Mechanisms of Pathogenicity
Mechanisms of Pathogenicity
Chapter Overview
Topics: Microbiome, Host-Microbe Interactions, Pathogenicity, Opportunistic Infections, Virulence Factors, Toxins, Quorum Sensing, Stages of Infectious Disease.
Microbiota
Definition
Microbiota refers to microorganisms that inhabit our bodies, replacing the outdated term "microflora."
Types
Normal Microbiota: Also known as resident microbiota; permanent residents in specific body areas.
Transient Microbiota: Temporary inhabitants; can be present under certain conditions but not permanently.
Acquisition of Microbiota
All sterile before birth, acquiring microbiota from the birthing process and environment afterward.
Differences in microbiota based on the method of delivery (vaginal vs. cesarean).
Host-Microbe Interactions
Contamination: Presence of an organism without causing harm.
Infection: Microorganism multiplies in host, potentially leading to illness (e.g., staph aureus on a cut).
Disease: Health disturbance caused by infection; symptoms worsen and disrupt normal bodily functions.
Infestation: Term reserved for parasitic infections (e.g., tapeworms).
Pathogenicity
Definition: Capability of an organism to cause infection or disease.
Factors Affecting Pathogenicity:
Ability to invade and multiply in hosts.
Quantity of microbes needed for infection (e.g., Shigella can cause illness from one cell).
Ability to evade the immune system (e.g., HIV infects immune cells).
Opportunistic Infections
Definition: They take advantage of a situation…when they see an opportunity they take it.
Factors for Opportunistic Infections:
Immunocompromised individuals: Vulnerabilities due to age, disease, or medications.
Unusual locations: Normal microbiota can cause infections if introduced into wrong sites (e.g., E. coli in the urinary tract).
Disturbance of Normal Microbiota: Antibiotics can wipe out beneficial microbiota, allowing opportunistic pathogens to flourish (e.g., yeast infections after antibiotics for UTIs).
Types of Infectious Diseases
Communicable Diseases: Spread easily from person to person.
Contagious: Highly communicable (e.g., influenza).
Less contagious examples (e.g., pneumonia).
Non-communicable Diseases: Cannot be spread person to person (e.g., tetanus, malaria).
Virulence Factors
Definition: Factors that help pathogens cause disease.
Examples:
Pili: Used for attachment to host tissues (e.g., Neisseria gonorrhoeae).
Glycocalyx: Enables adherence to surfaces and evasion of the immune system (slime layer vs. capsule).
Enzymes:
Urease: Neutralizes stomach acid, reaches the epithelial cells to create infections.
Hyaluronidase: Breaks down connective tissue, facilitating spread.
Collagenase: Destroys collagen, aiding penetration into tissues.
Toxins
Endotoxins: Found in gram-negative bacteria, released upon death (e.g., E. coli). Associated with low toxicity but serious effects.
Causes endotoxin shock
Exotoxins: Secreted by living bacteria, highly toxic (e.g., botulinum toxin), found more with gram positive bacteria but can be found in gram negative.
Categories:
Neurotoxins: Affect the nervous system (e.g., clostridium botulinum and clostridium tetani).
Cytotoxins: Affect cells (e.g., hemolysins- staphylococcus, streptococcus. leukocidins- staphylococcus, streptococcus).
Enterotoxins: Affect intestinal cells (e.g., vibrio cholera + staphylococcus aureus).
Mycotoxins: Fungal toxins causing health issues (e.g., aflatoxins linked to liver cancer).
aflatoxin: produced by aspergillus flavus; grows on grains and nuts, ha to be regulated,
ergot alkaloids: produced by a different mold, grows on grains and rye
Quorum Sensing
Definition: Communication among bacteria using chemical signaling molecules.
Importance in coordinating group behavior and developing strategies against hosts.
Concept of anti-quorum sensing molecules as potential broad-spectrum antibiotics.
Stages of Infectious Disease
Incubation Period: Time from infection to symptom onset; number of pathogens is low but increasing.
Prodromal Phase: Mild signs/symptoms; contagious.
Period of Illness: Most acute symptoms; pathogen loads peak.
Period of Decline: Symptoms decrease; susceptible to secondary infections.
Period of Convalescence: Recovery phase; pathogen levels drop back to normal.
Additional Concepts
Antigenic Drift: Minor antigenic changes over time due to mutations.
Antigenic Shift: Major changes resulting from gene mixing between different strains, leading to new viral strains (e.g., influenza).