Lecture 10 Flashcards

(21 cards)

1
Q

True Pathogen (Obligate Pathogen)

A

Definition: A microorganism that can cause disease in healthy individuals with normal immune defences.

Examples:

Vibrio cholerae – causes cholera.

Chlamydia trachomatis – causes sexually transmitted infections (STIs).

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2
Q

Opportunistic Pathogen (‘Opportunist’)

A

Definition: An organism that only causes disease when the host’s immune defences are compromised (e.g. weakened immunity, breached skin/mucosa).

Note: Some are normally harmless commensals (organisms living in the body without causing harm) but become harmful under certain conditions.

Examples:

Staphylococcus aureus

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3
Q

HOW DO WE PROVE A MICROBE CAUSES DISEASE? Koch’s Postulates

A

Presence: The pathogen must be found in every case of the disease.
⚠️ Problem: Asymptomatic carriers may have the pathogen without disease.

Isolation: The pathogen must be isolated and grown in pure culture.
⚠️ Problem: Viruses can’t be grown without a host cell.

Reproduction: When introduced into a healthy susceptible host, the same disease should occur.
⚠️ Problem: Not all hosts will respond the same (host immunity differences).

Re-isolation: The pathogen should be recoverable from the experimentally infected host.

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4
Q

Infectious Dose and LD50 (Lethal Dose 50%)

A

Infectious Dose
The number of organisms required to cause infection.

Affects whether or not an infection takes hold.

LD50 (Lethal Dose 50%)
The number of organisms required to kill 50% of test subjects.

Lower LD50 = more virulent.

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5
Q

VIRULENCE FACTORS

A

Toxins
Disrupt host cell function or kill cells.
Corynebacterium diphtheriae – diphtheria toxin

Capsules
Protect bacteria from phagocytosis by immune cells.

Adhesins
Help bacteria stick to host tissues

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6
Q

COMMENSAL FLORA

A

Microorganisms that naturally live on/in the human body without causing disease (under normal conditions).

Bacteria, Protozoa, Fungi, Archaea, Viruses

Found on:
Large Intestine
Skin
Mouth
Nose
Throat

More anaerobes in colon

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7
Q

HARMFUL EFFECTS OF COMMENSAL FLORA

A

When they escape their normal site:

Peritonitis from Bacteroides and E. coli after appendix rupture

UTI (Urinary Tract Infection) – E. coli from gut to urinary tract

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8
Q

ALTERATIONS TO GUT FLORA (e.g. antibiotics)

A

Antibiotics kill off sensitive gut bacteria

Resistant species overgrow, e.g. Clostridioides difficile

C. difficile produces toxins, causing:

Diarrhoea

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9
Q

ALTERATIONS TO GUT FLORA (e.g. antibiotics) treatment

A

Stop antibiotic

Give:

Oral metronidazole

Or vancomycin

Recovery depends on restoring normal flora

Use probiotics or faecal transplant

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10
Q

OPPORTUNISTIC INFECTION – WHO IS VULNERABLE?

A
  1. Immunosuppressed:
    Cancer
    Transplant patients
  2. Breached defences:
    IV line
    Catheter
    Wounds
  3. Foreign bodies:
    Prosthetics
    Splinters
  4. General weakness:
    Malnutrition
    Illness
    Old age
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11
Q

CLOSTRIDIOIDES DIFFICILE – INFECTION (oppurtunistic)

A

Features
Gram-positive rod
Spore-forming
Strict anaerobe

Symptoms
Frequent diarrhoea
Fever
Nausea, pain
Loss of appetite

At-risk groups:
Taking:

Broad-spectrum or multiple/long-term antibiotics

Proton pump inhibitors (reduce stomach acid)

Hospital stays

Age > 65

IBD, cancer, kidney issues

Weakened immunity

Digestive system surgery

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12
Q

CLOSTRIDIOIDES DIFFICILE – INFECTION (oppurtunistic) STEPS OF INFECTION

A

Contamination

Disruption of normal gut flora

Spore germination

Colonisation

Toxin production

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13
Q

Opportunistic Fungal Infection: Mucormycosis

A

Mucormycosis is a serious fungal infection caused by a group of molds called Mucorales.

commonly found in soil, decaying organic matter, and compost

These molds are opportunistic pathogens — they don’t usually cause disease in healthy people, but can cause severe and rapidly progressing infections in people with weakened immune systems.

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14
Q

Opportunistic Fungal Infection: Mucormycosis types

A

Rhinocerebral mucormycosis: Starts in the nose/sinuses and can spread to the brain — especially dangerous.

Pulmonary mucormycosis: Inhalation of spores into lungs — seen in transplant patients.

Cutaneous mucormycosis: Through broken skin (wounds or burns).

Gastrointestinal mucormycosis: Mostly in premature infants or immunocompromised.

Disseminated mucormycosis: Spread through the blood to multiple organs.

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15
Q

Opportunistic bacterial infection: Polar Leprosy

A

This describes the spectrum of disease caused by Mycobacterium leprae — the bacterium that causes leprosy

The form of disease depends on the host’s immune response, especially T-cell immunity.

Strong T-cell immunity = Tuberculoid Leprosy
Localised skin lesions and nerve damage. Low bacterial load. Less contagious.

Weak T-cell immunity = Lepromatous Leprosy
Widespread skin nodules, nerve damage, high bacterial load. Highly contagious.

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16
Q

Opportunistic infections: Latent pathogens

A

These are pathogens that can remain hidden in the body after the initial infection, and reactivate later, especially when immunity is low.

e.g. Mycobacterium tuberculosis (TB) — may stay dormant for years in lungs.

17
Q

Splenic Function

A

The spleen plays a major role in immune defence, especially against bloodborne pathogens.

🛡️ Functions:
Produces antibodies (especially IgM)

Filters the blood — removes damaged/aged red blood cells and bacteria

Helps with clearance of encapsulated bacteria (e.g., Streptococcus pneumoniae)

18
Q

Opportunistic infections: Post-splenectomy Sepsis (PSS)

A

After spleen removal (splenectomy), the person is at very high risk for rapid, overwhelming bacterial infection — called Overwhelming Post-Splenectomy Infection (OPSI).

🧨 Features:
Rapid onset — symptoms can develop within hours.

Very severe — leads to sepsis, organ failure, and death in up to 50–70% of cases if not treated early.

19
Q

Opportunistic infections: Post-splenectomy Sepsis (PSS) - prevention

A

⚠️ Prevention is vital:
Educate the patient:
Carry a splenectomy alert card

Educate healthcare providers:

Vaccination:
Against encapsulated bacteria:
Streptococcus pneumoniae
Neisseria meningitidis

Prophylactic antibiotics:
Often long-term penicillin

20
Q

Prevention of Infection

A

Immunisation — protect against key pathogens (e.g., HiB, pneumococcus).

Infection control — e.g., hand hygiene, PPE.

Engineering controls — physical systems to reduce exposure to pathogens.

Screening for latent infections — e.g., TB in immunosuppressed patients.

Prophylactic treatment — giving antibiotics, antivirals, or antifungals to prevent infection in high-risk individuals.

21
Q

Engineering Controls in Infection Prevention: Aspergillus

A

🦠 Aspergillus prevention:
Air filtration: HEPA filters remove spores from air.

Barrier protection: During hospital renovations/construction, spores in dust can cause infection.

Protective isolation: HEPA-filtered rooms for stem cell transplant patients.

Respiratory protection: When patients must leave protective rooms, they wear masks.