Apple scab is one of the greatest apple management problems throughout the world Much work has been done on cultivars resistant to Venturia inaequalis (Cke.) Wint., but few have been a commercial success. This frequently leaves fungicides as the only control method used. As Quebec growers select new cultivars for planting, more information is needed on their relative susceptibility for efficient scab control. In this light, 21 cultivars common to central and eastern Canada, were examined for their relative susceptibility using several components of partial resistance; disease severity, incubation period, latent period, lesion size, and conidial production. The cultivars used were Cortland, Early Geneva, Empire, Golden Delicious, Golden Russet, Idared, Jersey Mac, Jonagold, Jonamac, Lobo, Lodi, Summerland McIntosh, Mutsu (Crispin), Northern Spy, Paulared, Red Cortland, Red Delicious, Royal Gala, Spartan, Sunrise, and Vista Bella. A final ranking of the cultivars and selection of partial resistance components was done using the principal components analysis. (Abstract shortened by UMI.)

The use of a biofungicide on the perfect stage of V. inaequalis on leaf litter is one potential way to reduce the number of fungicides used to control apple scab. The previous in vitro screenings of Quebec mycoflora have shown that several isolates are able to significantly reduce the primary inoculum of the pathogen. Among the screened fungi, P176A and P130A, reduced over 98% of the ascospore production and were as effective as Athelia bombacina. However, because in vitro tests are generally poor predictors of in vivo assays a re-evaluation of the antagonists was done under field conditions. Eight fungal isolates, leaf shredding, and two comparative treatments (A. bombacina, 5% urea) were applied to intact scabbed leaves in October 1994 and 1995. After the treatments, the leaves overwintered on the orchard ground until the next spring. In April, samples of treated leaves were randomly selected and placed in spore traps to collect the ejected ascospores during rainfall. Since the primary inoculum was ejected during a four-month period, antagonism was based upon ratings taken throughout the whole ejection season. To evaluate the effect of incubation conditions on the antagonistic performance we incubated separately, in vitro and in vivo, sterile leaf disks which were artificially inoculated with V. inaequalis and fungal isolates. (Abstract shortened by UMI.)

The molecular basis for the gene-for-gene relationship of Vm-resistance in apple to Venturia inaequalis was investigated. Incompatible reactions involved a hypersensitive response (HR), which was accompanied by the accumulation of dark brown pigments and autofluorescent materials in epidermal and mesophyll cells at the site of invasion. Cell-free culture filtrates of the avirulent isolate elicited an HR in the Vm host (h5) leaves, but not in the susceptible host (h1). The elicitor activity was resistant to boiling but was abolished by proteinase K digestion. Elicitation of HR was used to monitor purification of the avirulence factor, AVRVm, from liquid cultures of the avirulent isolate following ultrafiltration, acetone precipitation and ion-exchange chromatography. The purest fraction contained three major proteins all with low isoelectric points (pI 3.0-4.5). The fraction also elicited HR on the differential host h4, but not on other resistant hosts (h2, h3 and h6) tested. Three candidate AVRVm proteins were identified and amino acid sequences were obtained using Edman degradation and mass spectrometry. Nucleotide sequences corresponding to these proteins were found in databases of V. inaequalis expressed sequence tags. There were no polymorphisms evident between avirulent and virulent isolates (representing races 1 and 5 respectively) either at genomic DNA or cDNA level of the full open reading frames. RT-PCR revealed that all genes were expressed in both avirulent and virulent isolates during in vitro and in planta growth. All three genes showed similar levels of expression between avirulent and virulent isolates during their in vitro growth. However, preliminary RT-PCR experiments showed that two of these genes were likely to be expressed at lower levels in the virulent compared with the avirulent isolate during compatible infection. Implications of this difference in expression and the future experiments to identify the genuine AvrVm gene were discussed.

The molecular basis for the gene-for-gene relationship of Vm-resistance in apple to Venturia inaequalis was investigated. Incompatible reactions involved a hypersensitive response (HR), which was accompanied by the accumulation of dark brown pigments and autofluorescent materials in epidermal and mesophyll cells at the site of invasion. Cell-free culture filtrates of the avirulent isolate elicited an HR in the Vm host (h5) leaves, but not in the susceptible host (h1). The elicitor activity was resistant to boiling but was abolished by proteinase K digestion. Elicitation of HR was used to monitor purification of the avirulence factor, AVRVm, from liquid cultures of the avirulent isolate following ultrafiltration, acetone precipitation and ion-exchange chromatography. The purest fraction contained three major proteins all with low isoelectric points (pI 3.0-4.5). The fraction also elicited HR on the differential host h4, but not on other resistant hosts (h2, h3 and h6) tested. Three candidate AVRVm proteins were identified and amino acid sequences were obtained using Edman degradation and mass spectrometry. Nucleotide sequences corresponding to these proteins were found in databases of V. inaequalis expressed sequence tags. There were no polymorphisms evident between avirulent and virulent isolates (representing races 1 and 5 respectively) either at genomic DNA or cDNA level of the full open reading frames. RT-PCR revealed that all genes were expressed in both avirulent and virulent isolates during in vitro and in planta growth. All three genes showed similar levels of expression between avirulent and virulent isolates during their in vitro growth. However, preliminary RT-PCR experiments showed that two of these genes were likely to be expressed at lower levels in the virulent compared with the avirulent isolate during compatible infection. Implications of this difference in expression and the future experiments to identify the genuine AvrVm gene were discussed.

The molecular basis for the gene-for-gene relationship of Vm-resistance in apple to Venturia inaequalis was investigated. Incompatible reactions involved a hypersensitive response (HR), which was accompanied by the accumulation of dark brown pigments and autofluorescent materials in epidermal and mesophyll cells at the site of invasion. Cell-free culture filtrates of the avirulent isolate elicited an HR in the Vm host (h5) leaves, but not in the susceptible host (h1). The elicitor activity was resistant to boiling but was abolished by proteinase K digestion. Elicitation of HR was used to monitor purification of the avirulence factor, AVRVm, from liquid cultures of the avirulent isolate following ultrafiltration, acetone precipitation and ion-exchange chromatography. The purest fraction contained three major proteins all with low isoelectric points (pI 3.0-4.5). The fraction also elicited HR on the differential host h4, but not on other resistant hosts (h2, h3 and h6) tested. Three candidate AVRVm proteins were identified and amino acid sequences were obtained using Edman degradation and mass spectrometry. Nucleotide sequences corresponding to these proteins were found in databases of V. inaequalis expressed sequence tags. There were no polymorphisms evident between avirulent and virulent isolates (representing races 1 and 5 respectively) either at genomic DNA or cDNA level of the full open reading frames. RT-PCR revealed that all genes were expressed in both avirulent and virulent isolates during in vitro and in planta growth. All three genes showed similar levels of expression between avirulent and virulent isolates during their in vitro growth. However, preliminary RT-PCR experiments showed that two of these genes were likely to be expressed at lower levels in the virulent compared with the avirulent isolate during compatible infection. Implications of this difference in expression and the future experiments to identify the genuine AvrVm gene were discussed.

The molecular basis for the gene-for-gene relationship of Vm-resistance in apple to Venturia inaequalis was investigated. Incompatible reactions involved a hypersensitive response (HR), which was accompanied by the accumulation of dark brown pigments and autofluorescent materials in epidermal and mesophyll cells at the site of invasion. Cell-free culture filtrates of the avirulent isolate elicited an HR in the Vm host (h5) leaves, but not in the susceptible host (h1). The elicitor activity was resistant to boiling but was abolished by proteinase K digestion. Elicitation of HR was used to monitor purification of the avirulence factor, AVRVm, from liquid cultures of the avirulent isolate following ultrafiltration, acetone precipitation and ion-exchange chromatography. The purest fraction contained three major proteins all with low isoelectric points (pI 3.0-4.5). The fraction also elicited HR on the differential host h4, but not on other resistant hosts (h2, h3 and h6) tested. Three candidate AVRVm proteins were identified and amino acid sequences were obtained using Edman degradation and mass spectrometry. Nucleotide sequences corresponding to these proteins were found in databases of V. inaequalis expressed sequence tags. There were no polymorphisms evident between avirulent and virulent isolates (representing races 1 and 5 respectively) either at genomic DNA or cDNA level of the full open reading frames. RT-PCR revealed that all genes were expressed in both avirulent and virulent isolates during in vitro and in planta growth. All three genes showed similar levels of expression between avirulent and virulent isolates during their in vitro growth. However, preliminary RT-PCR experiments showed that two of these genes were likely to be expressed at lower levels in the virulent compared with the avirulent isolate during compatible infection. Implications of this difference in expression and the future experiments to identify the genuine AvrVm gene were discussed.

The molecular basis for the gene-for-gene relationship of Vm-resistance in apple to Venturia inaequalis was investigated. Incompatible reactions involved a hypersensitive response (HR), which was accompanied by the accumulation of dark brown pigments and autofluorescent materials in epidermal and mesophyll cells at the site of invasion. Cell-free culture filtrates of the avirulent isolate elicited an HR in the Vm host (h5) leaves, but not in the susceptible host (h1). The elicitor activity was resistant to boiling but was abolished by proteinase K digestion. Elicitation of HR was used to monitor purification of the avirulence factor, AVRVm, from liquid cultures of the avirulent isolate following ultrafiltration, acetone precipitation and ion-exchange chromatography. The purest fraction contained three major proteins all with low isoelectric points (pI 3.0-4.5). The fraction also elicited HR on the differential host h4, but not on other resistant hosts (h2, h3 and h6) tested. Three candidate AVRVm proteins were identified and amino acid sequences were obtained using Edman degradation and mass spectrometry. Nucleotide sequences corresponding to these proteins were found in databases of V. inaequalis expressed sequence tags. There were no polymorphisms evident between avirulent and virulent isolates (representing races 1 and 5 respectively) either at genomic DNA or cDNA level of the full open reading frames. RT-PCR revealed that all genes were expressed in both avirulent and virulent isolates during in vitro and in planta growth. All three genes showed similar levels of expression between avirulent and virulent isolates during their in vitro growth. However, preliminary RT-PCR experiments showed that two of these genes were likely to be expressed at lower levels in the virulent compared with the avirulent isolate during compatible infection. Implications of this difference in expression and the future experiments to identify the genuine AvrVm gene were discussed.

La modélisation de la dynamique épidémiologique des ascomycètes parasites des arbres fruitiers présente deux aspects très importants : l’évaluation de la quantité d'inoculum et de son évolution, et l’identification des évènements climatiques donnant lieu à une contamination. Le travail présenté aborde ces deux aspects au travers de deux exemples : la tavelure du pommier, et la maladie de l’œil de paon de l’olivier, parasites majeurs pour les filières concernées.L’acquisition des connaissances sur la biologie des deux maladies a été abordée uniquement sur la base de données acquises sur le terrain, ce qui est original car généralement les modèles ont été réalisés sur la base de connaissances établies en conditions contrôlées.Dans le cas de Venturia inaequalis, agent de la tavelure du pommier, la vitesse de développement journalier de l’inoculum a été établie par optimisation numérique, sur la base d’observations réalisées en Provence. Un modèle de dynamique de projection des ascospores incluant la suspension de l’évolution de l’inoculum primaire lors des périodes sèches a été réalisé puis validé sur un jeu de données indépendantes. La transposabilité du modèle a été ensuite étudiée pour une autre région (Aquitaine). Dans le cas de Fusicladium oleagineum, agent de la maladie de l’oeil de paon, les conditions de contamination ont été établies en fonction de la température et de l’hygrométrie, d’une part par la réalisation d’un abaque sur la base de points sélectionnés par dires d’expert, et d’autre part de façon automatique à l’aide d’un système par apprentissage (réseau de neurones). Un modèle, liant la température moyenne après la contamination à l’apparition des symptômes a été ensuite réalisé. / Apple scab, caused by Venturia inaequalis, and peacoq leaf spot, cause by Fusicladiumoleagineum, are key diseases respectively for apple and olive growers. These disease usuallyrequire a large number of treatments. Adequate protection need a good evaluation ofquantitative disponibility of inoculum, and estimation of infection conditions.In this thesis, these two problems were studied using only field data. This is an originalaprroach to obtain knowledge about biology of fungi : most previous works were realised byregression of laboratory data obtained under controled conditions.In the case of Venturia inaequalis, primary inoculum consists of pseudothecia present in leaflitter. Treatments agains ascospore release period is the cornerstone of the strategy againstapple scab. However, the existing forecasting models are not reliable, and are all based ondegree-day time scale, proposed in 1982.Here, using a corpus of data acquired between 1996 and 2013, including observations ofascospore release and weather data, we assessed the daily rate of development of primaryinoculum by fitting generic new time scale functions. Further improvements were then studiedto take into account elements reported in litterature about the incidence of rain or wetness.Different methods were tested and adapted for the parameterisation of models by numericaloptimisation. Some forcasting models were proposed and adapted to the area where the studywas conducted, with parameters including rain and temperature. The validity was tested, andfurther developements of the forecasting tool was then proposed.In the case of Fusicladium oleagineum, a field-operational model predicting disease outbreakswas established as a function of temperature and relative humidity. First with the help ofpoints selected by experts, Secondly automaticaly using a neural network. A model defininglatent period as a function of average temperature after contamination was then realised.

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