Lecture 4 (20) Antibiotics Flashcards

1
Q

selective toxicity

A

kill or inhibit growth of microorganism without harming host cells

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2
Q

what’s another name for antimicrobial

A

antibiotic

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3
Q

bacteriostatic

A

inhibits the GROWTH of bacteria but doesn’t KILL it

relies on immnocompetent pt to kill it off itself

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4
Q

bacteriocidal

A

kills of bacteria itself; for pt that lack immune system to fight off infection

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5
Q

antibiotic synergism and antagonism

A

synergism- two antibiotics enhance eachother’s effects

antagonism-antibiotics that interfere with one another

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6
Q

broad vs. narrow spectrum-advantages/disadvantages

A

broad- effective against large number of bacteria so good for infection of unknown etiology but bad because may disrupt normal biota
narrow- effective against a small number of bacteria; good to not disrupt normal biota/ bad because need to know what infection is first

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7
Q

what causes antibiotic resistance?

A

it is NOT antibiotics, if mutations in bacteria that make it antibiotic resistant are developed, they can pass that mutation horizontally spreading that resistance

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8
Q

what are the categories of antibiotic resistance and what do they mean?

A

SIR
S-sensitive- infection may be treate with the dosage regimen of an antimicrobial agent recommended
I-intermediate- infection may be treated in body sites where the drug are physiologically concentrated or when a high dosage of drug can be used
R-resistant- resistant isolates are not inhibited by the usually achieved concentrations of the antimicrobial

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9
Q

why shouldn’t I prescribe antibiotics willy nilly

A

because giving antibiotics will help to select for antibiotic resistant bacteria and kill good ones off and cause an increase in resistance in the pop

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10
Q

empiric therapy

A

-treatment while waiting for lab results that usually includes broad spectrum antibiotics

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11
Q

targeted therapy

A
  • refined treatment

- usually narrow spectrum

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12
Q

what are 5 ways that a bacteria can develop antibody resistance

A

1) Breakdown of an antibiotic via hydrolysis
2) Chemical modification of an antibiotic to render it inactive
3) Alter target via mutation or gene acquisition
4) Altered permeability, decreased influx or increased efflux
5) lack of target

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13
Q

minimum inhibitory concentration (MIC)/minimumbacteriocidal (MBC) concentration

A

lowest amount of antibiotic that inhibits growth/ lowerest amount of antibiotic that kills 99.9% of bacteria

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14
Q

Kirby baur test

A

-measures bacterial resistance to antibiotics by dropping antibiotic capsules into plate of bacteria
if clear ring appears, bacteria is killed by antibiotic, if not, it is resistant

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15
Q

E test

A

put bacteria on a plate with strips of different antibiotic bacteria around
you can look at each strip and see where there is clearing
outside circle is hi conc of antibiotic, inside is low

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16
Q

Broth culture

A
  • GIVES MIC AND MBC
  • put bacteria in test tubes and then treat with different conc of antibiotics
  • to find MIC look for least light that visibly is blocked by color (meaning it looks like there is the least amount of bacteria in there without it being completely clear) then go one up
  • to find MBC go to the MIC and then go one up from that
17
Q

cell wall active antibiotics vs. membrane active antibiotics

A

cell wall active- disrupts peptidoglycan synth, effective ONLY against actively dividing bacteria
membrane active- disrupts with membrane synthesis or integrity and is effective against rest and actively dividing bacteria

18
Q

B-lactams

A
  • bactericidal

- inhibition of cell wall synthesis therefore only for dividing bacteria

19
Q

how are penicillin binding proteins involved in the synthesis of peptidoglycan

A
  • penicillin binding protein is used to bind the alanine on the pentapeptide of the NAM/NAg/ peptapeptide complex
  • it uses it’s serine site to cleave off the alanine and bind a neighboring pentapeptide alaning with its NAM and NAG alanine to create a larger peptidoglycan
20
Q

what’s the mechanism of action of beta lactams

A
  • they prevent the action of serine binding protein of the penicillin binding protein by binding to serine itself
  • therefore, if the bacteria is dividing, it wont have enough peptidoglycan and it will lyse
  • THIS IS WHY B LACTAMS ARE ONLY GOOD FOR DIVIDING BACTERIA- if not dividing, you have enough peptidoglycan
21
Q

beta lactam resistance

A

-bacteria have developed resistance against beta lactams by allowing sheltering the serine active site preventing the beta lactam from binding

22
Q

what are 4 ways beta lactams can be resisted by bacteria

A
  • altered peptidases where a mutation decreases affinity of antibiotic (described with antibiotic binding protein)
  • change in permeability of bacteria for antibiotics such as a change in porins
  • presence of efflux pumps where the bacteria can pump the antibiotic out of the bacteria and a usable amount of antibiotic is never reached
  • chemical modification of antibiotic via a bacterial enzyme like B-lactamase
23
Q

how does vancomycin work?

A

-recognizes and binds the two D-alanine residues o the end of the peptide chains of peptidoglycan
-vanco prevents the peptide chains from interacting properly with transpeptidase and crosslinks cant be formed
= non peptidoglycan formed, lysis

24
Q

how do bacteria become resistant to Vancomycin?

A

they last D alanine that vanco binds is replaced by a D lactate so vanco cant recognize it and bind
-crosslinks can forma and peptidoglycan can be formed

25
Q

Bacitracin

A
  • interferes with dephosphorylation of lipid carrier Bactoprenol that transfers peptidoglycan subunits (UDP-NAM and NAG) to the growing cell wall
  • thus renders it unable to form a cell wall
26
Q

tetracyclines
type: bacteriostatic/bacteriocidal, broad or limited spectrum
mech:
ex:

A

type: bacteriostatic, broad spectrum
mech: target ribosome 30s subunit of ribosome in bacteria and render it inactive
ex: tetracycline, doxycycline

27
Q

aminoglycosides
type: bacteriostatic/bacteriocidal, broad or limited spectrum
mech:
ex:

A

type: bacteriocidal/ oxygen dependent-limited
mech: bind 30s subunit and inactivates it
ex:gentamycin, kanamycin
NOTE: only effective against aerobic organisms so don’t use in organs like intestine that are mostly anaerobic

28
Q

macrolides
type: bacteriostatic/bacteriocidal
mech:
ex:

A

type: bacteriostatic
mech:bind 50s subunit of ribosome of bacteria
ex: erythromycin, azithromycin
NOTE: used as an alternate for individuals with penicillin allergy

29
Q

quinolones
type: bacteriostatic/bacteriocidal
mech:
ex:

A

type: bacteriocidal
mech: inhibits DNA replication, recombination and repair by preventing DNA unwinding by DNA gyrase (DNA topoisomerase II or IV)
ex: ciprofloxin, levofloxin

30
Q

Rifampin, rifabutin
type: bacteriostatic/bacteriocidal
mech:

A

type: bacteriocidal
mech: binds to DNA dependent RNA polymerase and inhibits initiation of RNA synthesis- no mRNA= cell death

31
Q

metronidazole
type: bacteriostatic/bacteriocidal
mech:
ex:

A

type: bacteriocidal
mech: reduced by bacteria =toxic compounds that damage DNA