Orientador: Márcio Garcia Ribeiro / Banca: Antonio Carlos Paes / Banca: Domingos da Silva Leite / Resumo: Escherichia coli e considerado o principal agente causal de infeccao de trato urinario (ITU) e piometra em caes. A patogenicidade das linhagens esta relacionada a presenca de adesinas e diferentes fatores de virulencia. Foram avaliadas alteracoes hematologicas e diferentes fatores de virulencia em 51 linhagens de E. coli isoladas de ITU, 52 de piometra e 55 de fezes de caes sem sinais entericos. A producao de ƒ¿-hemolisina foi verificada em 26 (51,0%) das estirpes de ITU e em 20 (38,5%) de piometra. Exames hematologicos revelaram principalmente anemia, trombocitopenia e leucocitose por neutrofilia e monocitose nos caes com ITU e piometra. Os maiores indices de sensibilidade nas 158 estirpes foram observados para norfloxacina, ciprofloxacina e enrofloxacina em mais de 60% dos isolados. Os maiores indices de resistencia foram encontrados em 60% ou mais das estirpes com o uso de sulfametoxazole/trimetoprim. Linhagens resistentes a tres ou mais antimicrobianos foram constatadas em 24 (47,1%) de ITU, 7 (13,5%) de piometra e 4 (7,3%) das fezes, das quais respectivamente, 17 (33,3%), 1 (1,9%) e 3 (5,5%), com resistencia multipla a cinco ou mais drogas. fimH foi observado em mais de 90% dos isolados. papC foi detectado em 12 (23,5%) linhagens de ITU, 19 (36,5%) de piometra e 10 (18,2%) das fezes. papGI nao foi detectado, enquanto papGII foi observado em 3 (5,8%) isolados de piometra. papGIII foi expressado em 10 (19,6%) linhagens de ITU, 15 (28,8%) de piometra e 9 (16,4%) das fezes. sfaS foi encontrado em 22 (43,1%) de ITU, 24 (46,1%) de piometra e 19 (34,5%) das fezes. afa foi detectado em 1 (1,9%) linhagem de ITU e de piometra...(Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Escherichia coli is considered the more important microrganism in urinary tract infection (UTI) and pyometra in dogs. The pathogenicity of strains is associated with different adhesins and virulence factors. Haematological exams and different virulence factors was evaluated in 51 E. coli strains isolated from UTI, 52 from pyometra and 55 from feces of dogs without enteric signs. Alpha-haemolysin was verified in 26 (51.0%) strains from UTI and 20 (38.5%) from pyometra. Haematological exams revealed mainly anaemia, thrombocytopenia and leucocytosis by neutrophilia and monocitosis in dogs with UTI and pyometra. Norfloxacin, ciprofloxacin and enrofloxacin were the most-effective drugs (>60%) for 158 E. coli strains. High rates of E. coli resistance to antimicrobials were observed in 60% or more of strains using sulfametoxazole/trimetoprim. Multiple drug resistance for three or more antimicrobials was observed in 2 (47.1%) strains isolated from UTI, 7 (13.5%) from pyometra and 4 (7.3%) from feces. From these, 17 (33.3%), 1 (1.9%) and 3 (5.5%), respectively, showed multiple resistance to five or more drugs. fimH was observed in 90% or more of 158 isolates. papC was detected in 12 (23.5%) strains isolated from UTI, 19 (36.5%) from pyometra and 10 (18.2%) from feces. None strain expressed papGI, while papGII was observed in 3 (5.8%) strains of pyometra. papGIII was detected in 10(19.6%) strains of UTI, 15 (28.8%) from pyometra and 9 (16.4%) from feces. sfaS was observed in 22 (43.1%) strains of UTI, 24 (46.1%) of pyometra and 19 (34.5%) of feces. afa was identified in 1 (1.9%) strains isolated from UTI and pyometra...(Complete abstract, click electronic address below) / Mestre

Rhodococcus fascians is a Gram-positive phytopathogenic bacterium which induces the development of leafy galls, local amplifications of multiple buds, on most infected plants. This process is linked to the production of phytohormones along with the presence of essential virulence-associated genes like the plasmid loci att and fas and the chromosomal gene vicA. However, the presence of these genes is not sufficient to ensure the infection phenotype development, indicating that other genes play a role in R. fascians pathogenicity. In this work, we studied the metabolic modifications occurring when the bacterium interacts with its host using a proteomic approach. A comparison between virulent and avirulent strains showed variations in the expression of catalases. In the virulent strain, besides the transitory induction of the att locus expression, the bacterium changes its metabolism from the Krebs cycle to the glyoxylate shunt, a process which is frequently observed in bacteria confronted to a hostile environment. The expression of the shunt-specific enzyme isocitrate lyase increased, while expression of fumarate hydratase and pyruvate dehydrogenase decreased. Hence, we focused on the link between the glyoxylate shunt and virulence. A screening of a R. fascians mutant library based on the capacity of bacteria to use acetate as the sole carbon source, a metabolic pathway depending on the glyoxylate shunt, resulted in the identification of a new gene essential for R. fascians pathogenicity. This gene encodes a glycosyl transferase, an enzyme known to be involved in the bacterial cell wall biosynthesis but possibly also implicated in cytokinin secretion. A mutant in this gene harboured an altered colony phenotype and could not induce malformations on infected plants. Accordingly, our results were integrated in the leafy gall pathology model recently presented by Stes et al. (2011). Finally, the several questions that are raised by this work, allowed us to suggest further research perspectives in order to unveil a little more of the R. fascians mysterious ways to interact with the plant./Rhodococcus fascians est une bactérie Gram-positive phytopathogène qui induit le développement de galles feuillées, des amplifications locales de multiples bourgeons, sur la plupart des plantes infectées. Ce processus est lié à la production de phytohormones ainsi qu’à la présence de gènes essentiels associés à la virulence tels que les loci plasmidiques att et fas et le gène chromosomique vicA. Cependant, la présence de ces gènes ne suffit pas à garantir le développement du phénotype d’infection, indiquant que d’autres gènes jouent un rôle dans la pathogénicité de R. fascians. Dans ce travail, nous avons étudié les modifications métaboliques qui se produisent lorsque la bactérie interagit avec son hôte par une approche protéomique. Une comparaison entre les souches virulente et avirulente a mis en évidence des variations d’expression au niveau des catalases. Dans la souche virulente, outre l’induction transitoire de l’expression du locus att, la bactérie change son métabolisme pour passer du cycle de Krebs au shunt du glyoxylate, un processus fréquemment observé chez les bactéries confrontées à un environnement hostile. L’expression de l’isocitrate lyase, enzyme spécifique au shunt, augmente, tandis que celle de la fumarate hydratase et de la pyruvate déhydrogénase diminue. Nous nous sommes donc intéressés au lien entre le shunt du glyoxylate et la virulence. Le screening d’une banque de mutants de R. fascians basé sur la capacité de la bactérie à utiliser l’acétate comme seule source de carbone, une voie métabolique dépendant du shunt du glyoxylate, a permis d’identifier un nouveau gène essentiel pour la pathogénicité de R. fascians. Ce gène code pour une glycosyl transferase, une enzyme impliquée dans la biosynthèse de la paroi bactérienne mais également dans la sécrétion des cytokinines. Un mutant dans ce gène présente un phénotype de colonie altéré et ne peut induire de malformations chez les plantes infectées. Finalement, nos résultats et les pistes d’interprétations que nous avons émisent nous permettent de compléter le modèle de l’interaction R. fascians-plante proposé récemment par Stes et al. (2011). Des perspectives de recherches visant une meilleure compréhension de ce pathosystème sont proposées. / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

Conselho Nacional de Desenvolvimento Científico e Tecnológico / Estreptococos do grupo B (EGB) é a principal causa de sepse e meningite neonatal e tem sido recentemente reconhecido como patógeno responsável por infecções invasivas em adultos imunocomprometidos (idosos ou portadores de doenças crônicas). Os EGB produzem inúmeras enzimas extracelulares, várias das quais interagem com o sistema imune do hospedeiro e são importantes durante a interação EGB-hospedeiro, bem como para o desenvolvimento da doença. Estudos anteriores mostraram que metaloproteases estão envolvidas em várias vias metabólicas em diferentes tipos celulares. Por esta razão, nós decidimos investigar o possível envolvimento de metaloproteases de EGB durante a interação celular e apoptose/necrose induzida pelo micro-organismo em células endoteliais da veia umbilical humana (HUVEC) e da linhagem de epitélio respiratório (A549). Tratamento de EGB com inibidores de metaloproteases (EDTA, EGTA e FEN) não induziu alterações no crescimento bacteriano, mas promoveu alterações na expressão de proteínas de superfície, capacidade adesiva e perfil de sobrevivência intracelular do patógeno. O EGB e o sobrenadante do crescimento bacteriano (meio condicionado; MC) promoveram a morte das células HUVEC e A549. Contudo, o tratamento com inibidores de metaloproteases restauraram a viabilidade celular induzida pelos EGB e o MC, sugerindo que metaloproteases bacteriana estão envolvidas no rompimento da barreira celular, promovendo a disseminação bacteriana. Este trabalho descreve pela primeira vez apoptose e necrose induzidas pelo EGB e MC em HUVEC e células A549 após 24h de incubação, respectivamente. Nós também observamos redução da pró-caspase-3 após infecção das HUVEC com EGB e MC, sugerindo ativação da caspase-3. Além disso, o aumento da expressão da proteína pró-apoptótica Bax e diminuição dos níveis da proteína anti-apoptótica Bcl-2 em HUVEC, demonstram o envolvimento do mecanismo apoptótico mitocondrial (via intrínseca). A melhor compreensão das bases moleculares da patogênese do EGB contribui para identificar novas moléculas bacterianas e hospedeiras que podem representar novos alvos terapêuticos ou imunoprofiláticos contra a doença causada por esse patógeno neonatal. / Group B streptococcus (GBS) is the leading cause of neonatal sepsis and meningitis and has recently been recognized as an increasingly common cause of invasive disease in immunocompromised adults (elderly or chronic diseases). GBS produces a number of extracellular enzymes, several of which interact with the host immune system and are important for the GBS- host interaction and for the development of disease. Previous studies showed that metalloproteases are involved in several metabolic pathways in different cellular types. For this reason, we decided to investigate the possible involvement of GBS metalloproteases during cell interaction and apoptosis/necrosis induced by microorganism in human umbilical vein endothelial cells (HUVEC) and epithelial respiratory cells line (A549). Treatment of GBS with metalloproteases inhibitors (EDTA, EGTA and PHEN) did not induce alteration on bacterial growth, but promoted changes in the expression of surface proteins, adhesive capacity and profile of intracellular survival of the pathogen. The GBS and supernatant of bacterial growth medium (conditioned medium; MC) promoted the death of HUVEC and A549 cells. However, the metalloproteases inhibitors treatment restored the cellular viability induced by GBS and MC, suggesting that GBS metalloproteases are involved in the disruption of cell barrier, promoting bacterial dissemination. This study describes for the first time apoptosis and necrosis induced by GBS and MC in HUVEC and A549 cells after 24h incubation, respectively. We also observe reduction of pro-caspase-3 after infection of HUVEC with GBS and MC, suggesting activation of caspase-3. Moreover, the over-expression of pro -apoptotic protein Bax and decrease of anti-apoptotic protein Bcl-2 levels in HUVEC show the involvement of mitochondrial apoptotic mechanism (intrinsic via). Enhanced understanding of the molecular basis of GBS pathogenesis may pinpoint novel bacterial and host molecules that can represent novel therapeutic or immunoprophylactic targets against disease caused by this foremost of neonatal pathogens.

A viticultura é uma atividade de grande importância econômica, destacando-se a sustentabilidade da pequena propriedade e o desenvolvimento territorial associados às atividades ligadas ao turismo. As plantas cultivadas se tornam vulneráveis a patógenos e insetos-praga e a videira apresenta diversas espécies consideradas pragas que reduzem sua produção e rentabilidade, entre estas, Spodoptera frugiperda, causando danos em diferentes partes da planta. Fungos entomopatogênicos podem oferecer uma alternativa aos pesticidas convencionais para o controle de pragas, pois produzem enzimas que degradam o exoesqueleto do inseto como quitinases e proteases facilitando o modo de infecção. Neste trabalho foi avaliado o potencial inseticida do fungo Nomurea rileyi, linhagem UCS03, contra S. frugiperda e o perfil eletroforético por SDS-PAGE das proteínas secretadas por N. rileyi em presença da cutícula do inseto em diferentes intervalos de tempo em gel unidimensional. O fungo N. rileyi apresentou virulência contra S. frugiperda, determinando um CL50 de 2 x 109conídios/mL com a linhagem UCS03 demonstrando atividade bionseticida. Na avaliação do perfil proteico do secretoma de N. rileyi em presença da cutícula do inseto, em diferentes tempos de cultivo, foi possível verificar um perfil altamente diferenciado. A maior concentração de proteína foi encontrada no 14° dia de incubação (0,3507 mg/mL) reduzindo a quantidade de proteínas após este período. Na análise por SDS-PAGE foi possível verificar diferentes proteínas de diferentes massas moleculares, nos intervalos de tempo considerados, sendo muitas inferiores a 75 kDa. Estas proteínas com diferentes massas moleculares podem estar envolvidas no metabolismo do fungo. Desta forma, estes resultados podem contribuir para a compreensão do processo de infecção de N. rileyi em S. frugiperda, oferecendo potencial para o desenvolvimento de novas pesquisas e aplicações destas em processos biotecnológicos. / Submitted by Ana Guimarães Pereira (agpereir@ucs.br) on 2017-03-14T12:21:21Z No. of bitstreams: 1 Dissertacao Ana Carolina Ruiz.pdf: 656327 bytes, checksum: 52c5a7db081b0ec94339972595956f52 (MD5) / Made available in DSpace on 2017-03-14T12:21:21Z (GMT). No. of bitstreams: 1 Dissertacao Ana Carolina Ruiz.pdf: 656327 bytes, checksum: 52c5a7db081b0ec94339972595956f52 (MD5) Previous issue date: 2017-03-14 / Viticulture is an activity of great economic importance with emphasis on the sustainability of small property and territorial development associated with tourism related activities. Cultivated plants become vulnerable to pathogens and insect pests and the vine has several species considered as pests that reduce their production and profitability, among them, Spodoptera frugiperda, with causes damage in different parts of the plant. Entomopathogenic fungi can provide an alternative to conventional pesticides for controlling pests, they produce enzymes that degrade the insect exoskeleton, such aschitinases and proteases facilitating the infection. In this work, the insecticide potential of the fungus Nomurea rileyi and S. frugiperda was evaluated, as well as the proteins secreted by N. rileyi in the presence of insect cuticle at different time intervals in one-dimensional gel. The fungus N. rileyi presented virulence against S. frugiperda, determining a CL50 of 2 x 109 con / mL with UCS03 strain demonstrating bionseticida activity. In assessing the protein profile of secretome N. rileyi in the presence of insect cuticle, at different times of cultivation, a highly differentiated profile was verified. The highest concentration of protein was found at day 14 of incubation (0.3507 mg / ml) reducing the amount of protein after this period. In the one-dimensional gel analysis was verified different molecular weights of proteins, in the time interval considered being many less than 75kDa. These proteins with different molecular weights may be involved in fungal metabolism. Thus, these results can contribute to the understanding of the infection process of N. rileyi in S. frugiperda, offering potential for the development of new researches and applications in biotechnological processes.

Conselho Nacional de Desenvolvimento Científico e Tecnológico / Estreptococos do grupo B (EGB) é a principal causa de sepse e meningite neonatal e tem sido recentemente reconhecido como patógeno responsável por infecções invasivas em adultos imunocomprometidos (idosos ou portadores de doenças crônicas). Os EGB produzem inúmeras enzimas extracelulares, várias das quais interagem com o sistema imune do hospedeiro e são importantes durante a interação EGB-hospedeiro, bem como para o desenvolvimento da doença. Estudos anteriores mostraram que metaloproteases estão envolvidas em várias vias metabólicas em diferentes tipos celulares. Por esta razão, nós decidimos investigar o possível envolvimento de metaloproteases de EGB durante a interação celular e apoptose/necrose induzida pelo micro-organismo em células endoteliais da veia umbilical humana (HUVEC) e da linhagem de epitélio respiratório (A549). Tratamento de EGB com inibidores de metaloproteases (EDTA, EGTA e FEN) não induziu alterações no crescimento bacteriano, mas promoveu alterações na expressão de proteínas de superfície, capacidade adesiva e perfil de sobrevivência intracelular do patógeno. O EGB e o sobrenadante do crescimento bacteriano (meio condicionado; MC) promoveram a morte das células HUVEC e A549. Contudo, o tratamento com inibidores de metaloproteases restauraram a viabilidade celular induzida pelos EGB e o MC, sugerindo que metaloproteases bacteriana estão envolvidas no rompimento da barreira celular, promovendo a disseminação bacteriana. Este trabalho descreve pela primeira vez apoptose e necrose induzidas pelo EGB e MC em HUVEC e células A549 após 24h de incubação, respectivamente. Nós também observamos redução da pró-caspase-3 após infecção das HUVEC com EGB e MC, sugerindo ativação da caspase-3. Além disso, o aumento da expressão da proteína pró-apoptótica Bax e diminuição dos níveis da proteína anti-apoptótica Bcl-2 em HUVEC, demonstram o envolvimento do mecanismo apoptótico mitocondrial (via intrínseca). A melhor compreensão das bases moleculares da patogênese do EGB contribui para identificar novas moléculas bacterianas e hospedeiras que podem representar novos alvos terapêuticos ou imunoprofiláticos contra a doença causada por esse patógeno neonatal. / Group B streptococcus (GBS) is the leading cause of neonatal sepsis and meningitis and has recently been recognized as an increasingly common cause of invasive disease in immunocompromised adults (elderly or chronic diseases). GBS produces a number of extracellular enzymes, several of which interact with the host immune system and are important for the GBS- host interaction and for the development of disease. Previous studies showed that metalloproteases are involved in several metabolic pathways in different cellular types. For this reason, we decided to investigate the possible involvement of GBS metalloproteases during cell interaction and apoptosis/necrosis induced by microorganism in human umbilical vein endothelial cells (HUVEC) and epithelial respiratory cells line (A549). Treatment of GBS with metalloproteases inhibitors (EDTA, EGTA and PHEN) did not induce alteration on bacterial growth, but promoted changes in the expression of surface proteins, adhesive capacity and profile of intracellular survival of the pathogen. The GBS and supernatant of bacterial growth medium (conditioned medium; MC) promoted the death of HUVEC and A549 cells. However, the metalloproteases inhibitors treatment restored the cellular viability induced by GBS and MC, suggesting that GBS metalloproteases are involved in the disruption of cell barrier, promoting bacterial dissemination. This study describes for the first time apoptosis and necrosis induced by GBS and MC in HUVEC and A549 cells after 24h incubation, respectively. We also observe reduction of pro-caspase-3 after infection of HUVEC with GBS and MC, suggesting activation of caspase-3. Moreover, the over-expression of pro -apoptotic protein Bax and decrease of anti-apoptotic protein Bcl-2 levels in HUVEC show the involvement of mitochondrial apoptotic mechanism (intrinsic via). Enhanced understanding of the molecular basis of GBS pathogenesis may pinpoint novel bacterial and host molecules that can represent novel therapeutic or immunoprophylactic targets against disease caused by this foremost of neonatal pathogens.

A viticultura é uma atividade de grande importância econômica, destacando-se a sustentabilidade da pequena propriedade e o desenvolvimento territorial associados às atividades ligadas ao turismo. As plantas cultivadas se tornam vulneráveis a patógenos e insetos-praga e a videira apresenta diversas espécies consideradas pragas que reduzem sua produção e rentabilidade, entre estas, Spodoptera frugiperda, causando danos em diferentes partes da planta. Fungos entomopatogênicos podem oferecer uma alternativa aos pesticidas convencionais para o controle de pragas, pois produzem enzimas que degradam o exoesqueleto do inseto como quitinases e proteases facilitando o modo de infecção. Neste trabalho foi avaliado o potencial inseticida do fungo Nomurea rileyi, linhagem UCS03, contra S. frugiperda e o perfil eletroforético por SDS-PAGE das proteínas secretadas por N. rileyi em presença da cutícula do inseto em diferentes intervalos de tempo em gel unidimensional. O fungo N. rileyi apresentou virulência contra S. frugiperda, determinando um CL50 de 2 x 109conídios/mL com a linhagem UCS03 demonstrando atividade bionseticida. Na avaliação do perfil proteico do secretoma de N. rileyi em presença da cutícula do inseto, em diferentes tempos de cultivo, foi possível verificar um perfil altamente diferenciado. A maior concentração de proteína foi encontrada no 14° dia de incubação (0,3507 mg/mL) reduzindo a quantidade de proteínas após este período. Na análise por SDS-PAGE foi possível verificar diferentes proteínas de diferentes massas moleculares, nos intervalos de tempo considerados, sendo muitas inferiores a 75 kDa. Estas proteínas com diferentes massas moleculares podem estar envolvidas no metabolismo do fungo. Desta forma, estes resultados podem contribuir para a compreensão do processo de infecção de N. rileyi em S. frugiperda, oferecendo potencial para o desenvolvimento de novas pesquisas e aplicações destas em processos biotecnológicos. / Viticulture is an activity of great economic importance with emphasis on the sustainability of small property and territorial development associated with tourism related activities. Cultivated plants become vulnerable to pathogens and insect pests and the vine has several species considered as pests that reduce their production and profitability, among them, Spodoptera frugiperda, with causes damage in different parts of the plant. Entomopathogenic fungi can provide an alternative to conventional pesticides for controlling pests, they produce enzymes that degrade the insect exoskeleton, such aschitinases and proteases facilitating the infection. In this work, the insecticide potential of the fungus Nomurea rileyi and S. frugiperda was evaluated, as well as the proteins secreted by N. rileyi in the presence of insect cuticle at different time intervals in one-dimensional gel. The fungus N. rileyi presented virulence against S. frugiperda, determining a CL50 of 2 x 109 con / mL with UCS03 strain demonstrating bionseticida activity. In assessing the protein profile of secretome N. rileyi in the presence of insect cuticle, at different times of cultivation, a highly differentiated profile was verified. The highest concentration of protein was found at day 14 of incubation (0.3507 mg / ml) reducing the amount of protein after this period. In the one-dimensional gel analysis was verified different molecular weights of proteins, in the time interval considered being many less than 75kDa. These proteins with different molecular weights may be involved in fungal metabolism. Thus, these results can contribute to the understanding of the infection process of N. rileyi in S. frugiperda, offering potential for the development of new researches and applications in biotechnological processes.

Indiana University-Purdue University Indianapolis (IUPUI) / Toxoplasma gondii, a single-celled eukaryotic pathogen, has infected one-third of the world’s population and is the causative agent of toxoplasmosis. The disease primarily affects immunocompromised individuals such as AIDS, cancer, and transplant patients. The parasites can infect any nucleated cell in warm-blooded vertebrates, but because they preferentially target CNS, heart, and ocular tissue, manifestations of infection often include encephalitis, myocarditis, and a host of neurological and ocular disorders. Toxoplasma can also be transmitted congenitally by a mother who becomes infected for the first time during pregnancy, which may result in spontaneous abortion or birth defects in the child. Unfortunately, the therapy currently available for treating toxoplasmosis exhibits serious side effects and can cause severe allergic reactions. Therefore, there is a desperate need to identify novel drug targets for developing more effective, less toxic treatments. The regulation of proteins via lysine acetylation, a reversible post-translational modification, has previously been validated as a promising avenue for drug development. Lysine acetyltransferases (KATs) are responsible for the acetylation of hundreds of proteins throughout prokaryotic and eukaryotic cells. In Toxoplasma, we identified a KAT that exhibits homology to Elongator protein 3 (TgElp3), the catalytic component of a transcriptional elongation complex. TgElp3 contains the highly conserved radical S-adenosylmethionine and KAT domains but also possesses a unique C-terminal transmembrane domain (TMD). Interestingly, we found that the TMD anchors TgElp3 in the outer mitochondrial membrane (OMM) such that the catalytic domains are oriented towards the cytosol. Our results uncovered the first tail-anchored mitochondrial KAT reported for any species to date. We also discovered a shortened form of Elp3 present in mouse mitochondria, suggesting that Elp3 functions beyond transcriptional elongation across eukaryotes. Furthermore, we established that TgElp3 is essential for parasite viability and that its OMM localization is important for its function, highlighting its value as a potential target for future drug development.

Indiana University-Purdue University Indianapolis (IUPUI) / Pseudomonas aeruginosa is a gram negative opportunistic pathogen with the capacity to cause serious disease by forming biofilms, most notably in the lungs of cystic fibrosis (CF) patients. Biofilms are communities of microorganisms that adhere to a solid surface, undergo global regulatory changes, secrete exopolysaccharides, and are innately antibiotic resistant. Virulence modulation is an important tool utilized by P. aeruginosa to propagate infection and biofilm formation in the CF airway. Many different virulence modulatory pathways and proteins have been identified including the protein, MgtE. MgtE has recently been discovered and has been implicated in virulence modulation, as an isogeneic mutation of mgtE leads to increased cytotoxicity. To further elucidate the role of MgtE in P. aerugionsa infections, transcriptional and translational regulation of this protein following antibiotic treatment has been explored. I have demonstrated that mgtE is transcriptionally upregulated following antibiotic treatment of most of the twelve antibiotics tested utilizing RT-PCR and QRT-PCR. A novel model system was employed, which utilizes cystic fibrosis bronchial epithelial (CFBE) cells homozygous for the ΔF508 mutation for these studies. This model system allows P. aeruginosa biofilms to form on CFBE cells modeling the P. aeruginosa in the CF airway. Translational effects of antibiotic treatment on MgtE have been attempted via Western blotting and cytotoxicity assays. Furthermore, to explore the possibility that mgtE is interacting with a known regulatory pathway, a transposon-mutant library was utilized and the regulatory proteins, AlgR and NarX, among others have been identified as possibly interacting with MgtE. Lastly, an MgtE homologue from Staphylococcus aureus was utilized to further demonstrate the virulence modulatory effects of MgtE by demonstrating the expression of the homologue results in decreased cytotoxicity, exactly like expression of the native P. aeruginosa MgtE. This research explores a newly discovered protein that impacts cytotoxicity and biofilm formation and provides valuable information about P. aeruginosa virulence.

Depuis quelques décennies, les bactéries pathogènes multi-résistantes aux antibiotiques sont de plus en plus répandues dans le monde. Cette situation a suscité le besoin et l'intérêt de trouver des médicaments antibactériens avec de nouvelles cibles potentiels. La découverte des systèmes de communication de type quorum sensing (QS) régulant la virulence bactérienne représente une des cibles privilégiées pour contrôler les bactéries pathogènes autrement qu’en interférant avec leur croissance bactérienne. Dans l’écosystème naturel, un grand nombre d'organismes (Eucaryotes et Procaryotes) co-existent en synthétisant chacun de leur côté des métabolites secondaires. Les plantes, étant en permanence en contact avec des bactéries, synthétisent des métabolites secondaires capables d’inhiber l’expression des gènes de virulence chez les bactéries sans pour autant affecter ni leur croissance ni leur viabilité. Notre objectif a été de contribuer à la valorisation de la biodiversité malgache en identifiant des plantes et en y isolant les composés actifs présentant une capacité à perturber le mécanisme de QS chez P. aeruginosa PAO1, une bactérie pathogène opportuniste de l’homme, des animaux et des plantes. Dans ce but, nous avons tout d’abord réalisé un criblage d’activité anti-QS de différents flavonoïdes commerciaux. De ce criblage, la narigenine et la naringine ont été sélectionnées pour être les molécules de contrôle positif et négatif des tests d’activité anti-QS, respectivement. Par la suite, 4 espèces de Dalbergia endémique de Madagascar ont fait l’objet de criblage pour leur activité anti-QS. Ce travail a fait ressortir l’activité anti-QS très intéressante de l’écorce de D. trichocarpa à partir de laquelle nous avons isolée le composé actif nommé la coumarate de l’aldéhyde-oléanolique (OALC). Le contrôle naringénine et l’OALC ne présente aucun effets inhibiteurs sur la croissance bactérienne de P. aeruginosa PAO1 et sur l’expression du gène QS-indépendant aceA suggérant une activité d’inhibition spécifiquement liée au QS. Cependant, ces deux molécules présentent des spectres d’inhibition différente. En effet, les deux molécules diffèrent dans le sens que la naringenine n’inhibe pas l’expression du gène gacA et la motilité de type twitching contrairement à l’OALC. Ces résultats suggèrent que l’OALC et la naringénine représente des candidats potentiels pour des investigations in vivo quant à leur effet anti-QS et anti-biofilm sur des modèles infectieux d’organismes supérieurs. Par ailleurs, ils démontrent la richesse des plantes malgaches comme sources de nouvelles molécules anti-virulence ainsi que l’importance de telle investigation afin de renforcer notre arsenal thérapeutique en composé antibactérienne dans la lutte continuelle contre les bactéries pathogènes/Since few decades, multidrug resistant bacteria spread all over the world. This situation gives rise to the need and interest in finding antibacterial drugs with novel potent target. Discovery of communication system termed Quorum Sensing (QS) which regulate bacterial virulence factor represent privileged target in another way than interfering with bacterial growth. In natural ecosystem, many organisms (Eukaryotes and Prokaryotes) produce secondary metabolites. As plants are permanently in contact with bacteria, they have synthetized secondary metabolites which inhibit bacterial virulence gene expression without affecting bacterial viability. Our goal was to contribute to the valorization of Malagasy biodiversity and specifically to identify plants and isolate bioactive compound presenting ability to disrupt QS mechanism in P. aeruginosa, opportunistic pathogen bacteria in plants, animals and human. In this purpose, screening of commercial available flavonoids has been firstly carried out. From this screening, naringenin and naringin have been selected to be used as positive and negative QS inhibitor controls, respectively. Subsequently, Four Malagasy endemic Dalbergia species have been screened for their anti-QS activity. This work pointed out the interesting anti-QS activity of D. trichocarpa bark extract which led to the isolation of oleanolic aldehyde coumarate (OALC) as one major bioactive compound. At the concentration tested, naringenin and OALC did not affect P. aeruginosa PAO1 viability and didn’t reduce QS-independent aceA gene expression suggesting a specific anti-QS activity. However, these two compounds present different inhibition spectrum. Indeed, naringenin didn’t inhibit gacA gene expression and twitching motility contrarily to OALC. These results suggest that OALC and naringenin represent potent candidates for in vivo investigations in their anti-QS and anti-biofilm activity onto eukaryotes infectious model. Besides, this finding demonstrated the potent source for novel anti-virulence compounds of Malagasy flora and the importance of this kind of research to strengthen our antimicrobial therapeutic arsenal with the ongoing struggle against bacterial infection. / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

Indiana University-Purdue University Indianapolis (IUPUI) / The Lyme disease agent, Borrelia burgdorferi, has a complex system that allows it to thrive in the harsh and distinct environments of its tick vector and mammalian host. Although it has been known for some time that the Borrelia oxidative stress regulator protein (BosR) plays a necessary role in mammalian infectivity and functions as a transcriptional regulator of alternative sigma factor RpoS, very little is known about its mechanism of action, other than the suggestion that BosR activates rpoS transcription by binding to certain upstream regions of the gene. In our studies, we performed protein degradation assays and luciferase reporter assays for further understanding of BosR function. Our preliminary findings suggest that BosR is post-transcriptionally regulated by an unknown protease and may not need to bind to any rpoS upstream regions in order to activate transcription. We also describe the construction of luciferase reporter systems that will shed light on BosR’s mechanism of action. We postulate the provocative possibility that unlike its homologs Fur and PerR in other bacterial systems, BosR may not utilize a DNA-binding mechanism in order to fulfill its role as a transcriptional regulator to modulate virulence gene expression.