Lecture 14 Flashcards

1
Q

Are antibiotics primary or secondary metabolites?

A

secondary, they have no use in organism production

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2
Q

Why is antibiotic resistance a growing problem?

A

because they are overprescribed and over used

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3
Q

What are the 5 basic forms of antibiotic resistance and an example for each?

A
Prevent access and accumulation 
- block entry 
- efflux
Destroy the antibiotic 
- damage cell
Modify the target to inhibit binding 
- ribosome mutations
Overproduce cellular target
- 'mop-up' drug
Target mimicry
- use to decoy protein with same drug-binding site as target
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4
Q

What are multi-drug resistance efflux pumps?

A

they can pump out multiple drugs; makes it harder for drugs to work

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5
Q

What is de novo antibiotic resistance?

A

antibiotic resistance as a result of mutation

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6
Q

How is de novo antibiotic resistance acquired?

A

horizontal gene transfer

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7
Q

How is drug resistance combatted?

A

dummy targets inactivate resistant enzymes
alter antibiotic structure
linking antibiotic
anti-virulence: disarms pathogens but do not kill

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8
Q

Why do some dormant (persister cells) become active?

A

they have a stalled metabolism so during treatment they are dormant but activate after

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9
Q

What is the minimal inhibitory concentration (MIC)?

A

lowest drug concentration that prevents visible growth

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10
Q

How are the MLC and the MIC related?

A

the MLC is always equal or greater than the MIC

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11
Q

Why are there so few antiviral agents in medicine?

A

since viruses take over host, it is hard to kill just the virus and not the host

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12
Q

What is the difference between the two groups of fungi?

A

Superficial mycoses: treated topically

Deep mycoses: treated systemically

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13
Q

Describe the drug discovery pipeline.

A
  • target discovery
  • screening
  • lead optimization
  • ADMET
  • development
  • registration
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