Microbial Control Flashcards

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1
Q

What is the difference between sterilisation and sanitisation?

A

Sterilisation: the destruction of all microbes
Sanitisation: the destruction of many microorganisms to reduce viable numbers

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2
Q

What is the difference between a disinfectant and an antiseptic?

A

Disinfectant: destroys microbes on inanimate objects
Antiseptic: a disinfectant for animate areas

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3
Q

What is pasteurisation?

A

A process developed by Louis Pastuer that reduces spoilage bacteria and increases the shelf life of food

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4
Q

What are the temperatures and times for LTLT and HTST relating to pasteurisation?

A

LTLT: 63 degress, 30 min
HTST: 72 degrees, 15 sec

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5
Q

List the 3 modes of action for disinfectants?

A
  • Protein coagulation/denaturation
  • Disruption of cell membrane
  • Chemical antagonism (inactivation of enzymes)
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6
Q

What is the optimal percentage of alcohol for disinfection?

A

70%

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7
Q

Betadine is a combination of iodophor and detergent which is used as a skin disinfectant in presurgical operations. List the advantages and disadvantages of Betadine for this use.

A
Advantages:
- good treatment for small wounds and infections
- effective on a wide range of microbes
- can be a pre-operation skin disinfectant
Disadvantages:
- can cause discolouration of skin 
- can lead to hypersensitivity of skin
- psuedonomas are able to grow from it
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8
Q

What is the mechanism of action for Quaternary Ammonium Compounds (QUATs) against bacteria?

A
  • They are surface active agents
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9
Q

Why are QUATS no longer used in some hospital settings?

A
  • Can be inactivated by soaps, low level disinfectants
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10
Q

What is the “decimal reduction time (D)”?

A

The ‘decimal reduction time’ (D) is the time (minutes) for the survivors to be destroyed by one log cycle which represents 90% of the initial population

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11
Q

What is Sterilisation?

A

The destruction of all microbes

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12
Q

Why are endospores difficult to kill?

A
  • They are the most heat resistant and difficult to kill microbial structure
  • The thick spore coat protects from radiation and chemicals
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13
Q

Why is moist heat better than dry heat?

A
  • Moist heat (autoclave) is more effective than dry heat (hot air oven)
  • Moisture is a better conductor of heat and has better heat penetration
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14
Q

In what circumstance would you probably use a dry heat oven in stead of autoclaving?

A
  • When sterilising glassware, oils and powders (it doesn’t make sharps blunt)
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15
Q

What methods are used to ensure an autoclave is working?

A
  • Autoclave prinouts/monitoring
  • Spore strips: endospores put on paper strip inside envelope, placed inside autoclave, transferred to broth and incubated at 55 degrees for 5 days, if there is growth then the autoclave is successful, if not, then it is not
  • Autoclave tape: Stripes on a strip of tape are white before sterilisation, tape is placed inside the autoclave, if there are neat lines on the tape then autoclave is successful, if they are faded out then it is unsuccessful, the brings an immediate result but does not indicate the time held
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16
Q

Name two chemicals used for “cold sterilisation”. How does ionizing radiation affect microbes and kill them?

A
  • Cold sterilisation works to denature proteins

- Formaldehyde and ethylene oxide can be used for cold sterilisation

17
Q

State the filtration pore size needed to filter out a) bacteria, b) viruses

A
  • Bacteria: 0.45 micrometres or less

- Virus: 0.01 mircrometre or less

18
Q

What is the difference between Bacteriostatic and Bactericidal agents?

A
  • Bacteriostatic: inhibit growth of bacteria

- Bactericidal: kill bacteria

19
Q

List the 6 modes of action for anti-bacterial agents (i.e. 6 target sites).

A
  • Inhibitors of cell wall synthesis
  • Membrane-active antimicrobial agents
  • Inhibitors of DNA replication
  • Inhibitors of RNA synthesis
  • Inhibitors of ribosome function - protein synthesis
  • Metabolic inhibitors
20
Q

Describe the action of the β-lactam antibiotics.

A
  • 𝛃- lactams inhibit the last stage of the cell wall production process
  • Not effective against resting bacteria
  • These agents binds to proteins at the cell wall/cell membrane interface (PBPs) that are involved in the cross linking of the peptidoglycan strands – results in cell lysis (all are bactericidal)
21
Q

How could incompletion of a prescribed course of antibiotics lead to bacterial resistance?

A
  • Not completing a course of antibiotics (that work) = selecting resistant mutants
22
Q

Why are antibiotics of no use against the common cold?

A
  • The common cold is a virus, antibiotics work on bacterial infections
23
Q

Define “antibiotic”. Define the ‘Antibiotic Creed’.

A
  • Antibiotic: natural compounds produced by microorganisms that kill or inhibit other microorganisms
  • Antibiotic Creed: the guidelines doctors go by in order to determine how much of an antibiotic to prescribe to a patient
24
Q

Why are the β-lactam agents good for treating susceptible bacterial infections in humans?

A
  • Because eukaryote cells (including humans) do not have a cell wall (only a plasma membrane) and no peptidoglycan, the β-lactams work well in that they kill bacteria without damaging cells of the host
25
Q

Why are many treatments for fungal infections often toxic to humans?

A
  • Fungi are difficult to treat because they are eukaryotic and so have similar structures to human cells
  • Can kill human cells along with fungal cells
26
Q

List two modes of action for anti-viral drugs.

A
  • Prevention of uncoating of virus (e.g. Amantadine for Influenza)
  • Inhibit viral replication (e.g. Aciclovir for Herpes)