Parasitism is a common phenomenon in nature, where one species benefits at the expense of another. In marine environments, fungal parasites are known to infect phytoplankton, causing disease and death, and contributing to the loss of phytoplankton populations. The impact of fungal parasites on phytoplankton communities can be significant, as selective parasitism on one species of phytoplankton can encourage the development of other species and may be one of the factors influencing communities' seasonal succession. Fungi parasites play a crucial role in sinking by inducing cell death and promoting cell aggregation, which can lead to the export of phytoplankton to the deep sea. Although fungal parasites are well studied in freshwater phytoplankton, there is still little information on marine phytoplankton parasites. Recent studies have shown that large diatoms are the preferred hosts for fungal parasites in cold waters, while the infection of dinoflagellates is reported in the oligotrophic Mediterranean Sea. However, the occurrence and impact of fungal parasites on phytoplankton communities in the Red Sea remain largely unknown. Therefore, the proposed project aims to investigate the occurrence of fungal parasites that infect phytoplankton and analyze their role in the export of phytoplankton to the deep sea in the Red Sea. By understanding the ecological impacts, life cycle, host range, and infection strategies of fungal parasites on populations of Red Sea phytoplankton, this study can provide critical information on the dynamics of marine ecosystems and carbon cycling.

The sudden appearance of chytridiomycosis, as the cause of amphibian deaths and population declines in several continents suggests that its etiological agent, the amphibian chytrid fungus Batrachochytrium dendrobatidis, was introduced into the affected regions. However, the origin of this virulent pathogen is unknown. Efforts were directed to determine the occurrence of chytridiomycosis in Africa, whether the disease had been introduced into South Africa in recent years and how wild frog populations were affected by infection. A chytridiomycosis survey of 2,300 archived and live specimens involving members of the Pipidae family in sub-Saharan Africa, as well as a number of unrelated frog species in South Africa was conducted by histological diagnosis of skin samples. The epidemiological evidence indicated that chytridiomycosis has been a stable endemic infection in southern Africa for 23 years before any positive specimens were found outside Africa. The occurrence of chytridiomycosis in South Africa can be described as widespread both in terms of geographical distribution and host species and generally infection is not associated with adverse effects at the individual or population level. It was proposed that the amphibian chytrid originated in Africa and that the international trade in the African clawed toad Xenopus laevis that commenced in the mid 1930s was the means of dissemination. A risk assessment of the X. laevis trade demonstrated that chytridiomycosis could spread through this pathway and culminated in the development of a management protocol to reduce the risks of spreading disease through this animate commodity. Initial comparative genetic analysis of B. dendrobatidis strains isolated from South African frogs with a global set of 35 strains, suggests that analysis of a more geographically diverse set of southern African strains is needed before this line of argument can support or reject the "out of Africa" hypothesis. / Thesis (Ph.D. (Zoology))--North-West University, Potchefstroom Campus, 2005.

The sudden appearance of chytridiomycosis, as the cause of amphibian deaths and population declines in several continents suggests that its etiological agent, the amphibian chytrid fungus Batrachochytrium dendrobatidis, was introduced into the affected regions. However, the origin of this virulent pathogen is unknown. Efforts were directed to determine the occurrence of chytridiomycosis in Africa, whether the disease had been introduced into South Africa in recent years and how wild frog populations were affected by infection. A chytridiomycosis survey of 2,300 archived and live specimens involving members of the Pipidae family in sub-Saharan Africa, as well as a number of unrelated frog species in South Africa was conducted by histological diagnosis of skin samples. The epidemiological evidence indicated that chytridiomycosis has been a stable endemic infection in southern Africa for 23 years before any positive specimens were found outside Africa. The occurrence of chytridiomycosis in South Africa can be described as widespread both in terms of geographical distribution and host species and generally infection is not associated with adverse effects at the individual or population level. It was proposed that the amphibian chytrid originated in Africa and that the international trade in the African clawed toad Xenopus laevis that commenced in the mid 1930s was the means of dissemination. A risk assessment of the X. laevis trade demonstrated that chytridiomycosis could spread through this pathway and culminated in the development of a management protocol to reduce the risks of spreading disease through this animate commodity. Initial comparative genetic analysis of B. dendrobatidis strains isolated from South African frogs with a global set of 35 strains, suggests that analysis of a more geographically diverse set of southern African strains is needed before this line of argument can support or reject the "out of Africa" hypothesis. / Thesis (Ph.D. (Zoology))--North-West University, Potchefstroom Campus, 2005.

No description available.

Blastocladiella emersonii é um fungo aquático da classe dos quitridiomicetos, notável pelas mudanças morfogenéticas que ocorrem durante o seu ciclo de vida. Neste trabalho isolamos 8.495 seqüências expressas (ESTs) deste fungo, que representam 3.226 seqüências únicas putativas. Destas seqüências, 37% foram classificadas segundo o processo biológico onde estariam envolvidas, de acordo com o sistema de anotação do Gene Ontology (GO). Analisamos os perfis de expressão in silico das ESTs usando estatística Bayesiana e os resultados obtidos foram validados por Northern blot para sete perfis de expressão selecionados. Pudemos encontrar boa correlação entre vários padrões de expressão e determinados processos biológicos. Foram selecionadas algumas seqüências potencialmente envolvidas com a esporulação do fungo para melhor caracterização. Analisamos a expressão de dois genes codificando centrinas (BeCenl e BeCen2) pertencentes a subfamílias distintas. Centrinas são proteínas ligantes de cálcio envolvidas em diferentes processos como o direcionamento do aparelho flagelar e a duplicação dos centros organizadores de microtúbulos (MTOCs). Observamos que os níveis da proteína BeCenl, que não havia sido descrita em fungos, apresentam um máximo aos 150 min da esporulação, defasado do pico de expressão do seu mRNA que ocorre aos 90 min deste estágio. A proteína BeCen2 está presente em níveis constantes durante todo a ciclo de vida do fungo, embora o seu mRNA apresente um pico de expressão aos 120 min da esporulação. Experimentos de imunofluorescência localizaram a proteína BeCenl no citoplasma e no corpo basal do zoósporo. Estes dados sugerem que BeCenl atue na re-orientação e movimento dos corpos basais e BeCen2 na duplicação dos MTOCs. Investigamos também a expressão de dois genes codificando proteína-quinases dependentes de ciclina putativas (BeCdkl e BeCdk2). Apenas uma Cdk (Cdkl) foi descrita em fungos como diretamente envolvida no controle do ciclo celular. Ambos os genes apresentam expressão diferencial, com níveis máximos de mRNA para os dois casos aos 90 min da esporulação. Por outro lado, a proteína BeCdkl está presente durante todo o ciclo de vida do fungo e foi localizada no núcleo e no capacete nuclear dos zoósporos. Um transportador putativo de hexose (Bemst) foi também analisado, com base na regulação por glicose de genes envolvidos com o ciclo celular observada em eucariotos. Verificou-se que os níveis do mRNA de Bemst diminuem drasticamente durante a esporulação, mas glicose ou outras hexoses não afetaram a expressão de Bemst. / Blastocladiella emersonii is an aquatic fungus that belongs to the class of chytridiomycetes, notable for the morphogenetic processes which occur during its life cycle. In this work we have isolated 8,495 expressed sequence tags (ESTs) from this fungus, representing 3,226 putative unigenes. From these unigenes, 37% were classified into a biological process, as a result of Gene Ontology (GO) annotation. Furthermore, we analyzed the expression profile in silico of each transcript using Bayesian Statistics and seven of these profiles were validated by Northern blot analysis. In addition, we found a good correlation between several of these expression patterns and certain biological processes. Some ESTs potentially involved in the sporulation of the fungus were selected to be further characterized. We analyzed the expression of two genes encoding two centrins (BeCenl and BeCen2) of distinct subfamilies. Centrins are calcium-binding proteins involved in different processes such as basal body orientation and duplication of the microtubuleorganizing centers (MTOCs). The amount of BeCenl, a centrin ortholog not previously described in fungi, presents a maximum at 150 min of sporulation, whereas the peak of its mRNA occurs at 90 min of this stage. Protein BeCen2 presents constant levels during the entire life cycle of the fungus, even though its mRNA shows a peak of expression at 120 min of sporulation. In addition, immunofluorescent studies localized BeCenl in the cytoplasm and the basal body of zoospores. These results suggest that BeCenl plays a role in re-orientation and movement of basal bodies and BeCen2 in MTOCs duplication. We also investigated the expression of two genes encoding putative cyclin-dependent protein kinases (BeCdkl and BeCdk2). Only one type of Cdk (Cdkl) directly involved in cell cycle control has been described in other fungi. Both genes were found to be differentially expressed, with maximum mRNA levels being detected in either case at 90 min of sporulation. In contrast, BeCdk1 is present throughout the life cycle of the fungus and was immunolocalized in the nuc1eus and the nuclear cap of zoospores. A putative hexose transporter (Bemst) was also investigated, taking into account the regulation by glucose of cell cycle controlled genes in eukaryotes. We found that Bemst mRNA levels decrease drastically during sporulation, but glucose and other hexoses had no effect on Bemst expression.

Les champignons sont des organismes hétérotrophes ubiquistes jouant des rôles pivots dans de nombreux écosystèmes (e.g. décomposeurs, symbiontes) et formant une lignée eucaryote majeure. Les Chytridiomycota constituent les branches basales du règne des Champignons, soit une position critique pour la compréhension de la radiation évolutive fongique. Or, ce groupe a été peu étudié, ce qui ne permet qu'une résolution partielle de ces relations évolutives. Ici, nous décrivons la diversité fongique, en ciblant principalement les Chytridiomycota via des analyses de génomique environnementale. Des échantillons de diverses natures ont été collectés au niveau de sources hydrothermales marines profondes qui sont connues pour être des hotspots de diversité, avec un fort taux d'endémisme. Pour l'analyse des séquences moléculaires obtenues, une base de données (PHYMYCO-DB) portant sur des marqueurs moléculaires fiables et dédiés à la phylogénie fongique, a été créée puis mise en ligne. Des outils moléculaires développés au cours de cette thèse ont permis de récupérer six phylotypes Chytridiomycota dont quatre produisent des branches non-décrites à ce jour. De plus, la diversité obtenue n'est pas limitée au clade des Opisthokonta (i.e. principalement les règnes des Animaux et des Champignons) puisqu'il a également été observé un phylotype Apusozoa et deux phylotypes ayant une position indéfinie à la base des Unikonta. Ces résultats offrent des perspectives pour la description de nouveaux organismes via le séquençage de génomes ou l'imagerie. Ces organismes sont également prometteurs pour la résolution des relations évolutives chez les Opisthokonta, les Unikonta, voire les Bikonta.

Blastocladiella emersonii é um fungo aquático da classe dos quitridiomicetos, notável pelas mudanças morfogenéticas que ocorrem durante o seu ciclo de vida. Neste trabalho isolamos 8.495 seqüências expressas (ESTs) deste fungo, que representam 3.226 seqüências únicas putativas. Destas seqüências, 37% foram classificadas segundo o processo biológico onde estariam envolvidas, de acordo com o sistema de anotação do Gene Ontology (GO). Analisamos os perfis de expressão in silico das ESTs usando estatística Bayesiana e os resultados obtidos foram validados por Northern blot para sete perfis de expressão selecionados. Pudemos encontrar boa correlação entre vários padrões de expressão e determinados processos biológicos. Foram selecionadas algumas seqüências potencialmente envolvidas com a esporulação do fungo para melhor caracterização. Analisamos a expressão de dois genes codificando centrinas (BeCenl e BeCen2) pertencentes a subfamílias distintas. Centrinas são proteínas ligantes de cálcio envolvidas em diferentes processos como o direcionamento do aparelho flagelar e a duplicação dos centros organizadores de microtúbulos (MTOCs). Observamos que os níveis da proteína BeCenl, que não havia sido descrita em fungos, apresentam um máximo aos 150 min da esporulação, defasado do pico de expressão do seu mRNA que ocorre aos 90 min deste estágio. A proteína BeCen2 está presente em níveis constantes durante todo a ciclo de vida do fungo, embora o seu mRNA apresente um pico de expressão aos 120 min da esporulação. Experimentos de imunofluorescência localizaram a proteína BeCenl no citoplasma e no corpo basal do zoósporo. Estes dados sugerem que BeCenl atue na re-orientação e movimento dos corpos basais e BeCen2 na duplicação dos MTOCs. Investigamos também a expressão de dois genes codificando proteína-quinases dependentes de ciclina putativas (BeCdkl e BeCdk2). Apenas uma Cdk (Cdkl) foi descrita em fungos como diretamente envolvida no controle do ciclo celular. Ambos os genes apresentam expressão diferencial, com níveis máximos de mRNA para os dois casos aos 90 min da esporulação. Por outro lado, a proteína BeCdkl está presente durante todo o ciclo de vida do fungo e foi localizada no núcleo e no capacete nuclear dos zoósporos. Um transportador putativo de hexose (Bemst) foi também analisado, com base na regulação por glicose de genes envolvidos com o ciclo celular observada em eucariotos. Verificou-se que os níveis do mRNA de Bemst diminuem drasticamente durante a esporulação, mas glicose ou outras hexoses não afetaram a expressão de Bemst. / Blastocladiella emersonii is an aquatic fungus that belongs to the class of chytridiomycetes, notable for the morphogenetic processes which occur during its life cycle. In this work we have isolated 8,495 expressed sequence tags (ESTs) from this fungus, representing 3,226 putative unigenes. From these unigenes, 37% were classified into a biological process, as a result of Gene Ontology (GO) annotation. Furthermore, we analyzed the expression profile in silico of each transcript using Bayesian Statistics and seven of these profiles were validated by Northern blot analysis. In addition, we found a good correlation between several of these expression patterns and certain biological processes. Some ESTs potentially involved in the sporulation of the fungus were selected to be further characterized. We analyzed the expression of two genes encoding two centrins (BeCenl and BeCen2) of distinct subfamilies. Centrins are calcium-binding proteins involved in different processes such as basal body orientation and duplication of the microtubuleorganizing centers (MTOCs). The amount of BeCenl, a centrin ortholog not previously described in fungi, presents a maximum at 150 min of sporulation, whereas the peak of its mRNA occurs at 90 min of this stage. Protein BeCen2 presents constant levels during the entire life cycle of the fungus, even though its mRNA shows a peak of expression at 120 min of sporulation. In addition, immunofluorescent studies localized BeCenl in the cytoplasm and the basal body of zoospores. These results suggest that BeCenl plays a role in re-orientation and movement of basal bodies and BeCen2 in MTOCs duplication. We also investigated the expression of two genes encoding putative cyclin-dependent protein kinases (BeCdkl and BeCdk2). Only one type of Cdk (Cdkl) directly involved in cell cycle control has been described in other fungi. Both genes were found to be differentially expressed, with maximum mRNA levels being detected in either case at 90 min of sporulation. In contrast, BeCdk1 is present throughout the life cycle of the fungus and was immunolocalized in the nuc1eus and the nuclear cap of zoospores. A putative hexose transporter (Bemst) was also investigated, taking into account the regulation by glucose of cell cycle controlled genes in eukaryotes. We found that Bemst mRNA levels decrease drastically during sporulation, but glucose and other hexoses had no effect on Bemst expression.