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1.
Quantitative resistance to Leptosphaeria maculans in Brassica napus was investigated in field and controlled environments using cultivars Darmor (with quantitative resistance) and Eurol (without quantitative resistance). In field experiments, numbers of phoma leaf spot lesions in autumn/winter and severity of stem canker the following summer were assessed in three growing seasons. There were no differences between Darmor and Eurol in number of leaf lesions in autumn/winter. However, stem cankers were less severe on Darmor than Eurol at harvest the following summer. In controlled-environment experiments, development of leaf lesions at different temperatures (5–25°C) and wetness durations (12–72 h) was investigated using ascospore inoculum; symptomless growth of L. maculans along leaf petioles towards the stem was quantified using quantitative PCR and visualized using GFP-expressing L. maculans ; growth of L. maculans within stem tissues was investigated using GFP-expressing L. maculans . There were more leaf lesions on Darmor than Eurol, although there was no difference between Darmor and Eurol in L. maculans incubation period. There were no differences between Darmor and Eurol in either distance grown by L. maculans along leaf petioles towards the stem or quantity of L. maculans DNA in leaf petioles, but L. maculans colonized stem tissues less extensively on Darmor than Eurol. It was concluded that quantitative resistance to L. maculans operates during colonization of B. napus stems by the pathogen.  相似文献   

2.
The influence of competitive effects between two isolates, of the number of infection sites on cotyledons and of host polygenic resistance on the systemic growth of Leptosphaeria maculans , the cause of phoma stem canker in oilseed rape ( Brassica napus ), were investigated. Controlled-condition experiments were conducted with two oilseed rape doubled haploid lines, one susceptible and the other with a high level of polygenic resistance, inoculated via wounded cotyledons with conidial suspensions obtained from two isolates. Expression of cankers in plants was enhanced by exposing inoculated plants to low temperature (6°C) followed by warm temperature (20°C). The fungus was detected by PCR amplifications of three minisatellite markers in all stems with visible canker symptoms and also in the stems of 14 of the 59 plants without visible cankers on the hypocotyls. Disease severity increased with the number of infection sites on cotyledons: in one of the three replicate experiments, the mean external necrosis length on the hypocotyl ranged from 6·47 to 35·3 mm for one and eight infections sites on cotyledons, respectively. The probability of an isolate reaching the hypocotyl from inoculated cotyledons decreased with increasing competing inoculum load on cotyledons: for instance, for isolate A290v it decreased from 1 when inoculated alone to 0·28 when coinoculated with six drops of competing isolate P27d. Polygenic resistance significantly reduced disease incidence and severity. For instance, in one of the three replicate experiments, disease incidence ranged from more than 74% in susceptible plants to 16% in resistant ones, while mean external necrosis length was up to 35·3 and 6·5 mm on susceptible and on resistant plants, respectively. This study offers new possibilities for assessing levels of polygenic resistance to stem canker in B. napus and studying the aggressiveness of L. maculans isolates.  相似文献   

3.
Effects of temperature on maturation of pseudothecia of Leptosphaeria maculans and L. biglobosa , closely related species which coexist on UK oilseed rape, were investigated. Stages in pseudothecial maturation on naturally infected oilseed rape debris were examined, both in controlled environments (5, 10, 15 or 20°C) under continuous wetness and in natural conditions (debris exposed in September and December 2000, and July, September and November 2002). Pseudothecia sampled weekly were assigned to maturation classes A (asci undifferentiated), B (asci differentiated), C (ascospores differentiated) or D (ascospores mature). Progress in pseudothecial maturation (assessed by time until 50% of pseudothecia reached each class) was similar for L. maculans and L. biglobosa at 15–20°C, but L. biglobosa matured more slowly at < 10°C. Maturation time decreased almost linearly with temperature from 5 to 20°C under continuous wetness but was longer in natural conditions, especially when periods of dry weather occurred. Differences in pseudothecial maturation are likely to contribute to epidemiological differences between L. maculans and L. biglobosa , which may explain their coexistence. It is appropriate to use the degree-day approximation to assess pseudothecial maturation at temperatures between 5 and 20°C, providing debris is wet.  相似文献   

4.
Among 146 accessions of Lycopersicon pimpinellifolium , 132 of L. esculentum var. cerasiforme and 53 of L. peruvianum screened for resistance to powdery mildew, caused by Oidium lycopersici , a wide variation in reactions was found. Two plants of L. esculentum var. cerasiforme accession LA-1230 were resistant. One resistant symptomless plant of accession LA-1230, designated LC-95, produced homozygous resistant progenies. LC-95 was crossed with cv. Marmande (susceptible parent) and F1, F2 and backcrosses to the resistant and the susceptible parents were derived. These genotypes were grown in glasshouses at 23°C and 95–100% RH and inoculated with O. lycopersici . The F1 plants were susceptible. F2 and backcross segregations fitted the hypothesis of a single recessive gene which is here designated ol-2 .  相似文献   

5.
In controlled environment experiments to study early development of light leaf spot, lesions developed with leaf wetness durations of 16 to 48 h after inoculation of oilseed rape with conidial suspensions of Pyrenopeziza brassicae at 12 or 18°C, but not with leaf wetness durations of 0 to 13h. The incubation period was 21 to 22 days at 12°C and 14 to 18 days at 18°C for leaf wetness durations of 16 to 48 h. The latent period was 21 to 23 days at 12°C and 18 to 19 days at 18°C, and the total number of lesions increased with increasing leaf wetness duration at both temperatures. In field experiments, light leaf spot always developed on oilseed rape with a leaf wetness duration of 48 h after inoculation in both 1990/1991 and 1991/1992, but the percentage leaf area affected was less on plants placed in an oilseed rape crop than on those placed in a glasshouse. Plants moved to an oilseed rape crop immediately after inoculation nearly always developed light leaf spot symptoms when they were inoculated between 19 October 1990 and 1 March 1991 or between 27 September 1991 and 14 February 1992, but plants inoculated between 31 August and 16 October 1990 or on 20 September 1991, when estimated leaf wetness duration was less than 16 h for several days after they were placed in crops, did not develop symptoms. The latent period of light leaf spot on plants transferred to the oilseed rape crop was 15 to 40 days, and there was an approximately linear relationship between 1 (latent period) and mean temperature during this period. The accumulated temperature during the latent period ranged from c. 150 to 250 day-degrees. The severity of lesions on these plants increased with increasing temperature from 5 to 15°C.  相似文献   

6.
Assessment of resistance to Plasmodiophora brassicae in swedes   总被引：1，自引：1，他引：0  
A method is described in which swede seedlings inoculated with standardized concentrations of resting spores of specific populations of Plasmodiophora brassicae can be evaluated for resistance in different environments. Similar ranking for resistance of four swede cultivars inoculated with one pathogen population was obtained from seedling tests in a glasshouse, from young plants in a polythene tunnel, and from mature plants in field trials. Differential resistance of the four cultivars to two pathogen populations evident in glasshouse seedling tests was more clearly demonstrated in the field where there was a highly significant cuitivar × pathogen population interaction (p<0 001) for both root fresh weight and mean disease category.
The inclusion of uninoculated control plants in field trials enabled a direct comparison of yield with that from inoculated plants. Cultivars were defined as resistant in terms of yield if they did not suffer any crop loss in comparison with uninoculated plants, even though some plants showed restricted gall development. The distribution of fresh weight to galls, roots and shoots could be used to characterize the relative resistance of cultivars; in the most susceptible cultivars there was rapid gall development but little increase in root or shoot fresh weight between 6 and 12 weeks after inoculation. Differential response was determined during the 6 weeks following inoculation; the implications of this observation are discussed in relation to growth stage and rate of development of host and pathogen.  相似文献   

7.
Relationships between development of eyespot, caused by Oculimacula yallundae (OY) or O. acuformis (OA) on stems of winter wheat (cv. Avalon), and thermal time (°C days after sowing) were investigated in field experiments in 1985/86, 1986/87 and 1987/88 (two experiments). In all experiments, the incidence and severity of stem eyespot (uninoculated plots, OY- and OA-inoculated plots) were linearly related to accumulated thermal time after sowing. There were ca. 600–800°C days from the time of the first sample when eyespot lesions were recorded on stems to the time when maximum eyespot incidence or severity was recorded. Relationships between stem eyespot incidence or severity and thermal time differed between seasons, with more severe eyespot in 1986/87 and 1987/88 than 1985/86. Both the severity and volume of stem lesions were initially greater in OY-inoculated plots than OA-inoculated plots in spring but differences were less by harvest in all seasons. The percentage of plants with stems colonized by OY or OA over all plots (including uninoculated) showed a consistent pattern in 1986/87 and 1987/88 (two experiments), with the percentage colonized by OY greater initially and the percentage colonized by OA gradually increasing with time towards harvest.  相似文献   

8.
The environmental factors that influence infection of lettuce by ascospores of Sclerotinia sclerotiorum , and subsequent disease development, were investigated in controlled environment and field conditions. When lettuce plants were inoculated with a suspension of ascospores in water or with dry ascospores and exposed to a range of wetness durations or relative humidities at different temperatures, all plants developed disease but there was no relationship between leaf wetness duration or humidity and percentage of diseased plants. Ascospores started to germinate on lettuce leaves after 2–4 h of continuous leaf wetness at optimum temperatures of 15–25°C. The rate of development of sclerotinia disease and the final percentage of plants affected after 50 days were greatest at 16–27°C, with disease symptoms first observed 7–9 days after inoculation, and maximum final disease levels of 96%. At lower temperatures, 8–11°C, disease was first observed 20–26 days after inoculation, with maximum final disease levels of 10%. Disease symptoms were always observed first at the stem base. In field-grown lettuce in Norfolk, 2000 and 2001, inoculated with ascospore suspensions, disease occurred only in lettuce planted in May and June, with a range of 20–49% of plants with disease by 8 weeks after inoculation. In naturally infected field-grown lettuce in Cheshire, 2000, disease occurred mainly in lettuce planted throughout May, with a maximum of 31% lettuce diseased within one planting, but subsequent plantings had little (≤ 4%) or no disease. Lack of disease in the later plantings in both Norfolk and Cheshire could not be attributed to differences in weather factors.  相似文献   

9.
Phytophthora infestans is able to produce oospores in leaves of potato and tomato plants after inoculation with a mixture of Al and A2 mating-type isolates. Various conditions for oospore formation were analysed. Under controlled conditions, oospores were produced in potato leaves at temperatures ranging from 5 to 25° C. In leaves of potato cultivar Bintje incubated at 15°C, oogonia and antheridia were observed 6 days after inoculation and thick-walled oospores appeared 3-4 days later. In field experiments oospores were found in leaves and stems of potato cultivars Bintje, Irene and Pimpernel and in leaves, stems and fruits of tomato cultivar Moneymaker within 2 weeks after inoculation. A bioassay was developed to test the survival of oospores in soil under various conditions. To determine whether late-blight infections derived from infectious soil were caused by oospwres, DNA fingerprinting was performed. DNA fingerprint probe RG-57 was suitable for distinguishing asexual progeny from recombinant progeny arising from soil-borne oospores. We demonstrated survival of viable, infectious oospores of P. infestans in soil during the winter of 1992–93. Oospores were not infectious from soil exposed to temperatures of 40°C or higher but in the range 35°C to as low as – 80°C for 48 h, oospores survived.  相似文献   

10.
A series of experiments was carried out over four years in a glasshouse with computer control of humidity and temperature to investigate the effect of humidity on the development of tomato powdery mildew. Four relative humidities (RHs) (80%, 87%, 90% and 95%) at constant 19°C were maintained over an eight-week experimental period during the Autumn. Disease was greatest at 80% RH and was progressively less with increasing RH to a minimum level at 95% RH on both inoculated plants, introduced to act as initial infection sources, and on adjacent uninoculated plants. The results indicate that high humidities may decrease severity of this disease in the glasshouse and may help management of this disease in the future.  相似文献   

11.
Hélias  rivon  & Jouan 《Plant pathology》2000,49(1):33-42
Transmission of pectinolytic Erwinia species from infected mother tubers to daughter tubers has been studied mainly through detection tests, carried out at harvest, on limited samples of tubers produced by plants grown from artificially inoculated mother tubers. However, detection has not been performed on samples collected at different stages of crop development, in order to follow the contamination progress in different organs through the plants to the progeny tubers. In this study the bacterial contamination of progeny tubers was investigated by detecting Erwinia carotovora ssp. atroseptica in different symptomless plant organs (stolons, stems, progeny tubers) and in the parts with or without symptoms of diseased stems, collected at various stages of crop development. Infection levels in below- and above-ground organs of plants of two cultivars differing in their resistance to Erwinia, infected by either vacuum infiltration or sand wounding, were monitored throughout the growing season and at harvest using DAS-ELISA and PCR. Detection tests showed that healthy organs from symptomless plants were less frequently contaminated than symptomless organs from diseased plants, and that stolons were precociously and more frequently contaminated than stems and daughter tubers, irrespective of the health of the plant. Stem infections were shown to progress latently in the stem, bacteria usually being recovered 10–15 cm past visible lesions. In many cases, typical aerial stem-rot symptoms could be related to this upward movement of bacteria from the infected mother tuber. Daughter tubers without symptoms were shown to be frequently contaminated, usually at heel ends, suggesting internal contamination from mother tuber to progeny.  相似文献   

12.
Pairwise combinations were carried out between the eight isolates originating from each of three asci of the B-group of Leptosphaeria maculans . Some of the pairings produced mature pseudothecia when incubated on wheat straws at 18°C and under a 12-h photoperiod of blue light. Isolates within a given tetrad could be attributed to one of two sexual compatibility groups, on the basis of combinations of isolates leading to fertile crosses. Within each tetrad, mating type segregated in a 1:1 ratio, suggesting the existence of one mating type gene ( MAT1 ) with two alleles MAT 1–1 and MAT 1–2. Under these same conditions, each individual isolate from an A-group ascus originating from Brassica juncea produced pseudothecia with one or other of two compatible A-group testers originating from B. napus . However, attempts to mate these eight A-group single-ascospore isolates with two B-group single-ascospore isolates of opposite mating types remained unsuccessful. This work is the first successful report of in vitro sexual reproduction between B-group isolates, and provides evidence for bipolar heterothallism in B-group isolates of L. maculans . The implications of this mating protocol for genetic studies of B-group isolates and the consequences of this work for the taxonomy of L. maculans are discussed.  相似文献   

13.
Summary Of the carnation varieties Pink Sim and Harvest Moon no virus-free plants were known. As therapy by means of heat treatment gave no satisfactory results, this method was combined with applacation of meristem culture. From plants kept for 6–8 weeks at 40°C, small portions from the tips of the stems, consisting of the meristem and some leaf primordia, were isolated and cultured in a nutrient agar under sterile conditions. The small plants that developed were transferred to soil. They grew into normal carnation plants in which no virus could be demonstrated either by serological test or by local lesion assays. From these plants virus-free stocks of these two varieties will be raised.  相似文献   

14.
Summary. Most freshly-matured seeds of Thlaspi arvense L. (Brassicaceae) were dormant at maturity in May. Seeds sown on soil germinated in autumn and spring, but mostly in autumn. Buried seeds exhumed at monthly intervals and tested in light and darkness over a range of thermoperiods exhibited annual dormancy/non-dormancy cycles. However, the dormant period was short, usually only in April, but sometimes May, and in some years 1–6% of the seeds remained conditionally dormant. After-ripening occurred during summer, and seeds were non-dormant during autumn. Seeds entered conditional dormancy in winter and dormancy in late winter or early spring. When buried dormant seeds were kept at 25/15, 30/15 or 35/20°C for 12 weeks, they gained the ability to germinate to 95–100% at 15/6, 20/10, 25/15, 30/15 and 35/20°C. After burial for 12 weeks at 15/6 and 20/10°C, seeds germinated to 80–100% at 15/6, 20/10 and 25/15°C. but to only 11–64% at 30/15 and 35/20°C. After 4 weeks at 5°C, initially-dormant seeds germinated to 100% at all thermoperiods except 35/20°C, where only 15% of them germinated. However, after 18 weeks at 5°C, only 0–1% of the seeds germinated at all thermoperiods. Most non-dormant seeds exposed to 1, 5 and 15/6°C for 16 weeks were induced into dormancy; 1–15% entered conditional dormancy and thus germinated only at 15/6, 20/10 and 25/15°C. This study indicates that seeds of winter annual plants of T. arvense are non-dormant in autumn and enter dormancy in winter, while those from summer annuals are dormant in autumn and become non-dormant during winter.  相似文献   

15.
Botrytis allii was incubated at 20, 10,4, 2,0, – 2 and –4° to investigate effects of temperature on growth, sporulation and germination on potato dextrose agar (PDA), and to estimate incidence and severity of disease on garlic bulbs inoculated with the pathogen during storage. B. allii-was capable of growing to a colony diameter of 17 mm after 20 weeks, sporulating and germinating on PDA at temperature as low as – 4°C. After 12 weeks at –4 and -2°C the mycelial growth was observed only on 45–54% of bulbs wound-inoculated with conidial suspension, and infection was limited to 5 mm in diameter on the surface of inoculation sites without producing any symptoms of the disease. Temperature responses were similar for mycelial growth, conidial germination and infection, but mycelial growth and sporulation was slower and later on garlic bulbs than in culture. Wounds were readily colonized by B. allii. No disease was found on unwounded bulbs that were inoculated with conidial suspensions and with mycelial plugs at various temperatures. Only 16–95% of cloves became infected by contact with other cloves within the same bulb after 12 weeks of storage at temperatures of 4–20 C.  相似文献   

16.
Alfalfa (Medicago sativa) cv. Beaver was screened for resistance to alfalfa mosaic virus (AIMV). A1MV infection in clonal plants was tested by double-antibody sandwich ELISA 4 and 8 weeks after inoculation with purified A1MV (1 mg/ml in 0025 M phosphate buffer, pH 7 0). Twelve clones showed a hypersensitive reaction 3–4 days after inoculation and the infection was restricted to the inoculated leaves. All the plants of hypersensitive clones consistently produced local lesions when inoculated with purified AIM V. In contrast, plants inoculated with AIMV in crude sap remained symptomless, although AIMV was detectable in inoculated leaves. The remaining 16 clones were susceptible to AIMV and showed systemic infection.  相似文献   

17.
Breeding tomatoes for resistance to tomato yellow leaf curl begomovirus   总被引：1，自引：0，他引：1  
Tomato yellow leaf curl begomovirus (TYLCV) can be devastating to tomato crops in tropical and subtropical regions. The development of resistant cultivars is the best option for the control of TYLCV. The TYLCV-resistance level of a new breeding line, TY172, alongside that of commercial cultivars known to be resistant to the virus, was evaluated in a field test by comparing the yield performance of inoculated plants with that of uninoculated plants of the same line or cultivar. There were substantial differences among the different entries tested in the extent of yield loss relative to the corresponding uninoculated control plants. This comparison between inoculated and uninoculated plants of the same entry provides a quantitative assay for resistance level. All resistant commercial cultivars tested developed different levels of disease symptoms. Only line TY172 showed no symptoms of the disease. A low level of viral DNA was detected in infected TY172, showing that it is a symptomless carrier of TYLCV. When TY172 was crossed with susceptible lines, the hybrids exhibited milder symptoms than the susceptible parent, yet higher than that of TY172, suggesting a partial dominance for TY172 resistance. Upon inoculation of F2 populations, the amount of symptomless individuals appeared in a ratio approximating 7:64. This suggests that at least three genes appear to account for the resistance.  相似文献   

18.
Symptoms of Cucumber mosaic virus (CMV) on yellow passion flower ( Passiflora edulis f. flavicarpa ) are characterized by bright yellow mottling on leaves, starting at random points on the vine and diminishing in intensity towards the tip, which becomes symptomless as it grows. To determine whether symptomless portions of vines are CMV-free or represent latent infection, leaves with and without symptoms were collected from infected vines in the field. Biological, serological (plate-trapped antigen enzyme-linked immunosorbent assay, PTA-ELISA), Western blot and dot-blot hybridization assays showed that portions of the vines without symptoms were CMV-free. Vegetatively propagated vines with symptoms showed remission of symptoms on newly developed leaves. One year later, no CMV was detected in the upper leaves of these plants. Mechanically inoculated passion flower seedlings behaved similarly; symptoms were shown by few leaves after inoculation. Afterwards, plants became symptomless and CMV was not detected in the upper leaves or root system, 40 or 85 days after inoculation. The mechanism responsible for remission of symptoms accompanied by CMV disappearance is not known.  相似文献   

19.
Exposure of banana bunchy top virus (BBTV)-infected plantlets of Cavendish banana to 40°C for 16 h daily for periods of up to 5 weeks did not free them from BBTV. However, BBTV was less readily transmitted by aphids from treated plants than from untreated controls. The same heat treatment applied for up to 12 weeks also failed to eliminate the virus from BBTV-infected tissue. When similar BBTV-infected tissue was cultured for 3 months at 35°C some of the buds started to produce healthy looking plantlets. Five out of 11 cultures produced healthy-looking plantlets in 6 months. Crude extracts from the leaves of these plantlets did not react with a monoclonal antibody prepared against BBTV. When heat-treated, healthy-looking plantlets were inoculated with viruliferous aphids all plants developed bunchy top symptoms indicating that they were not resistant to BBTV. The results suggest that the uneven distribution and low concentration of virus after treatment at high temperature leads to BBTV-free primordial cells which in turn may develop into healthy plantlets.  相似文献   

20.
Summary. Monthly samples of field-grown rhizomes and aerial stems of Polygonum amphibium were tested for innate dormancy during parts of 2 years in England and during 5 months of a third year in southern Germany. All stems and rhizomes were cut into two-node fragments, planted in soil in a warm glasshouse, and the new shoots counted after 3 weeks. Dormancy per month for different categories of stems varied from 0 to 23%, averaging 4–3% for all fragments tested but only 1–3% for mature buds. No evidence of a dormant period was found in either country.
Incidence de la darmance dans une tige à deux noeuds et des fragments de rhizome de Polygonum amphibium L.  相似文献   

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