Diss. (sammanfattning) Uppsala : Sveriges lantbruksuniv., 2001. / Härtill 4 uppsatser.

Oilseed rape is largely infected by several phytopathogens and two most economical important diseases are blackleg caused by fungus species complex Leptosphaeria maculans and L. biglobosa and clubroot caused by protist P. brassicae. The sequenced genomes of these phytopathogens provide opportunity to uncover various aspects related to disease infection, host pathogen interactions, plant disease resistance, and evolution of pathogens. Considering these we focused on one of the most conserved family called immunophilins (IMMs) in these genomes. IMMs are comprised of three structurally unrelated sub-families including cyclophilins (CYPs), FK506-binding proteins (FKBPs), and parvulin-like proteins (PARs). We identified putative members of IMMs in each phytopathogen using bioinformatics approaches. We further characterized the IMMs based on domain architecture, subcellular localization, exon-intron organization, transcriptomic expression patterns, gene ontology terms, conserved motifs presents and evolutionary analyses. IMMs are performing several vital roles in plants, animals and fungi. However, in phytopathogens their roles are not well established except for cyclophilin that implicates in pathogenicity in some phytopathogens. Therefore, we exploited the role of cyclophilin in L. maculans and L. biglobosa using expression profiles and in P. brassicae using Magnaporthe oryzae cyclophilin deletion mutant. Overall, we concluded that the cyclophilin acts as a virulence determinant in our studied phytopathogens. However, delineating the precise role of other IMMs would also be imperative. Taken together, our findings for the first time shed light on the highly conserved IMM family in the oilseed rape pathogens.

Detoxification of canola chemical defenses (phytoalexins and others) is an important mechanism used by the blackleg fungus Leptosphaeria maculans/Phoma lingam to overcome the plant’s natural defenses. Phytoalexins are anti-microbial defense metabolites produced de novo by plants in response to pathogen attack and other forms of stress. L. maculans is successful in detoxifying several cruciferous phytoalexins into different products. For example, brassinin, a key phytoalexin from crucifers, is transformed into indole-3-carboxaldehyde. This thesis includes investigation of phytoalexin metabolism by L. maculans and related work: (i) transformation pathways of cruciferous phytoalexins and analogues; (ii) design and synthesis of potential inhibitors of brassinin detoxification. In continuation of previous work, homologues, analogues and structural relatives of brassinin were analysed for metabolism by L. maculans. Products of metabolism of these compounds were identified and the overall metabolic pathways were established. It was concluded that structural relatives of brassinin metabolized differently from brassinin. Antifungal bioassays of the products suggested that all these transformations were detoxification reactions. Among the phytoalexins, rapalexin A was not metabolized whereas, erucalexin was metabolized. Results of these metabolism studies using L. maculans along with the syntheses and antifungal activities of the metabolites will be presented. In the second part of thesis, inhibition of the detoxification of brassinin by L. maculans using quinolines and isoquinolines was investigated. These compounds resulted from replacement of indolyl containing structures with quinoline and isoquinoline moieties, and various substitutions such as phenyl, thiazolyl, bromo, chloro, hydroxy and methoxy groups. All these compounds were tested for their effect on brassinin detoxification and antifungal activity. Overall, a significant effect on the rate of brassinin detoxification in cultures of L. maculans was detected in the presence of compounds 6-bromo-2-phenylquinoline, 2-phenylquinoline, 3-phenylquinoline, 1-thiazolylisoquinoline. 6-Bromo-2-phenylquinoline was the most effective compound in slowing down the metabolism of brassinin and also was a weak inhibitor of the growth of L. maculans (virulent on canola). Results of the syntheses and evaluation of the compounds are discussed.

Phoma stem canker (aka Blackleg) caused by the fungal pathogen Leptosphaeria maculans is a major disease affecting Canola (Brassica napus L.). This study examined 674 L. maculans isolates collected in 2010 and 2011 from western Canada at ten avirulence gene loci. Overall, certain alleles were more prevalent with AvrLm6 and AvrLm7 present in >85% of isolates and AvrLm3, AvrLm9, and AvrLepR2 present in <10% of isolates. This study also examined the genetic diversity of Leptosphaeria maculans populations around the world. Blackleg disease is found in most countries where Brassica spp. are cultivated and there are indications that L. maculans is an expanding species displacing the less aggressive Leptosphaeria biglobosa. Twenty two microsatellite primers were used to screen 96 isolates from 8 countries. A phylogenetic tree to assess the evolutionary relationship between regions was generated and the results indicated that genetic diversity was correlated with geographic location. / October 2015

Universiẗat, Diss., 2004--Kiel.

La maladie de taches noires (TN ; champignon Leptosphaeria lindquistii) est une maladie importante en France. L'étude présentée dans cette thèse fournit des informations utiles sur l’épidémiologie de TN et sur la résistance quantitative du tournesol contre TN. Des expérimentations ont été menées sur petites parcelles au champ, plantes adultes (serre), et plantules (phytotron) pour (1) caractériser la dynamique spatiotemporelle de TN, (2) identifier les traits morphologiques affectant TN via des processus d’esquive de la maladie et en utilisant une procédure standardisée d'évaluation de la maladie, et (3) identifier des prédicteurs de résistance quantitative à TN. Cette étude suggère que (1) TN est associée à des épidémies monocycliques dans le sud ouest de la France, (2) les niveaux faibles de TN sont associés à des plantes ayant un grand nombre de feuilles vertes et de de grande taille, et (3) des prédicteurs de résistance quantitative à BS peuvent être identifiés expérimentalement. / Phoma black stem (BS) is caused by the fungus Leptosphaeria lindquistii, and is an important disease in France. The study presented in this dissertation provides useful information on BS epidemiology and sunflower quantitative resistance against the disease. Experiments were conducted on plants grown in small plots (field), adult plants (greenhouse), and seedlings (growth chamber) in order to (1) characterize the spatiotemporal dynamics of BS, (2) identify morphological traits affecting BS through disease escape processes and utilizing a standardised disease assessment procedure, and (3) identify predictors of quantitative resistance to BS. This study suggests that (1) BS is primarily associated to monocyclic epidemics in south west France, (2) low BS levels are associated with sunflower plants characterized by a large number of green leaves and large height, and (3) predictors of quantitative resistance to BS can be experimentally identified.

Leptosphaeria maculans ‘brassicae’ (Lmb) est un champignon filamenteux de la classe des Dothideomycètes faisant partie du complexe d’espèces Leptosphaeria maculans-Leptosphaeria biglobosa composé d’agents pathogènes des crucifères. Lmb est particulièrement adapté au colza (Brassica napus) et provoque la maladie qui lui est la plus dommageable : la nécrose du collet. Dans le but de mieux comprendre et contrôler cette maladie, l’équipe d’accueil a initié un projet de génomique visant à identifier de façon systématique les gènes impliqués dans le pouvoir pathogène. Les premières données génomiques montraient deux aspects très importants et potentiellement spécifiques de Lmb : (i) tous les gènes d'avirulence caractérisés expérimentalement étaient localisés dans de grandes régions riches en bases AT et composées d'éléments transposables (ET), (ii) ces régions riches en AT préfiguraient une structure génomique particulière, qui, si elle se généralisait à l'ensemble du génome, aurait été totalement inédite chez un micro-organisme eucaryote. La première partie de cette thèse présente la description du génome de Lmb en se focalisant sur sa structure en isochores, résultant d’une invasion du génome par des ET qui ont ensuite été inactivés par un mécanisme de défense spécifique aux champignons ascomycètes, le RIP (Repeat-Induced Point mutation). Puis, l’impact potentiel de cette structure sur la diversification et l’évolution des protéines jouant un rôle clé lors de l’interaction agent pathogène-plante a été évalué, mettant ainsi en avant l’existence d’un génome à « deux vitesses ». Afin de mieux comprendre le rôle potentiel joué par les ET au niveau des capacités d’adaptation de Lmb au colza, une étude de génomique comparative et évolutive de cinq membres du complexe d’espèces a été réalisée. Ce travail montre que Lmb est la seule espèce du complexe dont le génome a été envahi par les ET, et que ces derniers sont impliqués dans (i) des réarrangements intrachromosomiques potentiellement liés à la spéciation entre Lmb et l’espèce la plus proche, (ii) la présence de gènes espèce-spécifiques et (iii) des déplacements dans des régions génomiques très dynamiques de gènes codant des effecteurs. Les travaux constituant cette thèse participent à la généralisation du concept selon lequel un lien fort existe chez les champignons filamenteux phytopathogènes entre ET et gènes impliqués dans la pathogenèse ou l’adaptation à l’hôte. / Leptosphaeria maculans ‘brassicae’ (Lmb) is a filamentous ascomycete from class Dothideomycetes. It belongs to the Leptosphaeria maculans-Leptosphaeria biglobosa species complex which comprises pathogens of crucifers. Lmb is specifically adapted to oilseed rape (Brassica napus) and is responsible for the most damaging disease of this crop: “stem canker”. In order to better understand and control the disease, the host team initiated a genomic project aiming at systematically identify genes involved in pathogenicity, analyse genome plasticity and evaluate their incidence on adaptability to host. Preliminary genome data firstly showed that all characterized avirulence genes were localized in large AT-rich regions, mainly composed of Transposable Elements (TEs). In addition, these AT-rich regions were the first hints that the Lmb genome may present a very unusual structure compared to other microorganisms. The first part of this thesis describes the Lmb genome with a special focus on its isochore structure, which is the result of a massive TE invasion of the genome followed by an inactivation of TEs by an ascomycete-specific defense mechanism called RIP (Repeat-Induced Point mutation). The potential impacts of this genome structure on diversification and evolution of proteins involved in the plant-pathogen interaction were assessed and highlighted the existence of a “two speed” genome. To better understand how TEs are involved in adaptation of Lmb towards oilseed rape, a comparative and evolutionary genomic analysis of five members of the species complex was conducted. This study shows that Lmb is the only species of the complex with genome invaded by TEs at such an extent, and that TEs are involved in (i) intrachromosomal rearrangements putatively related to the speciation event between Lmb and its closest relative species, (ii) the presence of species-specific genes, (iii) translocations of effector genes into highly dynamic genomic regions. Our data contribute to the generalization of the “two speed” genome concept in filamentous phytopathogens postulating that highly plastic regions of the genome are enriched in genes involved in niche adaptation and that a strong link exists between TEs and genes involved in pathogenesis or host adaptation.

Leptosphaeria maculans and L. biglobosa co-infect winter oilseed rape plants to cause phoma stem canker disease. The sexual spores of both species are produced in pseudothecia on infected winter oilseed rape stem debris after harvest and this is the most important source of inoculum for infection of newly-emerged plants in autumn. Field experiments investigated the effects of host resistance on proportions of pathogens Leptosphaeria maculans and L. biglobosa in most leaf and stem tissues during 2011/2012, 2012/2013 and 2013/2014 growing seasons and on the pseudothecial development on crop debris on nine winter oilseed rape cultivars; cvs Adriana (Rlm4 + quantitative resistance (QR)), Bilbao (Rlm4), Capitol (Rlm1), Drakkar (no R gene against L. maculans), DK Cabernet (Rlm1 + (QR), Es-Astrid (QR), Excel (Rlm7), Roxet (Rlm7) and NK Grandia (QR). Cultivars with a combination of R-gene resistance and QR [Adriana (Rlm4 + QR), DK Cabernet (Rlm1 + QR)] or cultivars with only QR [(Es-Astrid and NK Grandia)] had more numbers of L. maculans leaf spots than other cultivars in autumn but less stem canker damage. There was greater number of L. biglobosa leaf spots on leaves of cvs Roxet and Excel with resistance gene Rlm7 than those of other cultivars and later more L. biglobosa DNA was detected in their stems than in those of other cultivars. In all cultivars in the three growing seasons, there was a greater amount of L. biglobosa DNA than L. maculans DNA in basal stem canker and upper stem lesions. The cv. Drakkar (no R gene against L. maculans) was susceptible in all three growing seasons, with a great number of L. maculans and L. biglobosa leaf spots and severe stem cankers. There were four cultivars (Adriana, Bilbao, Drakkar and NK Grandia) selected for the study of pseudothecial development under natural conditions with different times of exposure and in controlled environment conditions (20oC, continuous wetness). The fastest development was on the susceptible cv. Drakkar (no R gene against L. maculans), followed by Bilbao (Rlm4), Adriana (Rlm4 + QR) and NK Grandia (QR) for stem base cankers and upper stem lesions in controlled conditions. Results for pseudothecial development on stems of the nine winter oilseed rape cultivars that were exposed in natural conditions at Bayfordbury support the controlled environment results, with pseudothecia on stems of cultivars with a combination R-gene and QR consistently maturing later than those on other cultivars, regardless of the weather conditions in three growing seasons. Ascospores produced in pseudothecia are the primary inoculum that initiate phoma stem canker epidemics in autumn. Ascospore release was later in autumn 2011 than in autumn/winter 2012/2013 or 2013/2014 because of dry weather. The pattern of ascospore release had a peak, or maximum in autumn/winter 2011/2012 (4958 spores/m-3 on 22 Jan 2012) and several maxima in autumn/winter 2012/2013 (1307 spores/m-3 on 5 Nov 2012, 1291 spores/m-3 on 15 Nov 2012, 1306 spores/m-3 on 25 Dec 2012) and 2013/2014 (4575 spores/m-3 on 27 Oct 2013, 4619 spores/m-3 on 3 Nov 2013, 3674 spores/m-3 on 9 Nov 2013, 3521 spores/m-3 on 12 Dec 2013). Results from the qPCR showed that ascospores of L. maculans were released earlier than ascospores of L. biglobosa at Bayfordbury in the 2013/2014 growing season. There were differences in phenotype of isolates amongst ninety-five isolates of L. maculans and forty-eight isolates of L. biglobosa obtained from different sources (phoma leaf spots, upper stem lesions or basal stem cankers) on different cultivars. Cotyledon tests showed that the resistance genes Rlm4, Rlm5, Rlm6 and Rlm7 are still effective in England. Most isolates from phoma leaf spots carried avirulent AvrLm4 (39 isolates; 97.5%), AvrLm5 (39 isolates; 97.5%) and AvrLm6 alleles (36 isolates; 90%) and all 40 isolates carried the avirulent allele AvrLm7 (100%). Fewer isolates from basal stem cankers carried avirulent AvrLm4 (4 isolates, 16.7%) or AvrLm6 alleles (16.7%) but all 24 isolates carried the avirulent AvrLm7 (100%). Fewer isolates from upper stem lesions carried the avirulent AvrLm4 allele (5 isolates; 16.1%), but 15 isolates carried avirulent AvrLm5 (48.4%), 21 isolates carried AvrLm6 (67.7%) and all 31 isolates carried AvrLm7 (100%). By contrast, all isolates were virulent against Rlm1, Rlm2, Rlm3 and Rlm9. This knowledge, together with knowledge about R genes present in current winter oilseed rape cultivars, should be useful to provide recommendations on cultivar selection to growers based on regional frequencies of avirulent alleles of Avr allele genes in the L. maculans populations (races) and improved understanding of the race structure of L. maculans. There is a need to further investigate any R genes that operate against L. biglobosa (possibly from wild brassicas) and to study if any R genes or QR can provide resistance against both L. maculans and L. biglobosa.

Leptosphaeria maculans est l'agent de la nécrose du collet des crucifères, principale maladie fongique du colza (Brassica napus). Lorsque des variétés de colza possédant la résistance Rlm7 ont été commercialisées au début des années 2000, la totalité des souches européennes étaient avirulentes vis-à-vis de ce gène de résistance. A l'inverse, AvrLm3 était considéré comme absent de ces populations. Un précédent projet de thèse réalisé dans l'équipe a montré la rapide capacité d'adaptation de L. maculans à la pression de sélection exercée par Rlm7 (Daverdin et al. 2012) et le phénotypage des populations isolées lors de cette étude avait montré que 98% des souches virulentes vis-à-vis de Rlm7 étaient avirulentes vis-à-vis de Rlm3. L'hypothèse d'un masquage du phénotype avirulent dû à la présence d'AvrLm4-7 a alors été validée par la complémentation d'une souche avirulente vis-à-vis de Rlm3 par AvrLm4-7. Sur ces bases, l'objectif de mon projet de thèse était d'identifier AvrLm3 afin d'analyser l'antagonisme entre les phénotypes AvrLm3 et AvrLm4-7, ainsi que les mécanismes menant au contournement de Rlm3 et Rlm7.Le gène AvrLm3 avait été identifié comme génétiquement lié à AvrLm4-7. Toutefois il n'avait pas été possible d'identifier un gène candidat. Par la combinaison d'approches de génétique et de génomique (clonage positionnel, RNA-seq, séquençage de novo d'une souche avirulente et de clones BAC), j'ai pu identifier AvrLm3, dont la séquence était absente du génome de référence de L. maculans. AvrLm3 est très fortement exprimé lors des phases précoces de l'infection et code pour une petite protéine sécrétée et ne présentant pas d'homologies avec d'autres protéines fongiques. Ce gène a donc les caractéristiques classiques des gènes codant pour des effecteurs, mais présente la particularité d'être le premier gène d'avirulence de L. maculans localisé en région télomérique. Bien que le mécanisme par lequel la présence du gène AvrLm4-7 supprime la reconnaissance d'AvrLm3 dans l'interaction entre B. napus et L. maculans n'ait pas été élucidé au terme de ma thèse, plusieurs hypothèses ont pu être invalidées, notamment l'absence de régulation de l'expression d'AvrLm3 par AvrLm4-7. De plus, une approche double hybride a mis en évidence une absence d'interaction directe entre les deux protéines d'avirulence. L'isolement de souches de L. maculans issues de parcelles expérimentales en 2012 et 2013 a mis en évidence le contournement actuel de la résistance Rlm7, avec environ 10 % de souches virulentes. Le phénotypage de ces collections a confirmé la présence majoritaire d'un allèle avirulent d'AvrLm3 chez celles-ci, moins de 0,5 % des souches isolées étant virulentes à la fois vis-à-vis de Rlm3 et de Rlm7. L'analyse de 592 souches d'origine mondiale a montré qu'AvrLm3 est toujours présent chez L. maculans, sous diverses formes alléliques, suggérant un rôle majeur d'AvrLm3 dans la fitness fongique. La résurgence du phénotype avirulent vis-à-vis de Rlm3 suite au contournement de Rlm7 fait envisager l'opportunité d'exploiter l'interaction entre les deux gènes d'avirulence pour une gestion plus durable des gènes de résistance de B. napus, par l'alternance de cultivars possédant Rlm3 et Rlm7 ou le pyramidage de ces deux gènes dans des variétés de colza. De plus, le rôle démontré d'AvrLm3 et d'AvrLm4-7 dans l'agressivité lors de l'infection suppose un fort coût de fitness lié à la virulence. Toutefois, des mécanismes originaux de compensation permettant au champignon d'échapper à la reconnaissance par Rlm3 et Rlm7 tout en conservant a priori fonctionnelle la fonction effectrice d'AvrLm3 et AvrLm4-7 ont été identifiés. Les résultats obtenus lors de ce travail de thèse ont permis la meilleure caractérisation d'une interaction gène-pour-gène inhabituelle. La diversité des mécanismes moléculaires permettant à L. maculans de contourner la résistance Rlm3 illustre la complexité de la course aux armements entre les plantes et les agents pathogènes. / Leptosphaeria maculans is a Dothideomycete responsible for stem canker on oilseed rape (Brassica napus). Genetic control, encompassing mostly the use of major resistance genes, is the most effective method to control this pathogen. When the first cultivars harboring Rlm7 have been deployed in the early 2000's, all of the European isolates were avirulent towards this resistance gene and AvrLm3 was considered to be absent from the populations. In 2012, Daverdin et al. showed that L. maculans has the ability to rapidly overcome the Rlm7 resistance whenever a strong selection pressure is applied. The phenotyping of isolates sampled by Daverdin et al. also showed that more than 98 % of the isolates virulent towards Rlm7 had become avirulent towards Rlm3. This result led to the hypothesis that the presence of AvrLm4-7 can suppress AvrLm3 recognition by Rlm3 and this was validated by the complementation of an isolate avirulent towards Rlm3 with a functional allele of AvrLm4-7. AvrLm3 is genetically linked to AvrLm4-7, at a distance of 20 cM. However, no candidate gene was identified before the beginning of my PhD. The objective of my PhD project was to identify AvrLm3, in order to better understand the antagonistic relationship between AvrLm3 and AvrLm4-7 phenotypes. The combination of genetic and genomic approaches (genetic mapping, RNA-seq, de novo sequencing of an isolate avirulent towards Rlm3 and BAC clone sequencing) allowed me to identify AvrLm3, whose sequence was absent from the reference genome assembly. AvrLm3 has common characteristics with others genes encoding fungal effector: it codes for a small, cysteine-rich protein, is highly expressed at early infection stages and shows no homology with others fungal genes. Although the mechanism allowing the suppression of AvrLm3 recognition due to the presence of AvrLm4-7 has not been elucidated, several hypotheses were invalidated: the presence of AvrLm4-7 has no impact on AvrLm3 expression and the two avirulence proteins do not interact physically.The sampling of field isolates in 2012 and 2013 showed the currently ongoing breakdown of Rlm7, with ca. 10% of virulent isolates, and the resurgence of the AvrLm3 phenotype in these populations, only 0.5 % of isolates being virulent towards both Rlm3 and Rlm7. A large collection of isolates from worldwide origin was genotyped for AvrLm3. It revealed that all isolates possess AvrLm3, with a high level of allelic diversity. The resurgence of the avirulent phenotype towards Rlm3 following the breakdown the Rlm7, along with the important role of AvrLm3 and AvrLm4-7 in fungal fitness, suggest that the antagonistic relationship between these two avirulence phenotypes could be an opportunity to propose original strategies to increase the durability of Rlm3 and Rlm7, by alternating both resistance genes at the landscape level or using pyramiding strategies. However, we identified novel isoforms of AvrLm4-7 allowing the fungus to escape Rlm7 recognition, while maintaining the suppression of Rlm3 recognition effective. This work allowed to better characterize an unusual gene-for-gene relationship. Indeed, only one other example of antagonism between avirulence phenotypes has been identified to date, in the phytopathogenic fungus Fusarium oxysporum (Houterman et al., 2008). The diversity of mechanisms allowing L. maculans to overcome the Rlm3 resistance illustrates perfectly the complexity of the arms race between plants and pathogens.

In the first part of this thesis the metabolism of the phytotoxins destruxin B and sirodesmin PL in crucifers and non-crucifers was studied using HPLC-ESI-MSn. Destruxin B and sirodesmin PL are phytotoxins produced by the phytopathogenic fungi Alternaria brassicae (Berk.) Sacc. (causative agent of blackspot disease) and Leptosphaeria maculans (Desm) Ces. et de Not.[asexual stage Phoma lingam (Tode ex Fr) Desm.] (causative agent of blackleg disease). Five cruciferous species were used in this study: Arabidopsis thaliana L., Brassica rapa L., B. napus L., Thellungiella salsuginea Pallas and Erucastrum gallicum O.E. Schulz. In addition, the cereals Avena sativa L. and Triticum aestivum L. were studied similarly. Destruxin B was metabolized by all crucifers to hydroxydestruxin B, a transformation similar to previously reported reactions in other crucifers. In addition, destruxin B elicited production of phytoalexins in A. thaliana, T. salsuginea and E. gallicum, while no phytoalexins were detected in case of B. rapa and B. napus. In cereals destruxin B was transformed differently. Several metabolites were detected and identified by HPLC-ESI-MSn analyses: hydroxydestruxin B, two isomers of dehydrodestruxin B and desmethyldestruxin B. On the other hand, no metabolites related to transformation of sirodesmin PL were detected in crucifers; however, in cereals sirodesmin PL was transformed to deacetylsirodesmin PL. In all crucifers sirodesmin PL was found to be a stronger elicitor of phytoalexin production than destruxin B. In the second part of this thesis, mycelia from different pathogenic fungi were screened for indolyl-3-acetaldoxime dehydratase. L. maculans isolate Laird 2 was chosen for isolation, characterization and substrate specificity of aldoxime dehydratase, as it showed the highest specific activity among the tested pathogens. The enzyme was partially purified using three chromatographic steps. It showed Michaelis–Menten kinetics and an apparent molecular mass of about 40 kDa. Based on its substrate specificity, the enzyme appears to be an indolyl-3-acetaldoxime dehydratase