Ch. 20 Antimicrobial Drugs Flashcards

1
Q

Paul Ehrlich

A

speculated about some “magic bullet” to destroy pathogens but not the host. This idea provided the basis for both selective toxicity and chemotherapy (term he coined)

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2
Q

which is the most ideal spectrum of activity (narrow vs broad)

A

narrow; less collateral damage

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3
Q

selective toxicity

A

drug affects pathogens, not host cells

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4
Q

superinfection

A

occurs with normal microbiota when they lose competitors and grow out of control. Kill normal microbiota that keep certain bacteria under control;

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5
Q

Five main actions of antimicrobial drugs

A

1) inhibition of cell wall synthesis
2) inhibition of protein synthesis
3) inhibition of nucleic acid replication and transcription
4) injury to plasma membrane
5) inhibition of essential metabolite synthesis

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6
Q

drugs that inhibit cell wall synthesis

A

penicillins, cephalosporins, bacitracin, vancomycin

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7
Q

inhibition of cell wall synthesis: penicillin

A

Inhibit formation of cross-bridges as you make peptidoglycan (more effective against gram positive)

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8
Q

drugs that inhibit protein synthesis

A

chloramphenicol, erythromycin, tetracyclines, streptomycin

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9
Q

inhibition of protein synthesis

A

Selective toxicity key (so it does not target our protein synthesis)
E.g. attacking 70s ribosome (prokaryotic) instead of 80s ribosome (ours)
Not all in the same way; target different parts of ribosome etc

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10
Q

drugs that inhibit nucleic acid replication and transcription

A

quinolones, rifampin

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11
Q

why are there not as many drugs that inhibit nucleic acid replication and transcription?

A

Not many since they are not many differences between prokaryotes and eukaryotes.

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12
Q

drug that injures plasma membrane

A

polymyxin B

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13
Q

function of injury to plasma membrane

A

Degrade integrity

Some antifungal drugs do the same

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14
Q

drugs that inhibit essential metabolite synthesis

A

sulfanilamide, trimethoprim

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15
Q

function of drugs that inhibit essential metabolite synthesis

A

Competitive inhibition
Both of these interfere with folic acid synthesis (we can’t make it)
Often prescribed together d/t synergism

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16
Q

antiviral drugs target…

A

steps in life cycle:
Entry
Uncoating
Nucleic acid synthesis (retroviruses) – specific enzymes
Genome integration (retroviruses) – specific enzymes
Assembly – potentially protease
Exit

17
Q

influenza disease spikes

A
HA spike (hemagglutinin spike) -- needed for entry into cells (attachment/entry)
NA spike (neuraminidase) -- needed for exit; binds to protein on inside of cell membrane
18
Q

Neuraminidase Inhibitors for influenza

A

Tamiflu (oseltamivir)
Relenza (zanamavir)
Rapivab (peramivir)

19
Q

Interferons and what they treat

A

Alpha-interferons: Viral hepatitis
Imiquimod: stimulates interferon production; Genital warts
HAART (highly active anti retroviral therapy): combination of 4 types of drugs; therapy for HIV (chronic disease)

20
Q

two tests to guide chemotherapy

A

Kirby-Bauer (disk diffusion method)

E-test: determines minimum inhibitory concentration (MIC)

21
Q

MIC vs MBC

A

If there is no visible growth, could still be live microbes (bacteriostatic, not bactericidal)
Minimum bactericidal concentration (MBC) using drug plates

22
Q

targets for resistance of antimicrobial drugs

A

Change of receptors
Inactivation by enzymes
Alteration of target molecule
Efflux of antibiotic (kicks it out)

23
Q

contributing factors to antimicrobial resistance

A

Failure to complete prescribed regimen
Using outdated, weakened antibiotics
Using antibiotics for the common cold and other inappropriate conditions
Use of antibiotics in animal feed
Using someone else’s leftover prescription

24
Q

synergism vs antagonism

A

Synergism: increases drugs effects
Antagonism: decreases drugs effects

25
Q

future of chemotherapeutic drugs

A

Target virulence factors rather than pathogen (new strategies)
Prevent organisms from getting essential nutrients (e.g. iron)
Develop methods to target slow-growing cells
Antimicrobial peptides (a lot of cells ake these)
Phage therapy

26
Q

antibiotic vs antimicrobial drugs

A

antibiotic: substance produced by microorg that in small amounts inhibits another microorg.
antimicrobial drugs: synthetic (e.g. sulfa drugs discovered by German industrial scientists in 1920s-1930s (Protonsil red)

27
Q

antibiotics are rather easy to discover, but…

A

few are of medical or commercial value.

28
Q

growing problem in antibiotic discovery…

A

antibiotic resistance

29
Q

common antibiotic produced by…

A

> 50%: Streptomyces spp.
endospore-forming bacteria
molds (mostly Penicillium and Cephalosporium)