Une caractéristique majeure de l’infection par Toxoplasma gondii est le contrôle rapide de la population parasitaire par une réponse immunitaire engageant des cellules résidentes et recrutées ainsi que des cytokines pro- et anti-inflammatoire. Dans ce contexte, l’IFNγ active une multitude d’activité anti- T. gondii des cellules immunes et non-immunes, mais peut aussi contribuer à l’immunopathologie. T. gondii a élaboré des mécanismes pour contrer les défenses de l’hôte en interférant avec la transcription des gènes stimulés par l’IFNγ. Nous avons identifié TgIST (T. gondii inhibitor of STAT1 transcriptional activity) comme un interrupteur moléculaire exporté par les parasites intracellulaires et qui est localisé dans le noyau des cellules hôtes, où il inhibe l’expression des gènes pro-inflammatoires dépendants de STAT1. Nous avons montré que TgIST séquestre STAT1 à des sites spécifiques, et promeut la formation de chromatine non permissive grâce à sa capacité à recruter le remodeleur chromatinien NuRD. Nous avons montré que durant l’infection aiguë en souris, les parasites déficients pour TgIST sont rapidement éliminés par les monocytes pro-inflammatoires GR1+, ce qui montre le rôle protecteur de TgIST contre les défenses médiées par l’IFNγ. En révélant les fonctions de TgIST, cette étude montre de nouvelles évidences sur la façon dont T.gondii a élaboré une arme moléculaire de choix pour prendre le contrôle sur la réponse immune, de façon à promouvoir le parasitisme à long terme / An early hallmark of Toxoplasma gondii infection is the rapid control of the parasite population by a potent multifaceted innate immune response that engages resident and homing immune cells along with pro- and counter-inflammatory cytokines. In this context, IFN-γ activates a variety of T. gondii–targeting activities in immune and nonimmune cells but can also con- tribute to host immune pathology. T. gondii has evolved mechanisms to timely counteract the host IFN-γ defenses by interfering with the transcription of IFN-γ–stimulated genes. We now have identified TgIST (T. gondii inhibitor of STAT1 transcriptional activity) as a critical molecular switch that is secreted by intracellular parasites and traffics to the host cell nucleus where it inhibits STAT1-dependent proinflammatory gene expression. We show that TgIST not only sequesters STAT1 on dedicated loci but also promotes shaping of a nonpermissive chromatin through its capacity to recruit the nucleosome remodeling deacetylase (NuRD) transcriptional repressor. We found that during mice acute infection, TgIST-deficient parasites are rapidly eliminated by the homing Gr1+ inflammatory monocytes, thus highlighting the protective role of TgIST against IFN-γ–mediated killing. By uncovering TgIST functions, this study brings novel evidence on how T. gondii has devised a molecular weapon of choice to take control over a ubiquitous immune gene expression mechanism in metazoans, as a way to promote long-term parasitism.

Résumé confidentiel / Résumé confidentiel

Apicomplexa, einschließlich Plasmodium sp. (Erreger der Malaria) und Toxoplasma gondii (Erreger der Toxoplasmose), sind ein großes Phylum einzelliger, obligat intrazellulärer Parasiten, welche ein essenzielles, Plastiden ähnliches Organell, den sogenannten Apicoplast, beherbergen. Aufgrund der Beteiligung an mehreren essenziellen Stoffwechselprozessen stellt das Ferredoxin Redoxsystem innerhalb der Apicomplexa ein vielversprechendes potentielles Wirkstoffziel dar. Eine kürzlich veröffentlichte Arbeit zeigt, dass ptFd in T. gondii (TgFd) ein essenzielles Protein ist. In der vorliegenden Arbeit konnte durch eine gezielte Analyse von Metaboliten der Isoprenoid-Biosynthese gezeigt werden, dass T. gondii Fd eine essenzielle physiologische Funktion als Elektronendonor für die letzten beiden Enzyme dieses Stoffwechselweges hat. Weiterhin zeigen im Zusammenhang mit dieser Arbeit generierte Daten, das der Einfluss auf die Isoprenoid-Biosynthese einen zusätzlichen Effekt auf die Proteinprenylierung hat. Darüber hinaus zeigen die Ergebnisse dieser Arbeit, dass die Hemmung der Isoprenoid Biosynthese des Wirtes zum langsamen Einsetzen des Absterbens bei TgFd Knockdown-Parasiten beiträgt, was darauf hindeutet, dass der Mangel an Isoprenoid Vorstufen nach induziertem Fd Knockdown bis zu einem gewissen Grad durch vom Wirt stammende Isoprenoide kompensiert werden kann. Zusammenfassend tragen die Ergebnisse dieser Doktorarbeit zu einem besseren Verständnis der metabolischen Rolle von Ferredoxin in T. gondii und P. falciparum bei und zeigen dessen Bedeutung für den Parasitenstoffwechsel und verdeutlichen damit das Potenzial Ferredoxins als Wirkstoffziel gegen das große Phylum der Apicomplexa. / Apicomplexan parasites, including Plasmodium sp. (the causative agent of malaria) and Toxoplasma gondii (causing toxoplasmosis), are a large phylum of unicellular, obligate intracellular organisms. The plant type ferredoxin redox system in apicomplexan parasites is a promising drug target due to its potential involvement in several essential metabolic processes. Recently published work demonstrated that ptFd in T. gondii (TgFd) is an essential protein. A tetracycline-inducible knock-down (ikd) approach was used to replace the endogenous single copy of TgFd with a myc-tagged copy (TgFdmyc) by double cross-over homologous recombination, and severe growth inhibition of parasites was observed upon Fd depletion. Metabolomic analyses show a 30% decrease in C14:0 fatty acids and a significantly lower gliding motility (20%) in the TgFd ikd strain compared to the TgFd ikd complemented (TgFd cikd) strain. In this thesis, targeted metabolomic analysis of the isoprenoid biosynthesis metabolites demonstrates that T. gondii Fd has an essential physiological function as an electron donor for the last two enzymes of the pathway. Furthermore, results of this work show that inhibition of the host isoprenoid biosynthesis contributes to the slow onset of death in TgFd knockdown parasites, indicating that the lack of isoprenoid precursors after induced Fd knockdown can to some extent be compensated by host-derived isoprenoids. Together, the findings of this study contribute to a better understanding of the metabolic role of Fd in T. gondii and P. falciparum, supporting its importance for the parasite’s metabolism and underlining its potential as a drug target in apicomplexan parasites.

Made available in DSpace on 2014-07-29T15:30:43Z (GMT). No. of bitstreams: 1 liliane.pdf: 1600508 bytes, checksum: e9fcd25a4570269e3820045946b731d2 (MD5) Previous issue date: 2008-04-01 / Toxoplasmosis is a protozoosis of high incidence in the world, caused by Toxoplasma gondii, transmitted by the ingestion of food contaminated by oocysts found in feline feces, or cists in raw or underdone meat, congenitally in other instances. The disease is usually asymptomatic, but in embryos or in imunodrepessive patients it may be devastating. In this work, the experimental serologic profile has been evaluated after specific therapy in isogenies mice Balbc, infected with a cystogenic lineage ME-49 of T. gondii. Fifty animals have been intra-peritoneal inoculated with 10 cists of T. gondii (lineage ME-49) obtained from the maceration of mice brains of previously inoculated mice. The mice have been divided into three groups of 15 animals each and a negative control group (not infected and not treated) of 5 animals. All the animals have been daily accompanied, and the symptoms were verified during 20 days. After this period, two groups of 15 animals underwent specific therapy schemes in which; group A: pirimetamin (12,5mg/kg/day) + folic acid; group B: pirimetamin + folic acid + sulfadiazine (500mg/kg/day), orally administrated during 10 consecutive days. After this period, all animals have been scarified, with an interval of 5 days, and the blood has been collected by a heart puncture and the serum separated for the Indirect Immuno-fluorescence Reaction. The samples from the treated animals presented a significant diminution in the quantity of (IgG) antibodies evaluated by the two schemes by the indirect immuno-fluorescence reaction (t=3,5, and t=7,6 respectively), in relation to the control group. There have been no significant differences between the two therapeutic schemes (t=0,36). Our results have shown that the experimental precocious treatment reduces significantly the IgG levels, suggesting a diminution of antigenic stimulus, and consequently a better prognosis for toxoplasmosis. / A Toxoplasmose é uma protozoose de alta prevalência mundial, causada pelo Toxoplasma gondii. É transmitida pela ingestão de alimentos contaminados com oocistos excretados em fezes de felinos, ou cistos, em carnes cruas ou mal cozidas, congenitamente entre outros mecanismos. A doença é usualmente assintomática, mas em fetos e/ou pacientes com imunodepressão, pode ser devastadora. Neste trabalho foi avaliado o perfil sorológico experimental após terapêutica especifica em camundongos isogênicos Balb/C infectados com cepa cistogênica ME-49 de T. gondii. Cinqüenta animais foram inoculados intraperitonealmente, individualmente, com 10 cistos da cepa ME-49 obtidos de macerado de cérebros de camundongos previamente inoculados. Os camundongos foram divididos em três grupos com 15 animais em cada grupo e um grupo controle negativo de 5 animais (não infectados e não tratados). Todos os animais foram acompanhados diariamente, observando-se sintomatologia, por 20 dias. Após este período dois grupos A e B, foram submetidos a esquemas terapêuticos específicos; Grupo A: pirimetamina (12,5mg/kg/dia)+acido fólico; grupo B: pirimetamina+acido fólico+sulfadiazina (500mg/kg/dia), por um período de 10 dias consecutivos, por via oral, onde as drogas foram ministradas de acordo com o peso dos animais. Após este período eles foram sacrificados, com intervalo de 5 dias, o sangue coletado por punção cardíaca, e o soro separado para a reação de imunofluorescência indireta. As amostras provenientes dos animais tratados apresentaram diminuição significativa nos títulos de anticorpos (IgG) avaliados com os dois esquemas, pela Reação de Imunofluorescência Indireta (t=3.5, e t=7,6 respectivamente), em relação ao grupo controle. Entre os dois esquemas terapêuticos não houve diferenças significativas (t=0,36). Nossos resultados demonstraram que o tratamento experimental precoce reduz significativamente os níveis de IgG, sugerindo uma diminuição do estimulo antigênico, e conseqüentemente um melhor prognóstico para a toxoplasmose.

No description available.

La toxoplasmose, dûe au parasite Toxoplasma gondii, est une zoonose dite à cycle complexe car le pathogène fait intervenir plusieurs espèces pour assurer sa transmission. Les félidés sont les hôtes définitifs de T. gondii et, lorsqu’ils sont infectés, peuvent excréter des millions d’oocystes dans l’environnement. L’ensemble des animaux à sang chaud, y compris l’homme, constituent les hôtes intermédiaires. L'infection des différents hôtes s'effectuent par transmission verticale ou via l'ingestion de tissus animaux contaminés ou d'oocystes présents dans l'environnement.Les objectifs de ma thèse étaient i) de mesurer la fréquence et la distribution spatiale des oocystes de T. gondii dans l’environnement en milieu rural, ii) d'estimer la prévalence et la distribution spatiale de l’infection dans la communauté locale de rongeurs, iii) de déterminer les principaux facteurs responsables de la structuration spatiale de la contamination environnementale et enfin, iv) d’évaluer l'importance de l'environnement en tant que source de contamination tant pour les animaux que pour l’homme.Nous avons mis en évidence une forte contamination des sols (29%) distribuée sur l'ensemble de la zone et, avons révélé un gradient spatial similaire de diminution de la contamination avec la distance aux bâtiments au niveau des sols et dans la communauté de rongeurs. Le modèle de simulation multi-agents a permis d'expliciter le rôle prépondérant de la configuration de l'habitat humain, qui de par son effet sur la structuration spatiale des populations de chats domestiques, détermine la fréquence et la distribution des points chauds de contamination. Par conséquent, en milieu rural, l'importante contamination des sols au niveau des fermes suggère que le risque d’infection pour l’homme est élevé, indirectement à travers la consommation de viande issue d’animaux d’élevage infectés, mais aussi directement via l’ingestion d’oocystes présents sur les substrats manipulés lors de diverses activités. / Toxoplasmosis, caused by the parasite T. gondii, is a zoonosis with a complex life cycle as the pathogen requires several different species to achieve it cycle. Felids, in particular domestic cats, are the definitive hosts of the parasite and when infected they can shed millions of oocysts in the environment. All warm blooded animals, including humans, are potential intermediate hosts. Host species can be infected through vertical transmission or by ingesting contaminated tissues or oocysts present on environmental substrates.My goals were: I) to precisely measure the frequency and spatial distribution of the environmental contamination to T. gondii in a rural area, ii) to estimate the prevalence and the spatial distribution of the parasite in the local community of rodents, iii) to identify the main factors driving the spatial structure of the environmental contamination and finally, iv) to assess the importance of the environment as a transmission source for animals and humans.First, we found a high frequency of contaminated soil samples (29%) that were largely distributed across the whole area, and, we found a similar spatial gradient of decreasing contamination with increasing distances from buildings for soils and rodents. Altogether, the results obtained allowed to identify and rank the determinants of the spatio-temporal dynamics of the environmental contamination to T. gondii. The agent-based model showed the primary role of the spatial configuration of human habitat, which, through its impact on the spatial structure of domestic cat populations, determines the frequency and distribution of the hot spots of soil contamination. Thus, in rural areas, the high level of contamination within and around agricultural buildings suggests that infection risks for humans are important, either indirectly through the consumption of contaminated meat or directly due to the ingestion of oocysts contaminating earth, water or vegetables.

Sendo uma patologia prevenível e tratável, o importante na toxoplasmose congênita é o diagnóstico precoce, fundamental para intervenção terapêutica imediata. Em Cascavel-PR a soroepidemiologia da toxoplasmose foi avaliada em 334 soros de gestantes, com prevalência de 54% e risco de 2,5%aa de infecção aguda. Para monitorar e instrumentar o pré-natal através da triagem de gestantes soronegativas por acompanhamento mensal foi desenvolvido um teste imunocromatográfico para detecção de anticorpos IgG anti-Toxoplasma gondii. (TIC-toxo). Conjugados de ouro coloidal com diferentes extratos antigênicos do agente e os reagentes controle e teste da reação foram preparados e avaliados por imunofiltração e controles intraexperimentais, incluindo microscopia eletrônica, sendo. selecionados na padronização o conjugado de ouro de 6nm recoberto com 2,5 ug/A 540nm de ouro de extrato antigênico alcalino de T. gondii, na linha teste da membrana, a Proteína A de S.aureus e na linha controle, o anticorpo anti-T. gondii,. No ensaio foram testadas 70 amostras de soro em duplicata, sendo 35 reagentes e 35 não reagentes, comparando com ELISA comercial, ELISA in house e IFI. Sensibilidade, especificidade, valor preditivo positivo, valor preditivo negativo e eficiência do TIC-Toxo foram, respectivamente: 88,6% (IC 72,3-96,3), 80,0% (IC 62,5-90,9), 81,6% (IC 65,1-91,7), 87,5% (IC 70,1-95,9) e 0,8429, havendo concordância e reprodutibilidade (Kappa=0,712171) entre o TIC-toxo e os métodos clássicos. O teste desenvolvido é rápido, de baixo custo, de fácil execução em única etapa para uso ambulatorial, precedendo a confirmação laboratorial, na triagem de gestantes ou grupos específicos, permitindo especialmente, o manejo adequado das gestantes de Cascavel em risco de toxoplasmose congênita. / As preventable and treatable condition, the main goal in congenital toxoplasmosis is early diagnosis, essential for adequate therapy. We study seroepidemiology of toxoplasmosis in 344 sera samples from pregnant women of Cascavel, PR, Brazil. By consistent serology, we demonstrate 54% prevalence and a 2.5% risk of acute infection/year, using several approaches. For supply the antenatal office care, it would be important a quick immunochromatographic assay for detection of anti T.gondii</I. IgG antibodies (TIC-Toxo), to be applied in the follow up of pregnant women at risk of infection. To develop the TIC-Toxo assay, we evaluate and standardize the gold particle conjugate adsorbed with several types of tachyzoite extracts, aside to specific reagents for the control and test area of the strip test, by immunofiltration assays, with several quality control steps including electron microscopy. Those analysis provide data for defining the reagents for mass production of TIC-Toxo, constructed with 6 nm colloidal gold conjugate recovered with 2.5ug/A540 of alcaline extract from T.gondii tachyzoites, with S.aureus Protein A at test dot and anti-T.gondii antiserum at control dot. Seventy sera samples were blind tested, 35 positive and 35 negative, comparing to ELISA and IFA assays. Sensitivity, specificity, positive predictive value, negative predictive value and accuracy were respectively: 88,6% (IC 72,3-96,3), 80,0% (IC 62,5-90,9), 81,6% (IC 65,1-91,7), 87,5% (IC 70,1-95,9) e 0,8429, with good agreement of TIC-Toxo and other assays (Kappa=0,712171), with good intra and inter test reproducibility. This TIC-Toxo is a quick, low cost, one step assay and easily performed, to be used for prenatal ambulatory diagnosis of toxoplasmosis, preceding the laboratorial confirming diagnosis and allowing adequate care of pregnant women or others selected groups at risk of acute toxoplasmosis and fetal congenital disease, specially at Cascavel-Pr.

Taquizoítos de T. gondii esterilizados por radiação ionizante é uma vacina interessante para induzir uma imunidade semelhante à infecção, mas sem a formação de cistos. Neste estudo avaliamos as populações celulares do sangue e do baço induzidas pela imunização, a resposta imune humoral, celular e a proteção após desafio com parasitas viáveis. Camundongos foram imunizados com taquizoítos de T. gondii irradiados por v.o. ou i.p.. Os animais foram desafiados com 10 cistos da cepa ME-49 ou VEG por via oral e apresentaram altos níveis de proteção com baixa carga parasitária. Camundongos imunizados por i.p. e v.o. apresentaram anticorpos específicos no soro e o aumento das populações de células B, plasmócitos, células TCD4+ e TCD8+ tanto no sangue como no baço. As células esplênicas de camundongos imunizados por i.p. mostraram a produção de IL-10, IFN-&#947; e IL-4. Células TCD4+ e células B do baço de camundongos imunizados por i.p. proliferaram após a estimulação com antígeno. A imunização com esse modelo vacinal induziu uma resposta imune mediada com células B, TCD4+ e TCD8+, com aumento da resposta imune humoral e celular que são necessárias para proteção do hospedeiro após uma infecção. Essa resposta imune induzida é uma resposta semelhante a uma infecção natural, sendo assim o desenvolvimento de vacinas utilizando a radiação ionizante como uma ferramenta, pode ser um modelo atrativo e eficiente para testar novos imunógenos no futuro. / Tachyzoites of T. gondii sterilized by ionizing radiation is an interesting vaccine for inducing immunity to infection similarly but without the formation of cysts. In this study we evaluated the cell populations from blood and spleen induced by immunization, the humoral immune response, cellular and protection after challenge with viable parasites. Mice were immunized with irradiated tachyzoites of T. gondii by v.o. or i.p.. The animals were challenged with 10 cysts of the ME-49 or VEG strain orally and showed high levels of protection with low worm burden. Immunized mice by i.p. and v.o. present specific antibodies in the serum and increased populations of B cells, plasma cells, CD4+ and CD8+ T cells in blood and spleen. The spleen cells of immunized mice by i.p. showed the production of IL-10, IFN-&#947; and IL-4. CD4+ T cells and B cells in the spleen of immunized mice i.p. proliferated upon stimulation with antigen. The immunization with this vaccine model induced an immune response mediated by B cells, CD4+ and CD8+ with increased humoral and cellular immune response are necessary for host protection after infection. This induced immune response is a response similar to natural infection, therefore the development of vaccines using ionizing radiation as a tool, can be an attractive and efficient model for testing new immunogens in the future.

Toxoplasma gondii é um protozoário pertencente ao filo Apicomplexa, de distribuição mundial, e que infecta diversas espécies hospedeiros, como mamíferos e aves, possuindo como hospedeiros definitivos o gato e outros felídeos, enquanto o homem e outros animais são os seus hospedeiros intermediários. O tratamento é feito, na maioria das vezes, com uma combinação de sulfadiazina e pirimetamina, agindo na via metabólica do ácido fólico, o qual é necessário para a biossíntese de purinas, pirimidinas e certos aminoácidos. Propusemos estabelecer um protocolo de avaliação sobre esse protozoário, assim como padronizarmos uma metodologia por espectroscopia para uma rápida avaliação ou triagem de substâncias potencialmente ativas contra o parasito. Verificamos a atividade das substâncias ácido ursólico e ácido oleanóico, as quais já demonstraram atividade biológica sobre outras espécies de protozoários, como Plasmodium, Trypanosoma cruzi e Leishmania sp. em sistemas in vitro e in vivo. A metodologia colorimétrica pelo MTT, pelo Alamar Blue®, do kit CyQUANT® NF e a contagem manual em meio líquido das formas taquizoítas do parasito em ensaios biológicos in vitro mostram-se inviáveis, pois há grande dificuldade em manter a integridade do parasita em meio de cultura líquido, o qual se mostra sensível à adição de qualquer outro componente que não aqueles necessários para manter sua viabilidade em ambiente extracelular. O ácido ursólico mostrou-se potencialmente ativo in vitro sobre formas intracelulares de T. gondii. Entretanto, o contato de células infectadas com as substâncias avaliadas por um período de 48 horas não resultou em diminuição mais acentuada na porcentagem de células infectadas do que a ocorrida no tratamento de 24 horas. A comparação dos resultados do tratamento pós infecção celular por 24 horas e do pré-tratamento das formas taquizoítas houve diferenças significativas, indicando principalmente maior ação do pré-tratamento sobre T. gondii. Quando administrado na dose de 7 mg/kg/ dia a camundongos infectados, o ácido ursólico não apresentou atividade sobre o parasita. / Toxoplasma gondii is an Apicomplexa protozoan, of worldwide distribution, that infects several species, from mammalians to birds; its definitive hosts are the cats and other felines, while man and other animals are considered as intermediate hosts. Treatment is, generally, a combination of sulfadiazine and pyrimethamine, triggering the metabolic pathway of folic acid, which is necessary for certain purines, pirimidines and aminoacids biosynthesis. We have proposed an evaluation protocol on this protozoan, and also to establish a methodology by spectroscopy for rapid evaluation of pottentialy bioactive substances against the parasite. The ursolic acid and oleanoic acid bioactivity were tested. These substances have already demonstrated to be effective on another protozoan species, like Plasmodium, Trypanosoma cruzi e Leishmania sp., either in vitro or in vivo. The colorimetric methodology by MTT, Alamar Blue®, CyQUANT® NF kit and manual counting of tachyzoite forms in liquid culture medium showed to be unviable, because there is a great difficult to maintain the parasite viability in liquid culture medium, wich one is sensible to addition of any other component different of that necessary for its survival in extracelular ambient. Ursolic acid was pottentialy active on T. gondii intracellular forms. However, the infected cells in contact with the tested substances for a period of 48 hours did not show a statistical greater reduction as compared to infected cells which underwent treatment for 24 hours. Significant results were observed when comparing pre-treatment of tachyzoite forms and treatment for 24 hours post-cellular infection. Our data pointed in the direction that pre-treatment exerted a higher effectiveness. Any parasiticidal activity was observed when ursolic acid on a concentration of 7 mg/kg/day was administered to infected mice.

Toxoplasma gondii é um protozoário coccídio intracelular obrigatório conhecido por sua habilidade em parasitar uma ampla gama de espécies hospedeiras. A região apical do parasito é rica em organelas que, em função dos produtos liberados, estão envolvidas no processo de adesão e invasão da célula hospedeira. As proteínas liberadas por micronemas (MICs), solúveis e transmembrana, possuem domínios adesivos essenciais para a virulência do parasita. Algumas dessas proteínas são encontradas associadas entre si na superfície do taquizoíta, formando complexos como TgMIC1/MIC4/MIC6 e TgMIC3/MIC8. Em estudos anteriores demonstramos a que o subcomplexo TgMIC1/MIC4 (Fração LAC+) liga-se à lactose e estimula macrófagos a secretar IL-12. Verificamos, utilizando células HEK293 transfectadas, que um dos principais mecanismos responsáveis pela produção de IL-12 decorria do reconhecimento de N-glicanos do ectodomínio de TLR2 pelo domínio de reconhecimento de carboidrato de TgMIC1. O objetivo do presente estudo foi o de investigar a capacidade de TgMIC1 e TgMIC4 de ativar macrófagos murinos e qual o papel desempenhado por TLR2 e/ou TLR4 no desencadeamento dessa ativação. Mostramos que macrófagos derivados de medula óssea de camundongos C57Bl/6, estimulados com TgMIC1 e TgMIC4, utilizadas isoladamente ou em combinação, secretam altos níveis de citocinas pró-inflamatórias, como TNF-?, IL-6, IL-12 e IL-1?, produzem altos níveis de óxido nítrico, e têm aumentadas suas capacidades migratória e fagocítica. Os ensaios que utilizaram macrófagos de camundongos C57Bl/6 nocauteados revelaram que a ausência de expressão de TLR2 ou de TLR4 prejudicou os efeitos ativadores exercidos por TgMIC1 e TgMIC4. Macrófagos TLR2-/- tiveram as manifestações de ativação celular significantemente reduzidas em relação aos macrófagos selvagens. Por outro lado, esses efeitos foram mais afetados pela ausência de TLR4, uma vez que as respostas obtidas frente ao estímulo com TgMIC1 ou TgMIC4 eram similares às verificadas em células não estimuladas (controle negativo). Concluímos que TgMIC1 e TgMIC4 interagem com os receptores do tipo toll 2 e 4 expressos por macrófagos, levando à ativação celular manifesta por alta produção de citocinas e outros mediadores inflamatórios, e aumento das capacidades migratória e fagocítica. A interação com TLR4 é preponderante em relação à estabelecida com TLR2 no desencadeamento de ativação celular / Toxoplasma gondii is an obligate intracellular coccidian protozoan known for its ability to parasitize a wide range of host species. The parasite\'s apical region is rich in organelles that, because of the products it releases, are involved in the processes of adhesion and invasion of the host cell. The soluble and transmembrane proteins released by the micronemes (MICs), have adhesive domains that are essential for the parasite virulence. Some of these proteins can be found associated with each other on the taquizoite surface, as it is the case of TgMIC1/MIC4/MIC6 or TgMIC3/TgMIC8 complexes. Our group has demonstrated in previous studies that the TgMIC1/TgMIC4 subcomplex (LAC+ fraction) binds to lactose and stimulates macrophages to release IL-12. Using HEK293 transfected cells, we showed that one of the main mechanisms leading to IL-12 release by macrophages, was the recognition of N-glycans of the TLR2 ectodomain by the carbohydrate recognition domain of TgMIC1. Thus, the objective of this study was to address whether TgMIC1 and TgMIC4 activate murine macrophages and what is the role of TLR2 and TLR4 in macrophage activation. Our results show that the stimulation of C57BL/6 mice bone marrow derived macrophages with TgMIC1 and TgMIC4, alone or in combination, induce the release of high levels of proinflammatory cytokines such as TNF-?, IL-6, IL-12 and IL-1?, and also nitric oxide; and increases phagocytic activity and cell migration activity. The assays using knockout C57Bl/6 macrophages showed that the absence of TLR2 or TLR4 expression impaired the activating effects of TgMIC1 e TgMIC4. TLR2-/- macrophages presented significantly reduced cell activation manifestations compared to WT macrophages. On the other hand, these effects were more affected in the absence of TLR4, once the responses obtained with TgMIC1 or TgMIC4 stimulation were similar to those observed in non stimulated cells (negative control). We conclude that TgMIC1 and TgMIC4 interact with the receptors Toll like 2 and 4 expressed in macrophages, leading to cell activation, resulting in high cytokine and inflammatory mediators production, and increased migratory and phagocytic capacity. The interaction with TLR4 is predominant over that established with TLR2 in the triggering of cell activation