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1.
Collimonas sp. IS343, isolated from an organically-farmed arable soil and characterized as a broad-range oligotrophic bacterium, was shown to degrade chitin and to suppress R. solani mycelium growth under in vitro conditions at high and low carbon availabilities. In contrast to C. fungivorans Ter331, strain IS343 did not respond with an increase in growth rate to higher carbon levels in liquid medium, it reached higher cell numbers in carbon-poor media and it showed better survival in bulk soil. Therefore, it was concluded that strain IS343 cells are better adapted to circumstances of low carbon availability as present in bulk soils than strain Ter331 cells. Further, strain IS343 cells were more suppressive towards R. solani than strain Ter331 cells in vitro. When introduced into soil, strain IS343 cells delayed disease development caused by R. solani AG2-2IIIB in sugar beet plants. These results suggest that strain IS343 cells are able to tentatively suppress R. solani AG2-2IIIB mycelium growth in soil. Potential mechanisms behind the observed suppressive effects can be competition for available nutrients between strain IS343 cells and R. solani mycelium in soil or the production of chitinase as shown for this and other Collimonas species.  相似文献   

2.
In general, the viability ofRhizoctonia solani in lesions of stored tulip and iris bulbs decreased rapidly after harvest. However, some of the mycelium remained viable and acted as source of infection after planting. Temperature had no influence on the rate of survival, as estimated by isolation on an agar medium, but after planting moreRhizoctonia grew out on iris bulbs which had been stored continuously at 30°C for 20 or 32 weeks than on bulbs kept at lower temperatures. The surviving fungus was also able to infect neighbouring iris plants. The presence of healthy iris bulbs close to similar but diseased bulbs promoted the development ofRhizoctonia on the latter after planting.Samenvatting De levensvatbaarheid vanRhizoctonia solani in lesies op tulpe- en irisbollen nam tijdens de bewaring na de oogst in het algemeen snel af. Er bleef echter enig mycelium in level, dat na het planten als infectiebron fungeerde. De temperatuur had geen invloed op de mate van overleving wanneer de mate van slaging van isolaties op een agarmedium als criterium werd genomen. Na planten groeide echter meerRhizoctonia uit op irisbollen die permanent gedurende 20 en 32 weken bij 30°C waren bewaard dan bij bollen die bij lagere temperaturen waren opgeslagen. De overlevende schimmel was ook in staat om naburige irissen aan te tasten. De aanwezigheid van gezonde irissen in de nabijheid van aangetaste bevorderde de ontwikkeling vanRhizoctonia op geplante zieke bollen.  相似文献   

3.
A common mycoparasite,Verticillium biguttatum, was found to kill sclerotia ofRhizoctonia solani placed on an inert material (perlite) as well as in soil at 15°C and 20°C, but not at 10°C. Compared with the effectivity ofV. biguttatum, that ofGliocladium roseum, Gliocladium nigrovirens, Hormiactis fimicola andTrichoderma hamatum on sclerotia was only low. In laboratory experiments, treatment of sclerotia-bearing seed potatoes withV. biguttatum reduced disease symptoms in the first stage of growth of the potato plant.V. biguttatum was found to occur on the subterranean part of the potato plant. On untreated plants the surface of the sprouts was colonised byV. biguttatum originating from the soil, presumably partly in response to the presence ofR. solani mycelium. In a preliminary field experiment,Verticillium treatment did not reduce symptoms on the stem. However, there was a marked reduction in sclerotium formation on the newly formed potato tubers. This offers perspectives for a commercial use ofV. biguttatum in the control ofR. solani.  相似文献   

4.
The infection process ofRhizoctonia solani AG-3 was studied on potato sprouts, cv. Bintje, in growth chamber trials at 15 °C. Initially hyphae ofR. solani grew predominantly in the longitudinal direction of the sprouts (runner hyphae). They tended to follow the junctions between epidermis cells as was observed by SEM. The hyphae formed side-branches mainly half-way of the subterranean parts of the sprouts. They branched several times with short swollen cells to form infection cushions. Lesions developed only underneath the infection cushions and were first observed five days after inoculation. The necrotic area was proportional to the area covered with infection cushions on the sprouts. Depth of the lesions could extend up to the vascular bundle. Sprouts were colonized only in healthy tissue in the epidermal layer underneath the infection cushion and in necrotic tissue. A few days after appearance of the lesions,R. solani formed brown, uninfective mycelium on and in the circumference of these lesions.Aldicarb did not influence any part of the infection process. Ethoprophos delayed the emergence of sprouts, but increased the number of sprouts per tuber. As soon as sprouts had emerged, growth was considerably promoted by ethoprophos. Ethoprophos delayed the appearance of lesions and reduced their size. Oxamyl showed the same effects to a smaller extent.As the size of lesions appears to be proportional to the size of the infection cushions, any agents that change the size of the infection cushions, such as pesticides or antagonists, may alter the severity of the disease.Samenvatting Het infectieproces vanRhizoctonia solani AG-3 werd bestudeerd op aardappelspruiten, cv. Bintje, in een klimaatcel bij 15C. Aanvankelijk groeide de schimmel met runnerhyfen voornamelijk in de lengterichting van de spruit. Via SEM kon waargenomen worden, dat de hyfen hierbij vooral over de begrenzingen van de epidermiscellen groeiden. Het mycelium vormde veel zijvertakkingen, bestaande uit iets gezwollen korte cellen, welke voornamelijk halverwege op het ondergrondse deel van de spruit gevormd werden. Een dichte massa van deze cellen vormde een infectiekussentje. Lesies, welke vanaf vijf dagen na inoculatie werden waargenomen, bevonden zich slechts onder spruitoppervlak bezet met infectiekussentjes. De lesiegrootte was recht evenredig met het spruitoppervlak dat bezet was met infectiekussentjes. De diepte van de lesies reikte tot aan de vaatbundels. De spruit werd alleen door de schimmel gekoloniseerd in gezond epidermisweefsel onder het infectiekussentje en in necrotisch weefsel. Enkele dagen na verschijning van lesies vormde R.solani bruin, niet infectieus, mycelium op en rondom de lesies.Aldicarb had geen effect op het infectieproces. Ethoprophos vertraagde de opkomst en verhoogde het aantal tot ontwikkeling gekomen spruiten per knol in gestoomd zand. Direct na opkomst had ethoprophos echter een sterk groeistimulerend effect. Ethoprophos vertraagde de lesievorming en reduceerde de lesiegrootte, vergeleken met onbehandelde planten. Oxamyl vertoonde deze effecten in geringere mate.Daar de lesiegrootte direct gecorreleerd blijkt met de grootte van het infectiekussentje, mag verwacht worden dat elke beïnvloeding van de ontwikkeling van het mycelium van R.solani, bijvoorbeeld door pesticiden of antagonisten, een verandering van de lesiegrootte ten gevolge heeft.  相似文献   

5.
拮抗性链霉菌对大丽轮枝菌微菌核形成与萌发的影响   总被引：4，自引：1，他引：3  
为探索拮抗性链霉菌对棉花黄萎病病原大丽轮枝菌Verticillium dahliae Kleb.的抑菌机制,采用菌丝生长速率法、微菌核萌发法研究了6株拮抗链霉菌无菌发酵滤液对大丽轮枝菌生长、微菌核形成与萌发的影响。链霉菌无菌发酵滤液对大丽轮枝菌菌落生长、菌核形成和微菌核萌发有明显抑制作用。其中菌株B49的抑菌效果最好,5倍稀释发酵液培养14天时对菌落生长的抑菌率达69.7%;菌株B49、D184和Act12的5倍稀释发酵液对微菌核形成的抑制率达100%;将经B49、D184和Act12发酵液处理后丧失形成微菌核能力的大丽轮枝菌菌株转接至不含发酵液的PDA培养基,连续传代至第5代,其仍然不能恢复形成微菌核的能力;微菌核在含有菌株D184 5倍稀释发酵液的培养基上培养168 h时,萌发率仅为38.3%。  相似文献   

6.
八种杀虫剂对黑粪蚊的防治效果及残留分析   总被引：2，自引：1，他引：1  
选择8种杀虫剂,分别在实验室和菇房条件下研究其对黑粪蚊的防治效果和对平菇菌丝生长的影响,并分析施药后不同时间平菇中的农药残留.结果表明,40%辛硫磷EC、40%氧乐果EC、48%毒死蜱EC对黑粪蚊具有很好的防治效果,但对平菇菌丝的抑制率明显高于其它药剂;10%吡虫啉WP、4.5%高效氯氰菊酯EC不仅对黑粪蚊成、幼虫具有良好的防治效果,而且使用后对平菇菌丝生长的影响较小;2.5%高效氯氟氰菊酯EW、4.5%高效氯氰菊酯EC、1.8%阿维菌素EC等使用5天后均未检测到农药残留,5%氟虫腈SC和10%吡虫啉WP药后15天仍能检测到残留.  相似文献   

7.
Effects of nematicides on growth and microbial antagonism toRhizoctonia solani were investigated as part of a study on the mechanisms involved in the increased incidence of this pathogen in nematicide-treated potato crops.Ethoprophos inhibited mycelial growth ofR. solani on potato dextrose agar (PDA), Czapek Dox agar (CDA) and on water agar (WA). Aldicarb stimulated its growth on PDA up to 14% but not on CDA and WA. Oxamyl inhibited mycelial growth on CDA and WA, but not on PDA.Ethoprophos and aldicarb stimulated development of the mycoparasiteVerticillium biguttatum on cultures ofR. solani. The effect was dependent on the medium on which the host fungus was grown. ForRhizoctonia cultures on PDA, growth of the mycoparasite was highly promoted by aldicarb and to a lesser extent by ethoprophos. WhenR. solani was grown on CDA, the development of the mycoparasite was not affected by aldicarb, slightly stimulated by ethoprophos and slightly inhibited by oxamyl. On water agar, its development on the host mycelium was not affected.In field trials on sandy soil, nematicides encouragedV. biguttatum probably by increased availability of substrate (i.e.Rhizoctonia mycelium) perhaps through reduced activity of the mycophagous fauna.Soil fungistasis was increased by ethoprophos and to a lesser extent by aldicarb at very high doses. At normal field rates, no effects can be expected on fungistasis. So the increased stem and stolon infection of potatoes in nematicide-treated fields was not caused by a direct effect of the nematicides on growth ofR. solani or by suppressing the microbial antagonism.Samenvatting De invloed van granulaire nematiciden op de groei vanRhizoctonia solani en op het microbiële antagonisme tegen deze schimmel werd onderzocht in het kader van een studie over de mechanismen die een rol spelen bij de toename van de aantasting in een met nematiciden behandeld aardappelgewas.Ethoprofos remde de myceliumgroei vanR. solani op aardappeldextrose agar (PDA), Czapek Dox agar (CDA) en op wateragar (WA). Aldicarb stimuleerde op PDA de groei met maximaal 14%. Op CDA en WA werd geen effect van aldicarb waargenomen. Oxamyl veroorzaakte groeiremming op CDA en WA, maar niet op PDA.Ethoprofos en aldicarb stimuleerden de ontwikkeling van de mycoparasietVerticillium biguttatum op cultures vanR. solani. De mate van groeistimulering was afhankelijk van de voedingsbodem waarop de waard,R. solani, werd gekweekt. De groei vanV. biguttatum werd sterk gestimuleerd door aldicarb en in geringere mate door ethoprofos, wanneer de waard gekweekt werd op PDA. Aldicarb had geen effect op de mycoparasiet wanneerR. solani op CDA gekweekt werd, terwijl ethoprofos de groei wel iets stimuleerde en oxamyl een gering remmend effect had. Op WA werd geen effect van de nematiciden op het mycoparasitisme vastgesteld.In veldproeven op zandgrond stimuleerden de nematiciden het voorkomen vanV. biguttatum op de stolonen. Het effect werd waarschijnlijk veroorzaakt door een verhoogde substraat beschikbaarheid (d.w.z. mycelium vanR. solani). De verhoogde beschikbaarheid van dit mycelium kan samenhangen met een door nematiciden gereduceerde activiteit van de fungivore bodemfauna.De bodemfungistase werd verhoogd door ethoprofos en, in geringere mate, door aldicarb bij hogere doseringen. Bij de in de praktijk aanbevolen doseringen kan echter geen effect op de fungistase verwacht worden. De toename in stengel- en stolonaantasting van aardappelen, geteeld in met granulaire nematiciden behandelde percelen, kon niet worden toegeschreven aan een direct effect van de nematiciden op de groei vanR. solani of aan een vermindering van het microbiële antagonisme.  相似文献   

8.
Antagonism of isolates ofAzotobacter chroococcum toRhizoctonia solani on agar plates was studied, and isolates were tested for their ability to controlR. solani infection of potato sprouts in sterilized and unsterilized soil. The degree of antagonism exhibited varied strongly among the isolates and was also found to be temperature-dependent. At 25, 20 and 15°C, all but one strongly antagonisticAzobacter isolate effectively prevented infection of sprouts of potatoes planted in a soil heavily infected with a pathogenic isolate ofR. solani. At 10°C none was effective.  相似文献   

9.
为获得对烟草黑胫病有较强生防效果的拮抗细菌,从健康烟草根际采集30份土壤样品,分离纯化得到347株细菌,经病原真菌定向筛选后得到1株对烟草黑胫病菌等病原真菌拮抗活性较好的细菌FB-16,其对烟草黑胫病菌的抑菌带宽为23mm。采用菌丝生长速率法、作用机制试验、温室防病试验测定FB-16的抑菌作用,并通过形态学特征、生理生化特征及16S rDNA序列分析对菌株进行鉴定。结果显示,菌株FB-16发酵液对烟草黑胫病菌菌丝生长抑制率为95.96%;其代谢产物对烟草黑胫病菌菌丝有致畸作用;菌株FB-16为解淀粉芽胞杆菌Bacillus amyloliauefaciens(Gen-Bank登录号为JN245982);饱和度25%硫酸铵获得的抑菌物质对烟草黑胫病菌的抑菌活性较高,抑菌圈直径达42.00 mm;FB-16活性产物处理的烟草植株在接种烟草黑胫病菌7天后的防治效果为69.96%。表明菌株FB-16在烟草黑胫病生物防治中具有潜在的利用价值。  相似文献   

10.
Fluxapyroxad,3-(difluoromethyl)-1-methyl-N-(3’,4’,5’-trifluorobiphenyl-2-yl) pyrazole-4-carboxamide (C18H12F5N3O, Fig. 1), is a SDHI fungicide, which is a new active ingredient that interferes with succinate ubiquinone reductase in the electron transport chain of fungi. Between 2008 and 2010, a total of 128 isolates of Rhizoctonia solani from Anhui Province of China were characterized for the baseline sensitivity to fluxapyroxad. The isolates collected between 2008 and 2010 all showed similar sensitivity to fluxapyroxad. Baseline sensitivity was distributed as unimodal curves with an average EC50 value of 0.054?±?0.014 μg ml?1. However, EC50 values of boscalid for inhibition of mycelial growth of R. solani isolates ranged from 1.89 to 2.68 μg/ml and the average (±SE) EC50 value was 2.212?±?0.228 μg/ml, indicating that the R. solani isolates were less sensitive to boscalid than that of fluxapyroxad. Fluxapyroxad exhibited excellent protective and curative activity against rice sheath blight and provided 82.6–94.2 % protective or curative control efficacy. In field trials, control efficacy of fluxapyroxad at 100 g a.i/ha 15 days and 30 day after second application was 83.4–88.0 %, suggesting excellent activity against sheath blight. Control efficacy of boscalid at a dosage of 600 g a.i/ha 15 days and 30 day after second application was about 51.7–57.0 %. There was a significant difference in the efficacy between fluxapyroxad and boscalid or jinggangmycin. These results suggested that fluxapyroxad is a good alternative fungicide to jinggangmycin for the control of rice sheath blight.  相似文献   

11.
Individual and combined effects of light‐trapping, biological and chemical control on Lycoriella solani (Winnertz) populations in experimental mushroom production cubicles were examined. During three weeks following the introduction of recorded numbers of adult L solani into experimental cubicles, light‐traps caught a maximum 74% of flies initially released. However, light‐trapping stimulated adult fly activity and immature stages in the growing substrate throughout the experiment. Consequently, no yield improvements, independently or in combination with biological control agents, were recorded. Incorporation of diazinon (25 mg AI kg−1) to compost following pasteurisation did not significantly reduce subsequent emergence of adult sciarids. Additional drench application of diflubenzuron (1 g AI m−2) to the casing layer reduced the number of immature sciarids during the first cropping period by 99% (P < 0.001). However, inclusion of chemical insecticides reduced the mushroom yield during this period by 14% (P < 0.001). Introduction of the predatory mite Hypoaspis miles (Berlese) to the compost during its colonisation by mycelium of Agaricus bisporus (Lange) reduced emergence of adult sciarids by 87% (P < 0.05). Later introduction of H miles at the beginning of the case‐run period was less effective. Application of the parasitic nematode, Steinernema feltiae (Filipjev (=S bibionis Bovien, after Poinar, 1990)) to the compost during its colonisation by mycelium of A bisporus had no immediate effect on sciarid emergence and provided only limited reduction at later crop stages. Similar application immediately after casing reduced sciarid emergence at first flush by 82% (P < 0.05). Irrespective of application time, a formulation of Bacillus thuringiensis (Berliner) var israeliensis had no significant effect on sciarid emergence or mushroom yields at any production stage. © Crown copyright 2000. Reproduced with the permission of Her Majesty's Stationery Office. Published by John Wiley & Sons, Ltd.  相似文献   

12.
The ectomycorrhizal fungus Amanita vaginata can control damping off (Rhizoctonia solani) and promote growth of Pinus tabulaeformis seedlings. The aim of this study was to investigate whether reactive oxygen species and antioxidative enzymes play a role in preventing damping off in ectomycorrhizal roots. Two months after P. tabulaeformis roots were inoculated with A. vaginata, the roots were inoculated with R. solani. During the early stages (2?C96?h) of R. solani infection, the quantity and localisation of hydrogen peroxide and the activities of superoxide dismutase and catalase were evaluated. A burst of hydrogen peroxide occurred in ectomycorrhizal roots and in non-ectomycorrhizal roots when attacked by R. solani. In ectomycorrhizal roots, hydrogen peroxide production peaked 12?h after R. solani inoculation, which coincided with an increase in the activity of superoxide dismutase and catalase, whereas in non-ectomycorrhizal roots, hydrogen peroxide production peaked 24?h after R. solani inoculation and did not coincide with changes in superoxide dismutase or catalase activity. The imbalanced activities of superoxide dismutase and catalase might cause excessive accumulation of hydrogen peroxide and consequent damage to cell walls. Electron microscopy revealed that there was a positive correlation between hydrogen peroxide levels and the number of amyloplasts, with seedlings inoculated with A. vaginata and/or R. solani showing higher levels. These results indicated that A. vaginata inoculation enhanced damping off resistance and stimulated seedling growth, which may be due to the activation of a burst of hydrogen peroxide and its scavenging enzymes and the production of biochemical substances such as amyloplasts.  相似文献   

13.
The relative importance of sclerotia and mycelia of Botrytis cinerea Pers ex Fr. as structures of survival in southeastern Spanish greenhouses was investigated. Sclerotia were not found in the SE region, neither on plant debris nor on living plant material, suggesting it may serve only a minor role in epidemic development. B. cinerea survived mostly as mycelium. The percentage of artificially inoculated tomato stem pieces from which mycelium was recovered, was used to quantify its survival rate. Outside the greenhouses, mycelium survived in 33% and 5% of the tomato stem pieces 110 days after inoculation in 1995 and 1997, respectively. After the same number of days inside the greenhouses, no mycelium was recovered from stem pieces in 1995, and in 1997 only 7% of the stem pieces contained mycelium. Survival of mycelium outside and inside the greenhouses was significantly (P < 0.05) different after 47, 83, and 110 days of exposure to field conditions in 1995, but they were not different in 1997. Under controlled conditions, mycelium of B. cinerea lost viability at 100% relative humidity at temperatures ranging from 5 to 40°C, suggesting that air temperature and relative humidity accounted for loss of viability of mycelium.  相似文献   

14.
Uptake of [14C]fenarimol (30 μM) by mycelium of wild-type Aspergillus nidulans was characterized by a rapid initial accumulation during the first 10 min of incubation with the fungicide and a subsequent gradual release with time. Uptake appeared to be the result of influx and efflux. Influx of fenarimol could not be inhibited by low temperature, anaerobiosis, starvation of mycelium, or incubation with several respiratory inhibitors and is, therefore, a passive process. Under identical test conditions efflux activity was severely inhibited and should, therefore, be regarded as an energy-dependent mechanism. After prolonged incubation (90 min) an equilibrium between influx and efflux was established, resulting in an energy-dependent permeability barrier, since uptake could instantaneously be enhanced by addition of oligomycin or N,N′-dicyclohexylcarbodiimide. It also indicates that efflux activity is inducible; this hypothesis is supported by the observation that pretreatment of mycelium with unlabeled fungicide prevented subsequent uptake of [14C]fenarimol. Uptake by fenarimol-resistant mutants J146, M193, and R264 of A. nidulans, all possessing the imaB gene for resistance, was relatively low and almost constant in time. In this case, uptake appeared to be considerably enhanced by low temperature, anaerobiosis, starvation of mycelium, and incubation with respiratory inhibitors. Low uptake by these mutants is ascribed to a higher energy-dependent efflux activity for fenarimol compared with the wild-type strain. Upon inhibition of the barrier activity, net uptake resulted from remaining passive influx, which in that case may be as high as in the wild-type strain. The results suggest that both wild-type and fenarimol-resistant mutants possess an energy-dependent efflux mechanism with different efficiencies to excrete fenarimol and probably other chemicals to which cross-resistance or collateral sensitivity is present.  相似文献   

15.
Experiments in the laboratory and on farms with potato tubers in storage are described in which sclerotia ofRhizoctonia solani were inactivated after inoculation of infected tubers with a suspension of conidia and hyphal fragments ofVerticillium biguttatum. Sclerotia on freshly harvested tubers can be killed in a period of six to eight weeks, provided that (1) a direct contact between sclerotia and conidia ofV. biguttatum is obtained, (2) the temperature during the storage period is at least 15 °C, but preferably closer to 20 °C during the first weeks, and (3) the relative humidity of the air between the tubers is at least 99%. Seed tubers are only certified as export quality if the infection withR. solani, visible as sclerotia on the tubers, is assessed as below a specified incidence. To restore the economical value of tubers with many sclerotia, living sclerotia can be inactivated byV. biguttatum. However, also dead sclerotia have to be removed, as dead and living sclerotia cannot be distinguished visually by inspectors. A satisfactory way to remove dead sclerotia from tubers has not yet been found.  相似文献   

16.
ABSTRACT Rhizoctonia solani anastomosis group (AG)-13 was collected from diseased roots of field grown cotton plants in Georgia in the United States. Isolates of AG-13 did not anastomose with tester isolates of AG-1 through AG-12. Mycelium of all isolates of AG-13 were light brown but darkened as cultures aged. All isolates produced aerial mycelium. Concentric rings were visible after 3 to 4 days of growth but disappeared as cultures aged and darkened. Individual sclerotia were up to 1.5 mm in diameter, similar in color to the mycelium, and generally embedded in the agar. Clumps of sclerotia up to 5 mm in diameter were produced on the agar surface. All attempts to induce basidiospore production were unsuccessful. The 5.8S region of the rDNA from isolates of AG-13 was identical in length and sequence to isolates of all other AGs of R. solani. Length and sequence of the internal transcribed spacer (ITS) regions of rDNA from isolates of AG-13 were unique among AGs of R. solani. Similarity between AG-13 and other AGs of R. solani ranged from 68 to 85% for ITS region 1 and 85 to 95% for ITS region 2. Selected isolates of AG-13 caused minor or no damage to barley, cauliflower, cotton, lettuce, potato, and radish in laboratory or greenhouse studies.  相似文献   

17.
The acylalanine fungicides CGA 29212 and metalaxyl inhibit colony growth of Phytophthora megasperma f. sp. medicaginis at much lower concentrations than structurally related chloroacetanilide herbicides. Metolachlor, among the latter, shows the highest antifungal activity, followed by propachlor. Dimethachlor and alachlor are only weakly inhibitory. A metalaxyl- and CGA 29212-resistant strain of P. megasperma f. sp. medicaginis shows cross-resistance to metolachlor and propachlor, but levels of resistance are much lower than observed with CGA 29212 and metalaxyl. Cross-resistance does not occur to dimethachlor and alachlor. All compounds except metalaxyl inhibit uptake of [3H]uridine by mycelium, propachlor being most effective. Effects are similar with both a metalaxyl-sensitive and a -resistant strain. CGA 29212, metalaxyl, and metolachlor inhibit incorporation of [3H]uridine into RNA by mycelium of the sensitive strain at concentrations not inhibitory to uptake. Metalaxyl slightly affects incorporation by mycelium of the resistant strain; the other compounds have a more pronounced effect but only at concentrations inhibitory to uptake. Metalaxyl, CGA 29212, and propachlor do not induce leakage of radioactivity from mycelium of both strains when added at high concentrations to cultures previously incubated with [3H]uridine; under these conditions incorporation by mycelium of the metalaxyl-resistant strain is significantly more affected by CGA 29212 and propachlor than by metalaxyl. Endogenous RNA polymerase activity of isolated nuclei from a metalaxyl-sensitive strain is inhibited by CGA 29212, metalaxyl, and metolachlor but not by propachlor, dimethachlor, and alachlor. Neither compound has any effect on endogenous RNA polymerase activity of isolated nuclei from a metalaxyl-resistant strain. CGA 29212 and metolachlor evidently have a metalaxyl-type of action. The presence of cross-resistance of the metalaxyl-resistant strain to propachlor also indicates a metalaxyl-type of action for this compound, although this could not be confirmed by an inhibitory effect of propachlor on endogenous RNA polymerase activity. In addition to a metalaxyl-type of action, CGA 29212, metolachlor, and propachlor have a second one that is also present in dimethachlor and alachlor, which lack the metalaxyl-type of action. The second mechanism of action, involving inhibition of [3H]uridine uptake, is most prominent with propachlor and might be related to the primary mechanism of action in plants of the chloroacetanilide herbicides.  相似文献   

18.
Mycelial uptake of [14C]fenarimol (10 μg/ml) by 20 fenarimol-resistant mutants of Aspergillus nidulans was compared with uptake by wild-type strain 003. Uptake of the fungicide during the initial 10 min of incubation was significantly lower in all mutant strains than in the wild-type strain indicating that resistance is related with reduced uptake. Upon prolonged incubation a gradual decrease of accumulated radioactivity in the wild-type strain was observed. A few mutants displayed resistance to unrelated chemicals such as p-fluorophenylalanine or d-serine; this phenomenon appeared not to be due to a decreased uptake of the corresponding natural amino acids. Incorporation of [3H]adenine and [14C]leucine by mycelium of mutant M193 was hardly inhibited after 5 hr of incubation with the fungicide, whereas a distinct effect was found with the wild-type strain. At this time also fungitoxicity to the wild-type strain became apparent. Probably, this effect is indirectly caused by inhibition of ergosterol biosynthesis. Mycelium of mutant M193 incorporated [14C]acetate slightly less effectively than the wild-type strain. After 2 hr of incubation with this radiochemical leakage of [14C]acetate metabolites from mycelium of the mutant strain was observed. This indicates that resistance might be correlated with increased excretion of fungal metabolites, which in turn may be related with reduced fitness of fenarimol-resistant mutants.  相似文献   

19.
A polynucleate Rhizoctonia isolate (R3) was analysed for virulence, growth characteristics, enzyme production and presence of dsRNAs. Taxonomic position was assessed morphologically and by anastomosis group (AG) testing and ITS sequence analysis. Results indicated that R3 is a hypovirulent R. solani AG 4. Mechanisms underlying biocontrol towards virulent R. solani and Botrytis cinerea were investigated and plant-mediated resistance was followed using biochemical markers of defence (PR1, laminarinase, chitinase). Control apparently relies on spatial and nutrient competition in soil, and on systemic induced resistance. This is the first report on induction of systemic resistance and of defence markers by a hypovirulent strain of R. solani.  相似文献   

20.
A two-year survey was conducted to investigate the level of genetic variability occurring across growing seasons within natural populations of Alternaria solani, the cause of early blight in potato. Genetic diversity among 151 isolates, taken from a disease resistance breeding trial, was assessed using seven random amplified polymorphic DNA (RAPD) primers and sequence analyses of portions of the internal transcriber spacer (ITS) region and Alt a1 gene. A. solani isolates were grouped into 19 RAPD profiles to examine the distribution patterns of genetically distinct isolates within and between years. Seven RAPD profiles were found spanning both years with profiles 6 and 13 being the most prevalent. Five unique profiles were found only in 2008 and seven were found only in 2009. No variation was observed among isolates of A. solani based on ITS and Alt a1 sequence analyses, but a distinction between A. solani and A. dauci, a close relative outgroup was identified. Pathogenicity was also assessed using a tissue culture plantlet assay on four isolates and two reference cultures. Differences in virulence were observed among the isolates examined.  相似文献   

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