Microsporidia are spore-forming, obligate intracellular pathogens typically associated with opportunistic infections in immunocompromised individuals. Treatment options for microsporidia infections in humans are limited and additional research is necessary to create better therapeutic agents. For many pathogenic organisms, adhesion to the host cell surface is a prerequisite for tissue colonization and invasion. Our previous research has demonstrated a direct relationship between adherence of microsporidia spores to the surface of host cells and infectivity in vitro. In an effort to better understand adherence, we have turned our attention to determining what proteins may be involved in this process. Examination of the Encephalitozoon cuniculi genome database revealed a gene encoding a protein with sequence homology to members of the ADAM (a disintegrin and metalloprotease) family of type I transmembrane glycoproteins. The microsporidia ADAM (MADAM) protein is of interest because ADAMs are known to be involved in a variety of biological processes including cell adhesion, proteolysis, cell fusion, and signaling. The objectives for this study were to examine the localization of MADAM, analyze its potential involvement during adherence and/or host cell infection, and to identify potential binding partners or substrates. Through the use of immunoelectron transmission microscopy, we demonstrated that MADAM is localized to the surface exposed exospore, plasma membrane, and the polar sac-anchoring disk complex (a bell-shaped structure at the spore apex involved in the infection process). Location of MADAM within the exospore and polar sac-anchoring disk suggests that MADAM is in a position to facilitate spore adherence or host cell infection. Thus far, we have been unable to conclusively demonstrate that MADAM is involved in either event. Through the use of a yeast two-hybrid system, we were able to identify polar tube protein 3 (PTP3) as a potential binding partner or substrate for the MADAM protein. The interaction between MADAM and PTP3 was confirmed by in vitro co-immunoprecipitation. PTP3 is hypothesized to be involved in the process of polar tube extrusion by stabilizing the interaction between PTP1-PTP2 polymers. Further analysis of the interaction between MADAM and PTP3 may lead to a better understanding of the events that occur during polar tube extrusion.

Pour faire face à des perturbations environnementales, les organismes ont développé des défenses antitoxiques couramment utilisés comme biomarqueurs dans l'évaluation de la qualité des milieux. Cependant, de nombreux facteurs confondants comme la température ou le genre, influencent la réponse de ces biomarqueurs. Il est ainsi nécessaire de connaitre les effets de ces facteurs afin d'imputer correctement la réponse biologique mesurée à la présence de polluants. Dans ce contexte, nous avons choisi d'étudier l'influence d'un parasite acanthocéphale, Polymorphus minutus, transmis horizontalement et de microsporidies à transmission verticale, sur les réponses physiologiques de leur hôte, Gammarus roeseli, un crustacé amphipode d'eau douce d'intérêt écotoxicologique. Pour cela, nous avons choisi d'étudier le glutathion, tripeptide jouant un rôle central dans les systèmes antitoxiques, sa synthèse (i.e. activité gamma-glutamylcystéine ligase), les réserves énergétiques (i.e. lipides, glycogène, protéines) et un biomarqueur d'effets toxiques, le malondialdéhyde. L'influence du parasitisme a été appréhendé dans différents cas d'études: (i) chez G. roeseli infecté par P. minutus, (ii) chez G. roeseli infecté par des microsporidies (Dictyocoela roeselum essentiellement) et (iii) chez G. roeseli co-infecté par ces deux types de parasite. Chaque cas d'étude a été réalisé en absence de stress et lors d'une exposition au cadmium. Nous avons mis en évidence qu'en absence de contamination, la présence de P. minutus et une co-infection par P. minutus et D. roeselum affectent les biomarqueurs de G. roeseli. Après exposition au cadmium, la présence de parasites (i.e. infection simple ou co-infection) modifie la mobilisation des défenses antitoxiques et accentue les effets toxiques subits par l'hôte. Les résultats obtenus au cours de ce travail mettent en avant le caractère confondant du parasitisme en écotoxicologie et souligne l'importance de prendre en compte ce paramètre lors de l'évaluation de la qualité des milieux / To cope with environmental disturbances, organisms have developed antitoxic defenses commonly used as biomarkers in environmental risk assessment. However, many confounding factors such as temperature and gender could influence biomarker responses. It seems hence necessary to investigate their effects, in order to attribute biological responses only to pollutants. In this context, we investigated the influence of parasitism by studying the acanthocephalan parasite Polymorphus minutus, horizontally transmitted, and microsporidia parasites, vertically transmitted, on the physiological responses of their common host, the freshwater amphipod Gammarus roeseli, a classical model used in ecotoxicology. We investigated the glutathione, a tripeptide having a key role in antitoxic systems, its synthesis (i.e. gamma-glutamylcysteine ligase activity), energy reserves (i.e. lipids, glycogen, proteins) and a toxicity biomarker, the malondialdehyde. The influence of parasitism was considered in different studies: (i) in G. roeseli infected by P. minutus only, (ii) in G. roeseli infected by microsporidia (mainly Dictyocoela roeselum) and (iii) in G. roeseli coinfected by both parasites. Each study was carried out in absence of pollutants and under cadmium stress. We highlighted that, in the absence of contamination, only P. minutus and the co-infection affect the G. roeseli biomarker assessments. After cadmium exposure, the presence of parasites (i.e. single infection or co-infection) influences the mobilization of antitoxic defences, and accentuates toxic effects in their hosts. Our results underline the confounding nature of parasitism in ecotoxicology and thus, highlight the importance to take into account this parameter in the environmental risk assessment

Immunodeficient honey bee (Apis mellifera) colonies suffer from broad range of parasites including eukaryotic protozoa. Despite this fact, the eukaryotic parasites are still poorly documented in the Czech Republic. The presence of eukaryotic parasites (Nosema ceranae, Nosema apis, Crithidia mellificae and Apicystis bombi) was observed in different apiaries in the Czech Republic. The samples were taken in 9 apiaries in 53 beehives during the 2014/2015 season. From each beehive, 10 adult of honey bees were taken from the peripheral comb in triplicate. DNA was isolated from every sample of honey bees. The parasites were detected by polymerase chain reaction (PCR) with specific primers. The treatment fall of parasitic mite Varroa destructor was obtained from beekeepers for season of 2014. Crithidia mellificae was detected by 5 types of specific primers (SEF, SER; SSU, SSU rRNA, Cyt b, Tryp cyt b) and positive amplicons were cloned and sequenced. The obtained sequences were compared with GeneBank and showed similarity from 98-100% to sequences of Lotmaria passim (Trypanosomatid). Crithidia mellificae was not detected. L. passim had prevalence of 79,2% and is reported in the Czech Republic for the first time. Primer Tryp-cyt b is recommended for the routine detection of L. passim. Nosema ceranae was...

Nosema ceranae est un parasite émergeant d’Apis mellifera décrit dans certaines régions comme la cause majeure de la mortalité des abeilles. Dans d’autres cas, il est soupçonné d’affaiblir les colonies par l’interaction avec d’autres facteurs de pression de l’environnement. Dans le cadre du phénomène global de la mortalité des abeilles, nous avons orienté nos recherches vers l’étude des effets N. ceranae, en faisant l’hypothèse que ce parasite est capable d’induire des changements comportementaux chez A. mellifera dus à des altérations physiologiques, ce qui pourrait éventuellement perturber l’organisation sociale et aboutir à la mort de la colonie. Etant donné cette hypothèse, trois domaines d’étude ont été inclus dans notre recherche, (i) les effets de N. ceranae sur l’organisation sociale de la colonie, (ii) les mécanismes moléculaires à la base des effets chez les abeilles parasitées, et (iii) les différences en virulence d’isolats de N. ceranae ce qui pourrait expliquer la variation des effets du parasite chez l’abeille. Nous avons obtenu trois résultats majeurs. D’abord, nous avons constaté des modifications dans la structure sociale des abeilles après l’infection. Ces changements sembleraient contribuer à la survie de la colonie constituant probablement un mécanisme d’immunité sociale. Ce mécanisme géré par un signal phéromonal, permettrait de diminuer la transmission du parasite au sein de la colonie et prolonger la survie des abeilles saines. Ensuite, nous avons mis en évidence des effets sur la physiologie de l’intestin de l’abeille qui pourraient causer sa mort : l’induction du stress oxydatif et l’inhibition du renouvellement cellulaire de l’épithélium. Finalement, nos résultats suggèrent que certaines caractéristiques de l’hôte et conditions environnementales augmenteraient la probabilité de N. ceranae d’induire la mort. En conclusion, N. ceranae a le potentiel de causer la mort des abeilles, cependant, la colonie pourrait contrer l’infection, par exemple, par de mécanismes d’immunité sociale, or, la réponse générale à l’infection dépendrait des caractéristiques de l’hôte en combinaison avec les conditions de l’environnement. Le phénomène d’effondrement de colonies à l’échelle mondiale a mis en évidence la fragilité du système colonie d’abeilles – environnement. L’étude de chaque facteur participant au système, en autres, parasites, pesticides, changements dans l’environnement, pratiques apicoles, est essentielle pour une meilleure compréhension de toutes les interactions qui maintiennent l’équilibre écologique des colonies / Nosema ceranae is an emergent parasite of the honey bee Apis mellifera. In some regions it has been found to be the main reason for bee mortality, while in others it is suspected of weakening honey bee colonies by interacting with other environmental stressors. In the context of worldwide colony losses, we focus our research on the study of N. ceranae, with the hypothesis that this parasite is able to induce behavioral changes in bees through physiological modifications, which could alter social organization and cause colony death. Given this hypothesis, the program of study falls into three areas; (i) N. ceranae effects on colony social organization, (ii) molecular mechanisms of N. ceranae infection underlying observed effects, and (iii) differences in virulence of N. ceranae strains which could explain the diversity of parasite effects. We obtained three main results. First, we observed modifications in honey bee social structure after infection. This mechanism under pheromone control, would reduce parasite transmission within the colony and increase the lifespan of healthy bees. These changes may contribute to colony survival as part of a mechanism of social immunity. Second, we found two mechanisms whereby the pathogen affects the physiology of bee midgut epithelium that could lead to host mortality: oxidative stress and the inhibition of cellular renewal. Finally, our results suggest that certain host and environmental conditions increase the probability that N. ceranae will cause bee mortality. In conclusion, N. ceranae has the potential to cause bee death, however at colony level bees might counteract infection through, for example, social immunity mechanisms; although, overall honey bee response to infection would depend on characteristics of the host in combination with environmental conditions. Worldwide colony losses phenomenon have highlighted the fragility of the “honey bee colony – environment” system. The study of each factor involve in this system, including parasites, pesticides, environmental changes and beekeeping practices, is essential to better understand all of the interactions that maintain the ecological balance of honey bee colonies

Tesis por compendio / [ES] La producción en acuicultura se ha visto menguada por aparición de enfermedades en los sistemas de cría de peces. En concreto, en la dorada (Sparus aurata), hay dos parásitos destacados: Enteromyxum leei (Myxozoa) y Enterospora nucleophila (Microsporidia). Hasta la fecha, para ninguno de los dos se ha establecido un cultivo in vitro, y solo para E. leei se ha conseguido establecer un modelo de mantenimiento de la infección in vivo. La presente tesis pretende incrementar el conocimiento sobre estos parásitos y sus relaciones con el hospedador, sentando las bases para generar soluciones que puedan ser aplicadas en la acuicultura. El objetivo con E. leei fue estudiar la inmunidad adquirida inducida en la dorada y la posibilidad de generar herramientas de diagnóstico y vacunas frente a esta enfermedad. Para ello, primero se demostró la resistencia del pez al parásito tras una segunda exposición, la cual duró hasta 16 meses. Además, la resistencia parece estar correlacionada con altos niveles de inmunoglobulina (Ig) M específica en sangre, y una alta expresión de Igs, incluso antes de la re-exposición al parásito. El siguiente paso fue afinar el protocolo de infección con E. leei. Los resultados mostraron que una semana es suficiente para transmitir la infección de E. leei por efluente, independientemente de la temperatura. Tras la demostración de la respuesta adaptativa eficaz frente a E. leei, y al disponer de un modelo de infección refinado, se realizó un ensayo de inmunización pasiva. Aquí, los resultados mostraron que los anticuerpos especi'ficos efectivamente consigue ralentizar la invasión del intestino por el parásito y disminuir los síntomas de la enfermedad. Paralelamente, el resultado del análisis del repertorio de las regiones variables de la IgM e IgT del intestino peces resistentes mostró la inducción de una respuesta policlonal en las ce'lulas B. En base a estos resultados, se realizó una búsqueda de antígenos de E. leei que pudieran ser utilizados como candidatos para la producción de vacunas (análisis proteómico) o herramientas de diagnóstico (análisis in silico). Para ello, se ensambló un transcriptoma de novo utilizando una muestra mixta de intestino de dorada y parásito. Los resultados dieron lugar a 7 y 12 candidatos en la búsqueda in silico y proteómica, respectivamente. En los estudios de E. nucleophila, debido a que fue descrita muy recientemente, el punto de partida fue más básico. Las muestras de este parásito solo se pueden obtener de brotes naturales en piscifactorias. Por ello, primero se realizó un estudio de caracterización de la patología de la infección a partir de peces infectados naturalmente. En etapas tempranas de la infección, el parásito se localiza principalmente en el intestino, pero meses después, la prevalencia en intestino baja e incrementa en los órganos hematopoyéticos y el esto'mago. Los signos clínicos de la infección consistieron en una reducción significativa del crecimiento, emaciación, y palidez de las paredes intestinales. A nivel celular, en los casos ma's graves se observó hipercelularidad en el epitelio intestinal y proliferación de ce'lulas rodlet, un elevado número de linfocitos en la base del epitelio e infiltración de granulocitos acidófilos en el epitelio intestinal. Finalmente se probaron varias formas de transmisión horizontal de E. nucleophila (cohabitación, efluente, intubación oral y anal) con para desarrollar un modelo de mantenimiento in vivo. Se consiguió la transmisión el parásito por todas las vías, pero con una disminución de prevalencia a lo largo del tiempo. Variables como la temperatura, la dosis, y el estado de los peces donantes parecen ser más determinantes que la ruta seleccionada para la transmisión. Entre las rutas probadas, la intubación anal parece ser la más prometedora, pero ninguna de ellas fue capaz de reproducir los signos clínicos observados en las infecciones naturales. / [CA] La producció en aqüicultura s'ha vist minvada per aparició de malalties en els sistemes de cria de peixos. En concret, en l'orada (Sparus aurata), hi ha dos paràsits destacats: Enteromyxum leei (Myxozoa) i Enterospora nucleophila (Microsporidia). Fins avui, per a cap dels dos s'ha establert un cultiu in vitro, i només per a E. leei s'ha aconseguit establir un model de manteniment de la infecció in vivo. La present tesi pretén incrementar el coneixement sobre aquests paràsits i les seves relacions amb l'hoste, establint les bases per a generar solucions que puguin ser aplicades en l'aqüicultura. L'objectiu amb E. leei va ser estudiar la immunitat adquirida induïda en l'orada i la possibilitat de generar eines de diagnòstic i vacunes enfront d'aquesta malaltia. Per a això, primer es va demostrar la resistència del peix al paràsit després d'una segona exposició, la qual va durar fins a 16 mesos. A més, la resistència sembla estar correlacionada amb alts nivells d'immunoglobulina (Ig) M específica en sang, i una alta expressió de Igs, fins i tot abans de la re-exposició al paràsit. El següent pas va ser afinar el protocol d'infecció amb E. leei. Els resultats van mostrar que una setmana és suficient per a transmetre la infecció de E. leei per efluent, independentment de la temperatura. Després de la demostració de la resposta adaptativa eficaç enfront de E. leei, i en disposar d'un model d'infecció refinat, es va realitzar un assaig d'immunització passiva. Aquí, els resultats van mostrar que els anticossos específics efectivament aconsegueix alentir la invasió de l'intestí pel paràsit i disminuir els símptomes de la malaltia. Paral·lelament, el resultat de l'anàlisi del repertori de les regions variables de la IgM i IgT de l'intestí peixos resistents va mostrar la inducció d'una resposta policlonal en les cèl·lules B. Sobre la base d'aquests resultats, es va realitzar una cerca d'antígens de E. leei que poguessin ser utilitzats com a candidats per a la producció de vacunes (anàlisis proteómico) o eines de diagnòstic (anàlisi in silico). Per a això, es va assemblar un transcriptoma de novo utilitzant una mostra mixta d'intestí d'orada i paràsit. Els resultats van donar lloc a 7 i 12 candidats en la cerca in silico i proteòmica, respectivament. En els estudis de E. nucleophila, pel fet que va ser descrita molt recentment, el punt de partida va ser més bàsic. Les mostres d'aquest paràsit només es poden obtenir de brots naturals en piscifactorias. Per això, primer es va realitzar un estudi de caracterització de la patologia de la infecció a partir de peixos infectats naturalment. En etapes primerenques de la infecció, el paràsit es localitza principalment en l'intestí, però mesos després, la prevalença en intestí baixa i incrementa en els òrgans hematopoètics i l'estómac. Els signes clínics de la infecció van consistir en una reducció significativa del creixement, emaciació, i pal·lidesa de les parets intestinals. A nivell cel·lular, en els casos més greus es va observar hipercelularidad en l'epiteli intestinal i proliferació de cèl·lules rodlet, un elevat nombre de limfòcits en la base de l'epiteli i infiltració de granulòcits acidòfils en l'epiteli intestinal. Finalment es van provar diverses formes de transmissió horitzontal de E. nucleophila (cohabitació, efluent, intubació oral i anal) amb per a desenvolupar un model de manteniment in vivo. Es va aconseguir la transmissió el paràsit per totes les vies, però amb una disminució de prevalença al llarg del temps. Variables com la temperatura, la dosi, i l'estat dels peixos donants semblen ser més determinants que la ruta seleccionada per a la transmissió. Entre les rutes provades, la intubació anal sembla ser la més prometedora, però cap d'elles va ser capaç de reproduir els signes clínics observats en les infeccions naturals. / [EN] Aquaculture production is hampered by the emergence of parasite diseases in fish farming systems. Among them, in Sparus aurata, there are two important enteric parasites described: Enteromyxum leei (Myxozoa) Enterospora nucleophila (Microsporidia). To date, no in vitro culture has been established for either parasite, and only for E. leei was it possible to establish a model for maintaining the infection in vivo. The aim of this thesis is to gain new knowledge about these parasites and their relationship with the host, also the basic foundations for generating solutions that can be applied in aquaculture. The general objective for E. leei was to study the acquired immunity induced in gilthead bream and the possibility of generating diagnostic tools and vaccines against this disease. To this end, resistance against the parasite was assessed with a second exposure against the parasite, which showed a resistance for at least 16 months. Besides resistance seemed to be correlated with high levels of specific immunoglobulin (Ig) M in blood, and a high expression of Igs, in particular, the soluble forms, even before re-exposure to the parasite. The next step was refining the protocol for effluent infection with E. leei by studying infection at different exposure time points, temperatures and population densities. The results showed that one week of exposure is sufficient to spread E. leei infection by effluent, regardless of temperature. After demonstrating the resistance against E. leei, and with a refined infection model, a passive immunization assay was performed. The results showed that the serum with specific antibodies effectively slows down the invasion of the gut by the parasite and reduces the symptoms of the disease. At the same time, the analysis of the repertoire of the variable regions of intestinal IgM and IgT showed an induction of a polyclonal response in B cells. On the basis of these results, a research was carried out for E. leei antigens that could have use as candidates for the production of vaccines (proteomic study) or diagnostic tools (in silico study) using the parasite transcriptomic data. To do this, a de novo transcriptome was assembled using a mixed sample of gilthead sea bream and parasite, with a posterior filtrate of the sequences. The In silico and proteomic analysis search resulted in 7 and 12 transcripts, respectively, which are being used for diagnostic and vaccine production. The starting point was more basic in E. nucleophila studies, since this is a recently described disease. The samples of this parasite can only be obtained from natural outbreaks in fish farms. Therefore, first study was carried out to characterize the pathology of the infection of naturally infected fish. In the early stages of the infection, the parasite is mainly located in the intestine, but months later, the prevalence is lower in the intestine and increases in the hematopoietic organs and the stomach. Clinical signs of infection were significant reduction in growth, wasting, and intestinal walls paleness. At the cellular level, in the most severe cases hypercellularity in the intestinal epithelium, proliferation of rodlet cells, high number of lymphocytes at the base of the epithelium and infiltration of acidophilic granulocytes in the intestinal epithelium were observed. Finally, horizontal transmission of E. nucleophila was tried using different transmission methods: cohabitation, effluent, and oral and anal intubation. Transmission of the parasite was achieved with all routes, but there was a decrease in prevalence over time in all cases except for the anal route. Variables such as temperature, dose, and the status of the donor fish appear to be more important than the selected route. Among the routes tested, anal intubation seemed to be the most promising, as it was sustained over a longer period of time, but none of them was able to reproduce the same clinical signs of infection observed in natural infections. / The authors kindly acknowledge the collaboration of anonymous fish farming companies allowing access to the animals during the disease outbreaks. We thank J. Monfort and L. Rodríguez (IATS-CSIC) for the technical assistance on histological processing.This work has been carried out with financial support from the European Union and the Spanish Ministry of Economy and Competitiveness (MINECO) under grant projects ParaFishControl (H2020-634429) and AGL2013-R-48560-C2-2-R, respectively. APS was contracted under ParaFishControl project. Primer sequences and access to the gilthead sea bream transcriptomic database were kindly provided by Prof. J. Pérez-Sánchez of the IATS- Nutrigenomics group. The authors thank I. Vicente for fish maintenance and technical assistance during samplings. The authors thank P. Boudinot (INRAE) for his help in designing and interpreting the immunoglobulin repertoire study and results, J. Pérez-Sánchez (IATS-CSIC) for providing access to the gilthead sea bream genome sequences to perform the repertoire analysis.This work was funded by the European Research Council (ERC Consolidator Grant 2016 725061 TEMUBLYM). / Picard Sánchez, MA. (2021). Control of enteric parasitic diseases of farmed gilthead sea bream: New insights into Enteromyxum leei (Myxozoa) and Enterospora nucleophila (Microsporidia) infections [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/167035 / TESIS / Compendio