Submitted by Marlene Santos (marlene.bc.ufg@gmail.com) on 2016-10-21T16:50:44Z No. of bitstreams: 2 Tese - Dunya Mara Cardoso Moraes - 2014.pdf: 1962001 bytes, checksum: 0651e62e269992f431e635168bd6edf9 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Approved for entry into archive by Jaqueline Silva (jtas29@gmail.com) on 2016-11-08T17:37:11Z (GMT) No. of bitstreams: 2 Tese - Dunya Mara Cardoso Moraes - 2014.pdf: 1962001 bytes, checksum: 0651e62e269992f431e635168bd6edf9 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) / Made available in DSpace on 2016-11-08T17:37:11Z (GMT). No. of bitstreams: 2 Tese - Dunya Mara Cardoso Moraes - 2014.pdf: 1962001 bytes, checksum: 0651e62e269992f431e635168bd6edf9 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2014-04-11 / Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPq / The purpose of this research was to investigate presence of Salmonella sp. by conventional bacterial identification and real-time PCR on eggshell, albumen, and yolk of washed and unwashed commercial white and brown eggs; in samples of flooring material from transport crates (meconium); raising environment (swab of cages and drinking fountains); cloacal swab; food and insects from growing, rearing and production phases in a commercial group of laying hens. Also, was examinated the susceptibility profile of Salmonella isolates to 14 antimicrobials: sulfamethoxazole (25μg), trimethoprim-sulfamethoxazole (25μg), enrofloxacin (5μg), tetracyclin (30μg) sulphonamides (300μg), ciprofloxacin (10μg), amoxicillin and clavulanic acid (3μg), ampicillin (20μg), ceftiofur (30μg), gentamicin (10μg), oxytetracycline (30μg), neomycin (30μg), doxycycline (30μg) and apramycin (15μg); and evaluated the presence of virulence gene spvC and resistence genes intl1, sul1 and blaTEM. A total of 68 dozens of white eggs and 61 dozens of brown eggs were randomly collected in poultry houses and 30 dozens and 34 dozens of white and brown eggs, respectively, were collected in egg-storage room (on the farm). Each collected dozen corresponded to three sample units: eggshell, albumen and yolk, totaling 387 samples. Salmonella spp. was detected by conventional bacteriology in 5.4% of analyzed samples and in 16% by qPCR. Salmonella Agona represented 18.2% of identified serovars, Salmonella enterica subs. enterica O:4.5 18.2%, Salmonella Schwarzengrund 18.2%, Salmonella Cerro 13.6%, Salmonella Anatum 13.6%, Salmonella Enteritidis 9.1%, Salmonella Johannesburg 4.5%, Salmonella Corvallis 4.5%, Salmonella Livingstone and Salmonella Senftenberg. From 864 samples collected (248 samples originated from growing, 392 from rearing and 224 from production phase), 2,8% where positives in bacteriologic technique and 15,3% in qPCR. Contamination was higher in growing and rearing phases and declined in production phase. Twenty four isolations of Salmonella where typified as Salmonella Agona (41,7%), Salmonella Livingstone (33,3%), Salmonella Cerro (16,7%), Salmonella Senftenberg (4,2%) and Salmonella Schwarzengrund (4,2%). The highest resistance percentage observed were to sulfamethoxazole (91,0%), sulphonamides (51%) and ceftiofur (28,9%) and 0% to ciprofloxacin. Only Salmonella Johannesburg and Salmonella Corvallis showed resistance to only one antibiotic and others serovars were resistant to at least two antimicrobials, noting that Salmonella Schwarzengrund presented resistance to 13 of them. The gene spvC was dectected only in serovar Enteritidis, while intl1 was present in six of ten analyzed serovars and the gene sul1 in three of them, always in association with intl1. The gene blaTEM was not identified. In conclusion, this research points numerous serovars circulating in commercial egg structures and phenotypic antimicrobials resistance investigation, along with antimicrobial resistance genes in isolates of Salmonella sp. are important investigation tools to determinate genetic profile of these bacteria. / Objetivou-se com esta pesquisa investigar a presença de Salmonella sp por bacteriologia por bacteriologia por bacteriologia por bacteriologia por bacteriologia por bacteriologia por bacteriologia por bacteriologia por bacteriologia por bacteriologia por bacteriologia por bacteriologia convencional convencionalconvencionalconvencionalconvencionalconvencional convencionalconvencional e PCR em tempo real em casca, albúmen e gema de ovos comerciais brancos e vermelhos, lavados e não lavados; em amostras de forros de caixa de transporte, amostras de ambientes de criação (suabes de gaiola e bebedouro), suabes de cloaca, ração e insetos oriundos das fases de cria, recria e produção de um lote de poedeiras comerciais e investigar o perfil de suscetibilidade de isolados de Salmonella frente 14 antimicrobianos sulfametoxazol (25μg), sulfametoxazol-trimetoprim (25μg), enrofloxacina (5μg), tetraciclina (30μg), sulfonamidas (300μg), ciprofloxacina (10μg), amoxilina ácido clavulânico (3μg), ampicilina (20μg), ceftiofur (30μg), gentamicina (10μg), oxitetraciclina (30μg), neomicina (30μg), doxiciclina (30μg) e apramicina (15μg) e avaliar a presença do gene de virulência spvC e dos genes de resistência intl1, sul1 e blaTEM. Foram colhidas, nos galpões, 68 dúzias de ovos brancos e 27 dúzias de vermelhos e nos entrepostos, após classificação e sanitização, 30 e 34 de dúzias de ovos brancos e vermelhos, respectivamente. Cada dúzia de ovos correspondeu a três amostras: uma amostra de pool casca, uma de pool de albúmen e uma de pool gema, totalizando 387 amostras. Obteve-se pela bacteriologia convencional 5,4% (21/387) e PCR em tempo real 16,0% (62/387) de amostras positivas para Salmonella. Os sorovares identificados foram Salmonella Agona, Salmonella enterica subs. enterica O:4,5, Salmonella Schwarzengrund, Salmonella Cerro, Salmonella Anatum, Salmonella Enteritidis, Salmonella Johannesburg e Salmonella Corvallis. Foram coletadas também 864 amostras no fluxo de produção de ovos e Salmonella sp. foi isolada pela bacteriologia convencional em 2,8% das amostras e pelo PCR em tempo real em 15,3%, sendo que 248 amostras foram originadas da cria, 392 na recria e 224 na produção. De acordo com a analise estatística a infecção evoluiu da fase de cria para a recria e ao chegar a fase de produção o nível de infecção declinou. Os 24 isolados de Salmonella foram tipificados e os sorovares identificados foram Salmonella Agona, Salmonella Livingstone, Salmonella Cerro, Salmonella Senftenberg e Salmonella Schwarzengrund. Foram analisadas também 45 isolados de Salmonella pertencentes aos sorovares Agona, Livingstone, Cerro, Schwarzengrund, Salmonella enterica subs. enterica O:4,5, Anatum, Enteritidis, Johannesburg, Corvallis e Senftenberg. Os maiores percentuais de resistência foram para sulfametoxazol (91,0%), sulfonamidas (51,0%) e ceftiofur (28,9%). O gene spvC foi detectado somente no sorovar Enteritidis, enquanto o gene intl1 esteve presente em seis dos dez sorovares analisados, o gene sul1 em três deles sempre em associação com intl1 e o gene blaTEM não foi identificado. Conclui-se com essa pesquisa que existe uma variedade de sorovares circulantes em granjas de postura e em ovos comerciais; a investigação fenotípica de resistência aos antimicrobianos aliada a pesquisa dos genes de virulência e de resistência aos antibióticos em isolados de Salmonella sp. circulantes em granjas de postura comercial são importante ferramenta de investigação para determinação do perfil genético dessas bactérias. Palavras

Abstract Streptococcus pneumoniae, pneumococcus, is a common cause of respiratory tract infections and also a common inhabitant of the upper respiratory tract of healthy people. At present, 93 different polysaccharide types have been identified and in addition to them, unencapsulated pneumococci are found especially in healthy carriers. Pneumococci are usually identified by using a bacterial culture combined with biochemical or immunochemical tests. Recently, new DNA-based methods, such as PCR, have been applied. Many PCR methods that detect pneumococci are targeted at genes which encode virulence factors such as pneumolysin, autolysin and pneumococcal surface antigen A. S. pneumoniae is a common causative agent of otitis media. In clinical trials, xylitol has been shown to decrease the occurrence of otitis media but the mechanism of action is not known. Xylitol has been shown to reduce pneumococcal growth and adherence to nasopharyngeal cells and its effect on the appearance of the pneumococcal polysaccharide structure has been shown by electron microscopy. Xylitol has also been demonstrated to inhibit biofilm formation of Staphylococcus aureus and Pseudomonas aeruginosa. Biofilms have been associated with otitis media and pneumococci have been shown to form biofilms. The purpose of this work was to study the role of capsular and other virulence genes in pneumococcal infection and biofilm formation. A new PCR method was developed to detect the pneumococcal capsule and it appeared to have potential when studying the pneumococcal etiology of pneumonia. Widely used PCR methods were used to study pneumococcal isolates, and conflicting results were obtained when the results were compared with conventional immunochemical methods. In addition, xylitol was shown to inhibit capsular gene expression and biofilm formation of pneumococci. Glucose and fructose appeared to enhance biofilm formation. The conflicting results between PCR and immunochemical methods suggest that further identification methods are needed in the diagnosis of pneumococcal infection. The observed inhibitory effect of xylitol on pneumococcal capsule gene expression and biofilm formation may partly explain the efficacy of xylitol in preventing acute otitis media in previous clinical trials. / Tiivistelmä Streptococcus pneumoniae, pneumokokki, on yleinen hengitystieinfektioiden aiheuttaja, joka esiintyy myös hengitysteiden normaalifloorassa. Pneumokokilla tunnetaan 93 kapselityyppiä ja näiden lisäksi etenkin oireettomilta nielukantajilta löytyy kapselittomia pneumokokkeja. Pneumokokin tunnistamiseen käytetään yleensä viljelyä sekä bio- ja immunokemiallisia testejä ja sittemmin tunnistuksen tukena on käytetty geeniteknologisia menetelmiä, kuten PCR. Useissa pneumokokin tunnistuksessa käytettävissä PCR-menetelmissä on käytetty kohdegeeninä virulenssitekijöitä, kuten pneumolysiiniä, autolysiinia ja pneumokokin pinta-antigeeni A:ta koodaavia geenejä. Pneumokokki on yleinen korvatulehdusten aiheuttaja. Kliinisissä tutkimuksissa ksylitolin on havaittu vähentävän korvatulehduksia, mutta vaikutusmekanismi on vielä epäselvä. Ksylitolin on osoitettu vähentävän pneumokokin kasvua ja kiinnittymistä nenänielun soluihin ja sen vaikutus polysakkaridikapselin ulkomuotoon on osoitettu elektronimikroskopialla. Ksylitolin on myös todettu vähentävän biofilminmuodostusta Staphylococcus aureus, ja Pseudomonas aeruginosa –bakteereilla. Biofilmin muodostuksen on ehdotettu liittyvän krooniseen korvatulehdukseen. Aiemmissa tutkimuksissa pneumokokin on osoitettu muodostavan biofilmejä. Työn tarkoituksena oli tutkia kapseli- ja muiden virulenssigeenien merkitystä pneumokokki-infektion diagnostiikassa ja biofilminmuodostuksessa. Työssä kehitettiin uusi PCR-menetelmä pneumokokin kapselin osoittamiseksi ja sillä todettiin olevan käyttömahdollisuuksia keuhkokuumeen pneumokokkietiologiaa tutkittaessa. Yleisesti käytettyjä PCR-menetelmiä tutkittiin pneumokokki-isolaateilla ja havaittiin vakavia ristiriitoja näiden ja perinteisten, immunokemiallisten tunnistusmenetelmien välillä. Lisäksi tutkimuksessa havaittiin ksylitolin vähentävän pneumokokin kapseligeenien ekspressiota ja biofilmin muodostusta. Sen sijaan glukoosi ja fruktoosi lisäsivät biofilmin muodostusta. Tutkimustulokset osoittivat ristiriidan perinteisten immunokemiallisten ja PCR-menetelmien välillä ja antavat aihetta uusien, tarkempien menetelmien käyttöönotolle pneumokokki-infektion diagnostiikassa. Tutkimuksen havainnot ksylitolin vaikutuksesta pneumokokin kapseligeeniekspressioon ja biofilmin muodostukseen voivat osittain selittää kliinisissä tutkimuksissa havaittua ksylitolin ehkäisevää vaikutusta korvatulehduksiin.

Philosophiae Doctor - PhD (Biotechnology) / Availability of genome sequences for numerous bacterial species comprising of different bacterial strains allows elucidation of species and strain specific adaptations that facilitate their survival in widely fluctuating micro-environments and enhance their pathogenic potential. Different bacterial species use different strategies in their pathogenesis and the pathogenic potential of a bacterial species is dependent on its genomic complement of virulence factors. A bacterial virulence factor, within the context of this study, is defined as any endogenous protein product encoded by a gene that aids in the adhesion, invasion, colonization, persistence and pathogenesis of a bacterium within a host. Anecdotal evidence suggests that bacterial virulence genes are undergoing diversifying evolution to counteract the rapid adaptability of its host’s immune defences. Genome sequences of pathogenic bacterial species and strains provide unique opportunities to study the action of diversifying selection operating on different classes of bacterial genes. / South Africa

As part of recognizing the interconnected nature of different sectors in relation to health, AMR (antimicrobial resistance) has emerged as an issue of high global importance. E. coli isolates were taken from pig farms in Thailand, which serves as a point of interest in the study of ARGs (antimicrobial resistance genes) in emerging economies. The fecal samples were collected from pigs, humans who came in contact with the pigs, and humans who did not have contact with pigs to be analyzed for ARGS, virulence genes, and plasmids. Data was analyzed with an automated pipeline in the form of ARG-MATEE, the Antimicrobial Resistance Gene Multi-Analysis Tool for Enteric E. coli, a tool designed in this study to be used here and in future investigations. ARG-MATEE regulates and records internal software versions in a produced report which also includes data tables for all non phylogeny results in Boyce–Codd normal form and data visualizations for plasmids, ARGs, virulence genes, and phylogeny. Through the use of ARG-MATEE, the iss virulence gene was seen to be significantly different between testing groups as it is present in only human testing groups, suggesting the loss of function of the iss gene in pigs, showing host specialization.

Listeria monocytogenes transporte le cellobiose principalement via le PTS (PEP:carbohydrate phosphotransferase system). La croissance sur cellobiose induit l'expression des opérons celBCA1, celBA2 ainsi que du gène lmrg_01989, qui codent respectivement le composant soluble EIIACel1, le transporteur EIICCel1, le composant soluble EIIBCel1, les protéines EIIBCel2 et EIIACel2, et une seconde EIICCel. La croissance sur glucose réprime fortement l'expression de ces gènes. La délétion de celC1 codant l'EIICCel1 ou des deux gènes, celA1 et celA2, ralentit considérablement la consommation cellobiose. L'expression des trois unités de transcription induite par le cellobiose dépend de CelR. CelR, qui code un régulateur transcriptionnel LevR- like, est situé en aval de l'opéron bicistronique celBA2. CelR est activé par phosphorylation par EI et HPr de l'His550. En revanche, la phosphorylation de l'His823, catalysée par P~EIIBCel1 et P~EIIBCel2, inhibe l'activité de CelR. Le remplacement de l'His823 par une Ala empêchant cette phosphorylation ou la délétion des deux gènes codants les EIIAsCel ou EIIBsCel entraîne l'expression constitutive des trois unités de transcription contrôlées par CelR. Comme le glucose, le cellobiose inhibe fortement l'activité de PrfA, l'activateur des gènes de virulence. Nous avons donc cherché à tester si l'un des composants PTSCel pouvait être impliqué dans la répression de gènes de virulence. Les mutants consommant faiblement le cellobiose, présentaient une levée de la répression des gènes de virulence par le cellobiose, alors que le glucose et les autres sucres-PTS les réprimaient toujours. De manière surprenante, la délétion du gène monocistronique lmrg_00557, qui code un autre composant EIIBCel du PTS, induisait la levée de la répression des gènes de virulence médiée par toutes les sources de carbone mais n'avait aucun effet sur la consommation de glucose ou de cellobiose. Ce gène lmrg_00557 a été appelé vgiB (virulence gene inhibitor B) et la protéine correspondante, qui semble jouer un rôle majeur dans la régulation de l'activité de PrfA, EIIBVir. Cette protéine est phosphorylée par le PEP et les composants PTS EI, HPr et EIIACel2 sur le résidu cystéine-8. La complémentation du mutant ΔvgiB avec l'allèle sauvage, mais également avec l'allèle Cys8Ala, restaurait le mécanisme général de répression des gènes de virulence par les sucres, suggérant ainsi que la forme non phosphorylée de EIIBVir inhibe l'activité de PrfA. / Listeria monocytogenes transports cellobiose mainly via a PEP:carbohydrate phosphotranseferase system (PTS). Growth on cellobiose induces the expression of the celBCA1 and celBA2 operons as well as lmrG01989, which encode the soluble EIIA Cel1 and EIIB Cel1 components, the transporter EIIC Cel1 , the EIIA Cel2 and EIIB Cel2 proteins, and a second EIIC Cel , respectively. Growth on lucose strongly repressed the expression of these genes. Deletion of the EIIC Cel1 –encoding celC1 or of both, celA1 and celA2, significantly slowed cellobiose consumption. The bicistronic operon celBA2 is located downstream from celR, which codes for a LevR-like transcription activator. Expression of the three cellobiose-induced transcription units depends on CelR. The gene encoding CelR is located upstream from the bicistronic operon celBA2. CelR itself is activated via phosphorylation by EI and HPr at His550. In contrast, phosphorylation at His823, which is catalyzed by both, P~EIIB Cel1 and P~EIIB Cel2 , inhibits CelR activity. Preventing this phosphorylation by replacing His823 with Ala or deleting the two EIIA Cel – or EIIB Cel -encoding genes caused constitutive expression of all three CelR-controlled transcription units. Similar to glucose, cellobiose strongly inhibits the activity of the virulence gene activator PrfA. We therefore tested whether one of the PTS Cel components might be involved in virulence gene repression. Mutants, that exhibit slow cellobiose consumption, were relieved from cellobiose-mediated virulence gene repression, whereas glucose and other PTS-sugars still repressed them. Strikingly, deletion of the presumed monocistronic lmrg_00557, which codes for another EIIB Cel -like PTS component, caused a general relief from carbon source-mediated virulence gene repression, but had no effect on cellobiose or glucose consumption. The gene lmrg_00557 was named vgiB (virulence gene inhibitor B) and the encoded protein, which seems to play a major role in PrfA regulation, was called EIIB Vir . It becomes phosphorylated by PEP and the PTS components enzyme I, HPr and EIIA Cel2 at cysteine-8. Complementation of the ΔvgiB mutant with wild-type vgiB, but also with the Cys8Ala allele restored general virulence gene repression, thus suggesting that it is the unphosphorylated form of EIIB Vir , which inhibits the activity of PrfA.

Le développement de la multirésistance chez Escherichia coli est un problème important en médecine animale et humaine. En outre, l’émergence et la diffusion des déterminants de résistance aux céphalosporines à larges spectres de troisième génération (ESCs) parmi les isolats, incluant des céphalosporines essentielles en médecine humaine (ex. ceftriaxone et ceftiofur), est un problème majeur de santé publique. Cette thèse visait trois objectifs. D’abord étudier la dynamique de la résistance aux antimicrobiens (AMR) ainsi que la virulence et les profils génétiques de la AMR des E. coli isolées de porcs recevant une nourriture post-sevrage supplémentée avec de la chlortétracycline et de la pénicilline G, et, accessoirement, évaluer les effets d'additifs alimentaires sur cette dynamique en prenant pour exemple d'étude un minéral argileux, la clinoptilolite, étant donné son possible lien avec le gène blaCMY-2 qui confère la résistance au ceftiofur. L'objectif suivant était d'investiguer les mécanismes menant à une augmentation de la prévalence du gène blaCMY-2 chez les porcs qui reçoivent de la nourriture médicamentée et qui n'ont pas été exposés au ceftiofur Ici encore,nous avons examiné les effets d’un supplément alimentaire avec un minéral argileux sur ce phénomène. Enfin, notre dernier objectif était d’étudier, dans le temps, les génotypes des isolats cliniques d'E. coli résistant au ceftiofur, isolés de porcs malades au Québec à partir du moment où la résistance au ceftiofur a été rapportée, soit de 1997 jusqu'à 2012. Dans l'étude initiale, la prévalence de la résistance à 10 agents antimicrobiens, incluant le ceftiofur, s’accroît avec le temps chez les E.coli isolées de porcelets sevrés. Une augmentation tardive de la fréquence du gène blaCMY-2, encodant pour la résistance au ceftiofur, et la présence des gènes de virulence iucD et tsh a été observée chez les isolats. La nourriture supplémentée avec de la clinoptilolite a été associée à une augmentation rapide mais, par la suite, à une diminution de la fréquence des gènes blaCMY-2 dans les isolats. En parallèle, une augmentation tardive dans la fréquence des gènes blaCMY-2 et des gènes de virulence iucD et tsh a été observée dans les isolats des porcs contrôles, étant significativement plus élevé que dans les porcs ayant reçu l'additif au jour 28. La diversité, au sein des E. coli positives pour blaCMY-2 , a été observée au regard des profils AMR. Certaines lignées clonales d'E.coli sont devenues prédominantes avec le temps. La lignée clonale du phylotype A prédominait dans le groupe supplémenté, alors que les lignées clonales du phylotype B1, qui possèdent souvent le gène de virulence iucD associé aux ExPEC, prédominaient dans le groupe contrôle. Les plasmides d'incompatibilité (Inc) des groupes, I1, A/C, et ColE, porteurs de blaCMY-2, ont été observés dans les transformants. Parmi les souches cliniques d'E.coli ESC-résistantes, isolées de porcs malades au Québec de 1997 à 2012, blaCMY-2 était le gène codant pour une β-lactamase le plus fréquemment détecté; suivi par blaTEM et blaCTX-M,. De plus, les analyses clonales montrent une grande diversité génétique. Par contre, des isolats d'E. coli avec des profils PFGE identiques ont été retrouvés dans de multiples fermes la même année mais aussi dans des années différentes. La résistance à la gentamicine, kanamycine, chloramphenicol, et la fréquence de blaTEM et de IncA/C diminuent significativement au cour de la période étudiée, alors que la fréquence de IncI1 et de la multirésistance à sept catégories d'agents antimicrobiens augmente significativement avec le temps. L'émergence d'isolats d'E. coli positifs pour blaCTX-M, une β-lactamase à large spectre et produisant des ESBL, a été observée en 2011 et 2012 à partir de lignées clonales distinctes et chez de nombreuses fermes. Ces résultats, mis ensemble, apportent des précisions sur la dissémination de la résistance au ceftiofur dans les E. coli isolées de porcs. Au sein des échantillons prélevés chez les porcs sevrés recevant l'alimentation médicamentée sur une ferme, et pour laquelle une augmentation de la résistance au ceftiofur a été observée, les données révèlent que les souches d'E. coli positives pour blaCMY-2 et résistantes aux ESCs appartenaient à plusieurs lignées clonales différentes arborant divers profils AMR. Le gène blaCMY-2 se répand à la fois horizontalement et clonalement chez ces E. coli. L'ajout de clinoptilotite à la nourriture et le temps après le sevrage influencent la clonalité et la prévalence du gène blaCMY-2 dans les E. coli. Durant les 16 années d'étude, plusieurs lignées clonales différentes ont été observées parmi les souches d'E. coli résistantes au ceftiofur isolées de porc malades de fermes québécoises, bien qu’aucune lignée n'était persistante ou prédominante pendant l'étude. Les résultats suggèrent aussi que le gène blaCMY-2 s'est répandu à la fois horizontalement et clonalement au sein des fermes. De plus, blaCMY-2 est le gène majeur des β-lactamases chez ces isolats. À partir de 2011, nous rapportons l'émergence du gène blaCTX-M dans des lignées génétiques distinctes. / Development of multidrug resistance in Escherichia coli is an important problem in animal and human medicine. Further, emergence and spread of determinants for resistance to third generation extended-spectrum cephalosporins (ESCs) such as the critically important cephalosporins in human medicine (e.g. ceftriaxone and ceftiofur) among isolates is a public health concern. Thus, the objectives of the present thesis were (1) to study the dynamic of antimicrobial resistance (AMR) phenotypes as well as virulence and AMR gene profiles in E. coli from pigs receiving a feed medicated with chlortetracycline and penicillin G following weaning and to study the effect of feed supplementation with a clay mineral, clinoptilolite, on this dynamic; (2) To investigate the mechanisms leading to an increase in the prevalence of blaCMY-2 conferring resistance to ceftiofur in pigs receiving medicated feed but which had not received ceftiofur, and to examine the effect of feed supplementation with a clay mineral on this phenomenon; and (3) to investigate the temporal characterization of clinical isolates of ceftiofur-resistant E.coli from diseased pigs in Quebec, Canada from 1997, when ceftiofur resistance was first reported, to 2012. In the initial study, prevalence of resistance to 10 antimicrobial agents, including ceftiofur, increased over time in E.coli isolates from weaned pigs. A late increase in the frequency of blaCMY-2, the gene encoding resistance to ceftiofur, and the presence of virulence genes iucD and tsh were observed in the isolates. Feed supplementation with clinoptilolite was associated with an early increase but later decrease in the frequency of the blaCMY-2 gene in isolates. Concurrently, a later increase in the frequency of the blaCMY-2 and the virulence genes iucD and tsh was observed in the control pig isolates, being significantly greater than in the supplemented pigs at day 28. Diversity among the blaCMY-2-positive E. coli isolates with respect to AMR patterns was observed. Certain clonal lineages of E. coli became predominant with time. The clonal lineage of phylotype A predominated in the supplemented group, whereas the clonal lineages of phylotype B1 which often possessed the ExPEC-associated virulence gene iucD, predominated in the control group. The blaCMY-2-carrying plasmids of incompatibility (Inc) groups, I1, A/C, and ColE were observed in transformants. In ESC-resistant E.coli clinical isolates from diseased pigs in Quebec, from 1997 to 2012, blaCMY-2 was the most frequently detected β-lactamase gene, followed by blaTEM and blaCTX-M and clonal analysis showed high diversity. E. coli isolates with identical PFGE patterns were found in multiple farms in the same year and also in different years. Resistance to gentamicin, kanamycin, chloramphenicol, and the frequency of blaTEM and IncA/C significantly decreased over the study time, whereas the frequency of IncI1 and multidrug-resistance to seven antimicrobial categories significantly increased over time. Emergence of blaCTX-M-positive, extended-spectrum β-lactamase (ESBL)-producing E. coli isolates was observed in 2011 and 2012 from distinct clonal lineages and multiple farms. Taken together, this work gives some insight into the spread of ceftiofur resistance in E.coli isolates from pigs. Results reveal that in weaned pigs receiving medicated feed on one farm in which an increase in ceftiofur resistance was observed, the blaCMY-2-positive E.coli resistant to ESCs belonged to several different clonal lineages with diverse AMR patterns. The blaCMY-2 gene spread both horizontally and clonally in E. coli. Feed supplementation with clinoptilolite and time period after weaning influenced the clonality and the prevalence of blaCMY-2 gene in E. coli. In ceftiofur-resistant E.coli strains isolated from diseased pigs in farms throughout Quebec over a 16 year period, several different pathogenic clonal lineages were observed, although none was persistent or predominant over the study time. The results suggest that blaCMY-2 gene spreads both horizontally and clonally on and between farms. Furthermore, blaCMY-2 was the major β-lactamase gene in these isolates. From 2011, we report the emergence of blaCTX-M in distinct clonal lineages.

Plants are continuously confronted with a multitude attack either abiotic but also biotic in nature. Interestingly, despite the abundance of bacteria that plant has to face, only few are able to induce death or disease in the host plant. It is therefore likely that, in addition to secondary metabolites with antimicrobial properties, plants also synthesize secondary metabolites which are able to inhibit the expression of virulence genes in bacteria without affecting either growth or viability, which allows plants to host willingly or not bacterial populations. This work focuses on the identification of such metabolites in Malagasy plants (genera Dalbergia and Combretum) and the demonstration of their inhibitory effect on the expression of virulence genes in two different pathosystems: Rhodococcus fascians (a phytopathogen) and Pseudomonas aeruginosa (an opportunistic pathogen). Thus, two metabolites were isolated using a combination of chromatographic techniques coupled with tests that evaluate the expression of certain genes involved in the virulence mechanisms of these bacteria. The first is a new prenylated isoflavanone, named perbergin, isolated from the bark extract of D. pervillei. It was shown that the perbergin target attR gene expression, encoding a LysR-type transcriptional regulator that plays a key role in regulating the expression of virulence genes of R. fascians and the transition from an epiphytic to a pathogenic lifestyle. Therefore, we have also shown that the expression of all virulence genes known to date in R. fascians is also affected while the expression of genes involved in epiphytic fitness of the bacteria is not altered. In addition, the application of perbergin at the time of infection of plants susceptible to R. fascians shows that this molecule reduces in vivo the virulence of R. fascians, highlighting the potential of perbergin as an anti-infective agent. The second is a flavonoid known as catechin, isolated from the bark extract of C. albiflorum. Catechin significantly inhibits the expression of genes that regulate the mechanism of quorum sensing in P. aeruginosa such as lasI, LasR, rhlI and rhlR but also lasB and rhlA which expression depends on quorum sensing. Therefore, the production of virulence factors such as pyocyanin and elastase is significantly affected. Because of the limited number of our arsenal of antibiotics and their increasing ineffectiveness, the identification of these compounds create a path to an alternative in the fight against pathogenic bacteria and multidrug resistance of pathogenic bacteria to antibiotics. Our results also demonstrate the richness of Malagasy plants as (re)sources of new therapeutic molecules and the importance of widening the range of bacterial targets to be investigated to develop new strategies to fight within the endless war that we are waging against bacteria pathogens.<p><p>Les plantes sont continuellement confrontées à une multitude d’attaques qu’elles soient de nature abiotique ou surtout biotique. Il est intéressant de noter que malgré la multitude de bactéries auxquelles les plantes doivent faire face, seules quelques unes sont capables d’induire la mort ou une maladie chez la plante hôte. Il est dès lors fort probable que, outre les métabolites secondaires ayant des propriétés antimicrobiennes, les plantes synthétisent également des métabolites secondaires capables d’inhiber l’expression des gènes de virulence chez les bactéries sans toutefois affecter ni leur croissance ni leur viabilité, ce qui permet aux plantes de contenir les populations bactériennes qu’elles hébergent de gré ou de force. Ce travail porte sur l’identification de ce type de métabolites dans des plantes malgaches (genres Dalbergia et Combretum) et la démonstration de leurs effets inhibiteurs sur l’expression de gènes de virulence chez deux pathosystèmes différents: Rhodococcus fascians (un phytopathogène) et Pseudomonas aeruginosa (un pathogène opportuniste). Ainsi, deux métabolites ont été isolés en utilisant une combinaison de techniques chromatographiques couplées avec des tests qui évaluent l’expression de certains gènes impliqués dans les mécanismes de virulence de ces bactéries. Le premier est un nouvel isoflavanone prénylé, nommé perbergine, isolé à partir de l’extrait d’écorces de D. pervillei. Il a été montré que la perbergine cible l’expression du gène attR, codant un régulateur transcriptionnel de type LysR qui joue un rôle clé dans la régulation de l’expression des gènes de virulence de R. fascians et qui assure la transition entre un mode de vie épiphyte et le mode pathogène. En conséquence, nous avons également montré que l’expression de l’ensemble des gènes de virulence connu à ce jour chez R. fascians est également affectée alors que l’expression de gènes impliqués dans l’aptitude épiphyte de la bactérie n’est pas altérée. Par ailleurs, l’application de perbergine au moment de l’infection de plantes sensibles à R. fascians montre que cette molécule atténue la virulence de R. fascians in vivo, mettant en exergue le potentiel de la perbergine comme agent anti-infectieux. Le deuxième est un flavonoïde, connu sous le nom de catéchine, isolé de l’extrait d’écorces de C. albiflorum. La catéchine inhibe significativement l’expression des gènes régulateurs du mécanisme du quorum sensing chez P. aeruginosa tels que lasI, lasR, rhlI et rhlR et également lasB et rhlA dont l’expression dépend du quorum sensing. En conséquence, la production des facteurs de virulence tels que la pyocyanine et l’élastase est significativement affectée. Compte tenu de l’appauvrissement de notre arsenal d’antibiotiques et de leur inefficacité croissante, l’identification de ces composés ouvre une voie alternative de lutte contre les bactéries pathogènes et la multirésistance des bactéries pathogènes aux antibiotiques. Nos résultats démontrent également la richesse des plantes malgaches comme (res)sources de nouvelles molécules thérapeutiques et l’importance d’élargir le champ des cibles bactériennes à investiguer pour développer de nouvelles stratégies de lutte dans la guerre sans fin que nous menons contre les bactéries pathogènes. / Doctorat en Sciences / info:eu-repo/semantics/nonPublished