
The Microbiology of Safe Food
Beschreibung
As our methods of food production advance, so too does the need for a fuller understanding of food microbiology and the critical ways in which it influences food safety. The Microbiology of Safe Food satisfies this need, exploring the processes and effects of food microbiology with a detailed, practical approach. Examining both food pathogens and spoilage organisms, microbiologist Stephen J. Forsythe covers topics ranging from hygiene regulations and product testing to microbiological criteria and sampling plans.
This third edition has been thoroughly revised to cater to the food scientists and manufacturers of today, addressing such new areas as:
* Advances in genomic analysis techniques for key organisms, including E. coli, Salmonella, and L. monocytogenes
* Emerging information on high-throughput sequencing and genomic epidemiology based on genomic analysis of isolates
* Recent work on investigations into foodborne infection outbreaks, demonstrating the public health costs of unsafe food production
* Updates to the national and international surveillance systems, including social media
Safe food for consumers is the ultimate goal of food microbiology. To that end, The Microbiology of Safe Food focuses on the real-world applications of the latest science, making it an essential companion for all those studying and working in food safety.
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Inhalt
- Cover
- Title Page
- Contents
- Preface to third edition
- Preface to second edition
- Preface to first edition
- Chapter 1 Foodborne infections
- 1.1 The microbial world and its relationship to food
- 1.2 Origins of safe food production
- 1.3 Overview of foodborne illness
- 1.4 Public perception of safe food
- 1.5 Causes of foodborne illness
- 1.6 Food poisoning due to common food commodities
- 1.6.1 Milk and milk products
- 1.6.2 Meat products
- 1.6.3 Fresh produce
- 1.6.4 Low-water activity (aw) and low-moisture foods
- 1.7 Host-related issues
- 1.8 Hygiene hypothesis
- 1.9 Chronic sequelae following foodborne illness
- 1.10 The size of the foodborne illness problem
- 1.11 The cost of foodborne diseases
- 1.12 Changes in antimicrobial resistance of foodborne pathogens
- 1.12.1 Bacterial antibiotic resistance in agriculture and aquaculture
- 1.12.2 Antibiotics of concern and resistance mechanisms
- 1.12.3 Polymyxin and plasmid-encoded colistin resistance
- 1.12.4 Livestock-associated methicillin-resistant Staphylococcus aureus (LA-MRSA)
- 1.13 Food safety following natural disasters, and conflict
- 1.14 Food microbiology, foodborne diseases and climate change
- Chapter 2 Basic aspects
- 2.1 The human intestinal tract
- 2.2 The normal human intestinal flora
- 2.3 Host resistance to foodborne infections
- 2.4 Bacterial cell structure
- 2.4.1 Morphology
- 2.4.2 Cell membrane structure and the Gram stain
- 2.4.3 Lipopolysaccharide (LPS, O antigen)
- 2.4.4 Flagella (H antigen)
- 2.4.5 Capsule (K and Vi antigen)
- 2.5 Bacterial toxins and other virulence determinants
- 2.5.1 Bacterial endotoxins and exotoxins
- 2.5.2 Pathogenicity islands
- 2.5.3 Bacterial toxins encoded in bacteriophages
- 2.6 Microbial growth cycle
- 2.7 Death kinetics
- 2.7.1 Expressions
- 2.7.2 decimal reduction times (D values) and z values
- 2.8 Factors affecting microbial growth
- 2.8.1 Intrinsic and extrinsic factors affecting microbial growth
- 2.8.2 Water activity
- 2.8.3 pH
- 2.8.4 Temperature
- 2.8.5 Interplay of factors affecting microbial growth in foods
- 2.9 Microbial response to stress
- 2.9.1 general stress response (GSR)
- 2.9.2 pH stress
- 2.9.3 Heat shock
- 2.9.4 Cold shock
- 2.9.5 Osmotic shock
- 2.10 Predictive modelling
- 2.10.1 Predicting modelling development
- 2.10.2 Primary models and the Gompertz and Baranyi equations
- 2.10.3 Secondary models
- 2.10.4 Tertiary models
- 2.10.5 Application of predictive microbial modelling
- Chapter 3 Food preservation and spoilage organisms
- 3.1 Spoilage micro-organisms
- 3.1.1 Spoilage micro-organisms
- 3.1.2 Spoilage of dairy products
- 3.1.3 Spoilage of meat products
- 3.1.4 Fish spoilage
- 3.1.5 Egg spoilage
- 3.1.6 Cereals and grain
- 3.2 Shelf life indicators
- 3.2.1 Glucose
- 3.2.2 Gluconic and 2-oxogluconic acid
- 3.2.3 L- and d-lactic acids, acetic acid and ethanol
- 3.2.4 Biologically active amines
- 3.2.5 Volatile compounds
- 3.2.6 Storage trials
- 3.2.7 Challenge tests
- 3.2.8 Predictive modelling
- 3.3 Methods of preservation and shelf life extension
- 3.4 Preservatives
- 3.4.1 Organic acids
- 3.4.2 Hydrogen peroxide and lactoperoxidase system
- 3.4.3 Chelators
- 3.4.4 Non-acidic preservatives
- 3.4.5 Preservation due to weak acids and low pH
- 3.4.6 Biopreservatives
- 3.5 Physical methods of preservation
- 3.5.1 Preservation by heat treatment
- 3.5.2 High-pressure treatment
- 3.5.3 Ohmic heating and radio frequency
- 3.5.4 Pulsed electric fields
- 3.5.5 Ultrasound
- 3.5.6 Intense light pulse
- 3.5.7 Food irradiation
- 3.5.8 Cold plasma and low-energy electrons for food surface decontamination
- 3.6 Packaging
- 3.6.1 Reduced oxygen packaging, modified atmosphere packaging and active packaging
- 3.6.2 Antimicrobial packaging and nanotechnology
- 3.7 Fermented food products
- 3.7.1 Fermented milk products
- 3.7.2 Fermented meat products
- 3.7.3 Fermented vegetables
- 3.7.4 Fermented protein foods: shoyu and miso
- 3.8 Organisms involved in the production of fermented foods
- 3.8.1 Lactic acid bacteria
- 3.8.2 Bifidobacterium species
- 3.8.3 Other organisms
- 3.9 Functional foods: probiotics and gut modulation
- 3.9.1 qualified Presumption of Safety (QPS) and Generally Regarded As Safe (GRAS)
- 3.9.2 Functional foods and probiotics
- 3.9.3 Probiotic studies
- 3.9.4 Novel organisms - modulation of gut microbiota
- Chapter 4 Bacterial foodborne pathogens
- 4.1 Indicator organisms
- 4.1.1 Coliforms
- 4.1.2 Enterobacteriaceae
- 4.1.3 Enterococci
- 4.1.4 Bacteriophages
- 4.2 Campylobacter jejuni, C. coli and C. lari
- 4.2.1 General description
- 4.2.2 Campylobacter infections
- 4.2.3 Campylobacter jejuni typing
- 4.2.4 Virulence factors
- 4.2.5 Whole-genome sequence analysis
- 4.2.6 Sources and control of Campylobacter jejuni
- 4.3 Salmonella serovars
- 4.3.1 General description
- 4.3.2 Salmonella serotypes
- 4.3.3 Infections caused by Salmonella serovars
- 4.3.4 Virulence factors of Salmonella serovars
- 4.3.5 Whole-genome analysis
- 4.3.6 Sources and control of Salmonella serovars
- 4.3.7 Salmonella serovar outbreaks
- 4.4 Pathogenic E. coli
- 4.4.1 General description
- 4.4.2 E. coli pathovars
- 4.4.3 Infections caused by E. coli pathovars
- 4.4.4 Virulence factors
- 4.4.5 Whole-genome analysis
- 4.4.6 Sources and control of E. coli pathovars
- 4.4.7 Outbreaks caused by E. coli pathovars
- 4.5 Sh. dysenteriae and Sh. sonnei
- 4.5.1 General description
- 4.5.2 Shigellosis
- 4.5.3 Virulence factors
- 4.5.4 Sh. sonnei outbreak
- 4.6 Cronobacter species
- 4.6.1 General description
- 4.6.2 Infections due to Cronobacter species
- 4.6.3 Identification and typing methods for Cronobacter species
- 4.6.4 Virulence factors
- 4.6.5 Sources and control of Cronobacter species
- 4.6.6 Cronobacter outbreaks
- 4.7 Vibrio cholerae, V. parahaemolyticus and V. vulnificus
- 4.7.1 General description
- 4.7.2 Infections due to Vibrio species
- 4.7.3 Virulence factors
- 4.7.4 Sources and control
- 4.8 Brucella melitensis, Br. abortus and Br. suis
- 4.8.1 General description
- 4.8.2 Brucellosis
- 4.9 Yersinia enterocolitica
- 4.9.1 General description
- 4.9.2 Yersiniosis
- 4.9.3 Sources and control
- 4.9.4 Outbreaks due to Y. enterocolitica
- 4.10 Aeromonas hydrophila, A. caviae and A. sobria
- 4.10.1 General description
- 4.10.2 A. hydrophila gastroenteritis
- 4.10.3 Sources and control
- 4.11 Plesiomonas shigelloides
- 4.11.1 General description
- 4.11.2 Plesiomonas infections
- 4.11.3 Sources and control
- 4.12 Listeria monocytogenes
- 4.12.1 General description
- 4.12.2 Listeriosis
- 4.12.3 Lineages and typing L. monocytogenes
- 4.12.4 Virulence factors
- 4.12.5 Whole-genome analysis of L. monocytogenes
- 4.12.6 Sources and control of L. monocytogenes
- 4.12.7 L. monocytogenes outbreaks
- 4.13 Staphylococcus aureus
- 4.13.1 General description
- 4.13.2 Infections associated with St. aureus
- 4.13.3 Virulence factors
- 4.13.4 Sources and control
- 4.14 Clostridium perfringens
- 4.14.1 General description
- 4.14.2 Cl. perfringens infections
- 4.14.3 Sources and control
- 4.15 Clostridium botulinum
- 4.15.1 General description
- 4.15.2 Cl. botulinum intoxication
- 4.15.3 Sources and control
- 4.16 B. cereus group
- 4.16.1 General description
- 4.16.2 B. cereus foodborne infections
- 4.16.3 Virulence traits
- 4.16.4 Sources and control
- 4.17 Enterococcus and Streptococcus species
- 4.17.1 General description
- 4.17.2 E. faecalis and E. faecium
- 4.17.3 Streptococcus pyogenes, group A streptococci
- 4.17.4 Virulence traits
- 4.18 Emerging and uncommon foodborne pathogens
- 4.18.2 Campylobacter concisus
- 4.18.3 EAEC, E. coli O55 and E. coli O26
- 4.18.4 Escherichia albertii
- 4.18.5 Providencia alcalifaciens
- 4.18.6 Clostridium difficile
- 4.18.7 Mycobacterium paratuberculosis
- 4.18.8 Acinetobacter species
- 4.18.9 Nanobacteria
- Chapter 5 Foodborne pathogens: viruses, toxins, parasites and prions
- 5.1 Foodborne viruses
- 5.1.1 Norovirus
- 5.1.2 Hepatitis A
- 5.1.3 Hepatitis E
- 5.1.4 Rotaviruses
- 5.1.5 Small round viruses, astroviruses, sapporo-like viruses, adenoviruses and parvoviruses
- 5.1.6 Human enteroviruses
- 5.2 Seafood and shellfish poisoning
- 5.2.1 Ciguatera poisoning
- 5.2.2 Scombroid poisoning
- 5.2.3 Paralytic shellfish poisoning
- 5.2.4 Diarrhoeic shellfish poisoning
- 5.2.5 Neurotoxic shellfish poisoning
- 5.2.6 Amnesic shellfish poisoning
- 5.3 Foodborne parasites: eucaryotes
- 5.3.1 Toxoplasma gondii
- 5.3.2 Taenia saginata and T. solium
- 5.3.3 Echinococcus multilocularis and E. granulosus
- 5.3.4 Cyclospora cayetanensis
- 5.3.5 Cryptosporidium parvum
- 5.3.6 Anisakis simplex
- 5.3.7 Trichinella spiralis
- 5.4 Mycotoxins
- 5.4.1 Aflatoxins
- 5.4.2 Ochratoxins
- 5.4.3 Fumonisins
- 5.4.4 Zearalenone
- 5.4.5 Trichothecenes
- 5.4.6 Prions and transmissible spongiform encephalopathies
- Chapter 6 Methods of detection and characterisation
- 6.1 Prologue
- 6.2 Conventional methods
- 6.2.1 Culture media
- 6.2.2 Sublethally injured cells
- 6.2.3 Viable but non-culturable bacteria (VBNC)
- 6.3 Rapid sampling methods
- 6.3.1 Sample preparation
- 6.3.2 Separation and concentration of target
- 6.4 Rapid end-detection methods
- 6.4.1 ELISA and antibody-based detection systems
- 6.4.2 Reversed passive latex agglutination
- 6.4.3 ATP bioluminescence techniques and hygiene monitoring
- 6.4.4 Protein detection
- 6.4.5 Flow cytometry
- 6.4.6 Biosensors
- 6.4.7 Impedance (Conductance) microbiology
- 6.5 DNA-based molecular typing and proteomic methods
- 6.5.1 Polymerase chain reaction (PCR)
- 6.5.2 Microarrays
- 6.5.3 Loop-mediated isothermal amplification (LAMP) technique
- 6.5.4 Pulsed-field gel electrophoresis (PFGE)
- 6.5.5 Restriction fragment length polymorphism (RFLP)
- 6.5.6 Amplified fragment length polymorphism (AFLP)
- 6.5.7 Random amplification of polymorphic DNA (RAPD)
- 6.5.8 Repetitive-element polymerase chain reaction (Rep-PCR)
- 6.5.9 Nucleic acid sequence-based amplification (NASBA)
- 6.5.10 Multiple-locus variable number tandem (VNTR) repeat analysis
- 6.5.11 PCR-probe based serotyping
- 6.5.12 Ribotyping
- 6.5.13 Matrix-associated laser desorption ionisation - time of flight (MALDI-TOF)
- 6.6 Identification and typing methods based on high-throughput DNA sequencing
- 6.6.1 Conventional seven-loci MLST
- 6.6.2 Genome sequence-based MLST
- 6.6.3 CRISPR-cas array typing
- 6.6.4 Single nucleotide polymorphism (SNP)-based analysis
- 6.7 Specific detection procedures and accreditation
- 6.7.1 Aerobic plate count (APC)
- 6.7.2 Salmonella serovars
- 6.7.3 Campylobacter species
- 6.7.4 Enterobacteriaceae and E. coli
- 6.7.5 Pathogenic E. coli, including E. coli O157:H7
- 6.7.6 Shigella species
- 6.7.7 Cronobacter genus
- 6.7.8 Aeromonas species
- 6.7.9 Arcobacter species
- 6.7.10 Listeria monocytogenes
- 6.7.11 Staphylococcus aureus
- 6.7.12 Clostridium perfringens
- 6.7.13 B. cereus, B. subtilis and B. licheniformis
- 6.7.14 Mycotoxins
- 6.7.15 Viruses
- Chapter 7 Microbiological criteria
- 7.1 Background to microbiological criteria and end-product testing
- 7.2 International commission on microbiological specifications for foods (ICMSF)
- 7.3 Codex Alimentarius principles for the establishment and application of microbiological criteria
- 7.4 Sampling plans
- 7.5 Variables plans
- 7.6 Attributes sampling plan
- 7.6.1 Two-class plan
- 7.6.2 Three-class plan
- 7.7 Principles
- 7.7.1 Defining a 'lot' of food
- 7.7.2 Sample unit number
- 7.7.3 Operating characteristic curve
- 7.7.4 Producer risk and consumer risk
- 7.7.5 Stringency of two- and three-class plans, setting n and c
- 7.7.6 Setting the values for m and M
- 7.8 Microbiological limits
- 7.8.1 Definitions
- 7.8.2 Limitations of microbiological testing
- 7.8.3 Examples of sampling plans
- 7.9 Implemented microbiological criteria
- 7.9.1 Microbiological criteria in the European Union
- 7.9.2 EU Directives specifying microbiological standards for foods
- 7.10 UK guidelines for ready-to-eat foods
- Chapter 8 Hygienic production practices
- 8.1 Contribution of food handlers to foodborne illness
- 8.2 Personnel hygiene and training
- 8.3 Cleaning
- 8.4 Detergents and disinfectants
- 8.5 Microbial biofilms
- 8.5.1 Microbial biofilm formation
- 8.5.2 Bacterial biofilm induction
- 8.5.3 Biofilm removal and control
- 8.6 Assessment of cleaning and disinfection efficiency
- Chapter 9 Food safety management tools
- 9.1 The manufacture of hygienic food
- 9.2 Microbiological safety of food in world trade
- 9.3 Consumer pressure effect on food processing
- 9.4 The management of hazards in food in international trade
- 9.5 Hazard analysis critical control point (HACCP)
- 9.6 Prerequisite programme
- 9.7 Outline of HACCP
- 9.7.1 Food hazards
- 9.7.2 Preparation for HACCP
- 9.7.3 Principle 1: hazard analysis (HA)
- 9.7.4 Principle 2: critical control points (CCPs)
- 9.7.5 Principle 3: critical limits
- 9.7.6 Principle 4: CCP monitoring
- 9.7.7 Principle 5: corrective actions
- 9.7.8 Principle 6: verification
- 9.7.9 Principle 7: record keeping
- 9.8 Microbiological criteria and HACCP
- 9.9 Microbiological hazards and their control
- 9.9.1 Sources of microbiological hazards
- 9.9.2 Temperature control of microbiological hazards
- 9.9.3 Non-temperature control of microbiological hazards
- 9.10 HACCP plans
- 9.10.1 Production of pasteurised milk
- 9.10.2 Swine slaughter in the abattoir
- 9.10.3 Chilled food manufacture
- 9.10.4 Generic models
- 9.11 GMP and GHP
- 9.12 Quality systems
- 9.13 Total quality management
- Chapter 10 Microbiological risk assessment
- 10.1 Risk analysis and microbiological risk assessment
- 10.2 Origin of MRA
- 10.3 MRA - an overview
- 10.4 MRA - structure
- 10.4.1 Risk assessment
- 10.4.2 Risk management
- 10.4.3 Risk communication
- 10.5 Risk assessment
- 10.5.1 Statement of purpose
- 10.5.2 Hazard identification
- 10.5.3 Exposure assessment
- 10.5.4 Hazard characterisation
- 10.5.5 Dose-response assessment
- 10.5.6 Dose-response models
- 10.5.7 Dose and infection
- 10.5.8 Risk characterisation
- 10.5.9 Production of a formal report
- 10.5.10 Triangular distributions and Monte Carlo simulation
- 10.6 Risk management
- 10.6.1 Risk assessment policy
- 10.6.2 Risk profiling
- 10.7 Food safety objectives (FSO)
- 10.8 Risk communication
- 10.9 Future developments in MRA
- 10.9.1 International methodology and guidelines
- 10.9.2 Risk assessment database
- 10.9.3 Training courses and use of resources
- Chapter 11 Application of microbiological risk assessment
- 11.1 Salmonella serovars
- 11.1.1 Salmonella enteritidis in shell eggs and egg products
- 11.1.2 Hazard identification and hazard characterisation of Salmonella in broilers and eggs
- 11.1.3 Exposure assessment of Salmonella serovars in broilers
- 11.1.4 Salmonella serovars in cooked chicken
- 11.1.5 Salmonella serovars in cooked patty
- 11.1.6 Poultry FARM
- 11.1.7 Domestic and Sporadic Human Salmonellosis
- 11.2 Campylobacter
- 11.2.1 C. jejuni risk from fresh chicken
- 11.2.2 Risk profile for pathogenic species of Campylobacter in Denmark
- 11.2.3 Risk assessment of C. jejuni in broilers
- 11.2.4 Campylobacter fluoroquinolone resistance
- 11.3 L. monocytogenes
- 11.3.1 L. monocytogenes hazard identification and hazard characterisation in ready-to-eat foods
- 11.3.2 L. monocytogenes exposure assessment in RTE foods
- 11.3.3 Relative risk of L. monocytogenes in selected RTE foods
- 11.3.4 L. monocytogenes in European Union trade
- 11.3.5 L. monocytogenes in meat balls
- 11.3.6 Listeriosis from RTE meat products
- 11.4 E. coli O157
- 11.4.1 E. coli O157:H7 in ground beef
- 11.5 Bacillus cereus
- 11.5.1 B. cereus risk assessment
- 11.6 Vibrio parahaemolyticus
- 11.6.1 Public health impact of V. parahaemolyticus in raw molluscan shellfish
- 11.7 Cronobacter species and Salmonella in powdered infant formula (PIF)
- 11.8 Viral risk assessments
- 11.8.1 Viral contamination of shellfish and coastal waters
- Chapter 12 International control of microbiological hazards in foods: regulations and authorities
- 12.1 Control of foodborne pathogens
- 12.1.1 Control of Salmonella serovars in poultry
- 12.1.2 Control of Escherichia coli pathovars and Salmonella serovars in fresh produce
- 12.1.3 Control of pathogens in low-moisture foods (LMFs)
- 12.2 World Health Organisation (WHO), global food security from accidental and deliberate contamination
- Box 12.1
- 12.3 Regulations in international trade of food
- 12.4 Codex Alimentarius Commission (CAC)
- 12.5 SPS measures, technical barriers to trade (TBT) and the WHO
- 12.6 EU legislation
- 12.7 International food safety agencies
- 12.7.1 European Food Safety Authority (EFSA)
- 12.7.2 Food authorities in the United States
- Chapter 13 Surveillance and foodborne outbreak investigation
- 13.1 Surveillance programmes
- 13.1.1 International Food Safety Authorities Network (IFSAN)
- 13.1.2 Surveillance systems in the United States
- 13.1.3 PulseNet international
- 13.1.4 European Centre for Disease Prevention and Control (ECDC) and European surveillance for salmonellosis and shiga toxin-producing E. coli (STEC)
- 13.1.5 European food-borne viruses in europe network (FBVE)
- 13.1.6 Rapid alert system for food and feed (RASFF)
- 13.1.7 Global salm-surv (GSS)
- 13.1.8 Surveillance of ready-to-eat foods in the United Kingdom
- 13.2 Outbreak investigations
- 13.2.1 Preliminary outbreak investigation
- 13.2.2 Case definition and data collection
- 13.2.3 Data collation and interpretation
- 13.3 Social media, crowd sourcing and reporting food poisoning cases
- 13.4 Mobile phones and food safety
- 13.5 Food terrorism and biocrimes
- Chapter 14 Whole-genome sequencing, microbiomes and genomic epidemiology
- 14.1 high-throughput DNA sequencing
- 14.2 Microbiome analysis
- 14.3 Genomic epidemiology
- 14.3.1 Whole-genome sequencing for microbial source tracking
- 14.3.2 Genome Trakr network (US)
- 14.3.3 NCBI pathogen detection site
- 14.3.4 Center for Genomic Epidemiology (denmark)
- 14.4 Key outbreaks investigated using genomic epidemiology
- 14.4.1 Ready-to-eat meat products L. monocytogenes outbreak, canada, 2008
- 14.4.2 E. coli O104:H4 outbreak, germany, 2011
- 14.4.3 C. jejuni outbreak investigations
- 14.4.4 Salmonella enteritidis in eggs, European outbreak, 2014
- 14.4.5 Multinational outbreak of Salmonella Agona through infant formula contamination, 2017
- 14.4.6 Retrospective Cronobacter sakazakii neonatal intensive care unit outbreak, france, 1994
- 14.4.7 L. monocytogenes ST6, polony sausages, south africa, 2017-2018
- Glossary of terms
- List of abbreviations
- Food safety resources on the world wide web
- Plates and credits
- References
- Index
- Supplemental Images
- EULA
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