Phage Therapy. Part A /
Clasificación: | Libro Electrónico |
---|---|
Otros Autores: | |
Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
Cambridge, MA :
Academic Press,
2023.
|
Colección: | Progress in molecular biology and translational science ;
200. |
Temas: | |
Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Front Cover
- Title page
- Copyright
- Contents
- Contributors
- Praface
- Chapter One: Exploring the potential of phage and their applications
- 1 Introduction
- 2 Life cycle of phage
- 3 Applications of phage
- 3.1 Phage for detection of bacterial pathogens
- 3.2 Phage therapy for bacterial infections
- 3.3 Phage in food industry
- 3.4 Phage clinical trails
- 3.5 Directed evolution and optimization of phage for enhanced therapy
- 4 Conclusion and future remarks
- Acknowledgements
- References
- Chapter Two: Isolation, screening and characterization of phageIsolation, screening and characterization of phage
- 1 Introduction
- 2 Become a phage-hunter: phage isolation
- 2.1 Sources for phage isolation
- 2.2 General scheme for phage isolation, with emphasis on jumbo phage
- 2.3 Biased and unbiased isolation methods in phage isolation with highlight on advanced techniques
- 2.4 Purification and amplification
- 3 Phage characterization
- 3.1 Phage screening
- 3.1.1 Host range
- 3.1.1.1 Solid-based methods
- 3.1.1.1.1 Spot test for determination of phage host range.
- 3.1.1.1.2 Relative efficiency of platting
- 3.1.1.2 Liquid-based methods
- 3.1.1.2.1 Microtiter plate host range assay.
- 3.1.1.2.2 High-throughput turbidimetric test.
- 3.1.2 Phage adsorption
- 3.2 Morphological characterization
- 3.2.1 Phage plaque morphology
- 3.2.2 Virion structure morphology
- 3.2.2.1 Transmission electron microscopy
- 3.2.2.2 Scanning electron microscopy
- 3.2.2.3 Atomic force microscopy
- 3.2.2.4 Cryo-electron microscopy
- 3.3 Biological characterization
- 3.3.1 One-step growth curve
- 3.3.2 Physical and chemical stability
- 3.3.2.1 Temperature stability
- 3.3.2.2 UV stability
- 3.3.2.3 Chemical stability
- 3.3.2.3.1 pH stability.
- 3.3.2.3.2 Salinity and ions
- 4 Genomic characterization.
- 4.1 Phage genome from extraction to annotation
- 4.2 Further screening of the phage genome
- 4.2.1 Safety
- 4.2.2 Temperate lifecycle gene-markers
- 4.2.3 tRNA and ncRNA genes
- 4.2.4 Holin-lysin lysis system
- 4.2.5 Polysaccharide depolymerases
- 4.2.6 Phage packaging mechanism
- 4.2.7 Regulator elements: promoters and terminators
- 4.3 Phage genome visualization and comparison
- 4.4 Phage phylogenetic analysis
- 4.4.1 At family level
- 4.4.2 At genus and species levels
- 5 Conclusion and future remarks
- References
- Further reading
- Chapter Three: Synthetic phage and its application in phage therapy
- 1 Introduction
- 2 Structure
- 2.1 Composition
- 2.2 Morphology
- 3 Classification
- 4 Development of synthetic phage
- 4.1 Homological remerging (HR)
- 4.2 Genetic data rebooting
- 5 Synthetic phages for substance redevelop
- 5.1 Chemical engineering cue in synthetic phage
- 5.2 Physical science cue control by synthetic phage
- 5.3 Multifunctional phage materials
- 6 Synthetic phage library
- 6.1 Reconstruction of synthetic phage
- 6.2 Genetic engineering of synthetic phage
- 7 Production synthetic phage parts from phage genomes
- 7.1 Phage RNA polymerases
- 7.2 Transcriptional regulators
- 7.3 Integrases
- 8 Application
- 8.1 Vaccine
- 8.2 Phage therapy (PT)
- 8.3 Selected protists Cells
- 8.4 Phage display
- 8.5 Nanomaterials
- 8.6 Phages developed through genetic engineering to promote tissue formation
- 8.7 Biofilms
- 8.8 Phage-based affection
- 8.9 Phage in the diagnostic of cancer
- 8.10 Multidrug resistant
- 8.11 Phage-based drug delivery
- 8.12 Phage as anti-infective
- 9 Conflicts in phage remedy of synthetic phage
- 10 Conclusions
- 11 Future with synthetic phage
- References
- Chapter Four: Phage engineering for development of diagnostic tools
- 1 Introduction.
- 3.1.4 Phage LUZ242s Igy peptide and DNA gyrase
- 3.1.5 Summary table
- 3.2 Interactions in Gram-positive bacteria
- 4 Phage lysis of the host
- 5 Modeling for phage therapy
- 5.1 In vitro cell line models
- 5.1.1 Cytotoxicity and pro-inflammatory characteristics
- 5.1.2 Mechanisms of interaction with tissues
- 5.2 Animal models
- 5.2.1 Invertebrate models
- 5.2.2 Vertebrate models
- 5.2.3 Immunogenicity and toxicity in animal models
- 5.3 Clinical trials in humans
- 6 Conclusions
- References
- Chapter Seven: Phage and phage cocktails formulationsPhage and phage cocktails formulations
- 1 Introduction
- 2 Formulation of phage cocktails
- 3 Applications of phage cocktails
- 3.1 Application of phages in oral infections
- 3.2 Application of phages in urinary tract infections
- 3.3 Application of phages in biofilms treatment
- 4 Conclusion and future perspectives
- Conflict of interest
- References
- Chapter Eight: Phages for treatment of Escherichia coli infectionsPhages for treatment of Escherichia coli infections
- 1 Introduction
- 2 T4-related phages for E. coli therapy
- 2.1 T4-related viruses infecting pathogenic E. coli strains
- 2.2 Characterisation of T4-related viruses for phage therapy
- 2.3 Isolation of bacteriophages from environmental sources
- 2.4 Large-scale phage preparation
- 2.5 Pharmaceutical formulation for phages
- 2.6 Evaluation of T4-related bacteriophage preparations in animal models
- 2.7 Case reports and clinical trials
- 2.8 Phage therapy against pathogenic E. coli: current state and outlook for the future.
- 3 Phage therapy of E. coli O157:H7
- 3.1 Introduction to E. coli O157:H7
- 3.2 General considerations for phages against E. coli O157:H7
- 3.3 Bacteriophages in food processing
- 3.4 Phage therapy in animals affected by E. coli O157:H7
- 4 Phage therapy
- HGT implications.
- 5 Conclusions
- References
- Chapter Nine: Phages for treatment of Klebsiella pneumoniae infections Phages for treatment of Klebsiella pneumoniae infections
- 1 Introduction
- 2 Know your enemy: K. pneumoniae
- 3 Limitations of antibiotic therapy for K. pneumoniae infections
- 4 Phage therapy of K. pneumoniae
- 4.1 Isolation of K. pneumoniae phages
- 4.2 Morphotypes and taxonomy K. pneumoniae phages
- 4.3 Forms of therapeutic K. pneumoniae phages
- 4.4 In vitro characterization of K. pneumoniae phages
- 4.5 In vivo experiments of phage therapy against K. pneumoniae
- 4.6 Clinical studies on cases treated with Klebsiella phages
- 4.7 Challenges in phage therapy for K. pneumoniae
- 5 Conclusion
- References
- Chapter Ten: Phages for treatment of Salmonella spp infection
- 1 Introduction
- 2 Conventional treatment vs phage therapy
- 3 Rapid screening and detection methods associated with bacteriophage for Salmonella
- 4 Phages as a tool against Salmonella infections
- 4.1 Salmonella phages
- 4.2 Commercially available phage products and regulatory status
- 4.3 Salmonella endolysins
- 5 Challenges in using phages
- 6 Future prospects
- 7 Conclusion
- Acknowledgments
- References
- Chapter Eleven: Phages for treatment of Staphylococcus aureus infection
- 1 Introduction
- 2 Identification, morphology and genomic characteristics of phages infecting S. aureus
- 2.1 Organization of S. aureus phages genomes
- 2.2 Structure and genome of phage K
- 2.3 Novel Staphylococcal phages with unique morphology and broad host range
- 2.3.1 Phage JD219
- 2.3.2 Phages V1SA19, V1SA20, and V1SA22
- 3 Phage cocktail development against S. aureus
- 3.1 APTC-C-SA01: A novel bacteriophage cocktail for S. aureus and MRSA Biofilms
- 3.2 Phage cocktail AB-SA01 targeting planktonic and biofilm cultures of S. aureus.