Effect of fenpropimorph and imazalil on sterol biosynthesis in penicillium italicum

Fenpropimorph was found to be highly active against Penicillium italicum (EC₅₀ 0.01/μg ml^?1). Conidia of P. italicum, treated with low concentrations of fenpropimorph, swelled in size and showed distorted germ tubes. During the initial stages of mycelial growth, fenpropimorph had little or no effect on the dry weight increase, which became strongly inhibited within 24 h after addition of the toxicant (0.05, 0.1 and 0.2 μg ml^?1). Irregular deposition of β–1,3 and β–1, 4 polysaccharides, probably chitin, was observed after treatment with fenpropimorph or imazalil. Fenpropimorph (0.05 and 0.2 μ ml^?1) caused the accumulation of a major demethyl-sterol that was different from ergosterol. It was identified as ergosta-8, 14, 24(28)-trien-3β-ol by mass, infrared, ultraviolet and proton nuclear magnetic resonance, spectrometric procedures. At both concentrations, the accumulation was already detected after incubation for 2 h. In contrast, imazalil (0.1 μg ml^?1) caused the accumulation of several methyl- and dimethyl-sterols which were tentatively identified as eburicol (24-methylene-24, 25-dihydrolanosterol), 4, 14α-dimethylergosta-8, 24(28)-dien-3-one, 14α-methylergosta-8, 24(28)-dien-3-one and obtusifoliol (4, 14α-dimethylergosta-8, 24(28)-dien-3α-ol). The accumulation of ergosta-8, 14,24(28)-trien-3β-ol indicates inhibition of the Δ¹⁴-reductase in P. italicum in a similar manner to that found previously in Ustilago maydis.     

Observations on the antisporulant activity of imazalil (enilconazole)

Imazalil, incorporated in a solid nutrient medium, had no effect on the sporulation of Penicillium italicum at concentrations that did not strongly inhibit mycelial growth. However, when the fungus was grown submerged in liquid culture, sporulation of P. italicum appeared to be more affected than vegetative growth; at 33 nM, imazalil completely prevented the formation of penicilli without adverse effects on growth. Imazalil was able to prevent sporulation in the vapour phase as shown by scanning electron microscopy on P. italicum and Aspergillus niger; the vapours of the compound were found to affect different stages of the sporulation process, depending on the timing of the experiment. Thus, in order to show antisporulant activity, imazalil had to reach the target site by means other than migration within the fungus.     

Effects of Sterol Biosynthesis Inhibitor Fungicides on Growth and Sterol Composition of Ustilago maydis,Botrytis cinerea and Pyrenophora teres

The effects of the sterol biosynthesis inhibitor (SBI) fungicides fenarimol, fenpropimorph, imazalil, prochloraz, propiconazole and triadimenol on growth and sterol composition of Ustilago maydis, Botrytis cinerea and Pyrenophora teres, grown from spores or sporidia in liquid culture, were determined. Growth of U. maydis was only slightly inhibited by SBI fungicides at concentrations which caused considerable changes in both sterol content and composition. Conversely, in B. cinerea and P. teres, growth was strongly inhibited under conditions where ergosterol was still the predominant sterol, suggesting that, in these two fungi, growth may be more sensitive to SBI fungicides than overall sterol production. Demethylase inhibitor fungicides behaved as a homogeneous group in their effects on growth and on sterol profiles of the three fungi studied.     

Fungitoxicity and growth regulation involving aspects of lipid biosynthesis

Triarimol and triforine inhibit ergosterol biosynthesis in fungi and cause accumulation of free fatty acids, 24-methylenedihydrolanosterol, obtusifoliol and 14α-methyl-δ^8,24(28)-ergostadienol. Triparanol also inhibits ergosterol synthesis and causes accumulation of free fatty acids, but not of the latter 3 sterols. Triparanol appears to inhibit prior to lanosterol in the sterol biosynthetic pathway of Ustilago maydis and at unidentified sites subsequent to lanosterol which lead to the accumulation of a sterol which migrates with desmethylsterols on TLC plates. Quantitative abnormalities in sterols and free fatty acids in U. maydis are not produced by the fungicides carbendazim, chloroneb, carboxin and cycloheximide. A deficiency in nitrogen leads to a marked increase in triglycerides, but a normal distribution pattern for other lipids.Inhibition of oxidative demethylation of the sterol 14α-methyl group is probably the prime mechanism of inhibition of ergosterol biosynthesis by triarimol. Rates of formation of obtusifoliol and 14α-methyl-δ^8,24(28)-ergostadienol in triarimol-treated U. maydis cells suggest that C-4 demethylation occurs along an abnormal pathway which operates effectively only at high substrate concentrations. The growth retardant action of triarimol and ancymidol in higher plants most likely results from inhibition of a reaction in the gibberellin biosynthetic pathway analogous to sterol C-14 demethylation.Free fatty acid accumulation in U. maydis cells treated with inhibitors of sterol synthesis are derived mainly from polar lipid degradation and from de novo synthesis as a consequence of the disproportionality between fatty acid synthesis and utilization. The free fatty acids may play a significant role in the lethality of these inhibitors in this organism.     

Resistance in mutagen-induced mutants of Ustilago maydis to fungicides which inhibit ergosterol biosynthesis

Resistance to a number of inhibitors of sterol C-14 demethylation, (clotrimazole, imazalil, miconazole, fenarimol, nuarimol and triadimefon), as well as resistance to inhibitors of sterol C-14(15) double bond reduction, (tridemorph and fenpropi-morph), was readily induced in Ustilago maydis. Resistant mutants were obtained after mutagenic treatment by ultraviolet irradiation, or by treatment with 1-methyl-3-nitro-1-nitrosoguanidine, of sporidia of the wild-type strain, followed by selection in the presence of the toxicant. The level of resistance of these mutants varied appreciably. Although not always reciprocal, cross-resistance to fungicides which inhibit ergosterol biosynthesis (EBIs) appeared to be present in most cases. Several of the U. maydis mutants which were resistant to inhibitors of sterol C-14 demethylation lacked cross-resistance to tridemorph and fenpropimorph, or displayed increased sensitivity to fenpropimorph (negatively correlated cross-resistance). Cross-resistance between EBIs and the antimicrobial agents climbazole and lombazole was also established. It is suggested that fungal mutants that possess a resistance mechanism based on a deficiency in sterol C-14 demethylation or sterol C-14(15) double bond reduction, have a greatly reduced chance of survival.     

Genetic control of resistance to fenpropimorph in Ustilago maydis

Fenpropimorph-resistant mutants of Ustilago maydis were obtained at high frequency (30 × 10⁻⁶) after UV-irradiation followed by selection on media containing fenpropimorph (50 μ g mL⁻¹). Genetic analysis of 30 such mutants resulted in the identification of two unlinked chromosomal loci, the U/fpm -1 locus with two allelic genes ( U/fpm- 1A and U/fpm -1B) and the U/fpm -2 locus. The mutant genes U/fpm- 1A and U/fpm -2 are responsible for high resistance levels (Rf: 75–100 or 257–286 based on MICs or ED_50s, respectively), while the U/fpm -1B mutation gives only a small reduction (approximately 7–10-fold) in fenpropimorph sensitivity. Cross-resistance studies with other SBIs showed that the major gene ( U/fpm- 1A and U/fpm -2) mutants were cross-resistant to the related compound fenpropidin (Rf: 15–20 or 53–66 based on MICs or ED_50s values, respectively) and to tridemorph (Rf: 5 or 7.1–9.5 based on MICs or ED_50s values, respectively), but not to the inhibitors of steps of ergosterol biosynthesis preceding the Δ¹⁴-reductase. The minor gene ( U/fpm -1B) mutants also had low-level resistance (approximately 5-fold) to tridemorph and to fenpropidin, but in contrast with the major gene mutants they were 2–10 times more sensitive to the triazoles studied (triadimefon, triadimenol, propiconazole and flusilazole) and to the pyridine, pyrifenox.
Studies of the fitness of U. maydis mutants showed that in major gene mutants, resistance was not associated with changes in growth rate in liquid culture or pathogenicity on young maize plants. The minor gene mutation reduced significantly the growth rate in liquid culture and the pathogenicity, either in homozygous or heterozygous condition in dikaryotic mycelium.     

Novel inhibitors of sterol C-14 demethylase and Δ14 Reductase/Δ8 → Δ7 isomerase for cereal disease control

The activity of five experimental fungicides combining structural elements responsible for sterol C-14 demethylase inhibition and sterol nuclear double-bond transformations has been investigated by examining sterol accumulation in Ustilago maydis (DC.) Corda, inhibition of sterol-biosynthesis enzymes in Saccharomyces cerevisiae Meyer using a cell-free system and protective activity in cereals against Erysiphe graminis DC. and Puccinia coronata Corda. Combining the fenpropidin/fenpropimorph basic structure with a pyridine moiety offered no advantage in fungicidal activity. However, the combination of the pyrifenox structure with a morpholine moiety yielded a compound which was a good inhibitor of C-14 demethylase and Δ⁸ → Δ⁷ isomerase in vitro and gave good cereal protection.     

Studies on the epidemiology of the tar spot disease complex of maize in Mexico

During the period 1986–1988 field studies were conducted on the epidemiology of the tar spot disease complex (TDC) of maize ( Zea mays ) caused by Phyllachora maydis, Monographella maydis and Coniothyrium phyllachorae. Under field conditions we found that P. maydis symptoms always appeared first, followed by symptoms of either M. maydis or C. phyllachorae. M. maydis causes leaf necrosis and has the most devastating effect. The primary symptoms covered about 12% of the leaf area below the ear leaf, whereas the total necrotic leaf area amounted to 30–60%, here considered as a secondary effect. Maximum TDC severity occurred during the winter season of 1988, which was characterized by a temperature range of 17–22°C, a mean RH >75%, and > 7h of leaf wetness per night. The highest numbers of windborne ascospores of P. maydis were trapped at an RH > 85% and at temperatures of 17 to 23°C in the winter of 1987 and 1988, although large numbers were also caught at temperatures of >23°C and RH <70%. Spore release was strongly influenced by light conditions and followed a similar diurnal curve throughout three seasons, reaching a maximum at 17.00–21.00 hours. The spread off. maydis within the field was very homogeneous. The incubation period of P. maydis was 12 to 15 days, and most of the ascospores were released within 3 weeks after formation of the ascostromata. M. maydis inoculum in plant debris was reduced by 90% within 3 to 4 months.     

Influence of Nutrient and Environmental Factors on Conidial Germination of Potebniamyces pyri

ABSTRACT Potebniamyces pyri is the causal agent of Phacidiopycnis rot, a postharvest disease of pears. Infection of fruit occurs in the orchard, and symptoms develop during storage. Conidial germination of P. pyri in response to nutrient, temperature, wetness duration, relative humidity (RH), and pH was determined in vitro. Conidia germinated by either budding or developing germ tubes in various concentrations of pear juice solutions. The mode of conidial germination was nutrient-dependent. Low nutrient levels favored budding, whereas high nutrient levels favored germ tube development. Conidia germinated at 0 to 30 degrees C but not at 35 degrees C, with optimum temperature between 20 and 25 degrees C. Wetness durations of 4 to 5 h and 6 to 8 h at optimum temperature were required for budding and developing germ tubes, respectively, and 20 to 24 h of wetness was required to reach germination peaks. Regardless of temperature, conidia germinated primarily by budding in 10% pear juice. Secondary conidia, produced by budding of conidia, initially increased their dimensions and later germinated at 0 to 25 degrees C in the same manner as mother conidia. No germination of secondary conidia occurred at 30 degrees C. Germ tubes from conidia elongated at 0 to 25 degrees C but not at 30 degrees C. No germination occurred at 相似文献   

Peronosclerospora maydis found on maize, sweetcorn and plume sorghum in Far North Queensland

Symptoms of a downy mildew disease were recognized on maize growing in the Atherton Tableland and Lakeland Downs areas of Far North Queensland in 1985. Quarantine measures were invoked to prevent the spread of this potentially serious disease to other parts of Australia.
The pathogen was identified as Peronosclerospora maydis in 1986 following examination of conidiophores with conidia and host range studies. An alternative host was strongly suspected and a survey near fields where the disease had been prevalent led to the identification of P. maydis on Sorghum plumosum, a grass indigenous to northern Australia. All downy mildew outbreaks on maize and sweetcorn in northern Australia since 1970 have been in areas where S. plumosum occurs. It seems likely that P. maydis has been present in Australia for many years.     

Conformational analysis of the fungicide fenpropimorph by molecular mechanics calculations and NMR spectroscopy

Fenpropimorph is an inhibitor of Δ8→Δ7-isomerase and Δ14-reductase in fungi and cycloeucalenol-obtusifoliol-isomerase and Δ8→Δ7-isomerase in higher plants. A detailed conformational analysis of the most potent enantiomer (S)-fenpropimorph is described. The conformational analysis is based on three different methods: molecular mechanics calculations. NMR spectroscopy and X-ray crystallography. In solution several conformations coexist. The molecular mechanics calculations using MM2(85) show a folded conformation of the unprotonated form of fenpropimorph to be stabilized by at least 3 kcal mol^?1 relative to the next lowest energy conformer, suggesting only one conformation of fenpropimorph to be present. A corresponding stabilization of the protonated form (5.4 kcal mol^?1) is obtained. However, this stabilization is found partly to be due to attractive steric interactions and may be a phenomenon occurring only in vacuum. In the solid state, fenpropimorph exists in an L-shaped conformation resembling one of the low-energy conformers obtained with MM2(85). Based on comparison with the natural substrate, a totally extended conformation of fenpropimorph is suggested to be the biologically active conformation for interaction with the Δ8 → Δ7-isomerase in fungi.     

Sterol composition of isolates of Erysiphe graminis f.sp. tritici differing in sensitivity to fenpropimorph

Isolates of Erysiphe graminis f.sp. tritici with wild-type or reduced sensitivity to fenpropimorph were similar in sterol composition, viz. ergosta-5,24(28)-dienol (±90%) and episterol (±10%). Following treatment with fenpropimorph, the relative content of episterol increased in conidia of all isolates tested, while that of ergosta-5,24(28)-dienol decreased. These results suggest that fenpropimorph, under the test conditions used, does not inhibit activity of sterol Δ¹⁴-reductase or Δ⁸→Δ⁷-isomerase but probably interferes with the final part of the demethyl sterol synthesis. However, modifications in this part of the pathway are probably not responsible for the decreased sensitivity of the pathogen to the fungicide. © 1998 SCI.     

Effect of Germination Initiation on Competitive Capacity of Trichoderma atroviride P1 Conidia

ABSTRACT Trichoderma biocontrol isolates are most effective as highly concentrated inocula. Their antagonism to other fungi may be a result of pregermination respiration. In a nutrient-rich medium, almost all Trichoderma atroviride P1 (P1) conidia initiated germination processes and increased respiration, even in dense suspensions. When 1 x 10(7) P1 conidia/ml were coinoculated with 1 x 10(5) Botrytis cinerea conidia/ml, dissolved oxygen fell to <1% within 2 h and the pathogen failed to germinate. More dilute P1 suspensions consumed oxygen slowly enough to allow coinoculated B. cinerea to germinate. On nutrient-poor media, fewer P1 conidia initiated germination. Oxygen consumption by the inoculum and inhibition of B. cinerea were enhanced when P1 conidia were nutrient activated before inoculation. Pregermination respiration also affected competitive capacity of the antagonist on solid substrates, where respiratory CO(2) stimulated germination rate and initial colony growth. These parameters were directly correlated with inoculum concentration (R(2) >/= 0.97, P < 0.01). After initiating germination, Trichoderma conidia became more sensitive to desiccation and were killed by drying after only 2 h of incubation on a nutrient-rich substrate at 23 degrees C. These results indicate that nutrient-induced changes preceding germination in Trichoderma conidia can either enhance or decrease their biological control potential, depending on environmental conditions in the microhabitat.     

海洋放线菌A3202的分离鉴定及其对柑橘采后病害的防效

为获得用于防治柑橘采后病害的海洋放线菌,以柑橘青霉病菌Penicillium italicum、柑橘绿霉病菌P.digitatum和柑橘炭疽病菌Colletotrichum gloeosporioides为指示菌,对分离到的25株海洋放线菌进行筛选。通过平板对峙法测定拮抗菌株的抑菌谱,并测定其发酵产物粗提物对柑橘果实采后病害的防效,根据形态特征、培养特征、生理生化特征及16S rDNA序列对其进行鉴定。结果表明,分离自鳞笠藤壶Tetraclita squamosa的菌株A3202对3种指示菌均具有强抑菌活性,对供试13种植物病原菌的菌丝生长具有不同程度的抑制作用,尤其对柑橘青霉病菌和柑橘绿霉病菌的抑制作用最强,抑菌带宽度分别可达2.33±0.05 cm和2.32±0.10 cm。该菌株800 mg/L粗提物溶液对接种后7 d的柑橘青霉病、柑橘绿霉病和柑橘炭疽病的相对防效均可达100%。初步鉴定该菌株为放线菌中的米修链霉菌Streptomyces misionensis。     

Biological Control of Botrytis cinerea in Cyclamen with Ulocladium atrum and Gliocladium roseum Under Commercial Growing Conditions

ABSTRACT The effect of treatments with conidial suspensions of Ulocladium atrum and Gliocladium roseum on leaf rot of cyclamen caused by Botrytis cinerea was investigated under commercial greenhouse conditions. Spraying U. atrum (1 x 10(6) conidia per ml) or G. roseum (2 x 10(6) conidia per ml and 1 x 10(7) conidia per ml) at intervals of 2 to 3 weeks during the production period and spraying U. atrum (1 x 10(6) conidia per ml) at intervals of 4 to 6 weeks resulted in a significant reduction of natural infections of petioles by B. cinerea. U. atrum or G. roseum (1 x 10(7)conidia per ml) was as effective as the standard fungicide program. B. cinerea colonized senesced leaves within the plant canopy and infected adjacent petioles and leaves later. The antagonists colonized senesced leaves and reduced B. cinerea development on these leaves. Thus, the inoculum potential on petioles adjacent to necrotic leaf tissues was reduced. The fate of U. atrum conidia on surfaces of green cyclamen leaves during a 70-day period after application was studied. The number of conidia per square centimeter of leaf surface remained relatively constant during the entire experiment. Sixty percent of the conidia sampled during the experiments retained the ability to germinate. When green leaves were removed from the plants to induce senescence and subsequently were incubated in a moist chamber, U. atrum colonized the dead leaves. Senesced leaves also were colonized by other naturally occurring fungi including B. cinerea. On leaves treated with U. atrum from all sampling dates, sporulation of B. cinerea was significantly less as compared with the untreated control. Our results indicate that early applications of U. atrum before canopy closure may be sufficient to achieve commercially satisfactory control of Botrytis leaf rot in cyclamen.     

柑橘内生燕麦镰刀菌Gds-1对柑橘青霉病的防治研究

柑橘青霉病是柑橘果实采后危害最大的病害。为得到一株可有效应用于柑橘青霉病防治的柑橘内生真菌菌株,进行了柑橘果实内生菌分离、离体与活体试验筛选、菌株形态学与多基因位点分子系统发育鉴定、菌株活体应用效果与作用特点以及菌株代谢产物稳定性与应用防效试验。结果表明:筛选所得的柑橘内生真菌Gds-1在离体与活体条件下均对柑橘青霉菌有较好的抑制效果;经多基因位点联合系统发育分析,将Gds-1鉴定为燕麦镰刀菌Fusarium avenaceum;提前48 h施用Gds-1菌体,对柑橘青霉病的预防效果最好 (防治效果为90.67%);Gds-1菌丝不会损害健康柑橘果实表皮,但可以在柑橘果实表皮伤口和被柑橘青霉菌感染的组织部位发挥作用,从而抑制柑橘青霉菌;当温度在 ?80~100 ℃和pH=5~10时,Gds-1无菌发酵液对柑橘青霉菌的拮抗作用高效稳定;单独施用Gds-1无菌发酵滤液28 d和56 d时,对柑橘青霉病的防效与100 μg/mL的抑霉唑相当,显著高于清水对照。本研究首次报道了生防镰刀菌F. avenaceum Gds-1对柑橘青霉病的防治作用,为柑橘果实采后生物源防腐剂的选择提供了新来源,为镰刀菌生物防治机理研究提供了新思路。     

Fungal derived cytokinins are necessary for normal Ustilago maydis infection of maize

Phytohormones derived from fungi play a key role in regulating plant–pathogen interactions; however, deciphering the separate contributions of pathogen and plant during infection has been difficult. Here, the Ustilago maydis–Zea mays pathosystem was used to investigate this chemical exchange. Ustilago maydis, the causative agent of maize smut, produces cytokinins (CK), which are a group of phytohormones responsible for directing plant development. The characteristic symptom of smut disease is the formation of tumours composed of plant and fungal tissue. Isopentenyltransferase (IPT) catalyses the rate‐limiting step in CK biosynthesis, and U. maydis strains in which the sole tRNA‐ipt gene was deleted no longer produced CKs. These deletion strains elicited fewer, smaller tumours than the pathogenic strain SG200. High performance liquid chromatography‐electrospray ionization tandem mass spectrometry (HPLC‐ESI MS/MS) was used to detect and quantify phytohormone levels in infected tissue. This revealed that key hormone changes in SG200 infections were not present in infections by deletion strains, suggesting that CK production by U. maydis is required for the altered phytohormone profile in infected tissue relative to uninfected tissue. Separate analyses indicated that U. maydis tRNA‐ipt mutants might be altered in their ability to metabolize CKs taken up from the environment. Mining the U. maydis genome identified genes encoding putative CK signalling and biosynthesis proteins.     

Ustilago maydis Infection of the Nonnatural Host Arabidopsis thaliana

ABSTRACT The experimental infection of Arabidopsis thaliana by the maize phytopathogenic hemibasidiomycete Ustilago maydis under axenic conditions is described. When plantlets were inoculated with mixtures of compatible haploids, the fungus was able to grow on the plant surface of inoculated seedlings in the form of white mycelium and invade the tissues, probably penetrating through stomata; however, it did not form teliospores. Symptoms of disease were increased anthocyanin formation, development of chlorosis, increased formation of secondary roots, induction of malformations in the leaves and petioles, induction of tissue necrosis, and stunting. In several cases, death of the invaded plants occurred. Interestingly, inoculation of single U. maydis haploid strains produced similar symptoms in Arabidopsis plantlets. In contrast, several mutants avirulent to maize also were avirulent or less virulent than wildtype strains on Arabidopsis. Collectively, the reported data suggest that the U. maydis-Arabidopsis pathosystem may constitute a useful experimental model for the analysis of some aspects of the virulence factors of the fungus. With the study of nonhost responses and their comparison to those occurring during maize infection, we will be able to elucidate some obscure aspects of U. maydis pathogenicity in the future.