No description available.

Quantitative trait loci (QTL) analysis for Sclerotinia stem rot resistance was carried out in five doubled haploid (DH) populations of Brassica napus. Sclerotinia stem rot is caused by the necrotrophic fungus Sclerotinia sclerotiorum (Lib.) de Bary. Sclerotinia stem rot has worldwide occurrence and causes significant yield losses in many crop species. Several screening methods have been recommended in the literature to evaluate plant resistance to Sclerotinia stem rot. Four controlled environment based screening methods: 1) excised leaf assay, 2) cotyledon assay, 3) mycelial stem inoculation technique and 4) petiole inoculation technique compared for their ability to differentiate between plant susceptibility/resistance, their reliability and suitability for large scale screening using eight B. napus cultivars/lines of varying reaction to S. sclerotiorum. The petiole inoculation technique and the mycelium stem inoculation technique were identified as reliable methods in this study. Previously developed, five B. napus DH populations (H1, H2, H3, DH179 and DH180) segregating for resistance to Sclerotinia stem rot were used in this study. The petiole inoculation technique was used to evaluate resistance to Sclerotinia stem rot. Data on days to wilting was recorded for a two week period. Twelve plants per line were screened in each evaluation and each population was evaluated three times. Two to three day-old mycelial cultures of S. sclerotiorum isolate Canada 77 was used. QTL analyses were carried out using a LOD threshold value of 2.5 on each individual replicate and on the average of all the replicates. In the H1 population, the number of QTL detected ranged from four to six in each analysis. In the H2 population, there were three to six QTL in each analysis. There were two to six QTL in each analysis of the H3 population. In the DH179 population, the number of QTL detected ranged from three to five in each analysis. In DH180 population, the number of QTL identified varied from three to six in each analysis. A number of common QTL were found between the replicates of each population. Five common QTL were identified between these populations. The markers linked to these QTL are now available for marker assisted selection.

Sclerotinia sclerotiorum is a widespread plant pathogen that produces structures known as sclerotia. When sclerotia germinate they give rise to infective hyphae, myceliogenic germination, or they produce ascocarps, carpogenic germination. Biological control has usually targeted sclerotia or ascospores. The main objectives of the research presented herein were to observe the effect of a mycoparasite and fungus gnats (Bradysia coprophila) on the survival of sclerotia in vitro and in field conditions, and to study the enzymatic activity of the mycoparasite when in contact with sclerotia damaged by fungus gnats. / In this research several mycoparasites were evaluated for their efficacy to degrade sclerotia in soil. From these tests, an isolate of Trichoderma hamatum, TMCS 3 proved to be the most effective. Larvae of fungus gnats have also been reported to feed on sclerotia. When both organisms were combined in laboratory tests, fewer sclerotia survived than when the organisms acted alone. Sclerotia recovered from this treatment contained fewer viable cells when compared to sclerotia recovered from treatments with TMCS 3 or fungus gnats alone. The results obtained from field trials showed that TMCS 3 was effective at degrading sclerotia. Unfortunately environmental conditions were not always optimal for the establishment of high populations of fungus gnats. Few larvae were observed feeding on sclerotia and no significant differences were found among treatments. / Growth of TMCS 3 was studied using different carbon sources as substrates, including sclerotia of S. sclerotiorum. Biomass obtained from this latter treatment was significantly larger than on the other carbon sources tested. Enzymatic activity was also induced by the presence of sclerotia. In many cases, sclerotial exudates from mechanically damaged sclerotia or sclerotia damaged by larval feeding showed that the concentration of amino acids, carbohydrates, and electrolytes was increased as damage to the sclerotia has increased. Exudation of protein was not different when damaged and undamaged sclerotia were compared. Exudates from sclerotia with the melanized rind completely removed by fungus gnats feeding accelerated the germination of conidia of TMCS 3. These heavily damaged sclerotia also enhanced the growth of TMCS 3 when both organisms were grown together. However enzymatic (i.e. glucanase and chitinase) activity of TMCS 3 was not increased by the damage to the sclerotia. When damaged sclerotia were buried in soil infested with TMCS 3 they were degraded faster when the medulla of sclerotia was completely uncovered by larval feeding.

Quantitative trait loci (QTL) analysis for Sclerotinia stem rot resistance was carried out in five doubled haploid (DH) populations of Brassica napus. Sclerotinia stem rot is caused by the necrotrophic fungus Sclerotinia sclerotiorum (Lib.) de Bary. Sclerotinia stem rot has worldwide occurrence and causes significant yield losses in many crop species. Several screening methods have been recommended in the literature to evaluate plant resistance to Sclerotinia stem rot. Four controlled environment based screening methods: 1) excised leaf assay, 2) cotyledon assay, 3) mycelial stem inoculation technique and 4) petiole inoculation technique compared for their ability to differentiate between plant susceptibility/resistance, their reliability and suitability for large scale screening using eight B. napus cultivars/lines of varying reaction to S. sclerotiorum. The petiole inoculation technique and the mycelium stem inoculation technique were identified as reliable methods in this study. Previously developed, five B. napus DH populations (H1, H2, H3, DH179 and DH180) segregating for resistance to Sclerotinia stem rot were used in this study. The petiole inoculation technique was used to evaluate resistance to Sclerotinia stem rot. Data on days to wilting was recorded for a two week period. Twelve plants per line were screened in each evaluation and each population was evaluated three times. Two to three day-old mycelial cultures of S. sclerotiorum isolate Canada 77 was used. QTL analyses were carried out using a LOD threshold value of 2.5 on each individual replicate and on the average of all the replicates. In the H1 population, the number of QTL detected ranged from four to six in each analysis. In the H2 population, there were three to six QTL in each analysis. There were two to six QTL in each analysis of the H3 population. In the DH179 population, the number of QTL detected ranged from three to five in each analysis. In DH180 population, the number of QTL identified varied from three to six in each analysis. A number of common QTL were found between the replicates of each population. Five common QTL were identified between these populations. The markers linked to these QTL are now available for marker assisted selection.

The fungal pathogen Sclerotinia sclerotiorum (Lib.) de Bary is capable of infecting over 400 plant species including canola (Brassica napus L.). The fungus secretes oxalic acid (OA), which plays an important role in infection and disease progression. An analysis of proteome-level changes associated with infection of susceptible canola leaves by S. sclerotiorum revealed significant changes in the abundance of 32 proteins, including proteins involved in photosynthesis and metabolism, hormone signaling, and antioxidant defense. A similar subset of 37 proteins was affected when leaves were treated with OA alone; this compound also caused a reduction in the activities of a number of antioxidant enzymes, suggesting an OA-mediated suppression of the oxidative burst. To further understand the mechanisms of pathogenesis, the role of Sssp, a predicted secreted protein from S. sclerotiorum, was targeted for analysis. Mutant strains of S. sclerotiorum were generated by disruption of the Sssp gene and characterized for virulence on canola. Based on the extent of symptom development, the virulence of the Sssp-disrupted mutants was significantly reduced relative to the wild-type, indicating that Sssp may play a role in the infection process. Finally, the development of sclerotia, long-term survival structures that serve as a primary source of inoculum for the fungus, was examined. A total of 88 proteins were found to exhibit temporal changes in abundance during sclerotium formation and maturation, including proteins involved in the regulation of melanogenesis. A total of 56 proteins were also identified in the sclerotial exudates, providing a basis for future studies. Collectively, the studies described in this dissertation represent the most comprehensive proteome-level analysis of the canola/S. sclerotiorum interaction and sclerotial development, and could contribute to the development of novel strategies for the management of S. sclerotiorum. / Plant Science

Thesis (M.Sc.). / Written for the Dept. of Plant Science. Title from title page of PDF (viewed 2009/06/23). Includes bibliographical references.

Universiẗat, Diss., 2003--Bonn.

No description available.

No description available.

Sclerotinia crown and stem rot (SCSR), caused by Sclerotinia trifoliorum Eriks., causes serious spring losses in some fall=sown, no-tillage alfalfa fields. In microplots artificially infested with sclerotia, greatest numbers of apothecia were found during November and December. Temperature and rainfall had significant impact on apothecium development. A proposed prediction method for apothecium appearance considers monitoring mean soil temperature. For apothecium initiation to occur, it was necessary for sclerotia to be subjected to an estimated 17 days of temperature at or below 15 C before apothecium production occurred. Soil temperatures were usually below 10 C at the time of apothecium appearance. Greatest numbers of apothecia occurred between 5-10 C. Rainfall influenced the number of apothecia, with significant increases occurring early in the 1984-85 production period. / Master of Science