Plusieurs études ont examiné la sensibilité aux antimicrobiens chez les bactéries d’organismes provenant de produits issus de l’aquaculture ou de leur environnement. Aucune information n’est cependant disponible concernant la résistance aux antimicrobiens dans les bactéries de la flore de poissons ou de fruits de mer vendus au détail au Canada. C’est particulièrement vrai en ce qui a trait aux bactéries des genres Aeromonas et Vibrio, dont certaines espèces sont des agents pathogènes zoonotiques connus. Au cours de cette étude, la sensibilité aux antimicrobiens d’isolats d’Aeromonas spp. et de Vibrio spp. provenant de poissons et de crevettes domestiques et importés a été mesurée à l’aide de techniques de micro dilution en bouillon et/ou de diffusion sur disque. Les classes d’antimicrobiens examinés comprenaient les tétracyclines (TET), les inhibiteurs de la voie des folates (sulfadiméthoxine-triméthoprime, SXT), le florfenicol (FLO), et les quinolones (acide nalidixique / enrofloxacine, NA/ENO). Des valeurs seuils épidémiologiques pour Aeromonas et Vibrio ont été établies en utilisant la méthode d’interprétation normalisée des données de résistance provenant de diffusion sur disque. La recherche de gènes de résistance associés au profil de résistance des isolats a été effectuée en utilisant des PCRs et des puces ADN. Le nombre d’isolats résistants aux divers antimicrobiens parmi les 201 isolats d’Aeromonas et les 185 isolats de Vibrio étaient respectivement les suivants: TET (n=24 et 10), FLO (n=1 et 0), SXT (n=2 et 8), NA (n=7 et 5) et ENO (n= 5 et 0). Diverses associations de gènes tet(A), tet(B), tet(E), floR, sul1, sul2, et intI1 ont été détectées, les gènes tet(E), intI1, sul2 et tet(B) étant les plus communs. Les espèces d’Aeromonas et de Vibrio isolées de poissons au détail et de fruits de mer peuvent héberger une variété de gènes de résistance, bien que peu fréquemment. Le risque que représente ces gènes de résistance reste à évaluer en considérant le potentiel infectieux des bactéries, l’utilisation des ces agents antimicrobiens pour le traitement des maladies en aquaculture et en médecine humaine et leur rôle en tant que réservoir de la résistance antimicrobienne. / Multiple studies have examined antimicrobial susceptibility in bacteria from aquacultured products microorganisms and their environment. However, no information is available concerning antimicrobial resistance in bacterial flora of fish and seafood available at the retail level in Canada. This is particularly true for the common aquatic commensals, Aeromonas and Vibrio, for which some species are known zoonotic pathogens. In the course of this study, the antimicrobial susceptibility among Aeromonas spp. and Vibrio spp. from domestic and imported fish and seafood was characterized. Aeromonas and Vibrio spp. isolates cultured from finfish and shrimp samples were evaluated for antimicrobial susceptibility by broth microdilution and/or disk diffusion techniques. Antimicrobial classes examined in detail included: tetracyclines (TET), folate pathway inhibitors (sulfadimethoxine-trimethoprim, SXT), florfenicol (FLO), and the quinolones (nalidixic acid / enrofloxacin, NA/ENO). Epidemiological cut-off values (ECV’s) for Aeromonas/Vibrio were established using normalized resistance interpretation (NRI) of disk diffusion data. Isolates were further examined by PCR and microarray for genes associated with their antimicrobial resistance. Of 201 Aeromonas and 185 Vibrio isolates, those classified as resistant were as follows, respectively: TET (n=24 and 10), FLO (n=1 and 0), SXT (n=2 and 8), NA (n=7 and 5) and ENO (n=5 and 0). Various combinations of tet(A), tet(B), tet(E), floR, sul1, sul2 and intI1 genes were detected with tet(E), intI1, sul2 and tet(B) being the most common. Vibrio and Aeromonas species isolated from retail fish and seafood sources can harbor a variety of resistance determinants, although their occurrence is not high. The risk represented by these resistances remains to be evaluated in view of the potential for bacterial infection and their role as a reservoir for antimicrobial resistance.

Les nématodes à galles (Meloidogyne spp.) sont des pathogènes cosmopolites extrêmement polyphages. L’emploi de la majorité des nématicides chimiques étant désormais interdit, la meilleure alternative repose sur l’utilisation de gènes majeurs de résistance (gènes R). Cependant, il existe un risque de contournement de ceux-ci et les ressources génétiques en termes de gènes R sont limitées. Une gestion qui permette de pérenniser l’utilisation de ces ressources d’intérêt agronomique est donc primordiale. Me1 et Me3 sont deux gènes R à large spectre du piment actuellement utilisés dans les programmes de sélection. La confrontation vis-à-vis de M. incognita de différents génotypes possédant l’un de ces deux gènes a montré que (1) le fond génétique de la plante joue un rôle clé sur l’efficacité de ces gènes R, (2) il n’existe pas d’effet du dosage d’allèles pour ces gènes R. Suite à ces résultats, une recherche de loci à caractère quantitatif (QTLs) a été réalisée afin d’identifier et de localiser des facteurs de résistance partielle susceptibles d’expliquer les différences observées entre les différents fonds génétiques. L’étude de tels facteurs vis-à-vis de M. incognita, M. arenaria et M. javanica, les trois principales espèces de nématodes à galles, a mis en évidence quatre nouveaux QTLs. Tous sont regroupés sur le chromosome P1 du piment, sauf un efficace vis-à-vis de M. javanica situé sur le chromosome P9. C’est la première fois que des facteurs de résistance aux nématodes à galles sont localisés sur le chromosome P1. Ce travail ouvre de nouvelles perspectives quant à la création de nouvelles variétés avec un potentiel accru en termes de résistance aux Meloidogyne. / Root-knot nematodes (RKNs), Meloidogyne spp., are extremely polyphagous plant parasites worldwide. Since the use of most chemical nematicides is being prohibited, genetic resistance is an efficient alternative way to protect crops against these pests. However, nematode populations proved able to breakdown plant resistance, and genetic resources in terms of resistance genes (R-genes) are limited. Sustainable management of these valuable resources is thus a key point of R-gene durability. In pepper, Me1 and Me3 are two dominant major R-genes, currently used in breeding programs to control M. arenaria, M. incognita and M. javanica, the three main RKN species. Challenging these two genes in different genetic backgrounds against M. incognita demonstrated that (1) the efficiency of the R-genes in reducing the reproductive potential of RKNs is strongly affected by the plant genetic background, (2) the allelic status of the R-genes has no effect on nematode reproduction. According to these first results, a QTL analysis was performed to identify and to localize partial resistance factors against RKNs which could explain the differences observed between the genetic backgrounds. Focusing on M. incognita, M. arenaria and M. javanica, four new major QTLs were localized. They are all regrouped on pepper chromosome P1 except one QTL efficient against M. javanica, which was located on pepper chromosome P9. The cluster on chromosome P1, regrouping most of the newly discovered resistance factors, is described for the first time with respect to RKN resistance. As a conclusion, this work should contribute to the breeding of new pepper varieties with a high level of resistance against RKNs.

Submitted by Renata Lopes (renatasil82@gmail.com) on 2016-02-15T10:47:06Z No. of bitstreams: 1 julianaalvesresende.pdf: 4187528 bytes, checksum: 3a29cc184829c26eb33ffecc869ae841 (MD5) / Approved for entry into archive by Adriana Oliveira (adriana.oliveira@ufjf.edu.br) on 2016-02-26T12:21:55Z (GMT) No. of bitstreams: 1 julianaalvesresende.pdf: 4187528 bytes, checksum: 3a29cc184829c26eb33ffecc869ae841 (MD5) / Made available in DSpace on 2016-02-26T12:21:55Z (GMT). No. of bitstreams: 1 julianaalvesresende.pdf: 4187528 bytes, checksum: 3a29cc184829c26eb33ffecc869ae841 (MD5) Previous issue date: 2013-12-16 / CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Digestão anaeróbia é uma alternativa sustentável para utilização de dejetos animais como insumo energético. Neste contexto, a dinâmica da comunidade microbiana, inativação de patógenos ou mesmo disseminação de genes de resistência durante o processo de biodigestão se torna relevante. Este trabalho avaliou a diversidade taxonômica (domínios Bacteria e Archaea) e a persistência de grupos bacterianos de relevância e resistência a drogas antimicrobianas, em dois biodigestores contínuos de escala piloto operados a temperatura ambiente em duas estações, verão e inverno. O substrato era composto de fezes bovinas frescas diluídas com água de lavagem dos pisos (sólidos totais de 2 a 3%). Amostras do biogás foram coletadas para determinação dos teores de metano. Para análises físico-químicas dos afluentes (carregamento inicial) e efluentes, alíquotas foram coletadas ao longo de 60 dias de fermentação para análises de sólidos totais, voláteis e pH. Análises das comunidades microbianas foram realizadas por PCR quantitativo (qPCR), PCR-single strand conformation polymorphism (SSCP) e análise metagenômica. A densidade de diferentes grupos bacterianos foi realizada por contagem direta. Linhagens bacterianas foram identificadas bioquimicamente utilizando kits comerciais. A susceptibilidade a drogas foi determinada por diluição em ágar. Quantificação de genes que codificam resistência aos macrolídeos (ermB), aminoglicosídeos (aphA2) e beta-lactâmicos (blaTEM-1) foram observadas por qPCR. A taxonomia de bactérias clinicamente relevantes foi ainda avaliada, por similaridade, a partir de um banco de dados criado com 30 sequências de DNA codificadoras para o 16S rRNA de bactérias potencialmente patogênicas. Independente da estação, o processo de biodigestão apresentou desempenho semelhante, com taxas de rendimento médio e teores de metano, 59,2% no verão e 53,7% no inverno. A dinâmica e os valores médios do número de cópias do gene V3 Bacteria e Archaea também foram semelhantes. Ocorreram alterações na composição (filo e famílias) das comunidades microbianas entre as estações e estas mudanças não influenciaram na produção de metano. Provavelmente, ocorreu uma redundância de grupos capazes de realizar funções similares. Foram verificadas reduções significativas de grupos bacterianos de relevância clínico-microbiológica viáveis em ambas as estações. Apesar disso, bactérias multirresistentes foram detectadas tanto nos afluentes como nos efluentes. Cocos Gram-positivos (CGP), o grupo mais prevalente, foi resistente à penicilina e levofloxacino, enquanto resistência à ampicilina, ampicilina-sulbactam e cloranfenicol foi observado com maior frequência entre os bacilos Gram-negativos da família Enterobacteriaceae (ENT) e não fermentadores (BGN NF). Enterococcus spp. foram os CGP isolados com maior frequência e entre os BGN, Escherichia coli foi o mais abundante. Houve redução no número de cópias de todos os genes de resistência (ermB, aphA2 e blaTEM-1) durante o processo de biodigestão, porém mantidos níveis preocupantes nos efluentes. Taxonomia bacteriana avaliada por similaridade das sequências mostrou Clostridium spp., Acinetobacter e Strenotrophomonas como as bactérias mais identificadas. Apesar dos dados apresentados nesse estudo endossarem a digestão anaeróbia como solução importante para reciclagem e produção de energia, levanta preocupações sobre riscos de caráter sanitários durante o processo. Além disso, discussões a respeito do uso de antimicrobianos na pecuária leiteira são necessárias. / Anaerobic digestion is a sustainable alternative to using animal waste as an energy source. In this context, the dynamics of the microbial community, inactivation of pathogens or even spread of resistance genes during the process of digestion becomes relevant. This study evaluated the taxonomic diversity (Bacteria and Archaea domains) and the persistence of bacterial groups of relevance and resistance to antimicrobial drugs, analyzing two continuous pilot scale digesters operated at ambient temperature in two seasons, summer and winter. The substrate was composed fresh cow dung diluted with water for washing floors (total solids 2 to 3%). Biogas samples were collected to determine the levels of methane. For physico-chemical analysis of influent (initial load) and effluent, aliquots were collected during 60 days of fermentation for analyzes of total volatile solids and pH. Analyzes of microbial communities were performed by quantitative PCR (qPCR), PCR-single-strand conformation polymorphism (SSCP) analysis and metagenomics. The density of different bacterial groups was performed by direct counting. Bacterial strains were identified biochemically using commercial kits. The drug susceptibility was determined by the agar dilution method. Quantification of genes encoding resistance to macrolides (ermB), aminoglycosides (aphA2) and beta-lactams (blaTEM-1) were observed by qPCR. The taxonomy of clinically relevant bacteria was further evaluated by similarity from a database created with 30 DNA sequences coding for 16S rRNA of potentially pathogenic bacteria. Independent of season, the process of digestion showed similar performance, with rates average yield and percent methane, 59.2% in summer and 53.7% in winter. The dynamics and the average values of the number of copies of the gene V3 Bacteria and Archaea were also similar. Changes occurred in the composition (phylum and families) of the microbial communities between seasons and these changes did not influence the production of methane. Probably occurred a redundancy group able to perform similar functions. Significant reductions of bacterial groups of clinical and microbiological relevance viable in both seasons were observed. Despite this, multiresistant bacteria were detected in both the affluents and effluents. Gram-positive cocci (GPC), the most prevalent group was resistant to penicillin and levofloxacin, while ampicillin, ampicillin-sulbactam, chloramphenicol was observed more frequently among Gram-negative rods of the Enterobacteriaceae family (ENT) and not fermenters (NF GNR). Enterococcus spp. were most frequently GPC isolated and among the GNR, Escherichia coli was the most abundant. There was reduction in the number of copies of all the resistance genes (ermB, aphA2 and blaTEM-1) during the process of digestion, however, the effluent still showing concerning levels. Bacterial taxonomy evaluated by similarity of the sequences showed Clostridium spp., Acinetobacter and Strenotrophomonas were the bacteria more identified. In spite the data presented in this study showed anaerobic digestion as an important solution to recycling and energy production, raises concerns about health risks of character during the process. In addition, discussions regarding the use of antimicrobials in dairy farming are needed.

Doctor of Philosophy / Department of Agronomy / Gina Brown-Guedira / Allan K. Fritz / Aegilops tauschii, the D-genome donor of modern wheat, has served as an important source of genetic variation in wheat breeding. The objective of this research was to characterize and utilize multiple Ae. tauschii-derived pest resistance genes contained in the germplasm KS96WGRC40. Two Ae. tauschii-derived genes, H23 and Cmc4, provide resistance to the Hessian fly (HF) and wheat curl mite (WCM), respectively. A linkage analysis of a testcross population estimated 32.67% recombination between H23 and Cmc4 on chromosome 6DS in wheat indicating that the two genes are not tightly linked as previous mapping reports show. Haplotype data of recombinant lines and physical mapping of linked microsatellite markers located Cmc4 distal to H23. Haplotype data indicated that both KS89WGRC04 and KS96WGRC40 have the distal portion of 6DS derived from Ae. tauschii. Microsatellite primer pairs BARC183 and GDM036 were more useful than the previously published linked markers in identifying lines carrying Cmc4 and H23, respectively. Through phenotypic selection and advancement within the testcross population, three TC1F2:4 lines were identified as homozygous resistant for H23 and Cmc4 and have the complete terminal segment of 6DS from Ae. tauschii. Two lines are more desirable than the original germplasm releases and can serve as a source of resistance to both HF and WCM in an elite background. A linkage analysis of a segregating recombinant inbred line population identified an Ae. tauschii-derived gene of major effect conferring resistance to Septoria leaf blotch (STB) and another Ae. tauschii-derived gene of major effect conferring resistance to soil-borne wheat mosaic virus (SBWMV) in the germplasm KS96WGRC40. The STB resistance gene in KS96WGRC40 is located in the distal 40% of the short arm of chromosome 7D flanked by microsatellite markers Xgwm044 and Xbarc126. Two previously reported STB genes, Stb4 and Stb5, have been mapped to 7DS in the same region as the STB resistance gene in KS96WGRC40. The uniqueness of the STB resistance genes on 7DS is questionable. The SBWMV resistance gene in KS96WGRC40 is located on chromosome 5DL linked to microsatellite marker Xcfd010. The SBWMV resistance gene within KS96WGRC40 was derived from TA2397 via KS95WGRC33.

Landfilling is the most widely used method for the disposal of municipal solid wastes (MSW) in the United States due to its simplicity and low cost. According to the 2014 report on Advancing Sustainable Materials Management by the USEPA, only 34% of the total MSW generated in the US was recycled, while 13% was combusted for energy recovery. In 2014, 53% of the MSW generated, (i.e. 136 million tons) in the US was landfilled. The treatment of landfill leachates, generated by percolation of water through the landfill, primarily due to precipitation, has been found to be one of the major challenges associated with landfill operation and management. Currently, leachates from most landfills are discharged into wastewater treatment plants, where they get treated along with domestic sewage. Issues associated with treatment of landfill leachates due to their high nitrogen and heavy metal content have been widely studied. Recently, it has been observed that the organic carbon in landfill leachates, specifically humic and fulvic acids (together referred to as "humic substances") contain aromatic groups that can absorb large amounts of ultraviolet (UV) light, greatly reducing the UV transmissivity in wastewater plants using UV disinfection as the final treatment step. This interference with UV disinfection is observed even when landfill leachates constitute a very small fraction (of the order of 1%) of the total volumetric flow into wastewater treatment plants. Humic substances are present as dissolved organic matter (DOM) and typically show very low biodegradability. Removing these substances using chemical treatment or membrane processes is an expensive proposition. However, the concentrations of humic substances are found to be reduced in leachates from landfill cells that have aged for several years, suggesting that these substances may be degraded under the conditions of long-term landfilling. The primary objective of this research was to use a two-stage process employing thermophilic pretreatment followed by a mesophilic anaerobic membrane bioreactor (AnMBR) to mimic the conditions of long-term landfilling. The AnMBR was designed to keep biomass inside the reactor and accelerate degradation of biologically recalcitrant organic carbon such as humic substances. The treatment goal was to reduce UV absorbance in raw landfill leachates, potentially providing landfills with an innovative on-site biological treatment option prior to discharging leachates into wastewater treatment plants. The system was operated over 14 months, during which time over 50% of UV-quenching organic carbon and 45% of UV absorbance was consistently removed. To the best of our knowledge, these removal values are higher than any reported using biological treatment in the literature. Comparative studies were also performed to evaluate the performance of this system in treating young leachates versus aged leachates. Next-generation DNA sequencing and quantitative PCR (qPCR) were used to characterize the microbial community in raw landfill leachates and the bioreactors treating landfill leachate. Analysis of microbial community structure and function revealed the presence of known degraders of humic substances in raw as well as treated landfill leachates. The total number of organisms in the bioreactors were found to be higher than in raw leachate. Gene markers corresponding to pathogenic bacteria and a variety of antibiotic resistance genes (ARGs) were detected in raw landfill leachates and the also in the reactors treating leachate, which makes it necessary to compare these ARG levels with wastewater treatment in order to determine if leachates can act as sources of ARG addition into wastewater treatment plants. In addition, the high UV absorbance of leachates could hinder the removal of ARBs and ARGs by UV disinfection, allowing their release into surface water bodies and aiding their proliferation in natural and engineered systems. / Ph. D.

Antibiotic resistance is a global threat that can severely imperil public health. To curb the spread of antibiotic resistance, it is imperative that efforts commensurate with a “One Health” approach are undertaken. Given that interconnectivities among ecosystems can serve as conduits for the proliferation and dissemination of antibiotic resistance, it is increasingly being recognized that a robust global environmental surveillance framework is required to promote One Health. The ideal aim would be to develop approaches that inform global distribution of antibiotic resistance, help prioritize monitoring targets, present robust data analysis frameworks to profile resistance, and ultimately help build strategies to curb the dissemination of antibiotic resistance. The work described in this dissertation was aimed at evaluating and developing different data analysis paradigms and their applications in investigating and characterizing antibiotic resistance across different resistomes. The applications presented in Chapter 2 illustrate challenges associated with various environmental data types (especially metagenomics data) and present a path to advance incorporation of data analytics approaches in Environmental Science and Engineering research and applications. Chapter 3 presents a novel approach, ExtrARG, that identifies discriminatory ARGs among resistomes based on factors of interest. The results in Chapter 4 provide insight into the global distribution of ARGs across human fecal and sewage resistomes across different socioeconomics. Chapter 5 demonstrates a data analysis paradigm using machine learning algorithms that helps bridge the gap between information obtained via culturing and metagenomic sequencing. Lastly, the results of Chapter 6 illustrates the contribution of phages to antibiotic resistance. Overall, the findings provide guidance and approaches for profiling antibiotic resistance using metagenomics and machine learning. The results reported further expand the knowledge on the distribution of antibiotic resistance across different resistomes. / Antibiotic resistance is a global threat that can severely imperil public health. To curb the spread of antibiotic resistance, it is imperative that efforts commensurate with a "One Health" approach are undertaken. Given that interconnectivities among ecosystems can serve as conduits for the proliferation and dissemination of antibiotic resistance, it is increasingly being recognized that a robust global environmental surveillance framework is required to promote One Health. The ideal aim would be to develop approaches that inform global distribution of antibiotic resistance, help prioritize monitoring targets, present robust data analysis frameworks to profile resistance, and ultimately help build strategies to curb the dissemination of antibiotic resistance. The work described in this dissertation was aimed at evaluating and developing different data analysis paradigms and their applications in investigating and characterizing antibiotic resistance across different resistomes. The applications presented in Chapter 2 illustrate challenges associated with various environmental data types (especially metagenomics data) and present a path to advance incorporation of data analytics approaches in Environmental Science and Engineering research and applications. Chapter 3 presents a novel approach, ExtrARG, that identifies discriminatory ARGs among resistomes based on factors of interest. The results in Chapter 4 provide insight into the global distribution of ARGs across human fecal and sewage resistomes across different socioeconomics. Chapter 5 demonstrates a data analysis paradigm using machine learning algorithms that helps bridge the gap between information obtained via culturing and metagenomic sequencing. Lastly, the results of Chapter 6 illustrates the contribution of phages to antibiotic resistance. Overall, the findings provide guidance and approaches for profiling antibiotic resistance using metagenomics and machine learning. The results reported further expand the knowledge on the distribution of antibiotic resistance across different resistomes. / Doctor of Philosophy / Antibiotic resistance is ability of bacteria to withstand an antibiotic to which they were once sensitive. Antibiotic resistance is a global threat that can pose a serious threat to public health. In order to curb the spread of antibiotic resistance, it is imperative that efforts commensurate with the "One Health" approach. Since ecosystem networks can act as channels for the spread and spread of antibiotic resistance, there is growing recognition that a robust global environmental monitoring framework is required to promote a true one-health approach. The ideal goal would be to develop approaches that can inform the global spread of antibiotic resistance, help prioritize monitoring objectives and present robust data analysis frameworks for resistance profiling, and ultimately help develop strategies to contain the spread of antibiotic resistance. The objective of the work described in this thesis was to evaluate and develop different data analysis paradigms and their applications in the study and characterization of antibiotic resistance in different resistomes. The applications presented in Chapter 2 illustrate challenges associated with various environmental data types (especially metagenomics data) and present a path to advance incorporation of data analytics approaches in Environmental Science and Engineering research and applications. The Chapter 3 presents a novel approach, ExtrARG, that identifies discriminatory ARGs among resistomes based on factors of interest. The chapter 5 demonstrates a data analysis paradigm using machine learning algorithms that helps bridge the gap between information obtained via culturing and metagenomic sequencing. The results of Chapters 4 provide insight into the global distribution of ARGs across human fecal and sewage resistomes across different socioeconomics. Lastly, the results of Chapter 6 illustrates the contribution of phages to antibiotic resistance. Overall, the findings provide guidance and approaches for profiling antibiotic resistance using metagenomics and machine learning. The results reported further expand the knowledge on the distribution of antibiotic resistance across different resistomes.

Les Escherichia coli pathogènes de la volaille (APEC) font partie des E. coli extra-intestinaux pathogènes (ExPEC) et seraient un réservoir possible de gènes de virulence et de résistance aux antimicrobiens (RAM) des ExPEC chez l’humain. L’objectif de cette étude était d’évaluer l’effet d’un prébiotique et d’un mélange d’acide organique et d’huiles essentielles encapsulés sur la prévalence des gènes de virulence des ExPEC et de RAM, ainsi que les associations entre ces gènes chez E. coli de l’intestin du poulet sain. Des échantillons de contenus caecaux de poulets de 29 jours d’âge ayant reçu un de ces ingrédients alimentaires comparativement à des témoins ont été analysés pour la présence des gènes de virulence iucD, tsh, papC et des gènes de RAM blaTEM, blaSHV, tetA, tetC, blaCMY-2, aadA1, aac3 par PCR. La prévalence d’iucD était supérieure dans le groupe témoin comparativement aux groupes «prébiotique» et «acide organique» et la prévalence de papC était affectée dans le groupe «acide organique». La prévalence d’isolats d’E.coli positifs pour blaCMY-2 était supérieure dans le groupe témoin comparée aux groupes «prébiotique» et «acide organique», tel que démontré par la technique d’hybridation de l’ADN sur HGMF (Hydrophobic Grid Membrane Filter). De plus, la prévalence des isolats d’E. coli positifs pour tetA, blaTEM, aadA1 ou tsh était affectée par les ingrédients alimentaires. Dans l’ensemble, des associations entre la présence de tsh et iucD, blaTEM et aadA1, et iucD et blaCMY-2 ont été observées. .Cette étude démontre l’utilité de certains ingrédients alimentaires pour dimunier le risque d’exposition en santé publique. / Avian Pathogenic E. coli (APEC) belong to the extra-intestinal pathogenic E. coli (ExPEC) pathotype, and may be a virulence and antimicrobial resistance (AMR) gene reservoir for ExPEC in humans. The aim of this study was to evaluate the effect of addition to the feed of a prebiotic or an organic acid on the prevalence of ExPEC-associated virulence genes and antimicrobial resistance (AMR) genes and the association between these genes in E. coli of the intestinal microflora of healthy chickens. Caecal contents from 29-day-old chickens having received one of these feed ingredients in comparison to a control group were examined for the presence of virulence genes iucD, tsh, and papC and AMR genes blaTEM, blaSHV, tetA, tetC, blaCMY-2, aadA1, and aac3 by PCR. The prevalence of iucD was significantly higher in the control group than in the prebiotic and organic acid groups and prevalence of papC was affected by the use of the organic acid. The prevalence of blaCMY-2-positive E. coli isolates was higher in the control group than the prebiotic or organic acid groups, as demonstrated by Hydrophobic–grid membrane filter (HGMF) DNA probe colony hybridization. In addition, the prevalence of E. coli isolates positive for tetA, blaTEM, aadA1 or tsh was affected by the use of these feed ingredients. Overall, associations between the presence of iucD and tsh, blaTEM and aadA1, and iucD and blaCMY-2 were observed. This study demonstrates that the use of certain feed ingredients could reduce the risk of exposure in a public health perspective.

L’utilisation massive des antibiotiques, depuis les années 50, génère une libération importante de ces molécules dans l’environnement (excrétion via les urines et les fèces) que l’on peut retrouver à des concentrations allant de 1 à 100 ng/L dans les eaux usées urbaines. Parce qu’elle réunit microorganismes résistants et antibiotiques, la station d’épuration d’eaux usées urbaines pourrait être une zone propice au transfert des gènes de résistance. Cependant, avec sa position stratégique à l’interface entre les activités humaines et l’environnement, la station d’épuration pourrait constituer un « rempart » contribuant à limiter leur dissémination dans l’environnement.Les paramètres qui influencent ces transferts dans les stations d’épuration sont encore mal connus, en particulier du fait de limitations méthodologiques. Aussi l’objectif de notre travail était de déterminer les facteurs environnementaux influant sur la stabilité et le transfert d’un élément génétique mobile modèle, le plasmide pB10, dans des communautés bactériennes (biomasses de stations d’épuration et sédiments de rivière) maintenues en microcosmes. Jusqu’à présent, les transferts de gènes de résistance ont été principalement étudiés avec des méthodes reposant sur la culture de microorganismes sur milieux sélectifs, dont nous savons aujourd’hui qu’elles sous-estiment les phénomènes observés. Aussi, nous avons élaboré une approche basée sur la PCR quantitative pour détecter la dissémination d’un ADN mobile modèle amené via une bactérie hôte E. coli DH5α. Les couples amorces/sondes très spécifiques ont pu être élaborés en tirant profit de la structure mosaïque du génome bactérien. L’approche proposée repose sur des mesures comparées du nombre de plasmide pB10 et de son hôte bactérien DH5α au cours du temps, où une augmentation du rapport (pB10/DH5α) implique une dissémination du plasmide vers les bactéries indigènes. Outre l’intérêt du développement méthodologique proposé, cette méthode a permis d’évaluer l’incidence de quelques paramètres environnementaux sur la dissémination d’un ADN au sein de communautés microbiennes complexes. Deux groupes de facteurs ont pu être distingués selon qu’ils influencent la persistance du plasmide pB10 dans les communautés dans son hôte initial (oxygénation/brassage, ajout d’antibiotiques en concentrations sub-inhibitrices comme l’amoxicilline et le sulfaméthoxazole fréquemment retrouvés en station d’épuration) ou/et qu’ils favorisent sa dissémination dans les communautés bactériennes (biofilms, sédiments). Sans induire de transferts génétiques, les antibiotiques testés, même en concentrations sub-létales, pourraient participer à la dissémination de gènes de résistance en favorisant leur persistance / The widespread use of antibiotics since the 50s, generates a significant release of these molecules in the environment (excretion via urine and feces) which can be found at concentrations ranging from 1-100 ng/L in wastewater. Due to the high microbial biomass and the abundance of nutrients, wastewater treatment plants (WWTP) represent a suitable habitat for horizontal gene transfer. Because they occupy a key position between human activities and the environment, WWTP may play a major role in limiting the dissemination of antibiotic resistance genes, therefore contributing to the preservation The parameters which influence these transfers in wastewater treatment plants are still poorly known, especially because of methodological limitations. Therefore the aim of our study was to identify environmental factors affecting the stability and transfer of a mobile genetic element model, the plasmid pB10 in bacterial communities (biomass from wastewater treatment plants and river sediments) maintained in microcosms. So far, the transfer of resistance genes have been studied mainly with methods based on the cultivation of microorganisms on selective media that we know now they underestimate the observed phenomena. Also, an approach based on quantitative PCR was developed for detecting the release of a mobile DNA template from the host bacterium E. coli DH5α. Couples of designed primers/probes were very specific and have been developed by taking advantage of the mosaic structure of the bacterial genome. The proposed approach is based on the over time measurements of the number of plasmids pB10 and its bacterial host DH5α, where an increased ratio (pB10/DH5α) implies a release of the plasmid to the indigenous bacteria. This method was used to assess the impact of some environmental parameters on the release of DNA in complex microbial communities. Two groups of factors could be distinguished according to whether they influence the persistence of plasmid pB10 in communities in microcosms (oxygenation / mixing, addition of antibiotics at sub-inhibitory concentrations as amoxicillin and sulfamethoxazole frequently found in treatment plant) and / or they favor his release in bacterial communities (biofilms, sediments). Without inducing genes transfers, the antibiotics tested, even at sub-lethal concentrations, could participate in the dissemination of resistance genes by facilitating their persistence

Les éléments génétiques mobiles (EGM) sont des structures génétiques fréquemment associées à la dissémination de gènes de résistance aux antibiotiques (GRA). Dans ce travail, nous avons utilisé deux EGM comme « proxies », les intégrons de classe 1 et les plasmides IncP-1, afin de mieux comprendre (i) le devenir possible des GRA une fois relargués dans un écosystème fluvial (l’Orne, France), ainsi que (ii) l’effet des pressions anthropiques sur leur persistance. À partir d'analyses de l'eau des rivières, nous avons pu montrer que les deux EGM ne se comportaient pas de la même manière. L'entrée des intégrons de classe 1 dans le système fluvial semblait être diffuse plutôt que ponctuelle, tandis que l'abondance du plasmide IncP-1 est relativement stable le long de la section de la rivière étudiée (23 km), indiquant ainsi une origine plutôt indigène. Les intrants anthropiques tels que les stations d’épuration des eaux usées ne semblent pas affecter l’abondance des EGM en raison d’un niveau trop élevé de dilution des effluents. Par ailleurs, il est intéressant de noter que les bactéries porteuses d’EGM semblaient être enrichies sur les matières en suspension, susceptibles de servir de véhicule pour amener des communautés de bactéries plus riches en EGM vers les sédiments. L'analyse de deux carottes de sédiment indique clairement que seules les couches supérieures présentent un niveau élevé de bactéries porteuses d’EGM. Ces abondances diminuent dans les couches plus profondes où seules des zones ponctuelles présentent des microréservoirs avec des abondances d’EGM plus élevées. Pour une carotte sédimentaire au moins, nous avons pu montrer que l'abondance relative d’EGM corrèle négativement la présence de polluants tel que le plomb ou certains HAP / Mobile genetic elements (MGEs) are genetic structures frequently associated to the dissemination of antibiotic resistance genes (ARGs). In this work, we used two of them as proxies, class 1 integrons and IncP-1 plasmids, to better understand (i) the possible fate of ARGs once released in a river ecosystem (Orne, France), as well as (ii) the effect of anthropogenic pressures on their persistence. From river water analyses, we could show that the two MGEs do not behave the same way. The entry of class 1 integrons in the river system appeared to be diffuse rather than punctual, while the abundance of IncP-1 plasmid is relatively stable along the river section studied (23 km) thus indicating a rather indigenous origin. Anthropic inputs such as wastewater treatment plant did not seem to affect the abundance of MGEs because a too high level of effluent dilution. Interestingly, MGE-bearing bacteria appeared to be enriched on suspended material, which is likely to serve as a vehicle to drive MGE-richer communities of bacteria toward the sediments. The analysis of two sediment cores clearly indicates that only the top layers displayed an elevated level of MGE-bearing bacteria. These abundances decrease in deeper layers where only localized zones display micro-reservoirs of elevated MGE abundances. For one sediment core at least, we could show that the relative abundance of MGE negatively correlates with pollutants such as lead or certain PAHs

Les Escherichia coli pathogènes de la volaille (APEC) font partie des E. coli extra-intestinaux pathogènes (ExPEC) et seraient un réservoir possible de gènes de virulence et de résistance aux antimicrobiens (RAM) des ExPEC chez l’humain. L’objectif de cette étude était d’évaluer l’effet d’un prébiotique et d’un mélange d’acide organique et d’huiles essentielles encapsulés sur la prévalence des gènes de virulence des ExPEC et de RAM, ainsi que les associations entre ces gènes chez E. coli de l’intestin du poulet sain. Des échantillons de contenus caecaux de poulets de 29 jours d’âge ayant reçu un de ces ingrédients alimentaires comparativement à des témoins ont été analysés pour la présence des gènes de virulence iucD, tsh, papC et des gènes de RAM blaTEM, blaSHV, tetA, tetC, blaCMY-2, aadA1, aac3 par PCR. La prévalence d’iucD était supérieure dans le groupe témoin comparativement aux groupes «prébiotique» et «acide organique» et la prévalence de papC était affectée dans le groupe «acide organique». La prévalence d’isolats d’E.coli positifs pour blaCMY-2 était supérieure dans le groupe témoin comparée aux groupes «prébiotique» et «acide organique», tel que démontré par la technique d’hybridation de l’ADN sur HGMF (Hydrophobic Grid Membrane Filter). De plus, la prévalence des isolats d’E. coli positifs pour tetA, blaTEM, aadA1 ou tsh était affectée par les ingrédients alimentaires. Dans l’ensemble, des associations entre la présence de tsh et iucD, blaTEM et aadA1, et iucD et blaCMY-2 ont été observées. .Cette étude démontre l’utilité de certains ingrédients alimentaires pour dimunier le risque d’exposition en santé publique. / Avian Pathogenic E. coli (APEC) belong to the extra-intestinal pathogenic E. coli (ExPEC) pathotype, and may be a virulence and antimicrobial resistance (AMR) gene reservoir for ExPEC in humans. The aim of this study was to evaluate the effect of addition to the feed of a prebiotic or an organic acid on the prevalence of ExPEC-associated virulence genes and antimicrobial resistance (AMR) genes and the association between these genes in E. coli of the intestinal microflora of healthy chickens. Caecal contents from 29-day-old chickens having received one of these feed ingredients in comparison to a control group were examined for the presence of virulence genes iucD, tsh, and papC and AMR genes blaTEM, blaSHV, tetA, tetC, blaCMY-2, aadA1, and aac3 by PCR. The prevalence of iucD was significantly higher in the control group than in the prebiotic and organic acid groups and prevalence of papC was affected by the use of the organic acid. The prevalence of blaCMY-2-positive E. coli isolates was higher in the control group than the prebiotic or organic acid groups, as demonstrated by Hydrophobic–grid membrane filter (HGMF) DNA probe colony hybridization. In addition, the prevalence of E. coli isolates positive for tetA, blaTEM, aadA1 or tsh was affected by the use of these feed ingredients. Overall, associations between the presence of iucD and tsh, blaTEM and aadA1, and iucD and blaCMY-2 were observed. This study demonstrates that the use of certain feed ingredients could reduce the risk of exposure in a public health perspective.