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Iran University of Medical Sciences

Dr. Dehghan

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microbiology rapid tests medical microbiology diagnostic methods

Summary

This document discusses rapid microbiological methods (RMMs) and their applications in various industries and medical microbiology laboratory settings. It covers different types of RMMs, their detection principles, and time to results.,

Full Transcript

Rapid Tests in Microbiology By: Dr. Dehghan Iran University of Medical Sciences Introduction Microbiology's Role: Transversal to various fields including pharmaceutical, biopharmaceutical, cosmetic, food, and water industries. Traditional Methods: Labor-intensiv...

Rapid Tests in Microbiology By: Dr. Dehghan Iran University of Medical Sciences Introduction Microbiology's Role: Transversal to various fields including pharmaceutical, biopharmaceutical, cosmetic, food, and water industries. Traditional Methods: Labor-intensive, culture-based methods with long result times (e.g., 14 days for sterility tests). Need for Rapid Methods: Faster results for quicker decision-making and process control. What are Rapid Microbiological Methods (RMM)? Definition: Analytical microbiological methods delivering faster results than traditional methods. Advantages: Automation potential, increased sensitivity and accuracy, reduced time to results. Classification of RMM By Determination Type: Qualitative: Presence or absence of viable bacteria. Quantitative: Enumeration of microorganisms. Identification: Classification of taxonomic groups. By Detection Principle: Detection of growth (e.g., CO2 production). Direct analysis (e.g., whole bacteria detection). Analysis of cell components (e.g., ATP, nucleic acids). Overview of Rapid Microbiological Methods (RMM) RMM Determination Detection method Detection Principle Time to Result Detects ATP Qualitative, bioluminescence Direct analysis 1 hour Bioluminescence Quantitative from ATP-luciferase reaction Detects Autofluorescence Quantitative Direct analysis fluorescence of 3 hours filtered colonies Detects bacterial reactions to Biochemical AssaysIdentification Direct analysis Time varies biochemical substances Detection of Indicates microbial Carbon Dioxide 24-72 hours for Qualitative growth via CO2 (CO2) Detection growth sterility tests production Overview of Rapid Microbiological Methods (RMM) RMM Determination Detection method Detection Principle Time to Result Direct Uses double Epifluorescent Qualitative, staining to Direct analysis Less than 1 hour Filter Technique Quantitative distinguish viable (DEFT) cells Direct Laser Laser scans filter Quantitative Direct analysis A few days Scanning surface Compares fatty acid Fatty Acid Identification Cell components composition to a 24-48 hours Profiling database Direct analysis Detects Qualitative, Flow Cytometry fluorophore-marked A few minutes Quantitative bacteria Fourier-Transform Direct analysis Infrared absorption Identification 6-8 hours Infrared (FTIR) analysis of bacteria Overview of Rapid Microbiological Methods (RMM) RMM Determination Detection method Detection Principle Time to Result Qualitative, Genotypic Nucleic acid Quantitative, Cell components Less than 2 hours Methods amplification Identification Detection of Measures gas Headspace Qualitative production/consump 72 hours Pressure growth tion Enzyme-Linked Immunosorbent Immunological Identification Cell components Assay (ELISA) and Time varies Methods Immunomagnetic Separation (IMS) Direct analysis Cell Ion profile Less than 40 Mass Spectrometry Identification components comparison minutes Overview of Rapid Microbiological Methods (RMM) RMM Determination Detection method Detection Principle Time to Result Detection of Measures heat from Microcalorimetry Qualitative 24-72 hours growth microbial activity Detects Phage-based Qualitative, Direct analysis protein/intracellular 48 hours Methods Identification Cell components material post-phage infection Solid Phase Qualitative, Detects fluorophore- Direct analysis 3 hours Cytometry Quantitative marked bacteria Measures optical Turbidimetry Qualitative Direct analysis Time varies density changes Applications of RMM Pharmaceutical Industry: Environmental monitoring, bioburden control, sterility testing. Food Industry: Detection and quantification of microorganisms in food products. Water Industry: Monitoring of microbial contamination in water supplies. Medical microbiology laboratory: used in medical microbiology laboratories to enhance the speed, sensitivity, and accuracy of pathogen detection and identification. RMMs and their applications in medical microbiology 1. Polymerase Chain Reaction (PCR) and Real-Time PCR (qPCR)  Application: Detection of bacterial, viral, and fungal pathogens.  Advantages: High sensitivity and specificity, rapid results (within hours), ability to quantify pathogen load.  Example: Diagnosis of viral infections like HIV, influenza, and COVID-19. 2. Next-Generation Sequencing (NGS)  Application: Comprehensive identification of microbial communities, detection of antibiotic resistance genes.  Advantages: High-throughput, detailed genetic information, useful in outbreak investigations.  Example: Sequencing of bacterial genomes to identify outbreak strains and track transmission. RMMs and their applications in medical microbiology 3. Matrix-Assisted Laser Desorption/Ionization-Time of Flight Mass Spectrometry (MALDI-TOF MS)  Application: Rapid identification of bacteria and fungi directly from clinical specimens or cultures.  Advantages: Fast (minutes), accurate, cost-effective for routine use.  Example: Identification of bacterial species in bloodstream infections. 4. Automated Blood Culture Systems  Application: Detection of bacterial and fungal growth in blood samples.  Advantages: Continuous monitoring, faster time to detection, reduced hands-on time.  Example: BacT/ALERT and BACTEC systems for sepsis diagnosis. RMMs and their applications in medical microbiology 5. Flow Cytometry  Application: Quantification and characterization of bacteria, detection of antibiotic resistance.  Advantages: Rapid, can analyze multiple parameters simultaneously.  Example: Detection of bacterial contamination in blood products. 6. Biosensors  Application: Detection of specific pathogens or toxins.  Advantages: Real-time detection, high sensitivity.  Example: Point-of-care testing for pathogens like MRSA. RMMs and their applications in medical microbiology 7. Immunological Methods (e.g., ELISA, Lateral Flow Assays)  Application: Detection of specific antigens or antibodies.  Advantages: Rapid, easy to use, suitable for point-of-care testing.  Example: Rapid diagnostic tests for diseases like malaria, dengue, and COVID-19. 8. Microfluidics and Lab-on-a-Chip Technologies  Application: Miniaturized platforms for pathogen detection and analysis.  Advantages: Low sample volume, fast processing, integration of multiple steps.  Example: Point-of-care diagnostic devices for infectious diseases. RMMs and their applications in medical microbiology 9. Automated Microscopy and Image Analysis  Application: Automated analysis of stained slides for pathogen detection.  Advantages: High throughput, objective results, reduced labor.  Example: Automated identification of tuberculosis bacteria in sputum samples. 10. Metabolomic and Proteomic Methods  Application: Analysis of microbial metabolites and proteins for identification and characterization.  Advantages: Detailed biochemical profiling, useful for understanding pathogen physiology.  Example: Identification of bacterial species based on metabolic profiles. Implementation Considerations  Integration with Clinical Workflows: Ensuring that RMMs can be seamlessly integrated into existing laboratory workflows and electronic health records (EHRs).  Cost and Accessibility: Balancing the cost of implementing RMMs with the benefits of faster and more accurate diagnostics.  Training and Expertise: Providing adequate training for laboratory personnel to use and interpret RMMs.  Regulatory and Quality Assurance: Adhering to regulatory standards and implementing rigorous quality control measures to ensure the reliability of RMM results.

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