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1.
Samples of heavily infested crop residues were incorporated in static compost heaps (2.5–4.6 m3) of the Indore type. Temperature increased to 50–70°C within 6 days depending on the type of crop residues used and the location within the heap. The heat phase (>40 °C) lasted 2–3 weeks and was followed by a c. 5-months maturation phase (<40 °C). Among the 17 pathogens tested, onlyOlpidium brassicae and one of the four formae speciales ofFusarium oxysporum that were tested survived composting, but also their inoculum was greatly reduced.Survival during specific phases of composting was studied by incorporation and retrieval of samples at various stages of the process.F. oxysporum f. sp.melonis was completely inactivated andO. brassicae andPlasmodiophora brassicae were almost completely inactivated during the short heat phase. The three pathogens survived the long-lasting maturation phase without loss of viability. Heat evolved during composting was found to be the most important factor involved with sanitation of crop residues. The possible involvement of fungitoxic conversion products and microbial antagonism is discussed.  相似文献   

2.
The effects of sublethal heat treatments on heat resistance were studied forFusarium oxysporum f.sp.dianthi (Fod) andVerticillium dahliae (Vd), one isolate of each pathogen. Treatments of propagule suspensions of Fod at 55°C and of Vd at 45°C for 30 min were survived by less than 0.001% and 0.01% of the propagules, respectively. Pretreatment of suspensions of Fod at 45°C increased survival of the 55°C treatment up to 0.73% of the propagules and pretreatment of suspensions of Vd at 40°C increased survival of the 45°C treatment up to 0.40%. Induction of heat resistance was dependent on duration of the exposure to the sublethal temperature. With Fod, this duration was shorter for propagules from old cultures than for those from young cultures. Pretreatment at 45°C of a suspension of an 1-week-old culture of Fod induced resistance when lasting 30 min or longer, but not when 20 min or shorter. With Vd, the duration of the pretreatment inducing heat resistance depended on type of culture — white or black — due to differences in microsclerotia formation. Implications of induced heat resistance for control of plant diseases by thermotherapy are discussed.  相似文献   

3.
A survey was made to identify the most important soilborne fungal pathogens of asparagus crops in the Netherlands. Ten plants were selected from each of five fields with a young (1–4 y) first planting, five fields with an old (6–13 y) first planting and five fields with a young replanting. The analysis included fungi present in the stem base and the roots of plants with symptoms of foot and root rot or showing growth decline without specific disease symptoms. Isolates of each species were tested for pathogenicity to asparagus on aseptically grown plantlets on Knop's agar. Symptoms were caused byFusarium oxysporum, F. culmorum, Botrytis cinerea, Penicillium verrucosum var.cyclopium, Cylindrocarpon didymum, Phialophora malorum, Phoma terrestris andAcremonium strictum. F. oxysporum was by far the most common species and was isolated from 80% of the plants. Not all of its isolates were pathogenic to asparagus. Symptoms were caused by 67%, 78% and 93% of the isolates obtained from young first plantings, old first plantings and replantings, respectively.F. culmorum was isolated from 31% of the plants. Two other notorious pathogens of asparagus,F. moniliforme andF. proliferatum, did not occur in our samples.Species causing symptoms in the vitro test that were found on more than 5% of the plants were additionally tested for their pathogenicity in pot experiments.F. oxysporum f.sp.asparagi caused severe foot and root rot, significantly reduced root weights and killed most of the plants.F. culmorum caused lesions on the stem base often resulting in death of the plant.P. terrestris, a fungus only once reported as a pathogen of asparagus, caused an extensive root rot, mainly of secondary roots that became reddish. The fungus was isolated in only a few samples and is not to be regarded as an important pathogen in Dutch asparagus crops.P. malorum caused many small brown lesions on the stem base and incidentally also on the upper part of small main roots. This is the first report of its pathogenicity to asparagus. The fungus is one of the organisms inciting spear rust and it reduced crop quality rather than crop yield.P. verrucosum var.cyclopium andC. didymum did not cause symptoms in pot experiments.Because of its predominance on plants with foot and root rot and its high virulence,F. oxysporum f.sp.asparagi was considered to be the main soilborne pathogen of asparagus in the Netherlands.  相似文献   

4.
Asparagus replant-bound early decline (ARED) was characterized and its etiology was elucidated in experiments under greenhouse and field conditions. Selective soil treatments were used to differentiate between autotoxic compounds and soil-borne pathogens as causal agents. In greenhouse experiments, there were symptoms of ARED within 12—15 weeks. Asparagus plants grown in soil formerly used for asparagus (asparagus soil) showed brown lesions on primary and secondary roots, and many secondary roots had rotted. Root weights of plants grown in asparagus soil were lower than those of plants grown in fresh soil.Fusarium oxysporum f. sp.asparagi (Foa) was by far the most common species among the fungi isolated from roots with lesions. Under greenhouse and field conditions, there were similar symptoms, which indicates that the results obtained under greenhouse conditions are similar to those in the field. The vertical distribution of the ARED-causing factor(s) was studied in a greenhouse experiment in which plants were grown in soil from three layers: 0–30, 30–60, and 60–90 cm. For all four asparagus soils tested, there were ARED symptoms and similar disease severity in samples from all three depths. The causal factor persisted at least 11 years after soil was no longer used for asparagus. When asparagus soil was diluted with fresh soil to give mixtures with 100%, 80%, 50%, 20% and 0% asparagus soil, disease severity did not decrease with increasing dilution of the asparagus soil from 100% to 20%. Disease severity of all mixtures with asparagus soil was significantly higher than that for fresh soil. The results imply that ARED is caused by a pathogen colonizing the soil rather than inhibition by autotoxins released from residues of the preceding asparagus crop. This conclusion is supported by the results of greenhouse and outdoor experiments with heat and fungicide treatments of soil. ARED was nullified by heat treatments of 30 min at 55 or 60 °C but not 45 and 50 °C, eliminating autotoxins as an important cause of ARED because they are heat-stable. Foa is eliminated by a 30-min soil treatment at 55–60 °C but not 50 °C. Prochloraz, known for its toxicity toF. oxysporum, also nullified ARED. Disease severity level was related to the density of Foa in soil. The results provide conclusive evidence thatF. oxysporum f. sp.asparagi is the main cause of ARED in the Netherlands, which largely removes the need to discriminate between early decline and replant-bound early decline, because Foa is the main cause of both diseases.  相似文献   

5.
Fusarium wilt-resistant Novada carnations responded both to stem inoculation with a conidial suspension ofFusarium oxysporum f. sp.dianthi orF. oxysporum f. sp.lycopersici and to root inoculation by planting in soil infected withF. oxysporum f.sp.dianthi by means of a localization mechanism comprising gel formation in the xylem vessels and hyperplasia of adjacent parenchyma cells. Dye translocation experiments showed that xylem transport was limited by the presence of vascular gels, although wilting did not occur. Overcapacity of the vascular system apparently allowed for sufficient water transport to compensate for local vascular dysfunction. Also, vascular regeneration in the hyperplastic tissue next to occluded xylem vessels created new pathways for water transport to compensate for those lost by occlusion. Regeneration of xylem vessels was eventually followed by regeneration of xylem fibers, xylem parenchyma, cambium, and phloem cells.Early Sam carnations, susceptible to Fusarium wilt, responded to stem inoculation withF. oxysporum f. sp.lycopersici by similar localization of infection and vascular regeneration. Stem inoculation withF. oxysporum f. sp.dianthi, however, resulted in colonization of the xylem vessels followed by lysis of the vascular tissues. Vascular gelation, hyperplasia of parenchyma cells, and vascular regeneration did generally not occur. However, if some hyperplasia occurred in attempted defence, some differentiation of hyperplastic cells into single xylem vessel elements was observed which only rarely resulted in complete vascular regeneration next to colonized xylem. In the absence of hyperplasia, differentiation of medulla parenchyma cells bordering destroyed vascular tissue into xylem vessel elements was even more exceptional. Apparently, vascular regeneration in carnation is a normal defence reaction to fungal invasion.Samenvatting Novada anjers, resistent tegen Fusarium-verwelkingsziekte, reageerden op stengelinoculatie met een conidiënsuspensie vanFusarium oxysporum f.sp.dianthi of vanF. oxysporum f.sp.lycopersici en op wortelinoculatie door te planten in metF. oxysporumf.sp.dianthi besmette grond met een lokalisatiemechanisme dat onder meer bestond uit vorming van gommen in de houtvaten en hyperplasie van naburige parenchymcellen. Uit proeven over kleurstoftransport bleek dat de sapstroom door de gomvorming beperkt werd, hoewel dit geen verwelkingssymptomen veroorzaakte. Overcapaciteit van het vaatstelsel zorgde kennelijk voor voldoende compensatie aan watertransport om plaatselijke verstoring van de sapstroom op te vangen. Daarnaast werd het verlies aan functionele houtvaten ook opgevangen door vaatweefselregeneratie in het hyperplastische weefsel grenzend aan door gommen verstopte houtvaten. Na verloop van tijd werden behalve houtvaten ook houtvezels, houtparenchymcellen, cambium- en floeemcellen geregenereerd.Early Sam anjers, vatbaar voor Fusarium-verwelkingsziekte, reageerden op stengelinoculatie metF. oxysporum f. sp.lycopersici met eenzelfde lokalisatiemechanisme en ook met vaatweefselregeneratie. Stengelinoculatie metF. oxysporum f.sp.dianthi echter had kolonisatie en vervolgens lysis van het vaatweefsel tot gevolg. Meestal trad er geen gomvorming, hyperplasie van parenchymcellen of vaatweefselregeneratie op. Als echter bij pogingen tot afweer toch enige hyperplasie optrad, bleken sommige hyperplastische cellen wel tot houtvatelementen te differentieren. Dit leidde echter maar zelden tot totale vaatweefselregeneratie parallel aan het gekoloniseerde vaatweefsel. In afwezigheid van hyperplasie differentieerden mergparenchymcellen vlak naast lyserend vaatweefsel slechts bij hoge uitzondering tot houtvatelementen. Vaatweefselregeneratie bij anjer is kennelijk een gewone afweerreactie op besmetting met pathogene schimmels.  相似文献   

6.
Seven experimental trials were carried out to evaluate the efficacy of the bacterial strains Achromobacter xylosoxydans AM1 and Serratia sp. DM1 obtained from suppressive soils and from soilless used rockwool substrates (Pseudomonas putida FC6B, Pseudomonas sp. FC7B, Pseudomonas putida FC8B, Pseudomonas sp. FC9B and Pseudomonas sp. FC24B) against Fusarium wilt on rocket caused by Fusarium oxysporum ff. spp. raphani and conglutinans. Along with these strains, two commercial bioproducts (RootShield—Trichoderma harzianum T22; Cedomon—Pseudomonas chlororaphis MA342) were also tested. Different application strategies such as soil treatment (trials I to VI; 107 and 108 CFU ml−1) and root dipping (trial VII; 108 and 109 CFU ml−1) were performed in a glasshouse in order to test the efficacy of the bacterial strains against Fusarium oxysporum ff. spp. raphani and conglutinans. The lowest disease incidence (16.7%) was observed with the application of Achromobacter sp. AM1, Serratia sp. DM1 at 108 CFU ml−1 and Pseudomonas sp. FC9B at 107 CFU ml−1 against F. oxysporum f. sp. conglutinans (experiment I). Maximum plant biomass (5.0 g/plant) was registered in Serratia sp. DM1 at 108 CFU ml−1 treated plants in trial IV. The trials against F. oxysporum f. sp. raphani (experiment II) showed that the application of Pseudomonas sp. FC7B, P. putida FC8B at 108 CFU ml−1 and P. chlororaphis MA342 at 7.5 × 106 CFU ml−1 significantly reduced disease incidence to values ranging between 87% and 92%. The highest plant biomass was recorded with the application of Achromobacter sp. AM1 and P. putida FC6B at 107 CFU ml−1 (3.9 to 4.2 g) carried out 7 days before the artificial inoculation of the pathogens (trial IV). The present study showed the potential biocontrol activity of the bacterial strains Achromobacter sp. AM1, Serratia sp. DM1 and Pseudomonas sp. FC9B against F. oxysporum f. sp. conglutinans and of Pseudomonas sp. FC7B, P. putida FC8B, P. chlororaphis MA342, Achromobacter sp. AM1 and P. putida FC6B against F. oxysporum f. sp. raphani. Growth-promoting activity of biocontrol bacteria used during the trials was observed.  相似文献   

7.
Susceptible interactions of Early Sam carnations with races 1,2,4, and 8 ofFusarium oxysporum f. sp.dianthi differed in pathogenesis, both after stem and after root inoculation. Race 1 induced pallescence and withering of leaves. Affected vascular tissue had a uniform pallid to pale brown colour; though heavily colonized, it was not or virtually not degraded. Defence reactions developed only slowly. Race 2 induced yellowing, of the midribs in particular, and withering of leaves. Affected vascular tissue was white with dark brown margins. Colonized tissue was degraded to leave vascular cavities. At lower heights of colonization, many defence reactions developed, which sometimes resulted in localization of the pathogen. Race 4 induced a similar pathogenesis as race 2, except for less intensive defence reactions. Race 8 induced midrib lesions on, and pallescence, withering and necrosis of leaves. Affected vascular tissue had a uniform light brown colour. Degradation of colonized vascular tissues was rare; instead, many defence reactions were observed, even at high heights in the plants.Races 1, 2 and 4 ofF. oxysporum f. sp.dianthi did not induce disease symptoms in Novada carnations, known to be highly resistant to race 2. Stem-inoculated plants localized the infection close to the inoculation site; stems of root-inoculated plants remained unaffected. The localization response also occurred in Early Sam and Novada carnations stem-inoculated withF. oxysporum f. sp.lycopersici.Samenvatting Tussen interacties van Early Sam-anjers met fysio's 1, 2, 4 en 8 vanF. oxysporum f. sp.dianthi werden verschillen in ziekteontwikkeling gevonden na wortel-zowel als stengelinoculatie. Fysio 1 gaf verbleking en verdroging van de bladeren. Aangetast vaatweefsel was gelijkmatig vaal of lichtbruin van kleur, en werd hevig gekoloniseerd, maar vrijwel niet afgebroken. Afweerreacties kwamen slechts traag op gang. Fysio 2 gaf vergeling, in het bijzonder van de hoofdnerven, en verdroging van de bladeren. Aangetast vaatweefsel was wit met donkerbruine randen. Gekoloniseerd weefsel werd afgebroken, hetgeen leidde tot de vorming van holten in het vaatweefsel. In de lagere gekoloniseerde delen traden veel afweerreacties op, hetgeen soms lokalisatie van het pathogeen tot gevolg had. Fysio 4 gaf eenzelfde ziekteontwikkeling als fysio 2, maar minder afweerreacties. Fysio 8 gaf lesies bij de hoofdnerven, en verbleking, verdroging en necrose van bladeren. Aangetast vaatweefsel was gelijkmatig lichtbruin van kleur. Afbraak van gekoloniseerd vaatweefsel werd zelden waargenomen; veel afweerreacties vergezelden de kolonisatie tot hoog in de stengel.Inoculatie van Novada anjers met fysio's 1,2 en 4 vanF. oxysporum f. sp.dianthi had geen ziektesymptomen tot gevolg. Via de stengel geïnoculeerde planten lokaliseerden de infectie ter hoogte van het inoculatiepunt; de stengels van via de wortels geïnoculeerde planten waren onaangetast. De lokalisatiereactie trad ook op in Early Sam en Novada anjers na inoculatie via de stengel metf. oxysporum f. sp.lycopersici.  相似文献   

8.
The Elegans fusaria causing wilt disease of carnation. I. Taxonomy   总被引：1，自引：0，他引：1  
The distinction of the wilt disease pathogen of carnationFusarium (oxysporum var.)redolens fromF. oxysporum (var.oxysporum) is considered. Previous reports that isolates of both taxa cause indistinguishable diseases in carnation are confirmed.F. (oxysporum var.)redolens andF. oxysporum were found to form one variable complex on morphological criteria. Apparently, host specialization rather than morphological variation reflects the evolutionary relationships in theFusarium sectionElegans. The distinction ofF. redolens fromF. oxysporum does therefore not seem justified, neither at specific nor at varietal level.Samenvatting Het onderscheid tussenFusarium (oxysporum var.)redolens enF. (oxysporum var.)oxysporum als verwekkers van verwelkingsziekte bij anjer wordt ter discussie gesteld. Fytopathologisch onderzoek bevestigde vermeldingen in de literatuur dat voor anjer pathogene isolaten van beide soorten ziekten veroorzaken die niet te onderscheiden zijn; dit is ook bekend voor andere gewassen. Op morfologische gronden blekenF. (oxysporum var.)redolens enF. oxysporum één variabel complex te vormen. Kennelijk geeft de pathogene specialisatie inFusarium sectieElegans de evolutionaire verwantschappen beter weer dan de morfologische variatie. Het onderscheiden vanF. redolens naastF. oxysporum is daarom noch als soort, noch als variëteit gerechtvaardigd.  相似文献   

9.
Nitrogen metabolism disorder in watermelon leaf caused by fusaric acid   总被引：1，自引：0，他引：1  
The effect of fusaric acid (FA) on the activity of leaf nitrogen (N) metabolism enzymes in watermelon seedlings supplied with different N forms was studied. The results showed that FA inhibited nitrogen uptake and caused decreased leaf amide and protein but increased the content of ammonium and amino acids. When treated with FA the activities of enzymes in the pathway for the synthesis of amino acid in leaves (GS, GOGAT, and GDH) were decreased by 15–23%, 13–40%, and 71–86%, respectively. The activity of asparagine synthetase was decreased by 34–57%. The proteinase activity was initially increased by 37–125% at 12 h after treatment of FA but then subsequently decreased. The activity of glutamate-pyruvate aminotransferase was increased by 280–400%, though the activity of glutamate-oxaloacetate aminotransferase was decreased by 30–63%. It was suggested that FA inhibited the uptake of ammonium in seedlings and suppressed the activities of amino acid and amide synthases, while stimulating proteinase activity.A new pathogenic mechanism of watermelon infection by Fusarium spp. was found as FA caused the complete disorder and collapse of the host plant's nitrogen metabolism. This work provides a new insight into the progression of watermelon wilting caused by Fusarium oxysporum f.sp. niveum.  相似文献   

10.
The mechanisms of suppression of fusarium wilt of carnation by two fluorescentPseudomonas strains were studied.Treatments of carnation roots withPseudomonas sp. WCS417r significantly reduced fusarium wilt caused byFusarium oxysporum f. sp.dianthi (Fod). Mutants of WCS417r defective in siderophore biosynthesis (sid–) were less effective in disease suppression compared with their wild-type. Treatments of carnation roots withPseudomonas putida WCS358r tended to reduce fusarium wilt, whereas a sid– mutant of WCS358 did not.Inhibition of conidial germination of Fod in vitro by purified siderophores (pseudobactins) of bothPseudomonas strains was based on competition for iron. The ferrated pseudobactins inhibited germination significantly less than the unferrated pseudobactins. Inhibition of mycelial growth of Fod by bothPseudomonas strains on agar plates was also based on competition for iron: with increasing iron content of the medium, inhibition of Fod by thePseudomonas strains decreased. The sid– mutant of WCS358 did not inhibit Fod on agar plates, whereas the sid– mutants of WCS417r still did. This suggests that inhibition of Fod by WCS358r in vitro was only based on siderophore-mediated competition for iron, whereas also a non-siderophore antifungal factor was involved in the inhibition of Fod by strain WCS417r.The ability of thePseudomonas strains to induce resistance against Fod in carnation grown in soil was studied by spatially separating the bacteria (on the roots) and the pathogen (in the stem). Both WCS417r and its sid– mutant reduced disease incidence significantly in the moderately resistant carnation cultivar Pallas, WCS358r did not.It is concluded that the effective and consistent suppression of fusarium wilt of carnation by strain WCS417r involves multiple mechanisms: induced resistance, siderophore-mediated competition for iron and possibly antibiosis. The less effective suppression of fusarium wilt by WCS358r only depends on siderophore-mediated competition for iron.  相似文献   

11.
甘草根腐病病原菌鉴定   总被引：10，自引：0，他引：10  
 甘草(Glycyrrhiza uralensis Fish.)别名甜草、蜜草、甜根子, 为豆科多年生草本植物, 以根与根茎入药, 具有补脾益气、清热解毒、祛痰止咳、缓急止痛、调和诸药之功效, 是我国临床常用的中药材, 也可用作食品添加剂。甘草主要分布在我国的内蒙古、甘肃和宁夏, 在青海、陕西、新疆、黑龙江、辽宁、吉林、河北、山西等地局部地区也有分布。宁夏盐池县是我国乌拉尔甘草的重要产区, 面积大、贮量多、品质好, 1995年被誉为“中国甘草之乡” [1]。近年来, 野生甘草遭到了大规模采挖, 甘草蕴藏量急剧减少, 目前主要通过人工种植来满足市场需求。随着甘草种植面积的不断扩大, 甘草病虫害日趋严重, 根腐病危害尤为突出, 直接影响甘草的产量和品质, 造成巨大经济损失。  相似文献   

12.
Defense responses to Fusarium oxysporum f. sp. asparagi and F. proliferatum were compared after root inoculation of the asparagus fern, Asparagus densiflorus vars. Myersii and Sprengeri, and cultivated asparagus, A. officinalis cv. Guelph Millennium. Both varieties of A. densiflorus exhibited a hypersensitive response with rapid death of epidermal cells within 8–24 h and restricted the fungal growth. In A. officinalis roots, rapid cell death was not found, and necrotic lesions were observed 8–14 d after fungal inoculation. Peroxidase and phenylalanine ammonia-lyase activities increased significantly in inoculated A. densiflorus but not A. officinalis plants. Local and systemic induction of peroxidase activity was detected after pathogen inoculation in root and spear tissues, respectively, of A. densiflorus. POX activity decreased in roots of inoculated A. officinalis by 8 d post-inoculation. Germination and germ tube growth were inhibited when spores of F. oxysporum f. sp. asparagi were incubated in root exudates and on root segment surfaces of inoculated A. densiflorus plants exhibiting hypersensitive cell death. Spore germination of F. proliferatum and three fungi non-pathogenic to cultivated asparagus was inhibited as well. Rapid induction of hypersensitive cell death in A. densiflorus was associated with restriction of fungal growth, and activation of peroxidase and phenylalanine ammonia-lyase, two defense enzymes thought to be important for plant disease resistance.  相似文献   

13.
A study was conducted in two greenhouses with a history of Fusarium crown and root rot (Fusarium oxysporum f.sp.radicis-lycopersici, Forl) and root-knot nematodes (Meloidogyne javanica andM. incognita). During the 2005–06 growing season, the effectiveness of soil disinfestation by solarization in combination with low doses of metham-sodium (500, 750, 1000 and 1250l ha−1) or dazomet (400 g ha−1), was tested against soilborne pathogens and nematodes in an attempt to find a suitable alternative to methyl bromide, which is soon to be phased out. Solarization alone was not effective in the greenhouse with a high incidence ofForl. In the greenhouse with a low level ofForl, all the treatments tested reduced disease incidence, and were therefore considered to be applicable for soil disinfestation. In addition, root-knot nematode density decreased with all the treatments tested in both of the greenhouses.  相似文献   

14.
The inheritance of resistance toFusarium oxysporum f.sp.cucumerinum race 1 was determined in the cucumber cv. WIS-248 by analyzing segregation of F1, F2, and BC populations of crosses with the susceptible cv. Straight-8. Resistance was conferred by a single dominant gene. In an allelism test, it was proven that theFcu-1 gene, which confers resistance toF. oxysporum f.sp.cucumerinum races 1 and 2 in cucumber cv. SMR-18 and theFoc gene, which confers resistance toF. oxysporum f.sp.cucumerinum race 2 in cucumber cv. WIS-248, are indistinguishable.  相似文献   

15.
Survival of a heat-tolerant pathogen Macrophomina phaseolina, causing dry root rot of clusterbean, was studied by incorporation and retrieval of infected residue samples at various stages of the composting process of pearl millet (Pennisetum glaucum) and clusterbean (Cyamopsis tetragonoloba) residues. During the heating phase, temperatures varied from 48–51°C at 30cm and 60–62°C at 60cm depth in compost pits. Reduction in survival of M. phaseolina propagules (13–23%) was significantly higher in the residues enriched with 4% urea-N and kept at 60cm compared to 2% urea-N and at 30cm. However, a heat phase (48–62°C) was not enough to completely eradicate M. phaseolina propagules from infected residues. Further reductions (54–61%) in survived propagules were achieved by sub-lethal temperatures (48–53°C) when moistened compost materials were exposed to heat during summer days. Beneficial effects of composts were ascertained on dry root rot intensity, seed yield of clusterbean and densities of M. phaseolina, Nitrosomonas and antagonists in soil. In a two-year field study, all the composts significantly reduced plant mortality due to dry root rot and increased the yield of clusterbean. The highest disease suppression and yield promotion were recorded in soil amended with pearl millet compost and cauliflower leaf residue compost, respectively. Soil amendment with compost also lead to a significant reduced density of M. phaseolina and an increased density of antagonistic actinomycetes, lytic bacteria and Nitrosomonas. Among composts, greater potential of cauliflower compost in enhancing population of antagonists in soil was discernible.  相似文献   

16.
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17.
In an earlier study, treatment of radish seed with the bacteriumPseudomonas fluorescens WCS374 suppressed fusarium wilt of radish (Fusarium oxysporum f. sp.raphani) in a commercial greenhouse [Leemanet al., 1991b, 1995a]. In this greenhouse, the areas with fusarium wilt were localized or expanded very slowly, possibly due to disease suppressiveness of the soil. To study this phenomenon, fungi were isolated from radish roots collected from the greenhouse soil. Roots grown from seed treated with WCS374 were more abundantly colonized by fungi than were roots from nonbacterized plants. Among these were several species known for their antagonistic potential. Three of these fungi,Acremonium rutilum, Fusarium oxysporum andVerticillium lecanii, were evaluated further and found to suppress fusarium wilt of radish in a pot bioassay. In an induced resistance bioassay on rockwool,F. oxysporum andV. lecanii suppressed the disease by the apparent induction of systemic disease resistance. In pot bioassays with thePseudomonas spp. strains, the pseudobactin-minus mutant 358PSB– did not suppress fusarium wilt, whereas its wild type strain (WCS358) suppressed disease presumably by siderophore-mediated competition for iron. The wild type strains of WCS374 and WCS417, as well as their pseudobactin-minus mutants 374PSB– and 417PSB– suppressed fusarium wilt. The latter is best explained by the fact that these strains are able to induce systemic resistance in radish, which operates as an additional mode of action. Co-inoculation in pot bioassays, ofA. rutilum, F. oxysporum orV. lecanii with thePseudomonas spp. WCS358, WCS374 or WCS417, or their pseudobactin-minus mutants, significantly suppressed disease (except forA. rutilum/417PSB– and all combinations with 358PSB–), compared with the control treatment, if the microorganisms were applied in inoculum densities which were ineffective in suppressing disease as separate inocula. If one or both of the microorganism(s) of each combination were applied as separate inocula in a density which suppressed disease, no additional suppression of disease was observed by the combination. The advantage of the co-inoculation is that combined populations significantly suppressed disease even when their individual population density was too low to do so. This may provide more consistent biological control. The co-inoculation effect obtained in the pot bioassays suggests that co-operation ofP. fluorescens WCS374 and indigenous antagonists could have been involved in the suppression of fusarium wilt of radish in the commercial greenhouse trials.Abbreviations CFU colony forming units - KB King's B - PGPR plant growth-promoting rhizobacteria - CQ colonization quotient  相似文献   

18.
 对分离获得的32株苦瓜枯萎病菌菌株进行形态学特征和寄主专化型测定, 结果表明, 测试的苦瓜枯萎病菌株均为尖孢镰刀菌苦瓜专化型 (Fusarium oxysporum f. sp. momordicae), 这些菌株可以侵染苦瓜和瓠瓜幼苗, 但不侵染其他葫芦科瓜类作物。对苦瓜枯萎病菌菌株的rDNA-ITS区 (ITS1、5.8S和ITS2)序列进行扩增测序, 结果显示其序列长度均为456 bp;聚类分析表明测序菌株与镰刀菌属中尖孢镰刀菌不同专化型的菌株聚为一群。利用RAPD标记技术分析苦瓜枯萎病菌的遗传多样性, 结果显示苦瓜枯萎病菌株与其他葫芦科瓜类作物枯萎病菌株间的遗传相似系数范围为0.59~0.99, 当遗传相似系数为0.85时, 供试的48个菌株分成10个类群 (G1~10)。在RAPD聚类树中所有苦瓜枯萎病菌株聚在一个分支上 (G1群), 菌株间的遗传相似系数范围为0.92~1.00, 具有较高的遗传相似性, 且菌株的聚群与地理来源存在一定的相关性。  相似文献   

19.
By random amplified polymorphic DNA (RAPD) analysis of the representative isolates of each race of Fusarium oxysporum f. sp. lactucae, RAPD fragments of 0.6, 1.6, and 2.9kb were obtained. The 0.6-kb RAPD fragment was common to the representative isolates of all three races. Amplification of the 1.6- and 2.9-kb fragments were unique to the isolates of races 1 and 2, respectively. Sequence tagged site (STS) marker FLA0001, FLA0101, and FLA0201 were generated from the 0.6-, 1.6-, and 2.9-kb RAPD fragments, respectively. Polymerase chain reaction (PCR) analysis showed that FLA0001 was common to all 49 isolates of F. oxysporum f. sp. lactucae. FLA0101 was specifically generated from all 23 isolates of race 1 but not from races 2 or 3. FLA0201 was specifically amplified from all 12 isolates of race 2 but not from races 1 or 3. In two isolates of F. oxysporum f. sp. lactucum, PCR amplified FLA0001 and FLA0101 but not FLA0201. On the other hand, these STS markers were not detected from isolates of five other formae speciales. Because these STS markers were not generated from isolates of other plant pathogenic fungi, bacteria, or plant materials examined in this study, PCR analysis combined with the three STS markers should be a useful means for rapid identification of races of F. oxysporum f. sp. lactucae.  相似文献   

20.
The antifungal glycoalkaloid -tomatine accumulates in tomato plants and may protect plants from fungal infection. Fusarium oxysporum f. sp. lycopersici, the causal agent of vascular wilt of tomato, produces a tomatinase (FoToml) that degrades -tomatine to the nontoxic compounds tetrasaccharide lycotetraose and tomatidine. Induction of tomatinases and the distribution of FoToml homologs were examined among 30 strains belonging to 16 formae speciales of F. oxysporum. Tomatinase activity was found in 27 strains belonging to 15 formae speciales, but FoToml homologs (>98% sequence identity) were detected in only six strains belonging to four formae speciales. To identify tomatinases other than FoToml, -tomatine-inducible proteins of another tomato pathogen F. oxysporum f. sp. radicis-lycopersici were analyzed by two-dimensional gel electrophoresis. A protein with a molecular mass of 64kDa accumulated in the -tomatine-induced culture filtrates, and the protein had tomatinase activity, degrading -tomatine to lycotetraose and tomatidine.  相似文献   

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