
Application of DNA Microarray Technology for Wastewater Analysis
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Content
- Cover
- Copyright
- Acknowledgments
- Abstracts and Benefits
- Table of Contents
- List of Tables
- List of Figures
- List of Acronyms
- Executive Summary
- Chapter 1.0: Literature Review on Pollution Indicators
- 1.1 Water Quality Indicators: Potential and Weaknesses
- 1.1.1 General Fecal Pollution Indicators
- 1.1.2 Usefulness of Indicators in Bacterial Source Tracking (BST)
- 1.1.3 Conclusions about Fecal Indicators
- 1.2 Waterborne Pathogens
- 1.3 Molecular Methods Used for Fecal Pollution Monitoring
- 1.3.1 Polymerase Chain Reaction (PCR)
- 1.4 DNA Microarrays
- 1.4.1 General Features
- 1.4.2 Sample Preparation Prior to Microarray Analysis
- 1.4.3 Current Status of Microarrays in Microbial Detection
- 1.4.4 Applications Relevant to Wastewater Analysis
- Chapter 2.0: Objectives of the Original Proposal
- 2.1 Background
- 2.2 Objectives
- Chapter 3.0: Sample Collection and Development of A DNA Extraction Method Suitable for Microarray Analysis
- 3.1 Description of the Sample Collection Procedures
- 3.1.1 Human Wastewater Samples
- 3.1.2 Animal Contaminated Water Samples
- 3.2 Bacterial Cell Counts
- 3.3 DNA Extraction Procedure Comparison
- 3.3.1 Choice of DNA Extraction Technique for Microarray Hybridization Tests
- 3.4 Conclusions about the DNA Extraction Procedure for Microarray Hybridization Tests
- Chapter 4.0: Development and Evaluation of Microarrays for Pathogen Detection
- 4.1 Total Escherichia coli DNA on 50-mer Oligonucleotide Versus Amplicon Arrays
- 4.1.1 Design
- 4.1.2 DNA Labeling Procedure
- 4.1.3 Microarray Hybridization
- 4.1.4 Results: Prototype 1.0 Detection Limit
- 4.1.5 Conclusions
- 4.2 16S rDNA and cpn60 Escherichia coli Amplicons on 70-mer Oligonucleotide Versus Amplicon Arrays
- 4.2.1 Design
- 4.2.2 Amplicon Generation and Labeling Procedure
- 4.2.3 Microarray Hybridization
- 4.2.4 Results: Microarray Prototype 2.0 Detection Limit
- 4.2.5 Conclusions
- 4.3 16S rDNA, cpn60, and wecE Amplicons on 18- to 26-mer Oligonucleotide Arrays with Short Amino-Linkers
- 4.3.1 Design
- 4.3.2 Amplicon Generation and Labeling Procedure
- 4.3.3 Microarray Hybridization
- 4.4 Conclusions
- 4.5 Final Prototype: 16S rDNA, cpn60, and wecE Amplicons on 18- to 26-mer Oligonucleotide Arrays
- 4.5.1 Design
- 4.5.2 Amplicon Generation and Labeling Procedure
- 4.5.3 Hybridization Procedure
- 4.5.4 Results: Microarray Prototype 4.0 Detection Limit
- 4.5.5 Conclusions
- Chapter 5.0: Development and Evaluation of Microarrays for Bacterial Source Tracking
- 5.1.1 Design
- 5.1.2 Slide Preparation
- 5.1.3 Amplification and Amplicon Labeling Procedures
- 5.1.4 Hybridization Procedure
- 5.1.5 BST Microarray Prototype Specificity Validation Using Pure Cultures
- 5.1.6 Results: Hybridization with Human Source Wastewater
- 5.1.7 Results: Hybridization with Animal Manure or Soil Runoff after Manure Application
- 5.1.8 Results: Hybridization with Animal Feces
- 5.1.9 Conclusions
- Chapter 6.0: Considerations on the Usability of DNA Microarrays in Wastewater Analysis
- 6.1 Time Required for Analysis
- 6.2 Estimated Cost of Analysis
- 6.3 Reproducibility
- 6.4 General Suitability in Wastewater Analysis
- Appendix A: Standard Wastewater Sample Concentration Procedure
- Appendix B: Standard Procedure for Heterotrophic Bacterial Counts on PCA Agar
- Appendix C: Standard Escherichia coli Count on mTEC Agar Procedure
- Appendix D: Standard Wastewater DNA Extraction Procedure
- Appendix E: Standard PCR Amplification Procedures
- Appendix F: Standard Labeling Procedure
- Appendix G: Standard Microarray Hybridization Procedure
- References
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