Des souches de Vibrio appartenant au clade Splendidus sont retrouvées de manière récurrente lors des mortalités estivales d’huîtres juvéniles. La souche V. tasmaniensis LGP32 est un pathogène intracellulaire facultatif des hémocytes d’huître, dont elle altère les fonctions de défense. Nous nous intéressons ici aux interactions entre les phagocytes et V. tasmaniensis LGP32, à diverses échelles (moléculaire, cellulaire et environnementale). Dans une première partie, nous avons découvert un mécanisme antimicrobien, encore inconnu chez C. gigas : la formation de pièges d'ADN extracellulaire (ETs). Ces ETs sont associés à des histones antimicrobiennes et sont capables de piéger des bactéries. Comme chez les vertébrés, la formation de ces ETs est dépendante de la production d'espèces réactives de l'oxygène. De plus, la présence de ces ETs a été confirmée in vivo et a été associée à une accumulation d'histones antimicrobiennes dans les tissus, suite à une blessure ou à une infection. Dans une seconde partie,nous avons étudié les interactions entre V. tasmaniensis LGP32 et des protistes hétérotrophes présents dans l’environnement des huîtres, tels que les amibes et les ciliés, qui se nourrissent de micro-organismes par phagocytose. Un résultat important de cette thèse a été de montrer que V. tasmaniensis LGP32 résiste également à la phagocytose des protistes hétérotrophes environnementaux, de manière intracellulaire. C'est à notre connaissance la première fois que les mécanismes d’interaction entre des bactéries pathogènes d'origine marine et des amibes marines sont décrits. Les amibes que nous avons isolées étant présentes dans l'environnement direct des huîtres, nous pouvons donc supposer que la pression de sélection exercée par les phagocytes environnementaux pourrait favoriser l’émergence de traits de virulence et/ou de résistance à la phagocytose parmi les bactéries marines, comme c’est le cas pour V. tasmaniensis LGP32. / Vibrio strains belonging to the Splendidus clade have been repeatedly found in juvenile diseased oysters affected by summer mortalities. V. tasmaniensis LGP32 is an intracellular pathogen of oyster hemocytes which has been reported to alter the oxidative burst and inhibit phagosome maturation.We here focus on the interactions between phagocytes and V. tasmaniensis LGP32, at molecular, cellular and environmental scales. In the first part of this work, we uncover anunknown antimicrobial mechanism of C. gigas hemocytes: the formation of DNA extracellular traps (ETs). These ETs are associated with antimicrobial histones and are able to entrap bacteria. As in vertebrates, ETs formation depends on reactive oxygen species production. In addition, the presence of ETs was confirmed in vivo and has been associated with antimicrobial histones accumulation in tissues, in response to injury or infection. In the second part of this work, we studied the interactions between V. tasmaniensis LGP32 and heterotrophic protists found in the oyster’s environment, such as amoebae and ciliates, which feed on microorganisms by phagocytosis. An important result of this workwas that V. tasmaniensis LGP32 resists to phagocytosis by environmental heterotrophic protists, as well as to oyster hemocytes. To our knowledge, this is the first mechanical description of an interaction between marine amoebae and marine pathogenic bacteria. As the amoebae were isolated from the direct environment of oysters, we can presume that the selective pressure exerted by environmental phagocytes could select for virulence and/or phagocytosis resistance traits in marine bacteria as in the case of V. tasmaniensis LGP32.

La différenciation cellulaire implique des facteurs clés. Chez la drosophile, le facteur de transcription Glide/Gcm est impliqué dans la différenciation de deux types de cellules immunitaires : les macrophages circulants, qui ont une origine hématopoïétique, et les cellules gliales, macrophages résidents du système nerveux central, qui sont issues des précurseurs neuraux. J'ai d'abord entrepris la caractérisation du potentiel hématopoïétique de Gcm et l'identification de ses cibles dans les hémocytes. Ensuite, pour comprendre comment plusieurs types cellulaires peuvent être spécifiés par un même facteur de transcription, j'ai étudié comment s'effectue le choix entre le destin glial et le destin hémocytaire de la cellule. J'ai en particulier misen évidence le rôle clé des gènes agissant en aval de Gcm, ceux impliqués dans la consolidation et le maintien de l'identité cellulaire. Finalement, j'ai participé à la caractérisation du territoire d'expression de Gcm au niveau protéique et découvert un nouveau rôle de Gcm dans la différenciation de cellules neurosécrétrices, cellules indispensable pour initier le signal hormonal déclenchant le phénomène de mue chez les insectes. / Cell fate determination involves key transcription factors. ln Drosophila, the transcription factor Glide/Gcm is required for the differentiation of two immune cell types: circulating macrophages,which arise from hematopoietic precursors, and glial cells, resident macrophages of the central nervous system, which differentiate from neural precursors. ln first, 1 characterized Gcm hematopoietic potential and identified its target genes in hemocytes. Then, to get an insight intomolecular mechanisms underlying the acquisition of several identities with a single fate determinant, 1 investigated how the choice between the hemocyte and the glial fates is regulated.Being necessary to consolidate and to maintain a specific fate, 1 highlight the key role of genes acting downstream of a fate determinant. Finally, 1 contribute to characterize Gcm expression profile at the protein level and highlight a new role of Gcm in the differentiation of neurosecretory cells, cells absolutely required to initiate the hormonal signal triggering the molting process in insects.

Spiroplasma citri est une bactérie phytopathogène transmise par la cicadelle Circuliferhaematoceps. L'absence de symptômes malgré la multiplication de S. citri dans l'hémolymphe, suggèreque le système immunitaire joue un rôle important dans la tolérance de la cicadelle vis-à-vis duspiroplasme.Le but de cette thèse a donc été d'étudier la réponse immunitaire de C. haematoceps aucours de l'infection par S. citri.Notre étude sur le système immunitaire de la cicadelle a montré la présence dans le plasma d'uneactivité antibactérienne et d'une activité phénoloxidase. Parmi les principaux types d'hémocytes unephagocytose des bactéries par les granulocytes et les plasmatocytes a été observée. Les gènessusceptibles d'être impliqués dans ces processus ont été recherchés par une approche par hybridationsoustractive. De manière étonnante, aucun gènes codant des récepteurs ni d'effecteurs connus del'immunité n'ont été identifiés. En revanche certains gènes (23 en tout) codent des protéines ayantpotentiellement un rôle immunitaire. Six de ces 23 gènes ont été retenus pour suivre leur expressionau temps précoce d'une infection bactérienne. Les résultats ont montré que les gènes codantI'Hexamérine, la DDBPl et la Thiorédoxine peroxydase étaient surexprimés lors de l'infection par 5.citri. Une approche fonctionnelle d'interférence par ARN a montré d'une part que I'Hexamérine étaitimpliquée dans l'activité phénoloxidase et d'autre part qu'elle jouait un rôle important dans la surviede C. haematococeps au cours de l'infection par 5. citri. En parallèle, le suivi de l'activité phénoloxidaseet de la phagocytose au cours de l'infection a montré que 5. citri était capable de s'adapter à laréponse immunitaire de l'insecte et d'y échapper. Ces résultats rejoignent ceux obtenus chez ladrosophile concernant S. poulsonii. / Spirop/asma citri is phytopathogenic bacteria transmitted by the leafhopper Circuliferhaematoceps. The absence of symptoms despite the multiplication of S. citri in the hemolymph,suggests that the immune system plays an important role in the tolerance of the leafhopper towardsthe spiroplasma infection. The purpose of this thesis was to study the immune response of C.haematoceps during the infection by 5. citri.The characterization of the immune system of the leafhopper showed that an antibacterial activity anda phenoloxidase activity were present in the plasma. The main types of hemocytes were identified.Among them, granulocytes and plasmatocytes are capable to phagocyte bacteria. The genes involvedin these immune processes were searched using subtractive hybridization method. lnterestingly, noneof the genes known to encode receptors or effectors of the immune system were identified. On theother hand 23 putative immune genes were identified. Six of these genes were retained to follow theirexpression in the early time of a bacterial infection. The results showed that the genes encodingHexamerin, DDBPl and Thioredoxin peroxidase were up-regulated during the infection by 5. citri. Afunctional approach by gene silencing showed that Hexamerin was involved in the phenoloxidaseactivity and played an important role in the survival of C. haematoceps during the infection by S. citri.Finally, the follow-up of the phenoloxidase activity and phagocytosis by hemocytes showed anadaptation and an evasion of S. citri from the immune response of the insect, according to the resultsobtained for 5. pou/sonii-infected drosophila.Keywords : 5piroplasma citri, phenoloxidase, phagocytosis, hemocytes, gene silencing, Hexamerine,subtractive hybridization.

Submitted by (edna.saturno@ufrpe.br) on 2016-11-24T16:26:34Z No. of bitstreams: 1 Jennifer Guimaraes.pdf: 774518 bytes, checksum: 992bf3a690cf42445cc397d5068f8f46 (MD5) / Made available in DSpace on 2016-11-24T16:26:34Z (GMT). No. of bitstreams: 1 Jennifer Guimaraes.pdf: 774518 bytes, checksum: 992bf3a690cf42445cc397d5068f8f46 (MD5) Previous issue date: 2012-02-01 / Diatraea flavipennella (Box) is considered a major pest of economic importance to the culture of sugar cane in Northeast Brazil. Biological control with the fungus Metarhizium anisopliae (Metch.) Sorok., may be a viable alternative, as this pathogen is already used for other pests in this crop. This work aimed to evaluate the effects of this fungus at different concentrations, against the third instar larvae of D. flavipennella and to investigate the immune response, by analysing the types of hemocytes, and phenoloxidase, total protein and nitric oxide, tritation as well as the possible differences in the biochemical profile of hemocytes. It was observed the effect of M. anisopliae against larvae of D. flavipennella, sprayed at concentrations of 103, 104, 105 conidia/mL, which showed differences regarding to the larval period,which extended up to 72.0 days and 25.0 days in treatment the control, respectively The results for hemocytes revealed that the most common cells when sprayed at concentrations of 103, 105, 107 conidia/mL were prohemocytes, spherulocytes, plasma cells and granulocytes in relation to adipohemocytes and oenocytoids. The of nitric oxide titration was different between the control and the concentration 107 conidia/mL (24), while phenoloxidase activity was similar among treatments at 24h and was higher only at the concentration 107 conidia/mL after 60h. The total protein concentration in 107 conidia/ml (60h) was higher relatively to the control. In the biochemical profile of hemocytes there was an alteration in carbohydrates, lipids and total proteins contents at reating to the fungus. The results indicate that M. anisopliae may be used in Integrated Pest Management of D. flavipennella in northeastern sugar crops, because of the its pathogenicity and interfere with their development even when exposed to small concentrations. / Diatraea flavipennella (Box) é considerada uma das principais pragas de importância econômica para a cultura da cana-de-açúcar no nordeste brasileiro. O controle biológico com o fungo Metarhizium anisopliae (Metch.) Sorok., pode ser uma alternativa viável, considerando que esse entomopatógeno já é empregado para outras pragas nesta cultura. Este trabalho teve como objetivo avaliar os efeitos deste fungo, em diferentes concentrações, sobre lagartas do terceiro ínstar de D. flavipennella e investigar sua resposta imune, através da análise quantitativa dos tipos de hemócitos, da produção de fenoloxidase, proteína total e óxido nítrico, e possíveis diferenças no perfil bioquímico dos hemócitos. Foi observado o efeito de M. anisopliae sobre lagartas de D. flavipennella, pulverizado nas concentrações de 103, 104, 105 conídios/mL, no qual apresentou diferenças com relação ao período larval, prolongando até 72,0 dias nos tratamentos e 25,0 dias na testemunha. Os resultados referentes aos hemócitos revelaram que as células mais freqüentes quando pulverizado nas concentrações de 103, 105, 107 conídios/mL foram prohemócitos, esferulócitos, plasmócitos e granulócitos, em relação aos adipohemócitos e oenocitóides. O nível de oxido nítrico apresentou diferença entre a testemunha e a concentração 107 conídios/mL (24h), enquanto a atividade de fenoloxidase foi semelhante entre os tratamentos em 24h e superior na concentração 107 conídios/mL em 60 h. A proteína total na concentração 107 conídios/mL (60h) foi maior diferindo da testemunha. No perfil bioquímico dos hemócitos, houve uma alteração em carboidratos, lipídeos e proteínas em reação ao fungo. Os resultados indicam que o fungo M. anisopliae pode ser utilizado no Manejo Integrado de D. flavipennella nos canaviais nordestinos, por apresentar patogenicidade e interferir no seu desenvolvimento mesmo quando expostas a pequenas concentrações.

Submitted by (edna.saturno@ufrpe.br) on 2016-11-28T11:56:50Z No. of bitstreams: 1 Lilian Maria da Solidade Ribeiro.pdf: 1291994 bytes, checksum: 217ae867676a57b323ee75ec19d87a49 (MD5) / Made available in DSpace on 2016-11-28T11:56:50Z (GMT). No. of bitstreams: 1 Lilian Maria da Solidade Ribeiro.pdf: 1291994 bytes, checksum: 217ae867676a57b323ee75ec19d87a49 (MD5) Previous issue date: 2010-02-01 / The resistance of Plutella xylostella (L.) (Lepidoptera: Plutellidae) has been attributed to many mechanisms as alterations in cell membrane receptors on midgut and the immune response to Bacillus thuringiensis Berliner toxin. The research tested the possibility that after expositions to Bt formulations, insects from a susceptible population (SP) and a resistant population (RP) presented qualitative and quantitative differentiated alterations of hemocytes and nitric oxide levels in hemolymph, histopathological and histochemical differenced alterations in midgut and that RP presented capacity of recovery midgut. SP and RP were exposed to Dipel® 1,35 mg/L (SP), 64,93mg/L (RP); XenTari® 5,17 mg/L (SP), 236,24 mg/L (RP) plus witness had hemolymph collected in intervals of 1, 6 and 12 h for total and differential counting of hemocytes and quantification of nitric oxide. The midgut was collected in the intervals: 0, 1, 6, 12 h. The regenerative cells quantification was made through the ImageLab 2000 program. In spite of RP had showed less number of hemocytes, it exhibited greater quantity of plasmatocytes, prohemocytes and spherulocytes, this can be related to resistance. Dipel® was effective in reduction of total numbers of hemocytes of SP and RP, while XenTari® changed significantly the differential counting. The nitric oxide increased in both populations and it not differed between the insecticides, indicating the no participation of it in the resistance. The insecticides induced alterations in different intensities on midgut in SP and RP, Dipel® showed to be more aggressive independently of population, taking to degeneration of epithelium. The presence of spherites covering the epithelial lamina, the hypertrophy of columnar cells and mucus abundance can be involved in midgut preservation in larvae of resistant population, however these features were not sufficient to avoid the degeneration of epithelium or induce the hyperplasia of regenerative cells. / A resistência de Plutella xylostella (L.) (Lepidoptera: Plutellidae) pode ser atribuída a vários mecanismos como alterações nos receptores de membrana celular no mesêntero e a resposta imune às toxinas do Bacillus thuringiensis Berliner. A pesquisa testou as hipóteses de que após exposição a formulações Bt: população suscetível (PS) e população resistente (PR) da traça apresentam alterações quantitativas e qualitativas diferenciadas dos hemócitos e dos níveis de óxido nítrico na hemolinfa, alterações histopatológicas e histoquímicas diferenciadas no mesêntero e de que PR apresenta capacidade de recuperação do mesêntero. PS e PR expostas ao Dipel® 1,35 mg/L (PS), 64,93mg/L (PR); XenTari® 5,17 mg/L (PS), 236,24 mg/L (PR), além da testemunha, tiveram hemolinfa coletada nos intervalos de 1, 6 e 12 h para contagem total e diferencial dos hemócitos e quantificação de óxido nítrico. O mesêntero foi coletado nosintervalos: 0, 1, 6 e 12 h. A quantificação das células regenerativas foi efetuada através do programa ImageLab 2000. Apesar de PR ter apresentado menor número de hemócitos, exibiu maior quantidade de plasmatócitos, prohemócitos e esferulócitos, podendo isto estar relacionado à resistência. Dipel® foi efetivo na redução do número total de hemócitos das PS e PR, enquanto que o XenTari® alterou significativamente a contagem diferencial. O óxido nítrico aumentou emambas as populações, não diferindo entre os inseticidas, indicando a não participação deste na resistência. Os inseticidas ocasionaram alterações, de intensidades diferentes, no mesêntero das PS e PR, Dipel® mostrou ser mais agressivo independente da população, levando a degeneração do epitélio. A presença de esferites revestindo a lâmina epitelial, a hipertrofia das células colunares e a riqueza de muco podem estar envolvidas na preservação do mesêntero em larvas da população resistente, porém essas características não foram suficientes para impedir a degeneração do epitélio ou induzir a hiperplasia das células regenerativas.

Dans l'environnement, les organismes sont soumis à des stress de multiples natures (e.g., polluants et pathogènes/parasites). Dans ce contexte, le système immunitaire joue un rôle fondamental. La pression chimique exercée par les polluants peut impacter leur système immunitaire, affaiblir leur santé et les prédisposer à contracter des maladies infectieuses. En écotoxicologie, l'évaluation de marqueurs d'immunocompétence peut servir à diagnostiquer l'état de santé des organismes et mieux comprendre le danger immunotoxique des xénobiotiques. Lymnaea stagnalis est un gastéropode d'eau douce représentatif de nombreux milieux lentiques sur la planète. Des tests OCDE de reprotoxicité sont disponibles mais peu d'études se sont focalisées sur des paramètres immunotoxiques. Le premier axe de la thèse se porte sur la connaissance et le développement de méthodes pour évaluer l'immunocompétence de manière répétée à l'échelle individuelle chez L. stagnalis. Le deuxième axe évalue cette approche multibiomarqueurs dans différents contextes écotoxicologiques. Plusieurs populations (élevages vs terrain), temps d'expositions (3 vs 29 – 44 jours), concentrations d'exposition (environnementales vs non réalistes) et contaminants ont été évalués : des médicaments (les anti-cancéreux Etoposide et cyclophosphamide, l'anti-rejet de greffes cyclosporine A et l'antiinflammatoire diclofenac), l'insecticide deltaméthrine, le métal cadmium et des effluents de station d'épuration. Des comparaisons entre des traits de vie et des traits immunitaires ont été réalisées. La réflexion est bâtie sur les questionnements relatifs à (i) la sensibilité de l'approche, (ii) le temps de réponse des marqueurs, (iii) leur précocité physiologique, (iv) la transposition d'immunotoxicité de xénobiotiques entre le phylum des chordata et L. stagnalis et (vi) l'utilisation pratique de L. stagnalis (élevages, collecte en milieu naturel, calibration, reproduction) / In natural environments, animals encounter multiple stresses (e.g., pollutants and pathogens/ parasites). In this context, the immune system plays a pivotal role. Chemical insults from pollutants can jeopardize the immune system of these animals, weaken their health and make them vulnerable to contracting infectious diseases. In ecotoxicology, assessment of immunocompetence markers can be used to diagnose the health of organisms and better understand the immunotoxic hazard of xenobiotics. Lymnaea stagnalis is a freshwater gastropod representative of several lentic ecosystems on the planet. OECD reprotoxicity tests are available using this species, but too few studies have focused on immunotoxic parameters. The first part of this thesis covers the description, comprehension and development of the methods used to assess the immunocompetence at an individual scale and repeatedly within an experiment in L. stagnalis. The second part assesses this multibiomarker approach in several ecotoxicological contexts. Several populations (laboratory-bred vs collected in the field), time exposures (3 vs 29–44 days), concentrations (environmental vs unrealistic) and contaminants were evaluated : pharmaceuticals (the anti-cancer drugs etoposide and cyclophosphamide, the anti-xenograft rejection drug cyclosporine A, the anti-inflammatory drug diclofenac), the insecticide deltamethrin, the metal cadmium and wastewater treatment plant effluents. The general reasoning is built on questions relative to (i) the sensitivity of the approach, (ii) the rapidity of the response, (iii) their physiological precocity of alteration (immune vs life-history traits), (iv) the transposition of xenobiotic immunotoxicity between L. stagnalis and the Chordata phylum and (vi) the pragmatic use of L. stagnalis (breeding, collection in the environment, calibration and reproduction)

Dans les écosystèmes marins côtiers, l‘activité anthropique et les paramètres naturels induisent chez lesorganismes aquatiques des situations de «multistress». Parmi ces paramètres, deux d‘entre eux ont été étudiés:La contamination métallique et l’infection bactérienne. Dans ce contexte la compréhension des réponsesmoléculaires et physiologiques de l’ormeau rouge Haliotis rufescens a été étudiée, en particulier, face l’impactmétallique (cuivre), et au pathogène (Vibrio parahaemolyticus) en interaction avec des bactéries probiotiquespendant le stade juvénile de ce mollusque en conditions contrôlées. Dans un première temps, une évaluation surl’effet d’un consortium probiotique formé de trois souches bactériennes: Vibrio sp C21, Agarivorans albus F1et Vibrio sp F15 a été testée et les paramètres de survie et de croissance des juvéniles de l’ormeau ont été suivis.Les résultats montrent que les probiotiques augmentent les performances de ces deux paramètres de trait de viecomparés aux individus témoins sans probiotiques. Dans un second temps, une approche génomique parbanques soustractives a été réalisée afin d’identifier les transcrits régulés par l’impact métallique. Cetteméthode a permis d’identifier 108 gènes potentiellement impliqués dans la réponse cellulaire et physiologiquedes organismes face au stress. La cinétique de l’expression génique a été suivie à l’aide de 14 transcrits et leurvariation temporelle pendant la phase critique révèle des régulations parfois complexes et différentielles chezles organismes. Ensuite, les réponses immunitaires des hémocytes d’ormeau face l'exposition au cuivre ont étérecherchées. Les résultats montrent que l’exposition au métal provoque des disfonctionnement importants desactivités hémocytaires. Enfin, l’interaction entre les bactéries pathogènes et probiotiques ont étés étudiées etleurs effets sur le mollusque ont été également recherchés. La présence des bactéries pathogènes régulel’expression génique des transcrits impliqués dans des fonctions physiologiques clés des organismes (lesdéfenses immunitaires et l’état énergétique). De plus, les résultats de cette interaction nous renseignent sur lerôle capital accompli par les bactéries probiotiques sur les performances en termes d’amélioration de la survieet de la croissance des jeunes ormeaux en condition de stress. / In coastal ecosystems, anthropogenic activity and natural factors induce “multi-stress” situations. Inthis study, we focused on two such stress-inducing factors: metal contamination and bacterial infection.Specifically, under controlled conditions, we examined the molecular and physiological responses of redabalone Haliotis rufescens toward the impact of a metal (copper) and a pathogen (Vibrio parahaemolyticus)with respect to this mollusk’s interaction with probiotic bacteria during the juvenile stage. First, we assessed theeffect of a consortium of three probiotic bacterial strains—Vibrio sp. C21, Agarivorans albus F1, and Vibrio sp.F15—on two abalone lifecycle-related parameters, namely, survival and growth. The results showed that,compared to the control treatment (no probiotics), the probiotics improved the performance of these twolifecycle parameters. In a second step, the molecular mechanisms underlying the juvenile abalone response tocopper stress were studied under experimental conditions, using a suppression subtractive hybridizationmethod. This method identified 108 partial sequences of genes involved in the cellular and physiologicalresponses to stress. The kinetics of gene expression were followed using 14 of these transcripts, and theirtemporal variations during the critical phase showed complex and differential regulation exerted by copper inthese organisms. We then investigated the immune response of abalone hemocytes to copper exposure. Theresults showed that exposure to the metal causes a significant dysfunction of hemocyte activities. Finally, theinteraction between probiotics and pathogenic bacteria (transcriptomic and cellular aspects) was studied and theeffects of these bacteria on mollusk performance were also investigated. The presence of pathogenic bacteriawas found to regulate gene expression of transcripts involved in key physiological functions, including thosethat regulate immune responses and energy metabolism. Examination of these interactions thus indicates therole of probiotic bacteria in performance in terms of the improved survival and growth of juvenile abaloneunder stress conditions.

Apoptosis-induced compensatory proliferation (AiP) is a mechanism that maintains tissue homeostasis after stress-induced cell death. During AiP, apoptotic cells induce proliferation of the neighboring surviving cells to compensate for tissue loss. AiP is important for wound healing and tissue regeneration in several model organisms. Additionally, AiP is an important feature of tumorigenesis and tumor relapse as it contributes to tumor repopulation following radiation or chemotherapy. Using an overgrowth tumor model (“undead tissue”) in Drosophila melanogaster, we determined that the initiator caspase Dronc promotes generation of extracellular Reactive Oxygen Species (ROS), which drive activation of the stress kinase JNK and downstream mitogens to promote AiP. We also observed increased numbers of Drosophila macrophages, termed hemocytes, which are attracted to undead tissue. However, the specific mechanisms by which macrophages are recruited to undead tissue are still unclear. Here, we report that the tissue microenvironment of the overgrown undead tissue directs macrophage recruitment during AiP. We demonstrate that ROS, JNK, and the matrix metalloproteinase Mmp2 are important for recruiting macrophages. Mechanistically, undead tissue-produced ROS and active JNK damage the basement membrane (BM) surrounding the undead tissue, by upregulating the expression and activity of Mmp2. The damaged BM then recruits macrophages to the undead tissue. Taken together, we propose a model in which the ROS-JNK-Mmp2 signaling axis damages the BM of undead tissue, resulting in changes in the tissue microenvironment that recruit macrophages to the area of damage to promote AiP and overgrowth.

No description available.

Universidade Federal de Uberlândia / CHAPTER II: Infection in insects stimulates a complex defensive response. Recognition of pathogens may be accomplished by plasma or hemocyte proteins that bind specifically to bacterial or fungal polysaccharides. Several morphologically distinct hemocyte cell types cooperate in the immune response. Hemocytes attach to invading organisms and then isolate them by phagocytosis, by trapping them in hemocyte aggregates called nodules, or by forming an organized multicellular capsule around large parasites. In the current investigation the cellular population in the hemolymph third instar larvae of M. scutellaris has been characterized by means of light microscopy analysis and phagocytosis assays were performed in vivo by injection of 0,5μm fluorescence beads in order to identify the hemocyte types involved in phagocytosis. Four morphotypes of circulating hemocytes were found in 3rd instar larvae: prohemocytes, plasmatocytes, granulocytes and oenocytoids. The results presented plasmatocytes and granulocytes involved in phagocytic response of foreign particles in 3rd instar larvae of M. scutellaris. CHAPTER III: Insects are continuously exposed to potentially pathogenic microorganisms and eukaryotic parasites, but only a few encounters result in infection. Insects possess a complex and efficient system of biological defense against pathogens and parasites. This system involves the following: the integument and gut as physical barriers to infection, coordinated responses of several subpopulations of hemocytes when these barriers are breached, and the induced synthesis of antimicrobial peptides and proteins, primarily by the fat body. The purpose in the present study was to verify a Toll receptor (MsToll) expression in Melipona scutellaris. By semiquantitative RT-PCR we evaluate the MsToll levels at different development stages and in different M. scutellaris workers tissues. The MsToll expression in the immune response was evaluated by real time RT-PCR in workers infected with Escherichia coli (gram-negative). Our data showed lower MsToll expression in the larval stage compared with other development stages. The specific tissue analysis showed that its expression in intestine was significantly higher compared with other tissues analyzed. Furthermore, the MsToll levels in innate immune response of M. scutellaris showed four folds enhanced in bees infected with E. coli compared with control. / CAPITULO II: Infecção em insetos estimula uma resposta defensiva complexa. O reconhecimento de patógenos pode ser realizado pelos hemócitos ou proteínas que se ligam especificamente em microorganismos com padrões moleculares específicos, os chamados (PAMPs). Diferentes células da hemolinfa cooperam na resposta imune. Os hemócitos reconhecem os patógenos e os isolam por fagocitose, formando nódulos ou, cápsula multicelular em torno do parasita. Nesse trabalho foram identificadas as células da hemolinfa da abelha sem ferrão Melipona scutellaris e caracterizados os hemócitos envolvidos no processo de fagocitose utilizando beads de 0,5μm de diâmetro, em média, com fluorescência vermelha. Na hemolinfa do 3° instar larval de M. scutellaris foram distinguidos quatro tipos de hemócitos: prohemócitos, plasmatócitos, granulócitos e oenocitóides. No ensaio de fagocitose foram identificados plasmatócitos e granulócitos, com beads fluorescentes fagocitados no citoplasma. CAPITULO III: Insetos são continuamente expostos a microrganismos potencialmente patogênicos, mas apenas alguns contatos resultam em infecção. Insetos possuem um complexo e eficiente sistema de defesa contra patógenos e parasitas, que envolve o tegumento e intestino como barreiras físicas para infecção; respostas coordenadas de vários tipos de hemócitos quando estas barreiras são violadas e a síntese de peptídeos antimicrobianos e proteínas, principalmente pelo corpo gorduroso. Nosso objetivo foi clonar e sequenciar parcialmente um gene do sistema imune inato MsToll da abelha Melipona scutellaris. Por análises de RT-PCR semiquantitativo avaliou-se os níveis de expressão de MsToll em diferentes estágios do desenvolvimento e em diferentes tecidos de operárias de M. scutellaris. A expressão de MsToll na resposta imune foi avaliada por RT-PCR tempo real em operarias infectadas com Escherichia coli (gram-negativa). Os resultados mostraram menor expressão do gene MsToll nos estágios larvais quando comparados com os demais estágios do desenvolvimento. A análise tecido específico de MsToll mostrou que em intestino sua expressão foi significativamente maior quando relacionado com os demais tecidos analisados. Com relação aos níveis de MsToll na resposta imune observou-se o aumentou de quatro vezes dos níveis desse transcrito em abelhas infectadas com E. coli comparadas com o controle. / Mestre em Genética e Bioquímica