<p>The purpose of this study was to investigate the occurrence<strong> </strong>of Verotoxin-encoding bacteriophages in mussels, cultured downstream the sewage treatment plant<strong> </strong>in Lysekil.</p><p>Mussels were collected in three growing areas from April 2008 to March 2009. Real-time PCR was performed for detection of <em>vtx1</em> and <em>vtx2</em> genes and enrichment of bacteriophages on non Verotoxin-producing <em>Escherichia coli</em> O157: H7 was carried out. All samples in real-time PCR analysis were negative; no presence of Verotoxin-encoding phages was shown. No plaque was formed on blood agar base plates, indicating that no bacteriophages had been taken up by <em>E. coli</em> bacteria</p><p>The levels of Verotoxin-encoding phages and <em>E.coli</em> outside the sewage treatment plant in Lysekil were not high enough to be able to form VTEC in mussels, indicating that the faecal contamination was low. This does not exclude the presence of other more common pathogens such as norovirus and campylobacter.</p><p> </p><p> </p>

The purpose of this study was to investigate the occurrence of Verotoxin-encoding bacteriophages in mussels, cultured downstream the sewage treatment plant in Lysekil. Mussels were collected in three growing areas from April 2008 to March 2009. Real-time PCR was performed for detection of vtx1 and vtx2 genes and enrichment of bacteriophages on non Verotoxin-producing Escherichia coli O157: H7 was carried out. All samples in real-time PCR analysis were negative; no presence of Verotoxin-encoding phages was shown. No plaque was formed on blood agar base plates, indicating that no bacteriophages had been taken up by E. coli bacteria The levels of Verotoxin-encoding phages and E.coli outside the sewage treatment plant in Lysekil were not high enough to be able to form VTEC in mussels, indicating that the faecal contamination was low. This does not exclude the presence of other more common pathogens such as norovirus and campylobacter.

The overall goal of this research was to understand the role of inter-kingdom signaling in enterohemorrhagic Escherichia coli (EHEC) infections of the human gastro-intestinal (GI) tract from the perspective of both the invading pathogen and the human intestinal epithelial cells, which they colonize. Differential gene expression of EHEC was studied upon exposure to the human neuroendocrine hormones epinephrine and norepinephrine. We determined that these hormones increase EHEC chemotaxis, motility, biofilm formation, colonization of host cells, and virulence gene expression. We also studied the EHEC response to the GI tract commensal bacterial signaling molecules indole and autoinducer-2 (AI-2). We observed that indole decreases all the EHEC phenotypes that are increased by the human hormones and represses EHEC virulence. However, the effect of AI-2 was similar to that observed with hormones and opposite to that observed with indole, i.e. AI-2 increases EHEC virulence phenotypes. We studied changes in host cell transcriptome in the presence of the commensal bacterial signal indole. Indole increases expression of genes involved in tight junction and gap junction formation, and production of mucins and actin cytoskeleton genes. Indole also down-regulates genes encoding for pro-inflammatory cytokines, chemokines, and Toll-like receptors. The gene expression results were confirmed with phenotypic assays where we observed an increase in trans-epithelial resistance, increase in the anti-inflammatory cytokine IL-10, decrease in the pro-inflammatory cytokine IL-8, decrease in the activity of the pro-inflammatory transcription factor NF-κB, and decrease in colonization by EHEC of the indole-pre-treated HCT-8 cells. We established that factors secreted by epithelial cells are important determinants of EHEC virulence. Gene expression studies showed that 34 out of 41 LEE virulence genes were induced when EHEC was cultured in conditioned medium. In addition, the data showed increased expression of the shiga toxin-2 prophage 933W. These changes in gene expression were corroborated by a 5-fold increase in HCT-8 cell colonization and increased intracellular Stx2 phage titers. We determined that the HCT-8-secreted factor(s) was protein-based and that it was greater than 3 kDa in size. In conclusion, we have characterized the pathogen response to various eukaryotic and prokaryotic GI tract signals. We have established, for the first time, that the commensal bacterial signal indole is an inter-kingdom signal for the host epithelial cells. Overall, our studies provide a greater understanding of host-pathogen interactions.

Shiga toxin-producing E. coli (STEC) have important public health and food safety implications. Cattle are the primary reservoir for STEC, which are transmitted to humans via contact with cattle or related food products. Dairy farms in particular have been incriminated as an important source of STEC. The broad aim of this study was to examine in depth the epidemiology of STEC on the dairy farm. The presence of STEC on three Australian dairy farms was surveyed. This aimed to provide data on the prevalence and nature of STEC on Australian dairy farms, as well as to examine in more detail the pre-harvest/slaughter ecology of STEC. STEC, E. coli O157:H7 and E. coli O26:H11 prevalences were similar to those from dairy farms in other countries. Replacement heifers were the most important source of STEC on the farms. Calves excreted STEC from an early age, with faecal prevalence peaking at weaning. Higher STEC prevalence was also associated with group housing of calves during weaning. Calf isolates were potential human pathogens based on serotype and virulence markers. Clonal relationships between isolates were analysed. Calf isolates were diverse and had a high clonal turnover. STEC isolated from within the same farm had a higher genetic similarity than those from different farms. Vertical and horizontal transmission were both identified among cattle. The farm environment was also identified as an important source of STEC. Reasons for increased levels of STEC excretion by calves were investigated. Two broad hypotheses for higher faecal shedding were proposed and examined individually. The first was that an animal is more likely to excrete STEC when its exposure to STEC is greater, thus promoting inoculation of the gastrointestinal tract. Calves were experimentally inoculated with a traceable STEC strain to examine the infection dynamics of STEC within cattle groups, and explore the effect of calf management procedures. Calves which were housed in groups and co-jointly fed and managed had a higher prevalence of the inoculation strain than animals housed individually. The test strain was readily isolated from the hides and saliva of inoculated calves, as well as their immediate environments. Calves become infected with STEC via the faecal-oral route, iv either by direct contact with other calves, or indirectly through contact with faecally contaminated materials. The second hypothesis was that individual animals are variably susceptible to intestinal colonisation by STEC, which leads to differing magnitudes and durations of STEC carriage. Factors influencing colonisation susceptibility to STEC and the mechanisms behind these factors were also examined. In order to compare enteric colonisation under a range of different conditions, a suitable experimental system was developed. In vitro organ culture of explanted ruminant colonic tissues provided a laboratory model that was representative of in vivo bacterial-mucosal attachment. The degree of STEC colonisation was enumerated using an immunofluorescent filtration technique. The quantitative colonisation assay was applied to determine the effects of host-dependant variables on STEC colonisation. Colonic tissues from weaning calves and adult cattle did not differ significantly in their susceptibility to colonisation; nor did tissues from cattle fed either high forage or high grain diets. Colonic explants from sheep, however, demonstrated significantly higher numbers of adherent STEC than bovine explants. It was therefore concluded that while species-specific differences in host tissues may mediate STEC carriage differences, this did not explain in vivo variability in age and diet related excretion. Factors that indirectly affect the susceptibility of host tissues to colonisation were examined. E. coli O157:H7 cultured in media designed to represent the enteric contents of a well-fed ruminant colonised the colonic mucosa in reduced numbers, indicating that age and diet may be correlated with differences in STEC carriage and excretion because of differing physiological augmentation of the intra-enteric environment. In conclusion, while group dynamics and management practices may increase STEC shedding prevalences for cattle via increased STEC exposure, factors that modulate an individual ruminant’s gastrointestinal carriage of STEC have a significant role in mediating STEC excretion. Either directly or indirectly, species, age and diet can affect the numbers of STEC that colonise the bowel wall, thereby influencing the magnitude and duration of STEC excretion. Both of these features of ruminant STEC ecology should be addressed in order to reduce the pre-slaughter/harvest presence of STEC.

abstract: In the United States, Escherichia coli O157:H7 (E. coli O157:H7) is the most frequent cause of hemolytic uremic syndrome (HUS) and it is also the primary cause of acute renal failure in children. The most common route of the infection is ingestion of contaminated meat or dairy product originating from cattle or vegetables contaminated with bovine manure. Since cattle are the main reservoir for human infection with E. coli O157:H7, the reduction of intestinal colonization by these bacteria in cattle is the best approach to prevent human infections. Intimin is an outer membrane protein of E. coli O157:H7 that plays an important role in adhesion of the bacteria to the host cell. Hence, I proposed to express intimin protein in tomato plants to use it as a vaccine candidate to reduce or prevent intestinal colonization of cattle with E. coli O157:H7. I expressed His-tagged intimin protein in tomato plants and tested the purified plant-derived intimin as a vaccine candidate in animal trials. I demonstrated that mice immunized intranasally with purified tomato-derived intimin produced intimin-specific serum IgG1and IgG2a, as well as mucosal IgA. I further demonstrated that mice immunized with intimin significantly reduced time of the E. coli O157:H7 shedding in their feces after the challenge with these bacteria, as compared to unimmunized mice. Shiga toxin is the major virulence factor that contributes to HUS. Since Shiga toxin B subunit has an important role in the attachment of the toxin to its receptor, I fused intimin to Shiga toxin B subunit to create multivalent subunit vaccine and tested the effects upon immunization of mice with the B subunit when combined with intimin. His-tagged intimin, Shiga toxin B subunit, and Shiga toxin-intimin fusion proteins were expressed in E. coli and purified. I demonstrated that this multivalent fusion protein vaccine candidate elicited intimin- and Shiga toxin B-specific IgG1, IgG2a, and IgA antibodies in mice. I also showed a reduction in the duration of the bacterial shedding after the challenge compared to the control sham-immunized groups. / Dissertation/Thesis / Ph.D. Plant Biology 2010

Submitted by Letícia Fernanda Lavezzo (leticialavezzo.unesp@hotmail.com) on 2016-03-23T20:23:19Z No. of bitstreams: 1 Dissertação_Letícia_Fernanda_Lavezzo.pdf: 1419993 bytes, checksum: 8e337d69094b988dba50c9a0bee85085 (MD5) / Approved for entry into archive by Ana Paula Grisoto (grisotoana@reitoria.unesp.br) on 2016-03-24T18:21:25Z (GMT) No. of bitstreams: 1 lavezzo_lf_me_jabo.pdf: 1419993 bytes, checksum: 8e337d69094b988dba50c9a0bee85085 (MD5) / Made available in DSpace on 2016-03-24T18:21:25Z (GMT). No. of bitstreams: 1 lavezzo_lf_me_jabo.pdf: 1419993 bytes, checksum: 8e337d69094b988dba50c9a0bee85085 (MD5) Previous issue date: 2016-02-25 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / O lodo de esgoto é uma alternativa como fertilizante orgânico na agricultura, porém em sua composição pode apresentar patógenos que oferecem risco ao homem e ao ambiente. Objetivou-se, com o presente estudo, avaliar a fertilidade do solo, e a presença de ovos viáveis de helmintos, coliformes termotolerantes, Escherichia coli para os patótipos EHEC, EPEC e STEC e a atividade enzimática das enzimas protease, redutase do nitrato e urease no solo após dezoito anos de aplicações anuais de lodo de esgoto em um Latossolo Vermelho eutroférrico (LVef) e Latossolo Vermelho distrófico (LVd). O lodo utilizado foi obtido na SABESP de Franca, São Paulo e o experimento foi instalado em delineamento de blocos cazualiados, sendo 4 tratamentos e 5 repetições. Os tratamentos foram T1: controle, apenas com aplicação de adubação mineral, T2: 5, T3: 10 e T4: 20 Mg ha-1 de LE. Antes de ser incorporado ao solo, realizou-se análise do lodo para ovos viáveis de helmintos e coliformes termotolerantes. Aos 40 dias, coletou-se amostras de solo na profundidade de 0-10 cm para avalição de ovos viáveis de helmintos no solo. Aos 70 dias, coletou-se amostras de solo na profundidade de 0-20cm para a análise da fertilidade. Para a análise de coliformes termotolerantes, seguindo a técnica de tubos múltiplos, as amostras foram coletadas no dia 0, 26, 40 e aos 78 dias. Para a realização da reação em cadeia da polimerase (PCR) para identificar a presença de Escherichia coli, coletou-se amostras de solo antes do início do experimento, no dia 0, aos 26 dias, 40, 58, 78, 110 e 146 dias. Para a avaliação da atividade enzimática, as amostras foram coletadas em profundidade de 0-10cm, nos dias 0, 40, 78 e aos 146 dias. Os atributos químicos do solo apresentaram efeito significativo entre os tratamentos utilizados. A análise do solo incorporado com o resíduo apresentou ausência total de ovos viáveis de helmintos no solo após 40 dias da aplicação do LE. Os valores de termotolerantes nos solos variaram entre zero a 1,1x106 Número Mais Provável de Sólidos Totais durante o período de 0 a 26 dias. Para análise de Escherichia coli do lodo e do solo, mostrou ausência dos patótipos de EHEC, EPEC e STEC por meio dos primers para os genes stx1, stx2 e aea. A atividade enzimática das enzimas proteases, redutase do nitrato e urease, ao londo do experimento, não apresentaram diferença estatística entre tratamentos. A aplicação do lodo de esgoto por 18 anos consecutivos influenciou nos atributos químicos do solo, não apresentou risco potencial de contaminação do solo por ovos de helmintos e Escherichia coli e não diferiu na atividade enzimática do solo. / The sewage sludge is an alternative as organic fertilizer to use in agriculture, but in its composition may have pathogens that offer to humans and the environment risks. The present study objective was to evaluate soil fertility, and the presence of viable helminth eggs, fecal coliforms, Escherichia coli for pathotypes EHEC, EPEC and STEC and the enzymatic activity of protease enzymes, nitrate reductase and urease in the soil after eighteen years of annual applications of sewage sludge in an Oxisol (LVef) and Oxisol (LVd). The sludge used was obtained in SABESP Franca, São Paulo and the experiment was installed in designing cazualiados blocks, 4 treatments and 5 repetitions. Treatments were T1: control, only with application of mineral fertilizer, T2: 5, T3: T4 10 and 20 Mg ha-1 LE. Before being incorporated into the soil, there was sludge analysis for viable helminth eggs and fecal coliforms. At 40 days, it is collected soil samples at a depth of 0-10 cm for viable helminth eggs evaluation in the soil. After 70 days it is collected soil samples at a depth of 0-20cm for fertility analysis. For fecal coliforms analysis, following the technique of multiple pipes, the samples were collected at day 0, 26, 40 and 78 days. To carry out the polymerase chain reaction (PCR) for the presence of Escherichia coli was collected from soil samples before the beginning of the experiment at day 0, after 26 days 40, 58, 78, 110 and 146 days . For the evaluation of enzyme activity, samples were collected at a depth of 0-10cm, on days 0, 40, 78 and 146 days. The soil chemical properties showed significant effects between treatments. Soil testing embedded with the residue showed complete absence of viable helminth eggs in the soil 40 days after the application of the LE. The values in thermotolerant soil ranged from zero to 1,1x106 Most Probable Number of total solids during the period from 0 to 26 days. For Escherichia coli analysis sludge and soil, showed absence of pathotypes EHEC, EPEC and STEC through primers for stx1, stx2 and aea. The enzymatic activity of protease enzymes, nitrate reductase and urease to the experiment, showed no statistical difference between treatments. The application for 18 consecutive years sewage sludge influenced the soil chemical properties, showed no potential risk of soil contamination by helminth eggs and Escherichia coli and did not differ in the enzymatic activity of the soil.

E. coli O157:H7 é um patógeno de importância em alimentos, tendo sido envolvido, nos últimos anos, em surtos de grandes proporções, principalmente por produtos cárneos. Entretanto sua ocorrência em alimentos, particularmente em carne crua, é baixa e poderia, eventualmente, ser atribuída à atividade antagônica expressa por outros microrganismos presentes. Assim sendo, foi avaliada a interferência de bactérias que fazem parte da microbiota normal de carne sobre a multiplicação de E. coli O157:H7 em carne bovina moída mantida em refrigeração e em temperatura ambiente. Com essa finalidade, foram realizados testes de desafio (\"challenge tests\") em porções de 25 g de carne bovina moída inoculadas com diferentes concentrações de E. coli O157:H7 (101, 103 e 106 CFC/g), desafiadas com diferentes inóculos de E. coli não patogênica, Pseudomonas putida e Leuconostoc spp. As cepas de Pseudamonas putida e de Leuconostoc spp., isoladas de carne, foram selecionadas em função de atividade inibitória contra E. calí O157:H7 observada \"in vitro\". Para o monitoramento de E. coli O157:H7, foram utilizados o método convencional, ou seja, plaqueamento em ágar Mac Conkey-sorbitol e identificação de colônias (testes bioquímicos e sorológicos), bem como um método considerado rápido, empregando o Petrifilm&#8482; Kit-HEC. De maneira geral, não foram observadas interferências significativas da presença de diferentes inóculos de E. coli não patogênica, P. putida e Leuconostoc spp., sobre a multiplicação de diferentes inóculos de E. coli O157:H7 à temperatura ambiente e à temperatura de refrigeração. Paralelamente, o Petrifilm&#8482; Kit-HEC revelou um alto índice de correlação com o ágar Mac Conkey-sorbitol (97,2%), com contagens da mesma ordem de grandeza. Os experimentos à temperatura ambiente revelaram um maior índice de correlação (99,0%), quando comparados àqueles à temperatura de refrigeração (94,9%). Aparentemente, a baixa ocorrência de E. coli O157:H7 em alimentos, particularmente em carne bovina crua, não pode ser atribuída à atividade antagônica de alguns microrganismos presentes. / Escherichia coli O157:H7 is a foodborne pathogen of increasing importance, since it has been involved in several threatening outbreaks, most of them associated with meat products. Though, it is possible that the low occurrence af E. coli O157:H7 in food, particularly in meat, may be due to antagonistic effects af other microorganisms present. Therefore, the influence of some bacteria isolated from meat, over E. coli O157:H7 in meat samples stored at chill and room temperatures was evaluated. For that purpose, studies were performed on 25 g of ground beef inoculated with different spiking levels of E. coli O157:H7 (101, 103 and 106 CFC/g), challenged with different spiking levels of non pathogenic E. coli, Pseudomonas putida or Leuconostoc spp. The Ps. putida and Leuconostoc spp. strains were selected based on deferred antagonism observed against E. coli O157:H7. Multiplication was monitored by means of cultural methods, employing sorbitol Mac Conkey agar and additional identification tests, and the rapid method Petrifilm&#8482; Kit-HEC. No significant influence of non pathogenic E. coli, Pseudomonas putida and Leuconostoc spp. over the multiplication of E. coli O157:H7 was observed. Results on Petrifilm&#8482; Kit-HEC showed high correlation with results on sorbitol Mac Conkey agar (97,2%). Experiments performed with meat kept at room temperatures resulted in higher correlation values (99,0%), when compared to those of meat kept at chill temperatures (94,9%). Apparently, the low occurrence of E. coli O157:H7 in food, particularly in raw meat, can\'t be attributed to antagonistic effects of other bacteria from natural microflora.

O objetivo deste trabalho foi a construção de linhagens geneticamente modificadas de B. subtilis capazes de expressar porções de intimina, principal componente envolvido na capacidade de colonização de linhagens enteropatogênicas de Escherichia coli (EPEC), como estratégia vacinal de administração oral contra diarréias infecciosas. As vacinas desenvolvidas empregaram cinco regiões da intimina de EPEC e linhagens de B. subtilis capazes de expressar e acumular proteínas recombinantes no citoplasma. Além disso, avaliamos o uso de esporos e células vegetativas como veículos vacinais para a entrega de antígenos recombinantes a partir de sistema de expressão epissomal. A eficácia do modelo vacinal foi demonstrada pela: (i) produção de anticorpos sistêmicos (IgG) e secretados (sIgA) contra intimina, (ii) capacidade de neutralização das intiminas expressas por diferentes linhagens de EPEC pelos anticorpos específicos gerados nos animais imunizados; e (iii) proteção a desafio com linhagens de EPEC a partir de modelo experimental que emprega camundongos recém-nascidos. Os resultados representam uma etapa importante na validação de uma nova estratégia vacinal para o controle de patógenos entéricos. Além disto, propomos a utilização de um modelo animal como uma nova ferramenta para se avaliar o potencial protetor de vacinas contra EPEC. / The objective of this work was the construction of genetically modified strains of B. subtilis able to express portions of intimin, the main component involved in colonization by enteropathogenic Escherichia coli strains (EPEC) as a strategy of oral vaccination against infectious diarrhea. The vaccines employed five regions of EPEC intimin and B. subtilis strains expressing recombinant proteins in the cytoplasm. Furthermore, we evaluated the use of spores and vegetative cells as vaccine vehicles for the delivery of recombinant antigens based on an epissomal expression system. The efficacy of the vaccines was demonstrated by: (i) production of systemic (IgG) and mucosal (sIgA) antibody responses to intimin, (ii) neutralizing of intimin expressed by different strains of EPEC by the antibodies generated in immunized animals, and (iii) protection to lethal challenges carried out with EPEC strains using an experimental model based in newborn mice. The results represent an important step in the validation of a new vaccine strategy for the control of enteric pathogens. Moreover, we propose the use of an animal model as a new tool to evaluate the protective potential of vaccines against EPEC.

Der zeitnahe und möglichst sichere Nachweis bakterieller Krankheitserreger und deren Empfindlichkeit gegenüber verfügbaren antibakteriell wirksamen Chemotherapeutika (Antibiotika) stellt einen Hauptaufgabenbereich der medizinischen mikrobiologischen Routinediagnostik dar. Hierzu wurden im Laufe der Jahre unterschiedliche Methoden entwickelt, womit von der genauen Beschreibung der Kolonie- und mikroskopischen Morphologie, Anfärbbarkeit und Formation über die Charakterisierung der biochemischen Leistungsfähigkeit bis hin zur genauen Sequenzierung des gesamten Genoms ein enormer Fortschritt zu verzeichnen war. Seit Mitte der 1990er Jahre etablierte sich die Massenspektrometrie als phänotypisches Nachweisverfahren und gewann zunehmend an Bedeutung. Ebenso konnten Erfolge beim Nachweis Antibiotika resistenter Bakterien verzeichnet werden. Um das Potential dieser noch jungen Nachweismethode weiter zu erforschen, wurden in dieser Arbeit Spezies der Familie Enterobacteriaceae und der Nonfermenter in eine eigene massenspektrometrische Datenbank aufgenommen, um diese als Grundlage zur Validierung des Identifizierungspotentials der Methode mittels Blindstudie zu nutzen. Im selben Arbeitsschritt wurde der Versuch unternommen, Antibiotika resistente Stämme im Zuge der Speziesidentifizierung zu detektieren, um so Aussagen über eine mögliche Einschränkung der therapeutischen Möglichkeiten und gegebenenfalls notwendigen Hygienemaßnahmen treffen zu können.

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Reconhecida como agente de doença humana em 1982, E.coli enterohemorrágica (EHEC) pode causar diarréia sanguinolenta, colite hemorrágica e síndrome hemolítica urêmica (SHU). EHEC constitui um subgrupo especialmente virulento das E.coli produtoras de toxina de Shiga (Stx). O fator crítico da sua virulência é a toxina Shiga, capaz de interromper a síntese proteica da célula eucariótica. São conhecidos dois subgrupos de Stx, Stx1 e Stx2. Stx1 possui duas variantes Stx1c e Stx1d. Stx2 possui muitas variantes. Estudos epidemiológicos sugerem que cepas com os perfis toxigênicos Stx2 ou Stx2/Stx2c seriam mais frequentemente associadas a pacientes com SHU. Além da expressão de Stx, EHEC do sorotipo O157:H7 colonizam a mucosa intestinal induzindo a formação de lesões denominadas attaching/effacing (A/E). Para a produção da lesão A/E, é necessária a presença de uma ilha de patogenicidade cromossômica denominada LEE, composta por cinco operons, LEE 1 a LEE5. Em LEE 5 são codificadas a adesina intimina e o seu receptor Tir, o qual é translocado por um sistema de secreção tipo III (SSTT) e em LEE 4 são codificadas as proteínas secretadas EspA,B e D. Em EHEC O157:H7 são descritos muitos fatores de virulência, codificados em ilhas de patogenicidade, no cromossomo e no megaplasmídio pO157. Bovinos são o principal reservatório deste patógeno e alimentos de origem bovina e produtos contaminados com fezes de bovinos são causadores de surtos epidêmicos. Em nosso país EHEC O157:H7 é isolada do reservatório animal mas é muito rara a sua ocorrência em doença humana. Notamos que nas cepas bovinas predomina Stx2c, enquanto nas cepas humanas predomina o perfil toxigenico Stx2/Stx2c. Quanto a interação com enterocitos humanos cultivados in vitro (linhagem Caco-2), verificamos que tanto cepas bovinas quanto humanas mostram idêntica capacidade de invadir e persistir no compartimento intracelular das células Caco-2. No entanto, em comparação com as cepas humanas, as cepas bovinas mostram uma reduzida capacidade de produzir lesões A/E. Empregamos qPCR para aferir a transcrição de três diferentes locus (eae, espA e tir) situados nos operons LEE4 e LEE5 de cepas bovinas e humanas, durante a infecção de células Caco-2. Verificamos diferenças na expressão dos genes, especialmente espA, entre cepas bovinas e humanas com maior expressão para estas ultimas, em linha com os achados dos testes FAS. Através de clonagem e expressão de proteínas recombinantes, purificamos as proteínas Eae, EspA e Tir e obtivemos anticorpos específicos, empregados para acompanhar a sua expressão ao longo da infecção de células Caco-2, por imunofluorescencia. Verificamos que as três proteínas são detectadas tanto em cepas bovinas quanto humanas, mas nestas ultimas, a marcação é precoce e torna-se mais intensa com o avanço da infecção. Nossos resultados indicam que cepas EHEC O157:H7 isoladas do reservatório bovino em nosso país apresentam diferenças importantes em relação ao perfil toxigenico e a capacidade de indução de lesões A/E, características apontadas na literatura como relevantes para a virulência do micro-organismo. Por outro lado, nossos achados quanto a capacidade de invadir e multiplicar-se no interior de enterócitos pode explicar a persistência do patógeno no reservatório animal e a sua capacidade de transmissão horizontal. / Recognized in 1982 as a human pathogen, enterohemorrhagic Escherichia coli (EHEC) causes bloody diarrhea, hemorrhagic colitis and hemolytic uremic syndrome (HUS). EHEC belonging to serotype O157:H7 are mostly important in North America, United Kingdom and Japan. Shiga toxin (Stx) is the critical factor of STEC. Stx is capable to interrupt the protein synthesis of the eukaryotic cell. Two subgroups of Stx are known, Stx1 and Stx2. Two variants of Stx1 are known (Stx1c and Stx1d), but several Stx2 variants have been described. Epidemiological studies suggest that STEC/EHEC strains carrying the toxigenic profiles Stx2 or Stx2/Stx2c are more frequently associated to HUS. Besides the expression of Stx, EHEC O157:H7 colonize the intestinal mucosa inducing the formation of characteristic histopathological lesions denominated attaching/effacing (A/E). To the production of A/E lesions, it is necessary the presence of a pathogenicity island called LEE (locus of enterocyte effacement), composed by five operons, LEE 1 to LEE5. An outer membrane adhesin (intimin) and its receptor Tir, which is translocated by a type three secretion sytem (TTSS), are both codified in LEE5 while the secreted proteins EspA, B and D, that constitute part of the SSTT, are codified in LEE4. Cattle are the main reservoir of this pathogen and foods of bovine origin and products contamined with bovine feces are common causes of epidemic outbreaks. In Brazil, EHEC O157:H7 can be isolated from the animal reservoir . Stx2c prevails among the bovine strains, while the toxigenic profiles Stx2 or Stx2/Stx2c are found among the human strains. Concerning the bacterial interaction with human enterocytes cultivated in vitro (Caco-2) we verified that both bovine and human strains showed almost identical ability to invade and to persist in the intracellular compartment of the Caco-2 cells. However, in comparison with the human strains, the bovine strains showed a reduced capacity to produce A/E lesions according to the FAS test. A quantitative FAS test confirmed the relative inefficiency of bovine strains to induce A/E lesions. We also used qPCR to follow the transcription of three genes (eae, espA and tir) of selected bovine and human strains, during the infection of Caco-2 cells. We verified differences in the gene expression, especially for espA, between bovine and human strains and these latter showed a larger expression, in line with the findings of the actin-aggregation tests. Through cloning and expression of recombinant proteins, we purified the Eae, EspA and Tir proteins and obtained specific antibodies, employed to follow the expression of those proteins, by immunofluorescence, along the infection of Caco-2 cells. We found that all proteins are detected both in bovine and human strains, but on these protein labeling occurs early and becomes more intense with the progress of the infection. Our results indicate that EHEC O157:H7 strains isolated from the bovine reservoir in Brazil shows, in comparison to strains isolated from human disease, important differences in relation to the toxigenic profile and the ability to induce A/E lesions. Our findings concerning the ability of the microorganism to invade and to multiply inside enterocytes can explain the persistence of the pathogen in the animal reservoir and its ability of horizontal transmission.