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Current and Emerging Technologies for the Diagnosis of Microbial Infections / edited by Andew Sails and Yi-Wei Tang.

Contributor(s): Series: Methods in microbiology ; v. 42.Publisher: London : Academic Press, 2015Description: 1 online resource (xix, 613 pages) : illustrationsContent type:
  • text
Media type:
  • computer
Carrier type:
  • online resource
ISBN:
  • 0128033312
  • 9780128033319
Subject(s): Genre/Form: Additional physical formats: Print version:: Current and emerging technologies for the diagnosis of microbial infections.LOC classification:
  • RC113.3 .C87 2015eb
NLM classification:
  • WC 100
Online resources:
Contents:
Front Cover; Current and Emerging Technologies for the Diagnosis of Microbial Infections; Copyright; Contents; Contributors; Preface; Chapter 1: Total Laboratory Automation in Clinical Bacteriology; 1. Clinical Bacteriology and Automation: background; 2. Specimen Collection: liquid Microbiology; 3. Pre-analytical Automation; 4. Pre-analytical Bacteriology Specimen Plating Instruments; 4.1. Isoplater; 4.2. Innova; 4.3. BD Kiestra InoqulA+; 4.4. Previ Isola; 4.5. Copan WASP; 4.6. Prelude: i2a; 4.7. deltalab AUTOPLAK; 5. Digital Plate Reading; 6. TLA Systems; 6.1. BD Kiestra; 6.2. Copan WASPLab.
6.3. i2a: ECITALS7. Change Management: A Holistic Approach to Automation in Bacteriology; References; Chapter 2: MALDI-TOF Mass Spectrometry for Microorganism Identification; 1. Introduction; 1.1. MALDI-TOF MS: Principles and Processes; 1.2. Commercially Available MALDI-TOF MS Platforms; 1.3. Factors Influencing the Performance of MALDI-TOF MS; 2. Microbial Identification by MALDI-TOF MS; 2.1. Comparison of MALDI-TOF MS and Conventional Methods for the Identification of Routine Isolates; 2.2. Comparison of Commercially Available MALDI-TOF MS Systems.
2.3. Laboratory Cost Savings Associated with Using MALDI-TOF MS for Isolate Identification3. Performance of MALDI-TOF MS for the Identification of Routine Clinical Isolates; 3.1. Identification of Gram-Positive Bacteria; 3.2. Identification of Gram-Negative Bacteria; 3.3. Identification of Anaerobes; 3.4. Identification of Mycobacteria; 3.5. Identification of Yeast; 3.6. Identification of Filamentous Fungi; 3.7. Identification of Select Agents; 4. Direct Identification from Clinical Specimens; 4.1. Identification of Microorganisms Directly from Positive Blood Cultures.
4.2. Identification of Bacteria Directly from Urine Specimens4.3. Identification of Bacteria Directly from Cerebrospinal Fluid; Limitations and Conclusions; References; Chapter 3: POC Tests in Microbial Diagnostics: Current Status; 1. Introduction; 2. The Current Utilisation of Infectious Diseases POC Testing; 2.1. Viral Respiratory Infections; 2.2. HIV/AIDS, Tuberculosis, Sexually Transmitted Infections; 2.3. Diarrhoea and Gastrointestinal Diseases; 2.4. Surveillance, Prevention, and Diagnosis of Healthcare-Acquired Infections.
2.5. Anticipated POC Testing Advances Through Biomarkers or Improved Technologies2.5.1. Sepsis; 2.5.2. Technological advances in rapid immunochromatographic platforms; 2.5.3. Paper-based diagnostics; 2.6. Patient Empowerment Is Key for Any POC Test; 3. The Road to POC Molecular Diagnostics Is Paved with Good Intentions and Technologies; 3.1. Near-POC Testing; 3.2. Isothermal Amplification Technologies; 3.3. Integrated Molecular Diagnostics Platforms; 3.3.1. The GeneXpert® platform; 3.3.2. The GenePOC platform; Conclusions; Acknowledgements; References.
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Text in English.

Print version record.

Front Cover; Current and Emerging Technologies for the Diagnosis of Microbial Infections; Copyright; Contents; Contributors; Preface; Chapter 1: Total Laboratory Automation in Clinical Bacteriology; 1. Clinical Bacteriology and Automation: background; 2. Specimen Collection: liquid Microbiology; 3. Pre-analytical Automation; 4. Pre-analytical Bacteriology Specimen Plating Instruments; 4.1. Isoplater; 4.2. Innova; 4.3. BD Kiestra InoqulA+; 4.4. Previ Isola; 4.5. Copan WASP; 4.6. Prelude: i2a; 4.7. deltalab AUTOPLAK; 5. Digital Plate Reading; 6. TLA Systems; 6.1. BD Kiestra; 6.2. Copan WASPLab.

6.3. i2a: ECITALS7. Change Management: A Holistic Approach to Automation in Bacteriology; References; Chapter 2: MALDI-TOF Mass Spectrometry for Microorganism Identification; 1. Introduction; 1.1. MALDI-TOF MS: Principles and Processes; 1.2. Commercially Available MALDI-TOF MS Platforms; 1.3. Factors Influencing the Performance of MALDI-TOF MS; 2. Microbial Identification by MALDI-TOF MS; 2.1. Comparison of MALDI-TOF MS and Conventional Methods for the Identification of Routine Isolates; 2.2. Comparison of Commercially Available MALDI-TOF MS Systems.

2.3. Laboratory Cost Savings Associated with Using MALDI-TOF MS for Isolate Identification3. Performance of MALDI-TOF MS for the Identification of Routine Clinical Isolates; 3.1. Identification of Gram-Positive Bacteria; 3.2. Identification of Gram-Negative Bacteria; 3.3. Identification of Anaerobes; 3.4. Identification of Mycobacteria; 3.5. Identification of Yeast; 3.6. Identification of Filamentous Fungi; 3.7. Identification of Select Agents; 4. Direct Identification from Clinical Specimens; 4.1. Identification of Microorganisms Directly from Positive Blood Cultures.

4.2. Identification of Bacteria Directly from Urine Specimens4.3. Identification of Bacteria Directly from Cerebrospinal Fluid; Limitations and Conclusions; References; Chapter 3: POC Tests in Microbial Diagnostics: Current Status; 1. Introduction; 2. The Current Utilisation of Infectious Diseases POC Testing; 2.1. Viral Respiratory Infections; 2.2. HIV/AIDS, Tuberculosis, Sexually Transmitted Infections; 2.3. Diarrhoea and Gastrointestinal Diseases; 2.4. Surveillance, Prevention, and Diagnosis of Healthcare-Acquired Infections.

2.5. Anticipated POC Testing Advances Through Biomarkers or Improved Technologies2.5.1. Sepsis; 2.5.2. Technological advances in rapid immunochromatographic platforms; 2.5.3. Paper-based diagnostics; 2.6. Patient Empowerment Is Key for Any POC Test; 3. The Road to POC Molecular Diagnostics Is Paved with Good Intentions and Technologies; 3.1. Near-POC Testing; 3.2. Isothermal Amplification Technologies; 3.3. Integrated Molecular Diagnostics Platforms; 3.3.1. The GeneXpert® platform; 3.3.2. The GenePOC platform; Conclusions; Acknowledgements; References.

Includes bibliographical references and index.

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