WEEK 5 - Alternative to Antibiotics Flashcards

1
Q

List 4 alternatives to antibiotics

A
  1. Bioicdes
  2. Bacteriophage
  3. Larva Therapy
  4. Antimicrobial peptides

AIM:
- To inhibit / stop microbial growth
- Prevent infection

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2
Q

Biocides - definition and examples

A

DEFINITION:
- is the active chemical molecule that controls the growth or kils bacteria / microorganisms (in a biocidal product)

Examples:
- Disinfectants ~ used on inanimate objects
- Antiseptics - applied topically to prevent / treat infections
- e.g. povidone-iodine ~ stains skin, used before making incision
- Preservatives ~ added to products to inhbit micro-organism growth
- prevents contamination
- biocide is present before microorganism

OTHER INFO:
- Usually chemically synthesised
- Do NOT cause toxicity to humans, animals, environment
- AIM is to sterilse

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3
Q

Biocide class examples

A
  1. Phenols e.g. m-cresol
  2. Bis-phenols e.g. triclosan
  3. Organic / Inorganic acids e.g. propionic or lactic acid
  4. Biguanides e.g. chlorhexidine
  5. Aldehydes e.g. formaldehyde
    - note e.g. is toxic = can NOT enter room disinfected using this gas unless all gas has been REMOVED
  6. Alcohols e.g. ethanol (hand gels)
  7. Quaternary ammonium compounds e.g. benzalkonium chloride
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4
Q

How are biocides used in healthcare

8 Uses

A
  1. Surface Disinfection
    - prevents cross-contamination between patients + HCP
    - clean frequently touched surfaces, equipment, walls etc.
    - e.g. alcohols, chlorine based compounds, quaternary ammonium
  2. Hand hygiene
    - ↓ spread of pathogens from HCP
    - inc. hand sanitiser, surgical scrubs
    - e.g. ethanol, isopropanol, chlorhexidine
  3. Sterilisation of medical equipment
    - remove microorganisms / spores from surgical tools
    - e.g. hydrogen peroxide, ethylene oxide
  4. Antiseptics for skin / wound care
    - ↓ microbial load on skin
    - for pre-operative skincare, wound cleaning
    - e.g. povidone-iodine, chlorhexidine, hydrogen peroxide
  5. Water treatments
    - ensure clean water supply to prevent waterborne infections
    - for drinking + washing water
    - e.g. chlorine, UV radiation
  6. Air disinfection
    - ↓ no. of airborne pathogens
    - for operating rooms, isolation wards
    - e.g. UV lights, hydrogen peroxide vapour
  7. Textile disinfection
    - ensure hospital linen, bed sheets, staff uniforms are free from pathogens
    - e.g. hydrogen peroxide
  8. Antimicrobial coating
    - provides long-term microbial resistance to surfaces
    - used on hospital bed rails, door handles, high touched surfaces
    - e.g. silver nanoparticles, copper ions, quat. ammonium
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5
Q

Explain the MoA for Biocides

A

Cell membrane disruption (MAJOR MoA)
- leads to inactivation / inhibition or death of microorganism
- NOT ALL bioicdes are membrantrophic

  1. Biocide disrupts microbial cell membrane or cell wall
    - interacts with lipid bilayer (phospholipids) or membrane proteins
  2. Compromises microbial cell membrane permeability
    - i.e. structure + function is disrupted
  3. Osmotic imbalance = leakage of cellular content
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6
Q

Bacteriophage - Structre INFO

2 types of bacteriophage

A

A virus that infects a bacterium / bacterial cell

STRUCTURE of Phage:
- Tail fibers which bind to bacterium surface receptors
- recepotrs are specific = specific phages can infect bacterium
- Injects genome into bacterium via phage central tail tube
- Tail tube and sheath gives specificity

LYTIC Phage:
- Causes LYSIS of bacterium
- Phage infects bacterium by injecting its genetic material into it
- Bacterial genome breaks down + phage genome replicates
- New phage burst bacterial host cell + infect other bacterium
- USED in therapy

LYSOGENIC (temperate) Phage:
- Does NOT cause LYSIS
- Phage injects its genetic material into bacterium
- Phage genome becomes integrated into bacteria genome = is rpelicated as bacterium duplicates
- Will produce bacterium containing phage material
- how resistance + virulence factors can transfer

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7
Q

How are bacteriophage used in healthcare

4 Uses

A
  1. Treat Antibioitc Resistant Infections
    - MoA: phage infect bacterium, injecting genome + replicating in bacteria until bacterium lyses = new phages released
    - Pathogens: MRSA, MDR pathogens, E.coli, Staph. aureus
    - Use: wounds, pneumonia, sepsis
  2. Wound care and Infections
    - ↓ microbial load in chronic wounds + surgical site infections
    - MoA: phages applied topically to selectively target + kill bacteria
    - e.g. apply phage-based dressings or gels
  3. Bacteria caused GI Infections
    - MoA: orally taken, phage target harmful bacteria in gut (+ preserve beneifcial micrbiota)
    - Pathogens: C.diff, salmonella
  4. Antibiotic-resistant Respiratory Infections
    - MoA: inhale phage preparation, targets bacterium in lungs
    - Pathogens: pneumonia
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8
Q

Explain what ‘personalised phage therapy’ is and what the beneifts are

A

Personalised phage therapy:
- Targeted therapy personalised to specific bacteria causing patient’s infection
- Phage is selected / engineered to target the specific bacteria
- may need to isolate bacteria to identify correct phage

ADVANTAGES:
- High specificity
- phage target specific bacteria without harming commensal microbiota
- Low resistance development
- bacteria develope resistance to phages slower than to antibioitcs
- Penetrate + disrupt bacterial biofilm
- Are biodegradable = environmentally friendly (break down easily)

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9
Q

What are the challenges with phage therapy

A
  • Not widely approved = frameworks still evolving
  • Host immune response may clear phage before they fully eradicate infection
  • More research required for their production and stability
  • Economic problem (companies may not see much profit in developing them)
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10
Q

Larval Therapy (MRSA) - INFO

a.k.a. Maggot therapy

A

Use of live, disinfected larvae / maggots to clean + promote healing in chronic wounds
- larvae is produced in sterile environment

Larvae is highly selective i.e. only eat necrotic tissue not live, healthy tissue

USE:
- For antibiotic resistant bacteria found in chronic wounds

Necrotic - dead / infected tissue

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11
Q

What is the MoA of Larval therapy

inc. antimicrobial and healing actions

A
  1. Larvae are applied directly to wound
  2. Larvae feed on dead tissue
    - secrete enzymes that break down infected tissue into a form they can inject
    - i.e. biosurgical debridement
  3. Removal of dead tissue speeds up healing process
    - i.e. wound cleaning process

Antimicrobial Action
- Larvae degrade + disrupt bacterial biofilm
- Larvae produce secretions that are antimicrobial
- secretions fight infection
- secretions have broad-spectrum antibacterial properties
- ↓ need for systemic antibiotics

Promote Healing
- Larvae secretions contain growth promoting factors
- stimulates wound healing
- encourages granulation / new tissue
- Larvae movement in wound stimulates blood circulation
- ↑ tissue O2 = accelrates healing

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12
Q

What is biofilm

A

Biofilm - produced by bacteria to protect it against antibiotics + immune system

Can be BROKEN BY:
- Bacteriphages
- Larvae therapy
Break down allows immune system + other tretaments to eliminate bacteria

  • They are typically resistant to antibiotics
  • Form in: chronic wounds
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13
Q

How is larval therapy used in healthcare

A

Used to treat wounds difficult to heal, infected or dead tissue

Examples:
- Chronic ulcers
- e.g. diabetic ulcers, pressure sores
- Necrotic wounds
- Post-surgical wounds
- Burns
- Amputation sites

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14
Q

What are the benefits of larval therapy

5 benefits

A
  1. Selective debridement
    • only consume dead, infected tissue
    • clean wounds without harming healthy tissue
  2. Have antimicrobial action
  3. Reduce the need for systemic antibiotics
  4. Promote healing
  5. Minimally invasive
    - therapy doesn’t require surgery
    - non-invasive
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15
Q

What are the challeneges and contraindications related to larval therapy

A

CHALLENGES:
- Patient perception and acceptance
- some patients may be uncomfortable with the idea of live maggots
- Cost
- cheaper than surgery but can still be expensive
- Wound care expertise
- larvae therapy has to be administered by specialist in wound care
- requires monitoring + management

CONTRAINDICATIONS:
May not be appropriate for:
- patients with allergies to larvae, componets of their secretions etc.
- patients with very sensitive skin
- wounds healing well with other methods

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16
Q

Antimicrobial Peptides (AMPs) - INFO

Inc. definition, challenges

A

Chains of naturally occuring amino acids that have broad-spectrum antimicrobial properties

  • Have activity agianst bacteria, viruses, fungi and parasites
  • Always have AMPs present in and on our bodies

CHALLENGES:
- Ensuring stability
- Minimise toxicity
- Avoid resistance development

17
Q

How is antimicropbial peptides used in healathcare

9 Uses

A
  1. Topical wound treatments
    • inc. AMP dressings and gels
    • promotes healing + prevents infection
  2. Medical device coating
    • ↓ infection risk, prevent bacterial adhesion + biofilm fomration
    • apply to cathers + impants
  3. Systemic antimicrobial therapy
    • AMPs used to treat systemic infections, esp. MDR bacteria
  4. Anticancer therapy
    • some AMPs target cancer cells
  5. Dental and oral health
    • help prevent dental caries + oral infections
  6. Antiviral therapies
    • effective against viruses like influenza, HIV, coronaviruses
  7. Immunomodulation
    • can control inflammation + enhance immune responses
    • useful in autoimmune diseases + sepsis
  8. Biofilm disruption
    • AMPs prevent / break down biofilms
  9. Synergistic use with antibiotics
    • can enhance effectiveness of antibiotics against resistant bacteria
18
Q

What is the pharmacists’ role in antibiotic alternatives

A
  • Educate + counsel patients on non-antibiotic treatment options
  • Promote vaccines
  • Prescribe / recommend alternative therapies
  • Antimicrobial stewardship
  • Create personalised alternative therapies
  • Contribute to development of new antimicrobial agents
  • Resistance monitoring (promote alternatives + adjust treatments as needed)
  • Advocate for changes to use non-antibiotic approaches