93 carboxamide compounds and the SDC of two carboxin-sensitive organisms, U. maydis and a Basidiomycetous yeast, Cryptococcus laurentii. It has been possible to elucidate substantially the requirement in molecular structure needed for inhibition of the mitochondrial SDC. With few exceptions, a good correlation exists between the inhibitory activity of carboxamides towards the SDC of U. maydis and C. laurentii and the inhibition of growth of carboxamide-sensitive fungi, both in vitro and in vivo on the diseased plant. The structure-activity results were used as a basis for the synthesis of new, fungicidally-active carboxamides. The compounds found to be most active against the mycelial growth of Rhizoctonia solani were also tested on spore germination or mycelial growth of non-Basidiomycete fungi. Three carboxanilides (3-methyl-thiophene-2-carboxanilide, 3′-methyl-2-methylbenzanilide and 3′-methyl-2-ethylbenzanilide) had a fungitoxic spectrum which extended beyond Basidiomycetes. The spectrum of fungicidal activity of carboxanilides appears to be altered not only by substitution in the aniline ring, but by the nature of the ring attached to the carbonyl. No correlation was found between the inhibitory activity of oxathiins and benzanilides and their calculated partition coefficients. 相似文献
7.
Tridemorph (2,6-dimethyl-N-tridecylmorpholine) was active against representative of nearly all taxonomic groups of fungi; gram-positive bacteria were also sensitive although gram-negative were not. Tridemorph, 3–10 μg/ml, inhibited the multiplication of sporidia of Ustilago maydis more strongly than the increase of dry weight. The treated sporidia appeared swollen, multicellular, and sometimes branched. Unsaturated lipophilic compounds like α-tocopherol and trilinolein alleviated the toxicity of tridemorph to Botrytis allii and U. maydis. Protein and RNA syntheses were inhibited slightly. DNA synthesis was rather strongly affected already after 2 hr. Lipid synthesis was first inhibited but later stimulated. At an early stage (2 hr) treated cells differed already from control cells by a higher content of free fatty acids. Tridemorph also inhibited sterol biosynthesis. The antimicrobial spectrum, the characteristic morphology of treated cells of U. maydis, the observations on cross-resistance, the alleviating effect of unsaturated lipophilic compounds, and the alterations in neutral lipid pattern suggest strong similarity of the mode of action of tridemorph with that of the known inhibitors of sterol biosynthesis. 相似文献
8.
In order to find the biorational pesticides, we have synthesized two series of daphneolone analogues including 5-methylfuryl chalcones and 5-nitrofuryl chalcones by optimizing daphneolone analogues from Stellera chamaejasme L. with the good insecticidal properties of Qinghai-Tibet Plateau. All the synthesized compounds have been evaluated for anti-plant pathogenic fungi activities. The bioactivity assay showed that some of these daphneolone analogues were potentially active against plant pathogenic fungi, Rhizoctonia solani, Gibberella zeae, Bipolaris maydis, Sclerotia sclerotium and Botrytis cirerea, while the most potent 1-(2,4-dichlorophenyl)-3-(5-methylfuran-2-yl)propenone (compound 7) in this study showed good inhibitory activity against R. solani at 200 mg L−1 with ca. 100% inhibition. 相似文献
9.
Effect of metabolites from different Trichoderma strains on the growth of Rosellinia necatrix,the causal agent of avocado white root rot 总被引：1，自引：0，他引：1
I. Arjona-Girona F. Vinale D. Ruano-Rosa M. Lorito C. J. López-Herrera 《European journal of plant pathology / European Foundation for Plant Pathology》2014,140(2):385-397
Seven different strains of Trichoderma isolated from avocado roots showed antagonism to Rosellinia necatrix, which is the causal agent of white root rot. We studied these Trichoderma strains on the basis of the secondary metabolites produced in liquid culture. Five different compounds, namely, 6PP (6-pentyl-α-pyrone), Harzianolide (4-hexa-2,4-dienyl-3-(2-hydroxy-propyl)-5H-furan-2-one), T39butenolide (4-hexa-2,4-dienyl-3-(2-oxo-propyl)-5H-furan-2-one), Dehydroharzianolide (4-hexa-2,4-dienyl-3-propenyl-5H-furan-2-one) and Cerinolactone [(3-hydroxy-5-(6-isopropyl-3-methylene-3, 4, 4a, 5, 6, 7, 8, 8a-octahydronaphthalen-2-yl) dihydrofuran-2-one); a recently discovered novel metabolite], were obtained. In vitro studies of the effects of these compounds on different R. necatrix strains isolated from avocado roots and with different virulence demonstrated that 6PP had the strongest effect even at a low concentration. Although unstable, Cerinolactone and T39butenolide also had large effects on R. necatrix, mainly at a concentration of 200 μg. Harzianolide and Dehydroharzianolide exhibited the lowest effects on the pathogen. In vivo studies of Trichoderma metabolites on Lupinus luteus plants demonstrated the delay of white root rot epidemic through preventive application of 6PP or Harzianolide to seeds or plantlets by immersion in solutions of these metabolites at 1 mg l?1 (minimum effective dosage). In contrast, Cerinolactone only was effective at 10 mg l?1 when applied by plantlet immersion. Thus, this study reports the role that these metabolites could play for controlling avocado white root rot caused by R. necatrix. 相似文献
10.
J. Dekker A. J. Gielink 《European journal of plant pathology / European Foundation for Plant Pathology》1979,85(3):137-142
In some cucumber and gherkin greenhouses in the Netherlands, where Curamil (a.i. pyrazophos) had been used for control of powdery mildew, unsatisfactory disease control was obtained in recent years. Laboratory tests revealed a decreased sensitivity of the pathogen to the fungicide. The fitness and the competitive ability of pyrazophos resistant strains in absence of the fungicide appeared to be somewhat lower than that of the normal, sensitive strains. The implications with respect to disease control in practice are discussed.Samenvatting In enkele kassen, waar Curamil (a.i. pyrazofos) in 1977 aangewend werd ter bestrijding van meeldauw op komkommers en augurken, werd onvoldoende effekt met dit middel tegen deze ziekte verkregen. Toetsing in het laboratorium bracht een verminderde gevoeligheid van het pathogeen voor het fungicide aan het licht (Tabel 1). Bij afwezigheid van pyrazofos bleek het competitief vermogen (Tabel 2) en de vitaliteit (Tabel 3) van de pyrazofos resistente isolaten wat lager te zijn dan die van het normale, gevoelige pathogeen. De betekenis hiervan met betrekking tot de ziektebestrijding wordt besproken. 相似文献
11.
Succinoxidase activity of mitochondria from an antimycin A-sensitive (ants) mutant of Ustilago maydis is approximately five times less sensitive to the fungicide carboxin than that of mitochondria from wild-type cells. The antimycin A sensitivity is due to the absence of an alternative electron transport pathway in mitochondria obtained from mutant cells grown in control medium. The same mutant, however, develops high rates of alternative respiration if grown in the presence of chloramphenicol. Substrate and oxygen affinity as well as resistance to hydroxamates indicate that this respiration is mediated by only one mitochondrial electron transport pathway, similar to the inducible system described earlier in wild-type mitochondria. Induction appears to be regulated by the activity of the cytochrome pathway. The absence of the constitutive system from the ants mutant mitochondria which are resistant to carboxin, a selective inhibitor of the succinate dehydrogenase complex, supports the view that this system must be related to succinic dehydrogenase. 相似文献
12.
M. A. De Waard J. G. M. Van Nistelrooy 《European journal of plant pathology / European Foundation for Plant Pathology》1983,89(1-2):67-73
The majority of fenarimol-resistant laboratory isolates ofAspergillus nidulans, Cladosporium cucumerinum, Penicillium expansum, P. italicum, andUstilago maydis testedin vitro, displayed a moderate degree of negatively correlated cross-resistance to dodine. A limited number of isolates also possessed an increased sensitivity to guazatine. Colonies of fenarimol-resistant isolates ofA. nidulans with increased sensitivity to dodine showed sector formation on dodine-amended agar. Subcultures from these sectors appeared to have the wild-type sensitivity to dodine and fenarimol. The results indicate that fenarimol resistance and increased sensitivity to dodine are closely linked. The potential practical significance of the results is discussed. 相似文献
13.
An ergosterol-deficient mutant of Ustilago maydis was compared to the wild type in regard to morphology, growth rate, lipid content, and sensitivity to ergosterol biosynthetic inhibitors. Morphology of mutant sporidia is abnormal and resembles that of fenarimol-treated wild-type sporidia. Doubling time of mutant sporidia is 6.3 hr compared to 2.5 hr for the wild type. The mutant produces 24-methylenedihydrolanosterol, obtusifoliol, and 14α-methylfecosterol; ergosterol is absent. The sterols of the mutant are the same as those which accumulate in wild-type sporidia treated with the sterol C-14 demethylation inhibitors fenarimol, etaconazole, and miconazole. The level of free fatty acids is higher in the mutant than in wild-type cells. Growth of mutant sporidia is not inhibited by fenarimol, etaconazole, and miconazole, or by the sterol Δ14-reductase inhibitor azasterol A25822B at low concentrations which inhibit growth of wild-type sporidia. The residual growth rate of wild-type sporidia treated with low concentrations of the sterol C-14 demethylation inhibitors is about the same as that of untreated mutant sporidia. Therefore, the mutant would not be recognized as resistant in a wild-type population. The mutant is deficient in sterol C-14 demethylation and is similar in all properties studied to wild-type sporidia treated with sterol C-14 demethylation inhibitors. These findings support the contention that inhibition of sterol C-14 demethylation in U. maydis is the primary mode of toxicity of fenarimol, etaconazole, and miconazole. A secondary mode of toxicity is evident for miconazole and etaconazole at higher concentrations but is doubtful for fenarimol. 相似文献
14.
Effects of sterol biosynthesis-inhibiting (SBI) fungicides on cytochrome P-450 oxygenations in fungi
The fungicides miconazole, fenarimol, and etaconazole block ergosterol biosynthesis in fungi by inhibiting sterol 14α-demethylation, which is mediated by a cytochrome P-450 enzyme. The sensitivity of cytochrome P-450-dependent hydroxylation or demethylation of several substrates to these fungicides and similar compounds was compared to that of fungal growth and sterol 14α-demethylation. Demethylation of p-chloro-N-methylaniline (PCMA) by sporidia of Ustilago maydis and 11α-hydroxylation of progesterone by Aspergillus nidulans were relatively insensitive to these compounds and to metyrapone. The ability of a sterol 14α-demethylation-deficient mutant to demethylate PCMA indicates that this substrate is not demethylated by the sterol 14α-demethylation system of U. maydis. The 14α-hydroxylation of progesterone by cells of Curvularia lunata was quite sensitive to the three fungicides, and also to metyrapone and isopropylphenylimidazole. This system was less sensitive to the three fungicides than sterol 14α-demethylation, but was appreciably more sensitive than PCMA demethylation. A study of progesterone 14α-hydroxylation in cell-free preparations of C. lunata showed the reaction to be inhibited by CO, and to be competitively inhibited by low concentrations of miconazole. These data suggest that the primary action of sterol biosynthesis-inhibiting (SBI) fungicides is competitive inhibition of sterol/steroid-type cytochrome P-450 enzymes rather than interference with the function of sterol carrier proteins or enzyme-modulating phospholipids. 相似文献
15.
H. T. A. M. Schepers 《European journal of plant pathology / European Foundation for Plant Pathology》1984,90(4):165-171
Isolates ofSphaerotheca fuliginea collected in 1981–1983 in cucumber glasshouses in the Netherlands were tested for their sensitivity to benzimidazole fungicides, dimethirimol, dinocap and pyrazophos.Resistance to dinocap was not observed, although this fungicide has been used for over 30 years. Resistance to benzimidazole fungicides and dimethirimol has been persistent since these fungicides were withdrawn for control of cucumber powdery mildew more than 10 years ago. Although pyrazophos has only been used incidentally after 1977, the level of resistance has not decreased.Factors possibly involved in the persistence of resistance and implications for disease control in practice are discussed.Samenvatting De gevoeligheid voor twee benzimidazool-fungiciden en dimethirimol, dinocap en pyrazofos werd getoetst vanSphaerotheca fuliginea isolaten die in 1981–1983 verzameld waren in komkommerkassen in Nederland. Resistentie tegen dinocap werd niet waargenomen, ofschoon dit fungicide al meer dan 30 jaar wordt gebruikt.De resistentie tegen benzimidazool-fungiciden en dimethirimol, die meer dan 10 jaar geleden werden teruggetrokken voor de bestrijding vanS. fuliginea, was persistent. Hoewel pyrazofos slechts incidenteel gebruikt is sinds 1977, is het resistentieniveau niet teruggelopen. Factoren die mogelijk betrokken zijn bij de persistentie van resistentie en de gevolgen voor de ziektebestrijding worden besproken. 相似文献
16.
Triarimol (2 μg/ml) strongly inhibited multiplication of Ustilago maydis sporidia after one doubling, but growth continued and sporidia became abnormally large, branched and multicellular. Oxidation of glucose or acetate was not affected, and only slight limitations occurred in DNA, RNA and protein syntheses. The toxicant did not inhibit triglyceride synthesis but markedly increased the quantity and altered the quality of free fatty acids. Incorporation of [14C]acetate into ergosterol and an unidentified sterol was inhibited more than 90%, but incorporation into two other unidentified sterols was almost unaffected. Inhibition in the sterol biosynthetic pathway at a point preceeding ergosterol is regarded as a primary site of triarimol action in U. maydis. 相似文献
17.
Carboxin (5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxanilide) was tested for its effect on the activities of mitochondria from several fungi, pinto beans and rat liver. Succinate oxidation by mitochondria from the sensitive fungus Ustilago maydis was inhibited by low concentrations of carboxin, the Ki being 0.32 μM. The inhibition was of a noncompetitive nature. Succinate oxidation was also inhibited in the mitochondria from other sources but not to the extent as in those from U. maydis. Carboxin had little effect on the oxidation of reduced nicotinamide adenine dinucleotide. The dioxide of carboxin, oxycarboxin, was not as effective in inhibiting succinate oxidation as was carboxin, but was more effective than the monoxide. Carboxin did not appear to uncouple oxidative phosphorylation in the presence of succinate in tightly coupled rat liver mitochondria but did decrease the respiratory control ratio. Carboxin was ineffective in releasing oligomycin inhibition in coupled rat liver mitochondria while dinitrophenol and salicylanilide were effective in this respect. It is believed that carboxin inhibits mitochondrial respiration at or close to the site of succinate oxidation and does not greatly affect the remaining portion of the electron transport system or the coupled phosphorylation reactions. 相似文献
18.
为明确我国禁止进境的植物检疫性有害生物——玉蜀黍霜指霉菌Peronosclerospora maydis在中国的适生性以及入侵风险,采用CLIMEX 2.0软件分析其适生性,用ArcGIS 10.2软件确定其适生范围和适生程度,并采用多指标综合评判法量化分析其入侵我国的风险等级。结果表明,玉蜀黍霜指霉菌在我国的适生范围主要分布在长江以南的西南山地丘陵玉米种植区和南方丘陵玉米种植区,高适生区主要分布在云南、贵州、四川、重庆、广东、广西、湖南、江西、福建、海南和台湾等省 （区、市）。玉蜀黍霜指霉菌作为专性寄生菌,可在玉米整个生长季侵染危害,经多指标综合评判法分析并计算得到其风险综合评价值R为2.12,表明该病菌入侵我国的风险等级属高度危险,一旦入侵,势必对粮食安全、农业安全和生态安全带来巨大威胁,建议加强检疫监测,严防该病菌入侵。 相似文献
19.
采用孢子萌发法,分别测定了代森锰锌、戊唑醇和噁霉灵对玉米褐斑病菌Physoderma maydis的室内毒力;并通过田间小区试验,研究了80%代森锰锌可湿性粉剂(WP)、430 g/L戊唑醇悬浮剂(SC)和70%噁霉灵可湿性粉剂(WP)对病原菌致病力的影响,以及在8叶期茎叶喷雾处理对该病害的田间控制作用。结果表明:代森锰锌对病原菌休眠孢子囊的萌发具有明显的抑制作用,EC50值为66.71 mg/L,而戊唑醇和噁霉灵的抑制效果较差;代森锰锌和戊唑醇能有效降低病原菌的致病力,处理小区植株发病叶片均控制在穗位叶以下,且穗位叶叶绿素含量、净光合速率和根系活力均明显高于对照区,防效分别达91.31%和88.99%;代森锰锌和戊唑醇处理小区玉米增产效果明显,增产率分别达13.8%和11.5%。 相似文献
20.
The strains of Botrytis cinerea or Ustilago maydis selected on fenarimol, triarimol, or triadimefon were also resistant to the other inhibitors of sterol C-14 demethylation; the sterol composition of the strains was normal. Among the isolates of U. maydis resistant to dodemorph, fenpropidin, fenpropimorph and tridemorph, some were resistant to the 15-azasteroid A 25822B and did not contain ergosterol. The other strains remained sensitive to A 25822B and had a normal sterol composition. All the resistant isolates and the wild-type were inhibited to the same extent by nystatin and pimaricin. 相似文献