Lecture 12 Flashcards

(14 cards)

1
Q

Emerging Bacterial Threats: Yersinia pestis (Plague)

A

Reservoir: Wild rodents are the primary carriers.

Forms of plague:

Pneumonic plague: Affects the lungs. Spread via droplets. Highly contagious and fatal if untreated.

Bubonic plague: Causes swollen lymph nodes (“buboes”). Spread by flea bites.

Septicemic plague: Bacteria in the bloodstream. Can develop from the other forms.

High fatality without rapid treatment

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2
Q

Emerging threats: Problems caused by biofilms:

A

Gum Disease: Dental plaque is a classic biofilm.

Medical devices:

Catheters (urinary or intravenous) – biofilms can block flow and cause infections.

Implants (e.g., joints, heart valves) – require surgical removal if infected.

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3
Q

Bacteriophage (Phage)

A

Viruses that infect and kill bacteria.

Extremely common – the most abundant lifeform on Earth.

Present in soil, water, animals’ intestines, etc.

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4
Q

Phage structure

A

Capsid (protein shell): encloses genetic material (DNA/RNA).

Genome can be: ssDNA, dsDNA, ssRNA, or dsRNA; circular or linear.

Collar and Core: structures supporting DNA injection.

Helical Sheath: contracts to push phage DNA into bacteria.

Tail spikes: used to attach to host bacteria.

Variation in length, capsid size, and tail presence.

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5
Q

Alternative Therapy: Phage Therapy

A

Phage therapy uses lytic bacteriophages to treat bacterial infections.
Especially useful when antibiotics fail (e.g., resistant infections).

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6
Q

Phage Sourcing & Isolation

A

Local environments with lots of bacteria (e.g. sewage)

Isolation Process:
Grow target bacteria in lab.

Introduce environmental sample.

Lytic phage infect and kill bacteria.

Filter to remove bacteria – retain pure phage solution.

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7
Q

Phage Therapy: Advantages over Antibiotics

A

Highly effective against target bacteria.

Co-evolve with bacteria – new phage can emerge to counteract resistance.

Self-limiting: phage stop multiplying once the infection is gone.

Can penetrate biofilms and deep tissues.

Environment-specific: Phages can be isolated from the same site as the infection.

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8
Q

Phage Therapy: Disadvantages and Challenges

A

Refrigeration required – not shelf-stable like some antibiotics.

Specialist training needed for doctors.

Difficult to treat polymicrobial infections (involving many bacterial types).
Solution: phage cocktails (mixtures).

Needs lab testing before use to ensure effectiveness:
Makes it unsuitable for acute/emergency infections.

High specificity:

Requires customized cocktails per region or patient.

Limited scope:

No lytic phage found for C. difficile (only temperate phage).

Delivery challenge: phages must reach infection site, which may differ from where antibiotics can reach.

Public perception: “viruses” can evoke fear and skepticism.

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9
Q

Phage Delivery Routes: Parenteral (non-oral)

A

Intramuscular (IM) Injection: Injection of phage directly into a muscle

Subcutaneous (SC) Injection: Injection of phage just under the skin, into the fatty tissue layer.

Intraperitoneal (IP) Injection: Injection of phage into the peritoneal cavity, the space within the abdomen that houses organs like intestines and liver.

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10
Q

Phage Delivery Routes: Oral

A

For gut infections, but must survive stomach acid.

Solution: microencapsulation.

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11
Q

Phage Delivery Routes: Local Application

A

Wound healing: hydrogel patches with phage (+ antibiotics).
Inhalation (nebulizer): lung infections.

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12
Q

Food Safety Uses of Phage

A

Raw meat: control Campylobacter.

Fresh produce: control Listeria.

Spoilage reduction.

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13
Q

Manuka Honey - Main components:

A

High sugar/osmolarity: draws water out of bacteria.

Hydrogen peroxide activity

Methylglyoxal (MGO): major antibacterial agent

Effective against ~80 bacterial species

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14
Q

Manuka Honey - targets and effects

A

Disrupts stress and membrane proteins in bacteria.

Decreases:

Quorum sensing: reduces coordination of bacterial behavior.
Siderophores: limits iron uptake.
Surface adhesion: prevents sticking to tissues.

Biofilms:

Inhibits formation
Disrupts existing biofilms

Reduces bacterial binding to human epithelial cells.

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