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The title of the book ""The Universe of Escherichia coli"" aims to present and emphasize the huge diversity of this bacterial species and our efforts to prevent the E. coli infections. As it is part of the gut microbiota, E. coli is a well-known commensal species, and probiotic E. coli strains are successfully used for improving host's health. Also many ""workhorse"" E. coli strain exist that are employed in laboratory and biotechnology settings. But certain E. coli strains can cause intestinal and also extraintestinal infections at many anatomical sites. Therefore many efforts are undertaken to prevent E. coli infections, among them food safety, vaccines, but also new antimicrobial agents are searched for.
Escherichia coli. --- E. coli (Bacterium) --- Escherichia --- Life Sciences --- Microbiology --- Genetics and Molecular Biology --- Biochemistry --- Bacteriology
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Shiga toxin-producing Escherichia coli (STEC) is an important foodborne pathogen associated with both outbreaks and sporadic cases of human disease, ranging from uncomplicated diarrhoea to haemorrhagic colitis (HC) and haemolytic uraemic syndrome (HUS). STEC affects children, elderly and immuno-compromised patients. STEC is capable of producing Shiga toxin type 1 (Stx1), type 2 (Stx2) or both, encoded by stx1 and stx2 genes, respectively. These strains are likely to produce putative accessory virulence factors such as intimin (encoded by eae), an enterohaemolysin (EhxA) and an autoagglutinating protein commonly associated with eae-negative strains (Saa), both encoded by an enterohaemorrhagic plasmid. Several studies have confirmed that cattle are the principal reservoir of STEC (O157 and non-O157:H7 serotypes) and many of these serotypes have been involved in HUS and HC outbreaks in other countries. Transmission of STEC to humans occurs through the consumption of undercooked meat, vegetables and water contaminated by faeces of carriers and by person-to-person contact. Diagnostic methods have evolved to avoid selective diagnostics, currently using molecular techniques for typing and subtyping of strains. Control is still a challenge, although there are animal vaccines directed against the serotype O157:H7.
Escherichia coli. --- E. coli (Bacterium) --- Escherichia --- environment --- Cattle --- STEC --- Virulence Factors --- Food
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This book illuminates the various aspects of Escherichia coli, including its pathotypes, virulence factors, and antimicrobial resistance. It also presents new insights into the scientometric analysis of the E. coli knowledge landscape, novel molecular diagnostic platforms, novel antimicrobial agents, and E. coli-based DNA amplification-expression technology for the automatic assembly of concatemeric open reading frames and proteins.
Escherichia coli. --- Escherichia coli --- Genetics. --- Bacterial genetics --- E. coli (Bacterium) --- Escherichia
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Although Escherichia coli is probably one off the best characterized organisms, very little is known about the mechanisms governing the biogenesis of its outer membrane and preserving its integrity during the bacterial cell cycle. For example, we have only a very limited knowledge of the way in which the various components of this membrane, namely phospholipids, lipopolysaccharides and β barrel proteins, are carried across the periplasm and then inserted in the membrane after synthesis in the cytoplasm or in the inner membrane.
My host team focuses on coming to a better understanding of the mechanisms permitting the folding and insertion of β barrel proteins in the outer membrane. In addition to the fundamental interest of studying these mechanisms, this research should lead to the development of new antibiotics that are effective against Gram negative bacteria. Indeed, the physicochemical properties of the outer membrane make these bacteria very resistant to many bacterial agents.
The β barrel proteins of the E. coli cell envelope are synthesized in the cytoplasm, and then carried through the inner membrane as unfolded polypeptides. They must then cross the periplasm before reaching the outer membrane as unfolded polypeptides. They must then cross the periplasm before reaching the outer membrane where they are assembled. According to the current model, β barrel proteins are escorted in the periplasm by chaperones that are present in this compartment. The precise role of these chaperones has however not been characterized.
FkpA is one of the four periplasmic chaperones identified so far. Its structure and in vitro chaperone activity have been well studied. However, we know nothing about FkpA’s in vivo role and about the nature of its substrates. The purpose of my work was therefore to characterize the function of this chaperone in the periplasm and to identify its physiological substrates.
To do this, I used a multidisciplinary approach. First, I carried out microbiological studies to characterize the phenotype of different bacterial strains lacking FkpA. The results of these studies have shown that strains lacking both DegP, the primary periplasmic protease, and FkpA were particularly sensitive to elevated temperatures. I’ve also shown that FkpA interacts with several β barrel proteins when purified from strains lacking one of the chaperones involved in the folding of these proteins. Finally, the in vitro tests that I carried out suggest that FkpA is capable of protecting these β barrel proteins from aggregation, without however participating actively in their folding. Put together, my results suggest that FkpA plays a role in the quality control of secreted proteins. Bien qu’Escherichia coli soit probablement l’un des organismes les mieux caractérisés, les mécanismes permettant la biogenèse de sa membrane externe et le maintien de l’intégrité de celle-ci durant le cycle cellulaire bactérien restent très peu connus. Par exemple, nous n’avons qu’une connaissance très partielle de la façon avec laquelle les différents constituants de cette membrane, à savoir les phospholipides, les lipopolysaccharides et les protéines en tonneau β, sont transportés au travers du périplasme puis insérés au sein de celle-ci après avoir été synthétisés dans le cytoplasme ou au niveau de la membrane interne.
Mon laboratoire d’accueil s’intéresse particulièrement aux mécanismes qui permettent le repliement et l’insertion des protéines en tonneau β dans la membrane externe. Outre l’intérêt fondamental que présente l’étude de ces mécanismes, ces recherches devraient ouvrir la voie au développement de nouveaux antibiotiques efficaces contre les bactéries à Gram négatif. En effet, les propriétés physicochimiques de leur membrane externe les rendent peu perméable à de nombreux bactéricides.
Les protéines en tonneau β de l’enveloppe d’E. coli sont synthétisées dans le cytoplasme, puis transportées sous forme non repliée au travers de la membrane interne. Elles doivent ensuite traverser le périplasme avant de gagner la membrane externe où elles sont assemblées et acquièrent leur conformation native. Selon le modèle actuel, les protéines en tonneau β seraient escortées au travers du périplasme par des chaperonnes présentes dans ce compartiment. Le rôle précis de ces dernières n’a cependant pas été caractérisé.
FkpA est lune des quatre chaperonnes périplasmiques identifiées jusqu’à présent. Sa structure et son activité chaperonne in vitro ont bien été étudiées. Cependant, on ne connaît rien du rôle que FkpA joue in vitro et de la nature de ses substrats. L’objectif de mon mémoire était donc de caractériser la fonction exercée par cette chaperonne au sein du périplasme et d’en identifier les substrats. L’objectif de mon mémoire était donc de caractériser la fonction exercée par cette chaperonne au sein du périplasme et d’en identifier les substrats physiologiques.
Pour ce faire, j’ai utilisé une approche multidisciplinaire. Tout d’abord, j’ai réalisé des études microbiologiques afin de caractériser le phénotype de différentes souches bactériennes dépourvues de FkpA. Les résultats de ces études ont fait apparaître que les souches dépourvues de FkpA et de la principale protéase périplasmique, DegP, étaient particulièrement sensibles à un stress thermique. J’ai aussi montré que FkpA interagit avec plusieurs protéines en tonneau β en purifiant la protéine. Pour finir, les tests in vitro réalisés suggèrent que FkpA est capable de protéger ces protéines en tonneau β de l’agrégation, sans toutefois participer activement à leur repliement. Mis ensemble, mes résultats suggèrent que FkpA joue un rôle dans le « contrôle qualité » des protéines sécrétées
Gram-Negative Bacterial Infections --- Cell Membrane --- Biogenesis --- FkpA protein, E coli --- Escherichia coli Proteins --- Periplasm
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Molecular biology --- General microbiology --- Escherichia coli --- Salmonella typhimurium --- Escherichia Coli --- Salmonella Typhimurium --- Escherichia coli. --- Salmonella typhimurium. --- #abib:almm --- Bacillus typhimurium --- Salmonella --- E. coli (Bacterium) --- Escherichia --- Salmonella typhimurium LT2 --- Diffusely Adherent E. coli --- Enteroaggregative E. coli --- Enteroinvasive E. coli --- Enteroinvasive Escherichia coli --- Alkalescens-Dispar Group --- Diffusely Adherent Escherichia coli --- E coli --- EAggEC --- Enteroaggregative Escherichia coli --- Escherichia coli Proteins --- Escherichia Coli. --- Salmonella Typhimurium. --- Biology --- Microbiology & Immunology --- Health & Biological Sciences --- Salmonella tyhimurmium --- Escherichian coli --- Monograph --- Bacillus coli --- Bacterium coli --- Bacterium coli commune --- Enterococcus coli
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Gene Expression Regulation, Bacterial. --- Escherichia coli --- 575.1 --- Diffusely Adherent E. coli --- Enteroaggregative E. coli --- Enteroinvasive E. coli --- Enteroinvasive Escherichia coli --- Alkalescens-Dispar Group --- Diffusely Adherent Escherichia coli --- E coli --- EAggEC --- Enteroaggregative Escherichia coli --- Escherichia coli Proteins --- Regulation, Gene Expression, Bacterial --- Bacterial Gene Expression Regulation --- Regulation of Gene Expression, Bacterial --- Heredity. Inheritance --- Escherichia coli. --- 575.1 Heredity. Inheritance --- Molecular biology --- Monera --- Bacillus coli --- Bacterium coli --- Bacterium coli commune --- Enterococcus coli --- Gene Expression Regulation, Bacterial
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The 2e of Escherichia coli is a unique, comprehensive analysis of the biology and molecular mechanisms that enable this ubiquitous organism to thrive. Leading investigators in the field discuss the molecular basis of E. coli pathogenesis followed by chapters on genomics and evolution. Detailed descriptions of distinct strains reveal the molecular pathogenesis of each and the causes of intestinal and extra-intestinal infections in humans. This work concludes with a presentation of virulence factors common to two or more pathotypes. The book is a great resource for references and up-to-date know
Escherichia coli infections. --- Escherichia coli. --- Virulence (Microbiology) --- Microbial virulence --- Pathogenic microorganisms --- E. coli (Bacterium) --- Escherichia --- Colibacillosis --- Gram-negative bacterial infections
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Escherichia coli --- Salmonella typhimurium --- Escherichia Coli --- Salmonella Typhimurium --- Escherichia coli. --- Salmonella typhimurium. --- 579.842.11 --- 579.842.14 --- Diffusely Adherent E. coli --- Enteroaggregative E. coli --- Enteroinvasive E. coli --- Enteroinvasive Escherichia coli --- Alkalescens-Dispar Group --- Diffusely Adherent Escherichia coli --- E coli --- EAggEC --- Enteroaggregative Escherichia coli --- Escherichia coli Proteins --- Salmonella typhimurium LT2 --- Escherichia --- Salmonella. --- 579.842.14 Salmonella. --- 579.842.11 Escherichia --- Bacillus typhimurium --- Salmonella --- E. coli (Bacterium) --- Bacillus coli --- Bacterium coli --- Bacterium coli commune --- Enterococcus coli --- Gene expression. --- Cell Division. --- Cell Division --- Genomic library --- ESCHERICHIA COLI --- SALMONELLA TYPHIMURIUM --- METABOLISM (MICROBIAL) --- MACROMOLECULAR COMPOUNDS --- DNA FORMATION --- CELL STRUCTURE --- LIPIDS --- AMINO ACIDS --- BIOLOGICAL STUDIES
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