BackMicrobe-Host Interactions, Immunity, Microbial Control, and Epidemiology
Study Guide - Smart Notes
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Microbe-Host Interactions
Microbiome
The microbiome refers to the collection of microorganisms living in and on the human body. These microbes play essential roles in health and disease.
Benefits: The microbiome aids in digestion, synthesizes vitamins, protects against pathogens, and modulates the immune system.
Composition Determinants: Microbiome composition is influenced by nutrients, physical and chemical factors, host defenses, and mechanical factors.
Microbial Antagonism
Microbial antagonism is the competition between microbes, often resulting in the inhibition of pathogenic organisms by normal flora.
Symbiosis
Symbiosis describes the relationship between microbes and their hosts. There are three main types:
Commensalism: One organism benefits, the other is unaffected.
Mutualism: Both organisms benefit.
Parasitism: One organism benefits at the expense of the other.
Opportunistic Pathogens
Opportunistic pathogens are normally harmless but can cause disease when the host's defenses are compromised.
Pathogenicity: The ability of a microbe to cause disease.
Virulence: The degree of pathogenicity.
Portals of Entry and Adherence
Microbes enter the host through specific portals of entry and must adhere to host tissues to establish infection.
Adhesins: Surface molecules that bind to host cells.
Glycocalyx, fimbriae, biofilms: Structures aiding in adherence.
Establishing Infection
Microbes establish infection by producing toxins, invading host tissues, and avoiding host defenses.
Destroy or evade antibodies, hide inside cells.
Use enzymes such as coagulases, kinases, hyaluronidase, collagenase, and IgA protease.
Antigenic variation: Changing surface proteins to evade immune detection.
Invasins: Facilitate entry and survival within host cells.
Toxins
Bacterial toxins are classified as endotoxins and exotoxins.
Endotoxins: Components of the bacterial cell wall (lipopolysaccharide, LPS), trigger inflammation, can cause shock, require high lethal dose.
Exotoxins: Secreted proteins, act specifically (e.g., neurotoxins), require low lethal dose, vaccines available.
A-B toxins: Consist of two parts: A (active) and B (binding).
Damage to Host
Disrupt cell function, use nutrients, produce waste, multiply within cells causing cell death, inflammation, cross-reactive antibodies.
Immunity
Innate Immunity
Innate immunity is the first line of defense, acting rapidly and generally against pathogens.
Physical barriers: Skin, mucous membranes.
Chemical barriers: Lysozyme, stomach acid.
Cellular defenses: Phagocytes, natural killer cells.
Adaptive Immunity
Adaptive immunity is the second line of defense, slower but highly specific.
Active immunity: Acquired through infection or vaccination.
Passive immunity: Acquired through maternal antibodies or monoclonal antibody treatment.
Antibodies
IgG: Indicates past infection, most abundant.
IgM: Indicates current infection.
IgG response: Faster and stronger upon second exposure.
Vaccines
The goal of vaccination is to stimulate a primary immune response. Types include:
Attenuated: Live but weakened microbes.
Inactivated: Killed microbes.
Toxoid: Inactivated toxins.
Subunit: Purified components.
Recombinant: Genetically engineered antigens.
VLP: Virus-like particles.
Polysaccharide: Sugar-based antigens.
Conjugate: Linked polysaccharide and protein antigens.
Nucleic acid-based: DNA or mRNA vaccines.
Adjuvant: Substance added to enhance immune response.
Physical Microbe Control
Physical methods are used to control microbial growth in various settings.
Sterilization: Complete elimination of all microbes.
Heat: Includes moist heat (autoclave, pasteurization), dry heat (flaming, incineration).
Filtration: HEPA and membrane filters remove microbes from air and liquids.
Cold: Refrigeration, deep-freezing, freeze-drying slow or halt microbial growth.
High pressure: Disrupts microbial structures.
Desiccation: Removal of water inhibits growth.
Drugs and Microbe Control
Antimicrobial drugs are used to treat infections, with most antibiotics being naturally occurring.
Selective toxicity: Drugs target microbes without harming host.
Therapeutic index: Ratio of toxic dose to effective dose.
Bacteriostatic: Inhibit growth.
Bactericidal: Kill microbes.
Spectrum: Broad-spectrum (many types), narrow-spectrum (few types).
Drug interactions: Antagonistic (reduce effect), synergistic (enhance effect).
Adverse effects: Allergic reactions, toxicity, dysbiosis.
Antibiotic Resistance
Innate resistance: Natural, due to inherent features.
Acquired resistance: Due to mutations or gene transfer.
Mechanisms: Enzymes inactivate drugs, alter target, decrease uptake, increase elimination.
Prevention: Responsible use by patients and professionals.
Mechanisms of Action
Antibacterial: Target cell wall, protein synthesis, nucleic acid synthesis, metabolic pathways.
Antivirals: Prevent integration, assembly, and release; few targets available.
Testing Methods
Kirby-Bauer disc diffusion: Tests antibiotic effectiveness.
MIC (Minimum Inhibitory Concentration): Lowest concentration preventing growth.
MBC (Minimum Bactericidal Concentration): Lowest concentration killing bacteria.
Epidemiology
Epidemiology is the study of disease occurrence and transmission in populations.
Communicable: Transmitted from person to person.
Non-communicable: Not transmitted between people.
Endemic: Constantly present in a population.
Epidemic: Sudden increase in cases.
Pandemic: Global epidemic.
Incidence: New cases in a time period.
Prevalence: Total cases at a given time.
Morbidity: Rate of illness.
Mortality: Rate of death.
Case-fatality: Proportion of deaths among diagnosed cases.
Reservoirs and Transmission
Reservoirs: Human, animal, or environmental sources of infection.
Transmission: Vertical (parent to offspring), horizontal (person to person), direct, droplet, vehicle-borne (objects, food, water), vector-borne (mechanical or biological).
Factors Impacting Epidemiology
Dose, incubation period, host population, environment.
Health Care Associated Infections
Importance of hygiene, careful use of in-dwelling devices, and antibiotics to prevent infections.
Example Table: Types of Vaccines
Type | Description | Example |
|---|---|---|
Attenuated | Live, weakened microbe | MMR vaccine |
Inactivated | Killed microbe | Polio vaccine |
Toxoid | Inactivated toxin | Tetanus vaccine |
Subunit | Purified antigen | Hepatitis B vaccine |
Recombinant | Genetically engineered antigen | HPV vaccine |
VLP | Virus-like particle | HPV vaccine |
Polysaccharide | Sugar-based antigen | Pneumococcal vaccine |
Conjugate | Linked polysaccharide and protein | Haemophilus influenzae type b vaccine |
Nucleic acid-based | DNA or mRNA | COVID-19 mRNA vaccine |
Example Table: Mechanisms of Antibiotic Resistance
Mechanism | Description |
|---|---|
Enzyme production | Inactivates drug (e.g., beta-lactamase) |
Altered target | Drug cannot bind to target |
Decreased uptake | Reduced entry of drug into cell |
Increased elimination | Efflux pumps remove drug |
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