The aim of this thesis was to study the evolution of reproductive systems and reproductive traits in the fungal genus Neurospora. More specifically, I have investigated the evolutionary forces shaping the genes involved in sexual reproduction, focusing on mating-type (mat) and pheromone receptor (pre) genes. Neurospora contains species exhibiting three different mating systems, i.e., heterothallism (self-incompatibility), homothallism (self-compatibility) and pseudohomothallism (partial self-incompatibility). First, a robust phylogeny of Neurospora was established. The phylogenetic analyses revealed multiple independent transitions in reproductive life style during the evolutionary history of the genus. We argued for a heterothallic ancestor of the genus, although our subsequent ancestral reconstruction analyses favored a homothallic ancestor. To be able to settle the ancestral mating system, we zoomed in on the structural architecture of the mat-locus in four homothallic species of Neurospora, thought to have arisen from independent transitions. Our results led us to suggest two different genetic mechanisms (translocation and unequal crossover) to explain the transitions in mating system from heterothallism to homothallism. We pointed out that the mating-system transitions in Neurospora are unidirectional, and suggested that transposable elements might be driving the transitions. In conclusion, we suggest a heterothallic ancestor for Neurospora, and that at least six transitions to homothallism and two transitions to pseudohomothallism have occurred in its evolutionary history. Further, we used the phylogeny of Neurospora as a framework to test if the evolution of pre-genes (pre-1 and pre-2) in hetero- and homothallic Neurospora is dependent on mating systems and/or even the homothallic clades themselves (i.e., mating-system and/or switch-dependent). The molecular evolution results suggest that pre-1 and pre-2 are overall functional in both homothallic and heterothallic Neurospora. The molecular evolution of pre-1 seems to be independent of mating-system or homothallic clade, and we detected signs for positive selection in the C-terminal tail. For pre-2 we found no support for mating-system dependent evolution, but indications for switch-dependent evolution. In this study we also included expression analyses of both pre- as well as mat-genes, with the prospect to assess functionality and regulation. During this thesis work, we also performed a phylogenetic study were we found that reproductive genes might be more permeable to introgression than other genes, which is in contrast to theoretical expectations. In the last study, we confirmed the co-existence of two alternative splice variants of the pheromone receptor gene pre-1 in Neurospora crassa, and performed expression profiles studies using quantitative RT-PCR. I hope this thesis work will further strengthen Neurospora as a model for research in evolutionary genetics.

To explore the similarities and differences of regulatory circuits among budding yeasts, we characterized the role of unscheduled meiotic gene expression 6 (UME6) and a novel mating type switching pathway in Kluyveromyces lactis. We found that Ume6 was required for transcriptional silencing of the cryptic mating-type loci HMLα and HMRa. Ume6 acted directly at these loci by binding to the cis-regulatory silencers. Ume6 also served as a block to polyploidy and was required for repression of three meiotic genes, independently of the Rpd3 and Sin3 corepressors. Mating type switching from MATα to MATa required the α3 protein. The α3 protein was similar to transposases of the mutator like elements (MULEs). Mutational analysis showed that the DDE-motif in α3, which is conserved in MULEs was necessary for switching. During switching α3 mobilizes from the genome in the form of a DNA circle. The sequences encompassing the α3 gene circle junctions in the MATα locus were essential for switching from MATα to MATa. Switching also required a DNA binding protein, Mating type switch 1 (Mts1), whose binding sites in MATα were important. Expression of Mts1 was repressed in MATa/MATα diploids and by nutrients, limiting switching to haploids in low nutrient conditions. In a genetic selection for strains with increased switching rates we found a mutation in the RAS1 gene. By measuring the levels of the MTS1 mRNA and switching rates in ras1, pde2 and msn2 mutant strains we show that mating type switching in K. lactis was regulated by the RAS/cAMP pathway and the transcription factor Msn2. ras1 mutants contained 20-fold higher levels of MTS1 mRNA compared to wild type whereas pde2 and msn2 expressed less MTS1 mRNA and had decreased switching rates. Furthermore we found that MTS1 contained several potential Msn2 binding sites upstream of its ORF. We suggest that these observations explain the nutrient regulation of switching. / At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Manuscript.

Transposable elements (TEs) have had immense impact on the structure, function and evolution of eukaryotic genomes. The work in this thesis identified Kat1, a novel domesticated DNA transposase of the hAT family in the yeast Kluyveromyces lactis. Kat1 triggers a genome rearrangement that results in a switch of mating type from MATa to MATα. Furthermore, Kat1 acts on sequences that presumably are ancient remnants of a long-lost transposable element. Therefore, Kat1 provides a remarkable example of the intricate relationship between transposable elements and their hosts. We showed that Kat1 generates two DNA double strand breaks (DSBs) in MATa and that the DDE motif and several other conserved amino acid residues are important for Kat1 cleavage activity. DNA hairpins were formed on one end of the DSBs whereas the DNA between the DSBs was joined into a circle. Kat1 was transcriptionally activated by nutrient limitation through the transcription factor Mts1 and negatively regulated by translational frameshifting. In conclusion, Kat1 is a highly regulated domesticated transposase that induces sexual differentiation.  In another study, we developed an assay to measure switching rates in K. lactis and found that the switching rate was ~6x10-4 events/generation. In a genetic screen for mutations that increased mating-type switching, we found mutations in the RAS1 gene. The small GTPase Ras1 regulates cellular cyclic AMP levels and we demonstrated that Mts1 transcription is regulated by the RAS/cAMP pathway and the transcription factor Msn2. Since Ras activity is regulated by nutrient availability, these data likely explains why nutrient limitation induces mating-type switching.

Orientador: Gonçalo Amarante Guimarães Pereira / Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia / Made available in DSpace on 2018-08-26T17:23:36Z (GMT). No. of bitstreams: 1 Almeida_LudimilaDias_M.pdf: 4371531 bytes, checksum: 15deaceac3a09118222822415b70daaf (MD5) Previous issue date: 2015 / Resumo: O ciclo sexual de basidiomicetos é controlado pelo sistema mating type. Este é formado por dois loci multigênicos não ligados A e B, o locus A codifica duas proteínas homeodomínio HD1 e HD2, capazes de heterodimerização, enquanto o locus B apresenta genes para receptores de feromônio e feromônios. Em fungos heterotálicos, o desenvolvimento sexual depende da especificidade entre os quatro alelos, sistema este chamado tetrapolar, e é ativado apenas por interações específicas entre alelos parentais necessariamente diferentes, assegurando que hifas geneticamente iguais sejam incompatíveis. Em contrapartida, a condição na qual hifas geneticamente iguais são compatíveis é denominada homotalismo. Fungos basidiomicetos são tipicamente heterotálicos, no entanto, apesar de pertencer a este filo, o fitopatógeno Moniliophthora perniciosa, causador da doença Vassoura de Bruxa no cacaueiro, é classificado como homotálico primário. Curiosamente, apesar desta classificação, M. perniciosa contém um sistema genético tetrapolar, sendo o primeiro fungo descrito com essa característica. Neste trabalho, foi realizada a caracterização dos loci mating type em M. perniciosa e verificamos o perfil transcricional destes genes com o objetivo de entender os mecanismos moleculares que atuam no seu comportamento homotálico. Primeiramente, foram identificados no genoma um locus A e um locus B, além de genes atuantes no processamento e sinalização em resposta aos feromônios. O estudo do perfil transcricional destes genes revelou que um receptor tem um perfil de expressão condizente com a fase do ciclo de vida do fungo na qual ocorre o processo de dicariotização. A análise funcional dos receptores foi realizada em um sistema expressão heteróloga, promissor para o estudo de GPCRs (G coupled proteins receptors), porém não permitiu confirmar a presença de alelos compatíveis de receptores e precursores de feromônios no genoma de M. perniciosa como uma possível explicação ao comportamento homotálico. Tendo em vista o locus A, este é formado por um par MpHD1 e MpHD2, o que difere de outros basidiomicetos devido a inserção de uma sequência (11,958kb) interrompendo seus promotores. A hipótese neste cenário é que o transposon encontrado no locus A poderia ter permitido um crossover desigual que trariam genes compatíveis para o mesmo alelo, sendo responsável pelo homotalismo na espécie. Contrariando essa hipótese, os dados obtidos neste projeto indicam que uma possível transição prévia ao homotalismo resultou em uma pressão seletiva relaxada sobre os loci mating type, cuja consequência foi a degeneração nos genes destes loci. Neste contexto, os genes do mating type poderiam não estar mais envolvidos na dicariotização. Este trabalho, portanto, fornece importantes dados para o entendimento da biologia sexual deste fungo, o que futuramente poderá ser correlacionado a sua fitopatogenicidade / Abstract: The basidiomycetes¿ sexual cycle is controlled by the mating type system. The structure of this system comprises two unlinked multigenic loci, A and B. The A locus codes for homeodomain proteins, HD1 e HD2 which form a heterodimer, and B locus presents pheromone receptors and pheromones. In outcrossing (heterothallic) fungi, sexual development depends on the compatibility of four genes in two different allelic versions in a so-called tetrapolar system, and is strictly activated by specific interactions between different parental alleles, ensuring that genetically identical hyphae are incompatible. The phytopathogen Moniliophthora perniciosa causes Witches¿ broom disease in cacao plants, and it is a typical basidiomycete fungi. However, it completes its sexual development through the crossing of genetically identical hyphae, and is the first described homothallic fungi with a complete tetrapolar genetic system. Here we show the characterization of the mating type loci of M. perniciosa and the transcriptional profile of these genes, to uncover the mechanisms underpinning its homothallic behavior. First, we identified an A locus, a B locus and a set of genes that participates in pheromone processing and signalization. Considering the transcriptional profile of these genes, one receptor shows an expression profile consistent with an involvement in dikaryotization. The functional evaluation of the receptors was performed in a heterologous expression system, a promising tool for GPCR (G coupled proteins receptors) proteins study. This system did not allow the confirmation if M. perniciosa contains compatible alleles for receptors and pheromones, one possible explanation for homothallism. Considering A locus, it codes for a pair MpHD1 and MpHD2, which has a sequence insertion (11,958kb) interrupting their promoters, differing from others basidiomycetes. The hypothesis in this scenario is that the insertion of a transposon could have allowed an unequal crossover that brought together compatible genes in the same allele, causing the homothallism in this species. Interestingly, in an opposite direction, our data indicates that a previous transition for homothallism could have resulted in a relaxed selective pressure on mating type loci, with consequences such as the presence of degenerated genes on these loci. In this context, the mating type genes could not necessarily play a role in dikaryotization process. This work provides valuable data for understanding the sexual biology of M. perniciosa, which hereafter could be correlated with its phytopathogenicity / Mestrado / Genetica de Microorganismos / Mestra em Genética e Biologia Molecular

No description available.

Le champignon filamenteux, Podospora anserina, possède deux types sexuels, mat+ et mat-, caractérisés chacun par une séquence spécifique. La séquence mat+ contient un seul gène FPR1; la séquence mat- contient trois gènes : FMR1, SMR1 et SMR2. La fonction moléculaire de SMR1 est inconnue, les autres gènes codent des facteurs de transcription qui contrôlent la fécondation (reconnaissance intercellulaire), et le passage d’un syncytium à un hyphe spécialisé binucléé contenant un noyau mat+ et un noyau mat- (reconnaissance internucléaire). Il n’y a pas eu d’analyse exhaustive des gènes impliqués dans la reconnaissance intercellulaire et le mécanisme de la reconnaissance internucléaire est encore inconnu. Afin de déterminer les cibles de FPR1 et FMR1, et les différents mécanismes impliqués, nous avons utilisé une approche microarray. Le profil transcriptomique des souches mat+ et mat- compétentes pour la fécondation a permis d’identifier 157 gènes cibles, et l’analyse transcriptomique des souches mutantes fpr1- et fmr1- a révélé que ces cibles peuvent être soit réprimées, soit activées par FMR1 ou FPR1, ou être sous le contrôle de ces deux facteurs. Ces expériences ont aussi détecté l’existence de 10 gènes activés ou réprimés au même niveau dans mat+ et mat-. La délétion de 32 gènes choisis parmi ces 167 gènes cibles n’a permis de mettre en évidence que deux gènes impliqués dans la fécondation. Les comparaisons des gènes cibles des facteurs de transcription MAT de Gibberella moniliformis et Sordaria macrospora avec ceux de P. anserina révèlent un nombre significatif de gènes cibles communs entre ces espèces, mais ces gènes ont des profils transcriptomiques différents, soulevant la question du rôle de ces gènes cibles. La recherche des gènes cibles de FPR1, FMR1 et SMR2 impliqués dans la reconnaissance internuléaire a été effectuée en comparant le transcriptome des périthèces issus de deux croisements, l’un n’exprimant que les gènes spécifiques mat+, l’autre que les gènes spécifiques mat-. Les résultats ont été interprétés selon le modèle d’identité nucléaire et le modèle de ségrégation aléatoire. Le premier modèle a conduit à l’identification de 27 gènes cibles, tandis que 154 gènes cibles ont été identifiés en appliquant le deuxième modèle. Au total 46 souches mutantes ont été construites. Cependant aucune délétion n’a affecté le développement sexué. En parallèle de ces expériences transcriptomiques, nous avons invalidé tous les gènes à HMG-box de P. anserina. Les résultats montrent que ces derniers ont un rôle très important dans le développement sexué, particulièrement Pa_1_13940 qui code un régulateur des gènes des types sexuels, le premier identifié chez les Pezizomycotina. / The filamentous fungus, Podospora anserina, has two mating-type idiomorphs, mat+ and mat-. The mat+ sequence contains one gene FPR1, while mat- contains three genes: FMR1, SMR1 and SMR2. The molecular function of SMR1 is unknown, FPR1, FMR1 and SMR2 encode transcriptional regulators which control the fertilization (intercellular recognition) and the transition from a syncytium to a specialized dikaryotic hypha which contains one mat+ and one mat- nucleus (internuclear recognition). No exhaustive analysis is available for the genes involved in the intercellular recognition, while the mechanism of the internuclear recognition is unknown. In order to understand the mechanism of these events and to identify the target genes of mating-type transcription factors, we used a microarray approach. The transcriptomic profiles of the mat+ and mat- strains that are competent for fertilization revealed 157 differentially transcribed genes, and transcriptomic analysis of fmr1- and fpr1- mutant strains was used to determine the regulatory actions exerted by FMR1 and FPR1 on these differentially transcribed genes. All possible combinations of transcription repression and/or activation by FMR1 and/or FPR1 were observed. Furthermore, 10 additional mating-type target genes were identified that were up- or down-regulated to the same level in mat+ and mat- strains. Of the 167 genes identified, 32 genes were selected for deletion, which resulted in the identification of two genes essential for the sexual cycle. A comparison with similar data set from the two ascomycetes, Gibberella moniliformis and Sordaria macrospora, reveals significant numbers of orthologous pairs, although transcriptional profiles were not conserved between species, questioning the function of these target genes. Internuclear recognition was investigated by the transcriptomic analysis of perithecia from two crosses expressing mat+ and mat- genes, respectively. The tow internuclear recognition models: nuclear identity and random segregation, were used to interpret our results. According to the former model, 27 target genes have been identified, while 154 target genes were identified with the latter model. A total of 46 mutant strains were constructed. However, these strains showed no defects in sexual development. Besides this microarray experiences, we have invalidated all HMG-box genes of P. anserina. The results show that the HMG-box genes have a very important role in sexual development, especially Pa_1_13940 which encodes the first identified regulator of Pezizomycotinan mating-type genes.

Plant pathogens have the ability to quickly overcome host resistance and shift to novel hosts. The (re)emergence of plant pathogens is a major concern in agriculture and in conservation of natural landscapes. The rapid adaptation to hosts and new environments depends on the genetic variability in pathogen populations. Despite of the importance of sugarcane for Brazilian agribusiness and the persistence of the smut pathogen Sporisorium scitamineum in most cropping areas, genetic variation studies are still missing for Brazilian isolates. In the chapters 1 and 2, molecular variability studies were performed for Brazilian and Argentine isolates of S. scitamineum, using molecular markers (AFLP, telRFLP) and sequencing (ITS and a candidate effector gene) strategies. No variation was found in ITS sequences. On the contrary, telRFLP marker generates almost a unique fingerprint for each strain. Two genetically distinct groups were formed by the joint analysis of the AFLP and telRFLP markers. The two groups were the same formed by haplotypes of a candidate effector gene. The presence of polymorphisms that causes non-synonymous mutations in a candidate effector gene potentially involved in the specific interaction with sugarcane may cause distinct performances on host genotypes. S. scitamineum is part of the highly diverse clade of Ustilaginomycetes fungi that includes several smut disease agents. Despite being phylogenetically close and present similar lifestyles, species of smut fungi have distinct and narrow host ranges. Hence, another objective in this thesis was to identify the genetic basis of host specialization in smut fungi using comparative genomics analyses. In chapter 3, the mating-type loci were described in S. scitamineum genome and compared among smut fungi. Transposable elements are the likely mechanism causing chromosomal rearrangements between mating-type loci. The presence of trans-specific polymorphisms at the genes encoding pheromone/receptor proteins suggests a hybridization potential among smut species. In the chapter 4, a broad comparative genomics analysis was performed among nine species of smut fungi infecting distinct hosts. The genetic basis of host specialization in smut fungi is complex and seems to involve a range of evolutionary processes, including gene gain/loss and episodic selection events. Species-specific effectors and positively selected genes will be good candidates for further characterization in regards to their role in host adaptation. / Fitopatógenos apresentam a habilidade de rapidamente suplantar os mecanismos de defesas da planta e adaptar-se a um novo hospedeiro. A (re)emergência de patógenos é uma das maiores preocupações na agricultura e na conservação de populações naturais. A rápida adaptação ao hospedeiro e a novos ambientes depende da variabilidade genética nas populações de patógenos. Apesar da importância da cana-de-açúcar para o agronegócio brasileiro e da persistência do patógeno Sporisorium scitamineum, o agente causal do carvão da cana-de-açúcar, na maioria das áreas canavieiras, estudos de variabilidade genética ainda não foram realizados para isolados brasileiros. Nos capítulos 1 e 2, estudos de variabilidade molecular foram realizados para isolados brasileiros e argentinos de S. scitamineum, usando marcadores moleculares (AFLP e telRFLP) e dados de sequenciamento (ITS e um gene candidato a efetor). Nenhum polimorfismo foi encontrado usando sequências ITS. Contrariamente, o marcador telRFLP gerou quase um fingerprint para cada linhagem. Dois grupos geneticamente distintos foram formados pela análise conjunta dos marcadores telRFLP e AFLP. Os dois grupos também foram formados pelos haplótipos obtidos pelo sequenciamento de um candidato a efetor. A presença de polimorfismos causando mutações não-sinônimas em um candidato a efetor pode acarretar em performances distintas em diferentes genótipos de cana-de-açúcar. S. scitamineum pertence à classe Ustilaginomycetes, a qual também abrange vários outros agentes causais de doenças do carvão. Apesar de filogeneticamente próximos e com estilo de vida similar, espécies de carvão apresentam uma faixa distinta e estreita de hospedeiros. Portanto, outro objetivo desta tese foi identificar a base genética da especialização ao hospedeiro por fungos causadores de carvão usando análises de genômica comparativa. No capítulo 3, os loci envolvidos na determinação do tipo de reação sexual (mating-type) foram caracterizados no genoma de S. scitamineum e comparados com sequências de outras espécies de carvão. Tranposons foram identificados como provável mecanismo de rearranjo cromossômico entre os loci de mating-type. Polimorfismos trans-específicos nos genes codificadores de feromônios e receptores sugerem o potencial de hibridização entre espécies de carvão. No capítulo 4, análises de genômica comparativa abrangendo nove espécies de carvão infectando hospedeiros distintos foram realizadas. A base genética da especialização ao hospedeiro em fungos causadores de carvão é complexa e parece envolver processos evolutivos de ganho/perda de genes e seleção positiva. Efetores espécie-específicos e sob seleção positiva são destacados como bons candidatos para serem caracterizados quanto ao papel que estabelecem na adaptação ao hospedeiro.

Submitted by Marlene Santos (marlene.bc.ufg@gmail.com) on 2017-09-29T19:13:24Z No. of bitstreams: 2 Dissertação - William Andrés López Arboleda - 2015.pdf: 1579315 bytes, checksum: 378fd0e65f3b2919d56630143950ed75 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2017-10-02T13:35:40Z (GMT) No. of bitstreams: 2 Dissertação - William Andrés López Arboleda - 2015.pdf: 1579315 bytes, checksum: 378fd0e65f3b2919d56630143950ed75 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Made available in DSpace on 2017-10-02T13:35:40Z (GMT). No. of bitstreams: 2 Dissertação - William Andrés López Arboleda - 2015.pdf: 1579315 bytes, checksum: 378fd0e65f3b2919d56630143950ed75 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2015-03-27 / Sclerotinia sclerotiorum is a phytopathogenic fungus that infects more than 400 plant species, including common bean. Genetic variability studies in connection with phenotypic traits of agronomic interest are important to drive the control strategies against this pathogen. The aims of this study were: to evaluate the genetic variability, fungicide sensitivity, aggressiveness and to determine the proportion of MAT (Mating Type) alleles of 79 isolates of S. sclerotiorum distributed in four populations from common bean. Two populations represented a single sampling location in two different times (2000 and 2013 growing seasons). To evaluate the fungicide sensitivity a cell viability test based on the alamarBlue dye using mycelial growth was standardized. Dose-response curves for fluazinam, procymidone and benomyl were estimated using this test and were compared with dose-response curves estimated by the mycelial growth inhibition on PDA plate and the FRAC (Fungicide Resistance Action Committee) protocol. Despite the differences to assess the fungicide sensitivity between the three methods, the dose-response curves showed similar trends for the three fungicides. The fungicide sensitivity assessment at the four populations showed low sensitivity to benomyl in the Planaltina population. Furthermore, this population presented a principally clonal population structure, with a haplotype represented by 18 out of 20 isolates. Significant population differentiation in all pairwise comparisons of phi, except the comparison between EV_2013-NH, was detected. Five genetically homogeneous groups were inferred by the DAPC analysis. No group was conformed by isolates from the four populations. Only two haplotypes between the two populations from the same sampling location were shared. The hypothesis of random mating was rejected at the four populations; however this hypothesis was not rejected at the two major populations inferred by the DAPC analysis. The screening of mating type locus showed a dominance of Inv+ isolates and a high proportion of Inv+/Inv- isolates (presumable heterokaryons). / Sclerotinia sclerotiorum é um fungo fitopatogênico capaz de colonizar mais de 400 hospedeiras, sendo o agente causal do mofo branco no feijoeiro. Estudos de variabilidade genética associados a características fenotípicas de interesse agronômico, como a sensibilidade a fungicidas, oferecem informações importantes para direcionar estratégias de controle sobre este patógeno. Os objetivos deste trabalho foram avaliar a variabilidade genética, sensibilidade a fungicidas e agressividade de 79 isolados de S. sclerotiorum distribuídos em quatro populações procedentes de culturas de feijoeiro em pivô central. Duas destas populações representaram um único local de coleta em duas épocas diferentes (2000 e 2013). Para avaliar a sensibilidade a fungicidas foi padronizado um teste de viabilidade celular baseado no corante alamarBlue® sobre o crescimento micelial em microplaca de 96 poços. Curvas de dose-resposta para os fungicidas fluazinam, procimidona e benomyl, usando um isolado de S. sclerotiorum, foram estimadas com este método, e comparadas com curvas de dose-resposta obtidas com os métodos de inibição do crescimento em placa e o proposto pelo Fungicide Resistance Action Committee (FRAC). Apesar das diferentes abordagens as curvas dose-resposta mostraram tendências semelhantes para os três fungicidas. A avaliação da sensibilidade a fungicidas nas quatro populações indicou uma alta insensibilidade ao benomyl na população de Planaltina. Por outro lado, a estrutura populacional foi principalmente clonal com um haplótipo representado por 18 dos 20 isolados desta população. Diferenciação populacional significativa foi detectada em todas as comparações par a par do phi, com a exceção da comparação EV-2013-NH. A analise DAPC identificou cinco grupos geneticamente homogêneos. Nenhum dos grupos esteve constituído por isolados das quatro populações. Só dois haplótipos foram compartilhados pelas populações EV_2000 e EV_2013. A hipótese de acasalamento aleatório foi rejeitada nas quatro populações, no entanto não foi rejeitada nas duas maiores populações sugeridas pelo DAPC. O screening do Mating type locus (MAT) mostrou uma prevalência de isolados Inv+ e uma alta proporção de isolados Inv+/Inv-

Stagonospora nodorum blotch (SNB), is a major foliar disease of wheat in the mid-Atlantic U.S., is caused by the necrotrophic fungus Parastagonospora nodorum. SNB is managed using cultural practices, resistant varieties, and foliar fungicides. There are increasing trends of severity and incidence of SNB in Virginia and the surrounding mid-Atlantic region, but it is not known if changes in the pathogen population are contributing to this trend. The overall goal of this research was to 1) determine the occurrence of quinone outside inhibitor (QoI) resistance in Virginia populations of P. nodorum infecting wheat, 2) quantify the distribution of G143A mutations conferring fungicide resistance in Virginia populations of P. nodorum, and 3) characterize genetic diversity of P. nodorum populations in Virginia and assess influences of cultivars and environments on population structure and SNB severity. For Objective 1, QoI resistant isolates of P. nodorum were identified from Virginia wheat fields, and this was the first report of QoI resistant P. nodorum in the United States. The G143A substitution in the cytochrome b gene of P. nodorum was associated with reduced QoI sensitivity, and in Objective 2, a state-wide, two-year survey of P. nodorum populations in Virginia determined that the G143A mutation was widespread in the state and among sampled fields the frequency ranged from 5-32% (mean = 19%). For Objective 3, P. nodorum was isolated from five different wheat cultivars across seven locations over two years in Virginia. SNB severity varied by cultivar but greater differences in disease severity were observed among locations and years suggesting environment plays an important role in SNB development. Among the necrotrophic effector (NE) genes examined, SnTox1 was predominant followed by SnTox3, and frequencies of NE genes did not vary by cultivar or location. P. nodorum populations in Virginia had high genetic diversity, but there was no genetic subdivision among locations or wheat cultivars from which individuals were isolated. Results also indicated that the P. nodorum population in Virginia undergoes a mixed mode of reproduction, but sexual reproduction made the greatest contribution to population structure. Overall, this work provides insights into the population biology of P. nodorum in Virginia and information on variability in fungicide sensitivity and cultivar susceptibility to SNB that has implications for the current and future efficacy of fungicides and host resistance for management of SNB. / Doctor of Philosophy / Wheat (Triticum aestivum L.) is one of the major cereal crops grown worldwide for food, feed, and other products. However, yields of this crop are often limited by fungal diseases including Stagonospora nodorum blotch (SNB) caused by Parastagonospora nodorum. Increasing trends of severity and incidence of SNB may be due to reduced sensitivity of P. nodorum to fungicides or increased virulence of P. nodorum populations on commonly grown cultivars. Fungicides such as quinone outside inhibitors (QoIs) are one of the major classes of fungicides used for disease control and G143A substitution is the most common point mutation associated with complete resistance to QoIs. Therefore, the overall goal of this research was to better understand genotypic and phenotypic variation in Virginia populations of P. nodorum in the context of fungicide sensitivity and susceptibility of wheat cultivars to SNB. The specific objectives were to 1) determine the occurrence of quinone outside inhibitor (QoI) fungicide resistance in Virginia populations of P. nodorum infecting wheat, 2) quantify the distribution of G143A mutations conferring QoI fungicide resistance in Virginia populations of P. nodorum, and 3) characterize genetic diversity of P. nodorum populations in Virginia and assess influences of cultivars and environments on population structure and SNB severity. Results from this research indicate that QoI fungicide resistance occurs in Virginia populations of P. nodorum due to a target site mutation (G143A substitution in the cytochrome b gene), and this mutation is widespread and relatively common in Virginia wheat fields. Based on a multi-year multilocation study, P. nodorum populations were genetically diverse, but there was no genetic subdivision among locations or wheat cultivars. SNB severity varied by location and cultivar, but disease severity was greatest at site-years with moderate springtime temperatures and high rainfall. Overall, this work contributes to a better understanding of P. nodorum populations including the current efficacy of fungicides and host resistance for management of SNB in the region.

The genus Arthroderma contains predominantly geophilic dermatophytes (naturally occuring in soil). Some species, especially those from Trichophyton terrestre complex, cause human and animal dermatomycosis. In the past, the species boundaries were determined mainly on the basis of biological species concept using in vitro mating experiments. But these nearly 70-years-old findings have not been tested by means of modern taxonomic methods. In total 194 species of the genus Arthroderma (including all available ex-type strains) originating predominantly in USA, Canada and Europe were studied in this thesis. They were mostly isolated from soil (n = 77), animals (n = 50), human clinical material (n = 41) and cave sediment (n = 9). The main goal of the thesis was to elucidate the species boundaries between species A. insingulare, A. lenticulare and A. quadrifidum, that were classified into the T. terrestre complex because of their seemingly identical asexual stage. Further, this work aimed to resolve the relationship between Arthroderma species using the multigene phylogeny and clarify which species are clinically relevant. A multigene phylogeny of the genus Arthroderma was based on the sequences of the ITS rDNA region, β-tubulin (TUB2) and translation elongation factor 1α (TEF1α) genes. The genus...