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  • 1
    Online Resource
    Online Resource
    Cham : Springer
    Keywords: Medicine ; Biomedicine ; Medicine ; Immunology ; Medical microbiology ; Infectious diseases ; Immunology ; Medical microbiology ; Infectious diseases ; Chlamydia ; Chlamydia
    Description / Table of Contents: The genus Chlamydia encompasses a number of species of obligate intracellular bacteria, including important human pathogens like the most common bacterial agent of sexually transmitted disease. This volume reviews current knowledge of chlamydial biology, covering the unusual structure of the bacteria - which alternate between metabolically almost inactive and fast-dividing forms. It also discusses the ways in which Chlamydia manipulates the host cytoskeleton and subverts the host cell’s defence, and illustrates how genomics have begun to uncover the diversity and complexity of chlamydial strains that look very similar but may cause distinct forms of disease. Further, it describes how techniques are now finally being established that can genetically modify Chlamydia, and discusses why such modification is still very difficult and what progress we can expect. Lastly, it presents our current understanding of chlamydial disease: what do we know about chronic infections, what are the mechanisms of inflammatory damage, and what are the prospects of a vaccine? Written be specialists in these various areas, the book is a valuable work of reference for students and scientists with an interest in the molecular, cellular and immunobiology of these fascinating bacteria
    Type of Medium: Online Resource
    Pages: Online-Ressource (X, 237 p, online resource)
    ISBN: 9783319712321
    Series Statement: Current Topics in Microbiology and Immunology 412
    RVK:
    Language: English
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  • 2
    Keywords: Forschungsbericht ; Pathogener Mikroorganismus ; Antibiotikum ; Arzneimittelresistenz ; Krankenhausaufenthalt ; Screening
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (4 Seiten, 258,62 KB)
    Language: German
    Note: Förderkennzeichen BMBF 031B0077E. - Verbund-Nummer 01166625 , Autor dem Berichtsblatt entnommen , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden
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  • 3
    Keywords: Forschungsbericht
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (9 Seiten, 38,07 KB)
    Language: German
    Note: Förderkennzeichen BMBF 0315837B , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Systemvoraussetzungen: Acrobat reader.
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  • 4
    Keywords: Forschungsbericht
    Type of Medium: Online Resource
    Pages: Online-Ressource (4 S., 18,1 KB)
    Language: German
    Note: Förderkennzeichen BMBF 0313935B. - Verbund-Nr. 01054952 , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Auch als gedr. Ausg. vorhanden , Systemvoraussetzungen: Acrobat reader.
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  • 5
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Emerging infectious diseases. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (243 pages)
    Edition: 1st ed.
    ISBN: 9783319712321
    Series Statement: Current Topics in Microbiology and Immunology Series ; v.412
    Language: English
    Note: Intro -- Preface -- Contents -- 34 Deconstructing the Chlamydial Cell Wall -- Abstract -- 1 Introduction -- 1.1 The Bacterial Cell Wall -- 1.2 Chlamydiae -- 2 On the Traces of PG in Chlamydiae -- 2.1 Early Experiments -- 2.2 Visualize the Invisible-The Discovery of PG Material in Chlamydiae -- 3 Functional and Genomic Studies of the Chlamydial PG Biosynthesis Pathway -- 3.1 Cytoplasmic and Membrane-Bound Steps of Chlamydial PG Biosynthesis -- 3.2 Periplasmic Steps of Chlamydial PG Biosynthesis -- 3.2.1 Penicillin-Binding Proteins -- 3.2.2 Amidase AmiA-A Bifunctional Target Protein of Penicillin -- 3.2.3 "NlpD"-A Septal Lipid II/PG-Binding Hydrolase -- 4 Organization of the Chlamydial Division Septum -- 5 Antichlamydial Activity of Cell Wall Antibiotics-Cellular Effects and Molecular Targets -- 5.1 Beta-Lactam Treatment of Chlamydiae -- 5.2 Beta-Lactamase Inhibitor Clavulanic Acid -- 5.3 Fosfomycin, d-Cycloserine, and Bacitracin -- 6 Role of PG Components in Chlamydial Immune Modulation -- 7 Missing Bricks in the Ring-Future Research and Perspectives -- Acknowledgments -- References -- 12 One Face of Chlamydia trachomatis: The Infectious Elementary Body -- Abstract -- 1 The Infectious Particle: Not so Elementary, My Dear Bedson! -- 1.1 A Morphology Tailored for Specific Needs -- 1.2 Non-dividing, But Not Inactive -- 1.3 A Metabolism Centred on Glucose Catabolism -- 2 From the Generation to the Conversion of EBs: A Chronological Perspective -- 2.1 EB Biogenesis -- 2.2 The Extracellular Episode -- 2.3 The Adhesion Step -- 2.4 The Entry Step -- 2.5 Still Space for Early Effectors -- 2.6 Setting Up the Decor Before Leaving the Stage to the RB -- 3 Conclusion -- Acknowledgments -- References -- 10 Manipulation of the Host Cell Cytoskeleton by Chlamydia -- Abstract -- 1 Cytoskeletal Dynamics in Epithelial Cells -- 1.1 Actin -- 1.2 Microtubules. , 1.3 Intermediate Filaments -- 2 The Host Cell Cytoskeleton and Chlamydia Invasion -- 2.1 Actin Recruitment During Invasion -- 2.2 Signaling to the Actin Remodeling Machinery -- 2.3 Direct Actin Nucleation by TarP -- 2.4 Disassembly of F-Actin at the Sites of Invasion -- 2.5 Microtubule and Chlamydia Invasion -- 2.6 Intermediate Filaments and Chlamydia Invasion -- 3 The Host Cell Cytoskeleton and the Vesicular Interactions and Structural Integrity of the Inclusion -- 3.1 Early Observations of Nascent Inclusion Trafficking to the Microtubule Organizing Center -- 3.2 Molecular Basis for MTOC Transport of Nascent Inclusions -- 3.3 Homotypic Fusion of Chlamydia Inclusions -- 3.4 Post-Translational Modification of Microtubules in Chlamydia-Infected Cells -- 3.5 The Role of Actin and Intermediate Filaments in Inclusion Integrity -- 4 The Host Cell Cytoskeleton and Chlamydia Egress -- 4.1 Chlamydia Egress by Extrusion of Intact Inclusions -- 4.2 The Role of the Chlamydia Plasmid in Extrusion Versus Lysis Decision -- 5 Summary -- References -- 13 Subversion of Cell-Autonomous Host Defense by Chlamydia Infection -- Abstract -- 1 Introduction -- 2 Innate Immunity Against Intracellular Bacteria -- 2.1 The Innate Immune System -- 2.2 Cell-autonomous Immunity -- 3 Subversion of Host Innate Defense by Chlamydia -- 3.1 Interference with IFN-Signaling and Autophagy -- 3.2 Interference with Inflammasome Activation and Inflammation -- 4 Inhibition of Host Cell Death -- 4.1 Manipulation of Survival Signaling Pathways -- 4.2 Enrichment of Anti-apoptotic Proteins -- 4.3 Depletion of P53 -- 5 Concluding Remarks -- References -- 39 The Hidden Genomics of Chlamydia trachomatis -- Abstract -- 1 Introduction -- 2 Next Generation Sequencing Techniques -- 2.1 Culture-Based Versus Culture-Independent Sequencing. , 2.2 Immuno-magnetic Separation and Multiple Displacement Amplification (IMS-MDA) -- 2.3 Target DNA Pull-Down -- 3 C. trachomatis in the Genomic Era: Genome Content -- 3.1 Comparative Genomics and Genome Synteny -- 4 The Link Between Tryptophan and Ocular Isolates -- 5 Species Phylogeny -- 6 Recombination -- 6.1 Direct Experimental Evidence of Recombination -- 6.2 Understanding C. Trachomatis Population Structure -- 6.3 Lineage-Specific Patterns of Recombination -- 7 Global and Temporal Population Structure of C. trachomatis -- 8 The Plasmid -- 9 The Swedish New Variant -- 10 Antimicrobial Resistance in C. trachomatis -- 11 Chlamydia trachomatis in the Field -- References -- 76 Advances and Obstacles in the Genetic Dissection of Chlamydial Virulence -- Abstract -- 1 Introduction -- 2 Chlamydial Genomes Are Malleable -- 3 Moving Genes Between and into Chlamydial Genomes with Recombination and Lateral Gene Transfer -- 4 Transformation of Chlamydia with Plasmid Shuttle Vectors -- 5 Applications of the Plasmid as a Shuttle Vector -- 6 Reverse Genetic Dissection of Chlamydia Plasmids -- 7 Genetic Manipulation of Chlamydial Chromosomes -- 8 Forward Genetic Analysis of Chlamydial Genomes -- 9 Overview and Future Perspectives -- Acknowledgements -- References -- 15 Chlamydia trachomatis as the Cause of Infectious Infertility: Acute, Repetitive or Persistent Long-Term Infection? -- Abstract -- 1 Introduction -- 2 Acute Infections with C. trachomatis -- 2.1 Prevalence, Incidence, Screening and Treatment of Acute Chlamydial Infection -- 2.2 What Are the Risk Factors? -- 2.3 Paradigms for the Development of Infectious Infertility -- 3 Multiple Infections -- 3.1 Is Reinfection a Common Problem? -- 3.2 Are Women More Susceptible to C. trachomatis upon Reinfection? -- 3.3 What Is the Risk for TFI After Chlamydial Infection and Is It Increased by Multiple Infections?. , 4 Chronic Infections -- 4.1 The Induction of Aberrant RBs In Vitro -- 4.1.1 Iron Depletion -- 4.1.2 IFN-γ -- 4.1.3 Antibiotics -- 4.1.4 Coinfection with Herpes Simplex Virus -- 4.2 What Would Be the Clinical Relevance, if We Could Translate the In Vitro Findings to the In Vivo Situation? -- 4.3 What Evidence Do We Have for Finding Persistence In Vivo? -- 4.4 Is the Induction of Chlamydial Aberrant RBs a Necessary Survival Mechanism or Merely a Stress Response to Unfavourable Circumstances? -- 4.5 Can a Human Fallopian Tube Cell Model Further Elucidate the Connection Between In Vivo and In Vitro? -- 5 Chronic Colonization of the Gastrointestinal Tract -- 5.1 How Does Intestinal Colonization Happen and How Often Does It Affect Humans? -- 5.2 What Would Be the Consequences? -- 6 Conclusions -- References -- 18 Immunopathogenesis of Chlamydial Infections -- Abstract -- 1 Introduction -- 2 Diseases Caused by Chlamydia in Humans -- 3 Animal Models of Chlamydial Pathogenesis -- 4 Chlamydial Immunopathogenesis -- 5 Role of Components of Innate Immune System in Chlamydial Pathogenesis -- 6 Role of Components of Adaptive Immune System in Chlamydial Pathogenesis -- 6.1 B Cells -- 6.2 T Helper Cells -- 6.3 Regulatory T Cells -- 6.4 Th 17 Cells -- 6.5 CD8+ T Cells -- 7 Summary -- 8 Outlook for Future -- Acknowledgements -- References -- 6 Chlamydia trachomatis: Protective Adaptive Responses and Prospects for a Vaccine -- Abstract -- 1 Overview -- 2 Obstacles to Vaccine Development -- 3 Immune Responses and Pathogenesis -- 4 Protective Adaptive Responses -- 4.1 CD4 T Cells -- 4.2 Resident Memory CD4 T Cells -- 4.3 CD8 T Cells -- 4.4 B Cells and Antibodies -- 5 Vaccinology -- 5.1 Antigens -- 5.2 Types of Vaccines -- 5.2.1 Live Vaccines -- 5.2.2 Subunits -- 5.2.3 Recombinant Protein -- 5.2.4 DNA Plasmid -- 5.3 Adjuvants -- 5.4 Vaccination Routes. , 6 Future Challenges and Conclusions -- References.
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 211 (2002), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Cell death by apoptosis is a common response to environmental stimuli and a frequent event in a multicellular organism. Not surprisingly, apoptosis is also found in microbial infections where it may contribute to progression and outcome. Perhaps less predictably, a number of bacteria have also been found to alleviate or even to inhibit apoptosis. Today we are at a point where our in some parts detailed knowledge of the molecular pathway to apoptosis allows us to probe situations in biology for the occurrence of apoptosis and to inquire into mechanisms of apoptosis induction and inhibition. In this brief article we will focus on anti-apoptotic activities exhibited by various bacteria. We will attempt to present the current knowledge on how the contact between mammalian and bacterial cell decrees resistance to apoptosis, what the respective contributions of the two partners are and how this interaction relates to the molecular path to apoptosis.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Toll-like receptors (TLRs) are activated by pathogen-associated molecular patterns to induce innate immune responses and production of pro-inflammatory cytokines, interferons and anti-inflammatory cytokines. TLRs activate downstream effectors through adaptors that contain ...
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 1. Over 100 different agents have been shown, under certain circumstances, to cause apoptosis, a form of cell death with characteristic morphology. In most cases, the mechanism of cell death is likely to be the same, as expression of the cell death inhibitory gene bcl-2 can frequently prevent apoptotic changes and/or delay cell death.2. These observations raise the question of how and why cells detect these agents and why they respond by implementing the suicide mechanism that bcl-2 can control. Our hypothesis is that apoptosis is used as an anti-viral strategy, and that cells interpret any metabolic disturbance as evidence of infection by a virus and thereby kill themselves in response to these toxins before they are killed by the action of the toxin itself.3. Experiments on the effect of sodium azide upon growth factor-dependent cells support this idea. Bcl-2 can delay cell death caused by azide, and inhibit apoptotic changes seen by electron microscopy, but cannot prevent the eventual death of the cells.4. These ideas suggest that drugs designed to regulate cell death may be useful for the treatment of ischaemic or neoplastic diseases. For example, human cells may activate a suicide pathway in response to sub-lethal amounts of anoxia following a stroke or heart attack and so blocking apoptosis may be a useful therapy to limit tissue damage. On the other hand, increasing the propensity of cells to activate their physiological cell death mechanisms may enhance the effectiveness of toxins designed to kill tumour cells.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 301 (2000), S. 5-17 
    ISSN: 1432-0878
    Keywords: Apoptosis Morphology Caspases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. The concept of apoptotic cell death as an essential part of the development and life of complex organisms has been devised in different situations and tested from various angles. This review article discusses the morphological changes during death by apoptosis. In cells undergoing apoptosis, an intracellular signalling pathway operates cell autonomously to implement the death and disposal of the cell. The similarity of the biochemical events during apoptosis in different situations is reflected by a high uniformity of morphological changes in many situations of naturally occurring or experimentally induced cell death. The unifying concept of apoptosis has been derived from the observation of this morphological consistency of dying cells almost 30 years ago. Since then, we have learned much about the intracellular signalling in the apoptotic process and the molecular background has been delineated which guides the initiation of the morphological changes. Here, an attempt is made to present the current knowledge about the molecular events in the development of these morphological alterations and to place these changes in the context of apoptotic cell death.
    Type of Medium: Electronic Resource
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