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  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Medical microbiology. ; Molecular microbiology -- Methodology. ; Molecular microbiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (2214 pages)
    Edition: 2nd ed.
    ISBN: 9780123977632
    DDC: 616.9041
    Language: English
    Note: e9780123977632v1 -- Front Cover -- Molecular Medical Microbiology, Volume 1 -- Copyright Page -- Contents -- List of Contributors -- Preface -- Preface to the First Edition -- 1 Molecular Medical Microbiology - The Expanding Concept -- A Brief History -- Molecular Medical Microbiology -- References -- 1 Bacterial Structure -- 2 Bacterial Ultrastructure -- General Morphology -- Surface Appendages -- Flagella -- Pili and Fimbriae -- Glycocalyx -- Capsules -- S-layers -- Cell Wall -- Gram-Negative Cell Walls -- Outer Membrane -- Periplasm and Peptidoglycan Gel -- Gram-Positive Cell Walls -- Peptidoglycan Layer and Periplasmic Gel -- Cell Wall Growth -- Cytoplasmic Membrane -- Nucleoid -- Cytoplasmic Inclusions -- Non-Membrane Inclusions -- Volutin Granules -- Polysaccharide Granules -- Non-Unit Membrane Inclusions -- Carboxysomes -- Lipid Bodies -- Gas Vesicles -- Photosynthetic Systems -- Cell Division -- Bacterial Conjugation -- Bacterial Sporulation -- Bacterial Germination -- Bacterial Biofilms -- Microscopy and Microbiology -- Acknowledgements -- References -- 3 Bacterial Capsules -- Introduction -- Chemistry of Capsules -- Primary Structures -- Secondary Structures -- Other Properties of CPSs -- Genetics of Capsular Biosynthesis -- Gram-Negative Bacteria -- Gram-Positive Bacteria -- Biosynthesis of Capsules -- Wzy-Dependent Polymerization -- ABC Transporter-Dependent Polymerization -- Synthase-Dependent Polymerization -- Attachment of Bacterial Capsules to the Cell Surface -- Regulation of Capsular Synthesis -- Modulation at the DNA Level -- Modulation at the Transcriptional Level -- Biological Functions of Capsules -- Capsules as a Virulence Factor -- Capsules as an Immune Evasion Factor -- Immunogenicity of CPSs as Vaccine Antigens -- Acknowledgements -- References -- 4 Genetics and Biosynthesis of Lipopolysaccharide -- Overview. , Classical Pathway of Lipid A-Kdo2 Biosynthesis -- Biosynthesis of Lipid IVA -- LpxA -- LpxC -- LpxD -- LpxBH -- LpxK -- Incorporation of Kdo Residues -- Late Acyltransferases -- Biosynthesis and Assembly of the Core Oligosaccharide -- Kdo and Ko -- Heptoses -- Isomerization -- Phosphorylation -- Phosphatase Reaction -- Synthesis of Nucleotide-Activated Heptose -- ADP-L-glycero-D-manno-Heptose-6-Epimerase -- Glycosyltransferases -- Enzymes Involved in the Completion of the Inner Core -- Assembly of the Outer Core -- Remodelling of the Lipid A-Inner Core Oligosaccharide -- Modification of the Lipid A Phosphate Groups -- Removal of Phosphate Groups -- Covalent Modifications of Phosphates -- Modification of Lipid A Acyl Chains -- Kdo Modifications -- Heptose Modifications -- Biosynthesis and Assembly of OAg -- Initiation -- Polyisoprenyl-Phosphate N-Acetylaminosugar-1-Phosphate Transferases -- Polyisoprenyl-Phosphate Hexose-1-Phosphate Transferases -- Assembly of OAg -- Wzy-Dependent O Antigen Assembly Pathway -- Und-PP-O Antigen Translocation -- Polymerization and Chain Length Regulation -- ABC Transporter-Dependent Pathway -- Synthase-Mediated Pathway -- O Antigen Ligation -- Synthesis and Recycling of Und-PP -- Export of LPS to the Outer Membrane -- Lipid A-Core Export Across the Inner Membrane -- Transport of LPS Across the Periplasm to the Cell Surface -- Acknowledgements -- References -- 5 Teichoic Acids, Lipoteichoic Acids and Other Secondary Cell Wall and Membrane Polysaccharides of Gram-Positive Bacteria -- Structure of Wall Teichoic Acids and their Attachment to the Cell Wall -- Structure and Properties of Lipoteichoic Acids -- The Cellular Roles of Teichoic Acids -- The Biological Activities of Wall Teichoic Acids -- Biological Activities of Lipoteichoic Acids -- Adhesion -- Cytokine Induction -- Nitric Oxide Induction. , Soluble Teichoic Acids In Vivo -- Genetics and Regulation of Anionic Polymer Synthesis -- Acknowledgement -- References -- 6 Peptidoglycan -- Introduction -- The Basic Chemical Structure of Peptidoglycan -- The Glycan Strands in Peptidoglycan -- The Stem Peptides in Peptidoglycan -- Peptide Cross-Links -- Variation of the Fine Structure -- Biophysical Properties of Peptidoglycan -- Thickness of Peptidoglycan -- Elasticity of Sacculi -- Pores in the Sacculus -- Architecture of Peptidoglycan -- Peptidoglycan Biosynthesis and Modifications -- Cytoplasmic Steps to UDP-MurNAc Pentapeptide -- Synthesis of the Lipid-Linked Precursor -- Variation in Lipid II Structure -- Peptidoglycan Synthases -- Peptidoglycan Hydrolases -- Secondary Modifications in the Peptidoglycan Structure -- Covalent Attachment of Secondary Cell Wall Polymers to Peptidoglycan -- Covalent Attachment of Proteins to Peptidoglycan -- Peptidoglycan Synthesis During the Cell Cycle -- Peptidoglycan Synthesis Complexes Active in Cell Elongation and Division -- Molecular Mechanism of Peptidoglycan Growth: The 3-for-1 Growth Model -- Regulation of Peptidoglycan Growth from the Inside and Outside -- Acknowledgements -- References -- 7 Flagella -- Flagellar Function -- Rate of Rotation -- Tumbling -- Energy Source -- Flagellar Structure -- Filament -- Flagellin (Hag or FliC) -- Phase Variation -- Filament Structure -- Filament Helicity -- Polymorphism -- Calladine Model -- Flagella Family -- Hook -- Universal Joint -- Hook Length Control -- Hook Protein -- Hook-Associated Proteins -- Basal Body -- The LP Ring Complex -- Rod -- The MS Ring Complex -- The C Ring -- C Rod -- Chaperones -- The Mot Proteins -- Assembly System of Flagella -- Morphogenesis -- Distal Growth -- Cap Proteins -- Export Apparatus -- Type III Secretion System -- Flil ATPase Activity -- Switching of the Export Gate. , Morphological Pathway -- In the Cytoplasm -- In the Periplasmic Space -- Outside the Cell -- Origin of Flagella -- Type III Secretion System -- F0F1-ATPase -- Conclusion -- Acknowledgement -- References -- 8 Pili and Fimbriae of Gram-Negative Bacteria -- Introduction -- Chaperone-Usher Pathway Pili -- CUP Pilus Architecture -- Subunit Structure -- Assembly Proteins and Mechanisms -- Periplasmic Chaperones -- The Chaperone Necessity -- Conserved Chaperone Surfaces and Donor Strand Complementation -- Donor Strand Exchange -- Ushers -- Functions of the Usher Domains in Pilus Assembly -- Usher Selectivity and Potential Binding Surfaces -- Current Model of Chaperone-Usher Pilus Biogenesis at the Usher -- Structural Insights into the Growing Pilus -- Pore-Gating Mechanisms of Usher -- Alternative Chaperone-Usher Pathways -- Diversity of CUP Systems in Disease -- Different Pilus Systems Involved in Adhesion and Disease -- Curli: Extracellular Nucleation/Precipitation Pathway -- Interfering With the Pilus -- References -- 9 Endospores, Sporulation and Germination -- Endospore Structure and Resistance -- Endospore Formation -- Endospore Germination -- Endospore Germination as a Therapeutic Target -- Endospore Detection -- Endospore-Based Technology -- Endospore-Borne Diseases -- Anthrax -- Bacillus cereus Syndromes -- Tetanus -- Botulism -- Clostridium sordellii and Toxic Shock Syndrome -- Clostridium difficile Infections (CDI) -- Clostridium perfringens Infections -- Opportunistic Infections -- Acknowledgements -- References -- 2 Bacterial Cell Function -- 10 Bacterial Growth, Culturability and Viability -- Introduction -- Bacterial Growth -- Patterns of Growth and Sources of Information -- Molecular Information Related to Bacterial Growth -- Ribosomal RNA -- Chromosome Replication -- Cell Division -- Global Regulatory Proteins -- Growth and Stasis. , Exponential Phase -- Exponential Phase Inocula: A Key Resource in Bacteriology -- Stress Responses -- Stationary Phase -- Dormancy and Sporulation -- Exit from Dormant or Stationary Cellular States and Re-entry into Growth -- Asymmetric Cell Division -- Culturability and Viability -- Culturability -- 'As Yet Uncultured' (AYU) Bacteria -- Cells of Culturable Organisms That Are Not Recovered in Culture -- Viability -- The VBNC Controversy -- Conclusions -- References -- 11 Bacterial Energy Metabolism -- Introduction to Energy Metabolism -- Scope of Chapter -- Chemiosmosis -- ATPase -- Na+-ATPase -- Fermentation -- Fermentations of Sugars and Polysaccharides -- Fermentation Pathways -- Ethanol Fermentations -- Lactate Fermentations -- Mixed Acid Fermentations -- Butyrate Metabolism in the Human Gut -- Utilization of Complex Carbohydrates -- Starch Utilization -- Xylan Utilization -- Cellulose Degradation -- Aerobic Respiration -- Components of Respiratory Chains -- Cytochrome Oxidases -- Cytochrome caa3 Oxidases -- Cytochrome cbb3 Oxidases -- Cytochrome bo3 Oxidase -- Cytochrome bd Oxidase -- Anaerobic Respiration -- Denitrification -- The Reductases Involved in Denitrification -- Nitrate Reductase Nar and Nitrate/Nitrite Transporter NarK -- Nitrite Reductases -- Nitric Oxide Reductases -- Nitrous Oxide Reductases -- Fumarate and Trimethylamine Oxide Reductases -- Regulation of Aerobic and Anaerobic Metabolism -- The Requirement for Regulation of Aerobic and Anaerobic Energy Metabolism -- Basic Principles of Regulatory Systems in Bacteria -- NarX-NarL Two-Component System -- Regulation at the Global Level by a Two-Component System: ArcB-ArcA -- Fnr - a One-Component System -- Diversity of Bacterial Energy Metabolism Regulators -- Regulatory Networks -- Energy Metabolism of Selected Bacterial Pathogens -- Campylobacter jejuni -- Helicobacter pylori. , Neisseria gonorrhoeae and Neisseria meningitidis.
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  • 2
    Online Resource
    Online Resource
    New York, NY :Springer,
    Keywords: Diagnostic microbiology -- Technique. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (553 pages)
    Edition: 1st ed.
    ISBN: 9780387328928
    DDC: 616.9041
    Language: English
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  • 3
    Online Resource
    Online Resource
    Oxford :Elsevier Science & Technology,
    Keywords: Medical microbiology. ; Molecular microbiology. ; Electronic books.
    Description / Table of Contents: The molecular age has brought about dramatic changes in medical microbiology, and great leaps in our understanding of the mechanisms of infectious disease. Molecular Medical Microbiology is the first book to synthesise the many new developments in both molecular and clinical research in a single comprehensive resource. This timely and authoritative 3-volume work is an invaluable reference source of medical bacteriology. Comprising over 100 chapters, organised into 17 major sections, the scope of this impressive work is wide-ranging. Written by experts in the field, chapters include cutting edge information, and clinical overviews for each major bacterial group, in addition to the latest updates on vaccine development, molecular technology and diagnostic technology. * The first comprehensive and accessible reference on Molecular Medical Microbiology * Two color presentation throughout * Full colour plate section * Fully integrated and meticulously organised * In depth discussion of individual pathogenic bacteria in a system-oriented approach * Includes a clinical overview for each major bacterial group * Presents the latest information on vaccine development, molecular technology and diagnostic technology * Extensive indexing and cross-referencing throughout * Over 100 chapters covering all major groups of bacteria * Written by an international panel of authors expert in their respective disciplines * Over 2300 pages in three volumes.
    Type of Medium: Online Resource
    Pages: 1 online resource (775 pages)
    Edition: 1st ed.
    ISBN: 9780080536880
    DDC: 616.01
    Language: English
    Note: Front Cover -- MOLECULAR MEDICAL MICROBIOLOGY -- Copyright Page -- Content -- PART 12: RESPIRATORY INFECTIONS -- Chapter 74. Respiratory Tract Infections: A Clinical Overview -- Chapter 75. Bordetella pertussis -- Chapter 76. Streptococcus pneumoniae -- Chapter 77. Klebsiella pneumoniae -- Chapter 78. Moraxella (Branhamella) catarrhalis -- Chapter 79. Mycoplasma pneumoniae and other Mycoplasmas -- Chapter 80. Coxiella burnetii -- PART 13: MYCOBACTERIAL INFECTIONS -- Chapter 81. Mycobacterium tuberculosis -- Chapter 82. Mycobacterium leprae -- Chapter 83. The Mycobacterium avium- intracellulare Complex -- PART 14: SEXUALLY-TRANSMITTED INFECTIONS -- Chapter 84. Sexually Transmitted and Genital Infections: A Clinical Overview -- Chapter 85. Treponema pallidum -- Chapter 86. Haemophilus ducreyi -- Chapter 87. Chlamydia -- PART 15: ANAEROBIC INFECTIONS -- Chapter 88. Anaerobic Infections: A Clinical Overview -- Chapter 89. Clostridium perfringens: Wound Infections -- Chapter 90. Clostridium tetani -- Chapter 91. Bacteroides -- PART 16: CENTRAL NERVOUS SYSTEM INFECTIONS -- Chapter 92. Central Nervous System Infections: A Clinical Overview -- Chapter 93. Haemophilus influenzae -- PART 17: ANIMAL AND ECTOPARASITIC SOURCE INFECTIONS -- Chapter 94. Brucella -- Chapter 95. Bacillus anthracis and Other Bacillus species -- Chapter 96. Yersinia pestis -- Chapter 97. Borrelia burgdorferi -- Chapter 98. Relapsing Fever Borrelia -- Chapter 99. Bartonella -- Chapter 100. Leptospira -- Chapter 101. Francisella -- Chapter 102. Rickettsia and Orientia -- Chapter 103. Identification of Uncultured Pathogens -- Index -- Colour Plates.
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  • 4
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Medical microbiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (760 pages)
    Edition: 3rd ed.
    ISBN: 9783319951119
    DDC: 616.9041
    Language: English
    Note: Intro -- Preface -- Contents -- Contributors -- Bacterial Identification Based on Universal Gene Amplification and Sequencing -- Introduction -- 16S rDNA Gene Sequencing for Bacterial Identification -- Routine Bacterial Identification in Clinical Laboratories -- Identification of Rare Bacteria and Bacteria with Unusual Phenotypic Profiles -- Identification of Slow-Growing and Uncultivable Bacteria -- Guidelines for Interpretation of 16S rDNA Gene Sequence Results -- Automation of 16S rDNA Gene Sequencing -- Other Gene Targets for Bacterial Identification -- Future Developments and New Technologies for Bacterial Identification -- References -- Molecular Techniques for Blood and Blood Product Screening -- Introduction -- Limitations for Current Technologies Used in Blood Safety -- Application of Advanced Molecular Techniques in Blood Safety Applications -- Major Different Generations of Nucleic Acid Detection Techniques -- Southern Blot Hybridization (1970s) -- Polymerase Chain Reaction (1980s) -- Microarrays (1990s) -- Screening of Donor Blood for Infectious Agents -- Confirmatory Testing of Donor Blood for Infectious Agents -- Application of Nucleic Acid Testing for Infectious Agents -- Hepatitis B Virus -- Hepatitis B Surface Antigen -- Antibodies to the Hepatitis B Core Antigen (Anti-HBc) -- Hepatitis C Virus -- Antibodies to the Hepatitis C Virus (Anti-HCV) -- HCV Confirmatory Tests -- Human Retroviruses -- Antibodies to Human Immunodeficiency Virus: Types 1 and 2 (Anti-HIV-1, -2) -- Antibodies to Human T-Lymphotropic Virus: Types I and II (Anti-HTLV-I, Anti-HTLV-I-II) -- West Nile Virus -- Syphilis -- Other Concerns -- Hepatitis Viruses -- Hepatitis Delta Virus -- TT Virus -- Cytomegalovirus -- Trypanosoma Cruzi -- Malaria -- Variant Creutzfeldt-Jakob Disease -- Dengue Viruses -- Babesia Species -- Chagas' Disease. , Severe Acute Respiratory Syndrome -- Ebola Virus -- Discovery of Unrecognized and Uncharacterized Viral Agents -- Conclusion -- References -- Molecular Diagnostics of Sexually Transmitted Diseases: Bacterial, Trichomonas, and Herpes Simplex Virus Infections -- Introduction -- Chlamydia trachomatis and Neisseria gonorrhoeae -- Signal Amplification -- Strand Displacement Amplification (SDA) -- Transcription-Mediated Amplification (TMA) -- Polymerase Chain Reaction (PCR) -- Treponema Pallidum -- Polymerase Chain Reaction (PCR) -- Haemophilus Ducreyi -- Nucleic Acid Hybridization -- Polymerase Chain Reaction (PCR) -- Mycoplasma and Ureaplasma -- Nucleic Acid Hybridization -- Transcription-Mediated Amplification (TMA) -- Polymerase Chain Reaction -- Trichomonas Vaginalis -- Nucleic Acid Hybridization -- Strand Displacement Amplification (SDA) -- Helicase-Dependent Amplification (HDA) -- Transcription-Mediated Amplification (TMA) -- Polymerase Chain Reaction (PCR) -- Herpes Simplex Virus -- Loop-Mediated Isothermal Amplification (LAMP) -- Strand Displacement Amplification (SDA) -- Polymerase Chain Reaction (PCR) -- Conclusion -- References -- Advances in the Diagnosis of Mycobacterium tuberculosis Infection -- Introduction -- Mechanism of Mycobacterium tuberculosis Infection -- Epidemiology of Tuberculosis -- Epidemiology of Drug-Resistant TB -- Epidemiology of Tuberculosis and HIV Coinfection -- New Compounds in Development -- Cell- and Culture-Based Methods of TB Diagnosis -- Bacilloscopy -- In Vitro Culturing -- BACTEC MGIT960 System -- Molecular Methods -- NAAT (Nucleic Acid Amplification Test) -- Xpert MTB/RIF -- Cobas TaqMan MTB Test -- Abbott RealTime MTB Automated Assay -- BD ProbeTec ET TB System -- Gen-Probe Amplified Mycobacterium tuberculosis Direct Test -- Multiplex Allele-Specific PCR (MAS-PCR) -- PCR-Reverse Blot Hybridization Assay (REBA). , Line Probe Assay -- Genotype MTBDRplus -- Nipro NTM + MDRTB Detection Kit 2 -- Genotype MTBDRsl® V 1.0 and V 2.0 -- GenoQuick® MTB VER 1.0 -- GenoType MTBC VER 1.X -- IS6110-Based Restriction Fragment Length Polymorphism (RFLP) -- Spacer Oligonucleotide Typing (Spoligotyping) -- Mycobacterial Interspersed Repetitive Units-Variable Number Tandem Repeats (MIRU-VNTR) -- Loop-Mediated Isothermal Amplification PCR (LAMP) -- Next-Generation Sequencing -- Whole Genome Sequencing -- Immunological Methods -- Tuberculin Skin Test (TST) -- Interferon-Gamma Release Assay -- Urine Lipoarabinomannan Rapid Test -- Nanodisk-MS Platform -- Microscopy Methods -- Automated Microscopic System, TBDx -- Sputum Smear Light-Emitting Diode Fluorescent Microscopy (LED-FM) -- Concluding Remarks -- References -- Advanced Microbial Strain Subtyping Techniques for Molecular Epidemiology Investigations -- Introduction -- Definition of Molecular Epidemiology -- Genotyping Techniques Used to Conduct Epidemiologic Investigations -- Repetitive Element PCR Genotyping Tests -- Broad-Spectrum Repetitive Element PCR Genotyping Tests -- Limitations of Broad-Spectrum Rep-PCR Genotyping Tests -- Species-Specific Repetitive Element PCR Genotyping Tests -- Pulsed-Field Gel Electrophoresis (PFGE) -- Multilocus Sequence Typing (MLST) -- Whole-Genome Sequence (WGS)-Based Genotyping Tests -- Applications of Genotyping Tests in Epidemiologic Investigations -- Foodborne Diseases -- Tuberculosis -- Healthcare-Associated Infections -- Other Applications of NGS Technology in Epidemiologic Investigations -- Next-Generation Molecular Epidemiology -- References -- Molecular Detection and Characterization of Carbapenem-Resistant Enterobacteriaceae -- Introduction -- Rapid Nucleic Acid-Based Tests -- Conventional PCR Assays -- Real-Time PCR Assays -- In-house Real-Time PCR -- Commercial Real-Time PCRs. , FDA-Approved Real-Time PCR Assays -- Commercially Available Research Use-Only (RUO) Assays -- PCR/ESI-MS -- Loop-Mediated Isothermal Amplification -- Microarray -- Next-Generation Sequencing (NGS) -- Rapid Non-nucleic Acid-Based Tests: MALDI-TOF MS -- Conclusion -- References -- Advanced Methods for Screening and Identification of Methicillin-Resistant Staphylococcus aureus -- Clinical Relevance -- Molecular Epidemiology -- Culture-Based MRSA Detection -- Molecular Methods for MRSA Screening for Surveillance -- Molecular Methods for MRSA Diagnosis in Active Infection -- Detection of MRSA/MSSA in Positive Blood Cultures -- Detection of MRSA in Other Sites -- Direct Detection of MRSA in Blood -- Next-Generation Sequencing (NGS) for Rapid Detection of MRSA -- Conclusions -- References -- Advanced Techniques in Diagnostic Parasitology -- Introduction -- Advanced Technologies in Clinical Parasitology -- Mobile Phone Microscopy -- Digital Image Analysis -- Molecular Diagnostics -- Nucleic Acid Amplification Methods -- Sequencing-Based Approaches -- Proteomics -- Conclusions -- References -- Advanced Methods for Detection of Foodborne Pathogens -- Introduction -- Traditional Methods -- Serotyping -- Enzyme-Linked Immunosorbent Assay (ELISA) -- Bacteriophage -- Polymerase Chain Reaction (PCR), Real-Time PCR, and Reverse Transcriptase PCR -- Microarray -- PFGE -- Whole Genome Sequencing (WGS) -- Metagenomics -- Conclusions -- References -- Technical and Clinical Niches for Point-of-Care Molecular Devices -- Defining POCT: The Debate -- Why Point-of-Care for Clinical Microbiology? -- Technologies for POCT: The Right Technology for the Right Job -- Clinical Situations for Which POCT for Microbiology Are Used -- The Transition of POC to "On-Demand" Hospital Testing -- Infectious Syndromes and Syndromic POC Testing in Clinical Microbiology. , Limitations of Current POC Technologies -- References -- The Human Coronaviruses -- Introduction -- HCoV Genome Organization -- Clinical Symptoms -- Epidemiology -- Human Coronavirus 229E (Group 1/Alpha-Coronavirus) -- Human Coronavirus NL63 (Group 1/Alpha-Coronavirus) -- Human Coronavirus HKU1 (Group 2/Betacoronavirus, Lineage A) -- Human Coronavirus OC43 (Group 2/Betacoronavirus of Lineage A) -- SARS Coronavirus (Group 2 Coronavirus/Betacoronavirus of Lineage B) -- MERS Coronavirus (Group 2/Betacoronavirus, Lineage C) -- Virus Ecology of Human Coronaviruses -- Diagnostics -- Advanced Molecular Techniques Relevant to Human Coronaviruses -- Concluding Remarks -- References -- The Role of the Human Bocavirus (HBoV) in Respiratory Infections -- Introduction -- HBoV Biology -- Epidemiology -- Clinical Features -- Coinfections and Persistence -- Diagnostics -- Advanced Molecular Techniques in HBoV Research and Diagnostics -- Summary and Perspective -- References -- Technical Advances in Veterinary Diagnostic Microbiology -- Introduction -- Identification -- Typing -- Virulence Determination -- Antimicrobial Susceptibility Testing -- Conclusion -- References -- Recent Advances in Veterinary Diagnostic Virology -- Introduction -- Standardization of Diagnostic Assays -- Sample Collection, Transportation, Storage, Enrichment, and Nucleic Acid Preparation -- Sample Collection -- Transportation -- Sample Storage -- Sample Enrichment -- Nucleic Acid Preparation Processes -- Nucleic Acid Amplification-Based Assays -- Quantitative PCR Assays -- Multiplex PCR: Detection of Multiple Viruses, Variants of a Virus, Including Vaccine Strains -- Molecular Tests for the Improved Detection of Food and Waterborne Zoonotic Pathogens -- Proximity Ligation Assays -- Isothermal Nucleic Acid Amplification -- Digital PCR -- Genomic Sequencing and Viral Metagenomics. , xMAP Technology (Suspension Array Technology).
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  • 5
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Medical microbiology. ; Molecular microbiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (3535 pages)
    Edition: 3rd ed.
    ISBN: 9780323899925
    DDC: 616.9041
    Language: English
    Note: 9780323899925v1_WEB -- Front Cover -- Molecular Medical Microbiology -- Copyright Page -- Contents -- List of contributors -- About the editors -- Preface -- 1 Molecular medical microbiology-from bench to bedside -- 1.1 The concept -- 1.2 The evolving concept -- 1.3 From bench to bedside -- References -- 1 Bacterial structure -- 2 Classification of medically important bacteria -- 2.1 Introduction -- 2.2 Basics of bacterial taxonomy -- 2.3 Gram-negative bacteria -- 2.3.1 Enterobacterales -- 2.3.1.1 Enterobacter spp -- 2.3.1.2 Klebsiella spp -- 2.3.1.3 Citrobacter spp -- 2.3.1.4 Escherichia and Shigella -- 2.3.1.5 Pseudomonas spp -- 2.3.1.6 Other glucose nonfermenting gram-negative bacilli -- 2.3.1.7 Acinetobacter spp -- 2.3.1.8 Burkholderia spp -- 2.4 Gram-positive bacteria -- 2.4.1 Mycobacterium -- 2.4.1.1 Staphylococci -- 2.4.1.2 Viridans group streptococci -- 2.5 Conclusion and summary -- References -- 3 Bacterial ultrastructure -- 3.1 Introduction -- 3.2 Overview of bacterial ultrastructures -- 3.3 Surface appendages -- 3.4 Flagella -- 3.5 Pili and fimbriae -- 3.6 Capsules and S-layers -- 3.7 Membrane vesicles -- 3.8 Bacterial cell walls -- 3.9 Gram-negative bacterial cell wall -- 3.10 Gram-positive bacterial cell walls -- 3.11 Mycobacteria -- 3.12 Cell wall-deficient bacteria -- 3.13 Cell walls of Archea and surface appendages -- 3.14 Cytoplasmic membrane -- 3.15 Nucleoid -- 3.16 Bacterial cell division -- 3.17 Cytoplasmic inclusions -- 3.18 Outlook -- References -- 4 Bacterial cell walls: peptidoglycan -- 4.1 Introduction -- 4.2 The basic chemical structure of peptidoglycan -- 4.2.1 The glycan strands in peptidoglycan -- 4.2.2 The stem peptides in peptidoglycan -- 4.2.3 Peptide cross-links -- 4.2.4 Variation of the fine structure -- 4.3 Biophysical properties of peptidoglycan -- 4.3.1 Thickness of peptidoglycan -- 4.3.2 Elasticity of sacculi. , 4.3.3 Pores in the sacculus -- 4.4 Architecture of peptidoglycan -- 4.5 Peptidoglycan biosynthesis and modifications -- 4.5.1 Cytoplasmic steps to UDP-MurNAc pentapeptide -- 4.5.2 Synthesis of the lipid-linked precursor -- 4.5.3 Variation in the lipid II structure -- 4.5.4 Peptidoglycan synthases -- 4.5.5 Peptidoglycan hydrolases -- 4.5.6 Secondary modifications in the peptidoglycan structure -- 4.6 Covalent attachment of secondary cell wall polymers to peptidoglycan -- 4.7 Covalent attachment of proteins to peptidoglycan -- 4.8 Peptidoglycan synthesis during the cell cycle -- 4.8.1 Peptidoglycan synthesis complexes active in cell elongation and division -- 4.8.2 Molecular mechanism of peptidoglycan growth: the 3-for-1 growth model -- 4.8.3 Regulation of peptidoglycan growth from the inside and outside -- Acknowledgments -- References -- 5 Bacterial capsules -- 5.1 Introduction -- 5.2 Chemical and structural properties of the capsules -- 5.2.1 Primary structures -- 5.2.2 Secondary structures -- 5.2.3 Other properties of capsular polysaccharides -- 5.3 Genetics of capsule biosynthesis -- 5.3.1 Gram-negative bacteria -- 5.3.2 Gram-positive bacteria -- 5.4 Biosynthesis of the capsules -- 5.4.1 Wzy-dependent polymerization -- 5.4.2 ABC transporter-dependent polymerization -- 5.4.3 Synthase-dependent polymerization -- 5.4.4 Attachment of bacterial capsules to the cell surface -- 5.5 Regulation of capsule production -- 5.5.1 Modulation at the DNA level -- 5.5.2 Modulation at the transcriptional level -- 5.5.3 Posttranscriptional regulation -- 5.5.4 Metabolic regulation -- 5.6 Biological functions of the capsules -- 5.6.1 Capsules as a virulence factors -- 5.6.2 Capsules as an immune evasion factor -- 5.6.3 Other functions of capsules -- 5.7 The capsules as targets for host immunity and therapeutics. , 5.7.1 Molecular recognition of bacterial capsules by host immune systems -- 5.7.2 Capsules as vaccine antigens -- 5.7.3 Capsules as therapeutic targets -- 5.8 Conclusion and prospect -- Acknowledgments -- References -- 6 Flagella -- 6.1 Flagellar function -- 6.1.1 Estimation of torque -- 6.1.2 Tumbling -- 6.1.3 Energy source -- 6.2 Flagellar structure -- 6.2.1 Filament -- 6.2.1.1 Flagellin (Hag or FliC) -- 6.3 Phase variation -- 6.4 Filament structure -- 6.5 Filament helicity -- 6.5.1 Polymorphism -- 6.6 Calladine model -- 6.6.1 Flagella family -- 6.7 Hook -- 6.7.1 Hook protein -- 6.7.2 Universal joint -- 6.7.3 Hook length control -- 6.8 Hook-associated proteins -- 6.8.1 Basal body -- 6.9 Rod -- 6.10 The LP ring complex -- 6.10.1 The MS ring complex -- 6.11 The cytoplasmic ring -- 6.12 Flagellar protein export apparatus -- 6.13 Chaperones -- 6.14 The Mot proteins -- 6.15 Assembly system of flagella -- 6.15.1 Morphogenesis -- 6.15.2 Distal growth -- 6.15.3 Cap proteins -- 6.16 Protein export apparatus -- 6.16.1 Type 3 secretion system -- 6.16.2 Substrate specificity switching -- 6.17 Morphological pathway -- 6.18 In the cytoplasm -- 6.19 In the periplasmic space -- 6.20 Outside the cell -- 6.21 Origin of flagella -- 6.21.1 Type 3 secretion system -- 6.21.2 FOF1-ATPase -- 6.22 Conclusion -- Acknowledgment -- References -- 7 Bacterial pili and fimbriae -- 7.1 Introduction -- 7.2 Chaperone-usher pathway pilus represented by type I fimbriae and P pilus of Escherichia coli -- 7.2.1 Structure of type I fimbriae and pili -- 7.2.2 Biogenesis model of type I fimbriae and P pili -- 7.2.3 Alternative chaperone/usher pathways -- 7.2.4 Regulation of type I fimbriae and P pili -- 7.2.5 Function of type I fimbriae and pili -- 7.3 Type IV fimbriae and P pilus -- 7.3.1 Structure and biogenesis of type IV fimbriae and pili. , 7.3.2 Regulation of type IV fimbriae and pili -- 7.3.3 Function of type IV fimbriae and pili -- 7.3.4 Type V pilus -- 7.3.5 Structure of type V fimbriae and pili -- 7.3.6 Biogenesis model of type V fimbriae and pili -- 7.3.7 Regulation of type V fimbriae and pili -- 7.3.8 Function of type V fimbriae and pili -- 7.4 Development of novel therapeutics via targeting the pilus biogenesis -- 7.5 Emerging themes and future directions -- Acknowledgment -- References -- 8 Endospores, sporulation, and germination -- 8.1 Introduction -- 8.2 Sporulation as a survival strategy -- 8.3 The endospore structure and resistance -- 8.4 Endospore formation -- 8.5 Spore awakening: germination -- 8.6 Endospore formers pathogens -- 8.7 Pathogenic spore formers control -- 8.8 Endospore detection -- 8.9 Endospore-based technology -- 8.9.1 Probiotics -- 8.9.2 Biocides -- 8.9.3 Biofuels and organic compounds -- 8.9.4 Bioparticles -- References -- 2 Bacterial cell function -- 9 Bacterial growth and cultivation -- 9.1 Introduction -- 9.2 Bacterial growth -- 9.2.1 Patterns of growth and sources of information -- 9.2.2 Molecular information related to bacterial growth -- 9.2.2.1 Ribosomal RNA -- 9.2.2.2 Chromosome replication -- 9.2.2.3 Cell division -- 9.2.2.4 Global regulatory proteins -- 9.2.3 Growth and stasis -- 9.2.3.1 Lag phase -- 9.2.3.2 Exponential phase -- 9.2.3.3 Stationary phase -- 9.2.3.4 Death phase -- 9.2.3.5 Exit from dormant or stationary cellular states and re-entry into growth -- 9.2.4 The Environmental factors that affect bacterial growth -- 9.2.4.1 Temperature -- 9.2.4.2 Oxygen -- 9.2.4.3 pH -- 9.2.4.4 Osmotic pressure -- 9.2.5 Unique growth forms: spores, biofilms, and persisters -- 9.3 Bacterial growth and antibiotics treatment -- 9.4 Bacterial cultivations -- 9.4.1 Historic perspective of cultivation -- 9.4.2 "As-yet-unculturable" bacteria. , 9.4.3 The renaissance of bacterial cultivation -- 9.4.3.1 Cocultivation -- 9.4.3.2 Community cultivation -- 9.4.3.3 In situ cultivation -- 9.4.3.4 Single-cell isolation and cultivation -- 9.4.3.5 High-throughput cultivation -- 9.4.3.6 Culturomics -- 9.5 Final remarks -- Acknowledgments -- References -- 10 Bacterial energy metabolism -- 10.1 Introduction -- 10.1.1 Scope of chapter -- 10.2 Fermentation -- 10.2.1 Bacterial fermentation of sugars -- 10.2.2 Bacterial ethanol fermentation -- 10.2.3 Bacterial lactate fermentation -- 10.2.4 Propionate fermentation -- 10.2.5 Bacterial organic acid fermentation -- 10.2.6 Bacterial biogas fermentation -- 10.2.7 Its role in human health -- 10.2.8 Industrial bacterial fermentation -- 10.2.8.1 Chemiosmosis -- 10.2.9 Complete steps of chemiosmosis and adenosine triphosphate synthesis -- 10.2.10 Adenosine triphosphate synthase -- 10.2.11 Evolutionary significance -- 10.2.11.1 Aerobic respiration -- 10.2.12 Glycolysis -- 10.2.13 Formation of acetyl-CoA -- 10.2.14 Tricarboxylic acid cycle -- 10.2.15 Pyruvate dehydrogenase complex -- 10.2.16 Citrate synthase -- 10.2.17 Isocitrate dehydrogenase -- 10.2.18 α-Ketoglutarate dehydrogenase complex -- 10.2.18.1 Anaerobic respiration -- 10.2.19 Nitrate respiration -- 10.2.20 Denitrification -- 10.2.21 Applications of denitrification -- 10.2.22 Sulfate respiration -- 10.2.23 Fumaric acid respiration -- 10.2.23.1 Metabolism of complex carbohydrates -- 10.2.24 Starch metabolism -- 10.2.25 Cellulose degradation -- 10.2.26 Lignin degradation -- 10.2.27 Xylan degradation -- 10.2.27.1 Energy metabolism in selected bacteria -- 10.2.28 Obligate aerobes -- 10.2.29 Obligate anaerobes -- 10.2.30 Facultative anaerobes -- 10.2.31 Microaerophile -- References -- 11 Biofilms, quorum sensing, and crosstalk -- 11.1 Communal behavior of bacteria -- 11.2 A conceptual overview of quorum sensing. , 11.3 Quorum signals and circuits.
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  • 6
    Online Resource
    Online Resource
    New York, NY :Springer,
    Keywords: Diagnostic microbiology -- Technique. ; Electronic books.
    Description / Table of Contents: This newly updated edition of the well informed guide covers the more advanced and less cumbersome methods of analysis that embattled hospital microbiology labs must adopt to replace the slow and cumbersome culture-based assays of pathogenic microorganisms.
    Type of Medium: Online Resource
    Pages: 1 online resource (942 pages)
    Edition: 2nd ed.
    ISBN: 9781461439707
    Language: English
    Note: Intro -- Advanced Techniquesin Diagnostic Microbiology -- Preface -- Contents -- Contributors -- Part I: Methods -- Chapter 1: Automated Blood Cultures -- Introduction -- Principles -- Automated Culturing Systems -- Blood Culture and CMBCS for Mycobacteria -- Concluding Remarks -- References -- Chapter 2: Breath Tests for Detection of Helicobacter pylori and Aspergillus fumigatus -- Introduction -- Helicobacter pylori -- Aspergillus spp. -- Conventional Diagnostic Tests -- Detection of H. pylori -- Detection of Aspergillus spp. -- Breath Tests -- Introduction -- Sample Collection -- Urea Breath Test for H. pylori -- Breath Test for Aspergillosis -- Conclusions -- References -- Chapter 3: Rapid Antigen Tests -- Introduction -- Principles of the Techniques -- Agglutination -- Immuno uorescence -- Enzyme Immunoassay -- Chemiluminescent Methods -- Lateral Flow Immunochromatography and Fluoroimmunoassay -- Characteristics of the Techniques -- Applications of the Techniques -- Bacteria -- Fungi -- Parasites -- Viruses -- References -- Chapter 4: Antibody Detection: Principles and Applications -- Introduction -- Principles and Characteristics of Techniques -- Colorimetric or Chromogenic Substrate -- Radioimmunoassay -- Chemiluminescence-Immunoassay -- Electrochemiluminescent -- Fluorescent Immunoassays -- Multi-Analyte Pro le Technology -- Contrast of These Techniques -- Application of the Techniques in the Diagnostic Microbiology -- Clinical Applications -- Automation -- Summary -- References -- Chapter 5: Cytometry-Based Antimicrobial Resistance Techniques -- Introduction -- Flow Cytometry Setup -- Antimicrobial Resistance Measurements -- Assay Turnaround Time -- Comparator Methods -- Flow Cytometry Challenges -- Conclusions and Future Prospects -- References -- Chapter 6: Biochemical Pro le-Based Microbial Identi cation Systems. , Introduction -- Conventional Microbial Identi cation Systems -- Single Enzyme Rapid Tests -- Catalase Test -- Oxidase Test -- Spot Indole Test -- Slide Coagulase Test -- Microdase -- Bile Solubility Test -- PYR -- Leucine Aminopeptidase Test -- MUG Test -- Indoxyl Butyrate Disk -- Chromogenic Enzyme Substrate Test -- Gonocheck II -- Bacticard Neisseria -- Hippurate -- Lysostaphin -- CLO Test -- Overnight Biochemical Tests -- Tube Coagulase Test -- DNA Hydrolysis -- Vancomycin Disk Test -- Bacitracin Inhibition Test (Taxo A Disk) -- Bacitracin and STX Susceptibility Test -- Taxo P Disks (Optochin) -- CAMP Test -- Reverse CAMP Test -- Bile Esculin Agar Slant -- 6.5 % Salt Broth -- Indole Test -- Nitrite Test -- ALA ( Haemophilus in uenzae Porphyrin Test) -- Motility Indole Lysine Sul de (MILS) Medium -- O -Nitrophenyl-b- d -Galactopyranoside Test -- Methyl Red Test -- Voges-Proskauer Test -- Pseudosel Agar Slant -- Urea Agar Slant -- Citrate Agar Slant -- Cetrimide Agar -- Gelatin -- Acetate Utilization -- Lead Acetate for Hydrogen Sul de Detection -- Lysine Iron Agar -- Triple Sugar Iron Agar Slant -- Phenylalanine Deaminase -- Decarboxylase (Moeller's Method) -- OF Glucose Medium -- OF Sugars -- Commercial Microbial Identi cation System -- API Identi cation System -- API Gram-Negative Identi cation -- API Gram-Positive Identi cation -- API Anaerobe Identi cation -- BBL™ Crystal™ Identi cation System -- BBL Phoenix Identi cation and Susceptibility System -- VITEK and VITEK 2 Identi cation System -- MicroScan WalkAway -- Sensititre ® Microbiology Systems -- MIDI Sherlock -- BioLog ID System -- References -- Chapter 7: Infectious Disease Biomarkers: Non-Antibody-Based Host Responses -- Introduction -- Procalcitonin -- The Roles of PCT and Other Biomarkers in Sepsis -- The Roles of PCT in Sepsis -- The Roles of CRP in Sepsis. , The Roles of CRP and PCT in Infectious States Other than Sepsis -- The Roles of Miscellaneous and Novel Biomarkers in Infectious States -- Serum Amyloid A -- Lipopolysaccharide-Binding Protein -- Coagulation Markers -- Angiopoietins -- Neopterin -- Toll-Like Receptor-2 -- Triggering Receptor Expressed on Myeloid Cells-1 -- Soluble Urokinase-Type Plasminogen Activator Receptor -- Soluble Receptor for Advanced Glycation End Products -- CD64 -- HLA-DR -- Presepsin -- Cytokines -- Proadrenomedullin -- Alpha-1 Antitrypsin and Other Hepatitis Biomarkers -- Gelsolin -- Interferon-Gamma-Inducible Protein-10 -- Neutrophil Distribution Width -- Regulatory T Lymphocytes (Treg) -- Summary of Miscellaneous Biomarkers -- Newer Platforms for Measurement of Biomarkers -- Conclusions and Future Directions -- References -- Chapter 8: Functional Assessment of Microbial and Viral Infections by Real-Time Cellular Analysis System -- Introduction -- RTCA and Its Principle of Detection Using Impedance Microelectrode Sensor Arrays -- Analysis of Host Cell Responses to Bacterial Infections on RTCA System -- Detection of Clostridium dif cile Toxin -- Detection of Clostridium botulinum Toxin -- Detection of Meningococcal Infection -- Virus-Induced CPE and Neutralizing Antibody Detection on RTCA System -- West Nile Virus and St. Louis Encephalitis Virus CEP and Neutralizing Antibody Detection -- In uenza Virus and Neutralizing Antibody Detection -- Hand-Foot-Mouth Virus Detection -- Helminth Motility and Egg Hatching Activity on RTCA System -- Host Immune Function Assessment on RTCA: Nature Killer Cells and T Cells -- Natural Killer Cell Function Assessment -- T Cell Surface Receptor Detection -- Perspectives -- References -- Chapter 9: Cellular Fatty Acid-Based Microbial Identi cation and Antimicrobial Susceptibility Testing -- Introduction. , General Principles and Methods of Cellular Fatty Acid Analysis -- CFA Testing Platforms for Bacterial Identi cation -- Library Expansion and Fatty Acid Polymorphisms -- Identi cation of Agents of Bioterrorism and Other Select Agents -- Mycolic Acid Analysis for Identi cation of Mycobacteria -- HPLC and Susceptibility Testing -- Advantages and Disadvantages of Fatty Acid-Based Identi cation Methods -- References -- Chapter 10: MALDI-TOF Mass Spectrometry-Based Microbial Identi cation -- Introduction -- General Remarks on Mass Spectrometry -- MALDI and ESI MS -- Species Identi cation Using MALDI-TOF MS -- Limitations and Shortcomings of MALDI-TOF MS -- Further Challenges Approaching MALDI-TOF MS for Species Diagnosis -- Conclusion -- References -- Chapter 11: Nucleic Acid Extraction Techniques -- Introduction -- Nucleic Acid Extraction Techniques -- Cesium Chloride/Ethidium Bromide Density Gradient Centrifugation -- Phenol-Chloroform Extraction -- Solid-Phase Extraction -- Magnetic Bead Method -- Applications to Clinical Specimens -- Cellular Component -- Serum, Plasma, and Whole Blood -- In uence of Speci c Pathogen -- PCR Inhibitors -- Measurement of DNA Quality -- Comparison of Nucleic Acid Extraction Methods -- Manual Method -- Automatic Methods -- Conclusion -- References -- Chapter 12: Nonampli ed Probe-Based Microbial Detection and Identi cation -- Introduction -- Probe-Based Assay Design -- Target Selection -- Probe Selection -- Nucleic Acid Hybridization Formats -- Clinical Application of Nonampli ed Probe-Based Assays -- Gen-Probe Nucleic Acid Detection Methods -- Hybrid Capture Assay -- Af rm DNA Assay -- Line Probe Assay -- In Situ Hybridization Assays -- Peptide Nucleic Acid FISH Assays -- Future Considerations -- References -- Chapter 13: Molecular Typing Techniques: State of the Art -- Introduction. , What Does "State of the Art" Mean? -- The Ultimate Foundation for Epidemiological Comparison: The Bacterial Genome -- Methods with Electrophoretic Output -- Pulsed-Field Gel Electrophoresis -- Optical Mapping -- PCR-Based -- Repetitive Sequence-Based PCR -- PCR Ribotyping -- Staphylococcal Cassette Chromosome mec Typing -- Multiple-Locus VNTR Analysis -- DNA Sequence-Based Methods -- Single-Locus Sequence Typing -- S. aureus Protein A Typing -- Strepcococcus pyogenes M Protein ( emm) Typing -- mec -Associated Direct Repeat Unit Typing -- Multi-Locus Sequence Typing -- Other Multi-Locus Approaches: Hybridization-Based Typing -- Whole Genome Sequence Typing -- Non-Sequence-Based Whole Cell Typing -- Strain Typing in the Context of the Epidemiological Window -- References -- Chapter 14: An Introduction to In Vitro Nucleic Acid Ampli cation Techniques -- Target Ampli cation Systems -- Probe Ampli cation Systems -- Signal Ampli cation Systems -- References -- Chapter 15: PCR and Its Variations -- PCR: The Quintessential Nucleic Acid Ampli cation Method -- Principles of PCR -- Enzymatic Ampli cation of DNA: Components of the PCR -- The PCR Cycle -- Denaturation -- Annealing -- Extension -- Detection and Analysis of the PCR Product -- Conventional PCR -- Real-Time PCR -- PCR Variations -- Allele-Speci c PCR -- Hot-Start PCR -- Touchdown PCR -- Degenerate PCR -- Nested and Heminested PCR -- Multiplex PCR -- Reverse Transcription-PCR -- Quantitative PCR -- Real-Time PCR -- PCR-Based Strain Typing Techniques -- Arbitrarily Primed-PCR and Random Ampli ed Polymorphic DNA -- Ampli ed Fragment-Length Polymorphism -- ERIC-, Rep-, BOX-, IS-, and VNTR-PCR -- Appendix -- Primer Design Resources -- References -- Chapter 16: Non-PCR Target Ampli cation Techniques -- Introduction -- Isothermal Transcription-Based Ampli cation. , Strand Displacement Ampli cation.
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