BACTE AMR Flashcards

1
Q

a chemical substance produced by microorganisms
with the capacity to inhibit (bacteriostatic) or kill
(bactericidal) other microorganisms

A

ANTIBIOTICS

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2
Q

effective against a limited number of
pathogens

A

Narrow-spectrum

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3
Q

destroys different kinds of organisms

A

Broad spectrum

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4
Q

examples for Broad spectrum

A

ampicillin, cephalosporins, chloramphenicol,
ciprofloxacin, rifampicin, sulfonamides,
trimethoprim, tetracycline

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5
Q

examples for Narrow spectrum

A

bacitracin, clindamycin, dapsone,
erythromycin, gentamicin, isoniazid,
penicillin, polymyxin b, and vancomycin

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6
Q

produced by bacteria or fungi

A

Natural drugs

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7
Q

modified natural drugs with
added chemical groups (ampicillin, carbenicillin,
methicillin)

A

Semi-synthetic drugs

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8
Q

chemically-produced drugs
(sulfonamides, trimethoprim, chloramphenicol,
ciprofloxacin, isoniazid, dapsone)

A

Synthetic drugs

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9
Q

Bacillus subtilis

A

Bacitracin

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10
Q

Bacillus polymyxa

A

Polymyxin

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11
Q

Cephalosporium

A

Cephalosporins

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12
Q

Micromonospora purpurea

A

Gentamicin

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13
Q

Streptomyces erythraeus

A

Erythromycin

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14
Q

Streptomyces fradiae

A

Neomycin

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15
Q

Streptomyces nodosus

A

Amphotericin B

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16
Q

Streptomyces noursei

A

Nystatin

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17
Q

Streptomyces venezuelae

A

Chloramphenicol

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18
Q

agents that inhibit bacterial growth; but generally, they
do not kill the microorganisms

A

Bacteriostatic agents

19
Q

example for Bacteriostatic agents

A

(chloramphenicol,
dapsone, erythromycin, clindamycin, isoniazid,
sulfonamides, and tetracycline)

20
Q

agents that usually kill or destroy organisms; used for
life-threatening infections

A

Bactericidal agents

21
Q

example for Bactericidal agents

A

(aminoglycosides
—gentamicin, amikacin, and streptomycin;
beta-lactams, glycopeptides, isoniazid, rifampicin,
quinolones, bacitracin, and metronidazole)

22
Q

These are the most selective antibiotics with a high
therapeutic index

A

CELL-WALL INHIBITORS

23
Q

● They inhibit the activity of the transpeptidase
enzymes in which cell growth stops and the death of
the cells often follows
● These drugs are effective against Gram-positive
bacteria

A

CELL-WALL INHIBITORS

24
Q

CELL-WALL INHIBITORS examples

A

Bacitracin, B-lactams, carbenicillin

25
Q

Binds to the penicillin-binding proteins
(transpeptidase-transglycosylase) —involved
in cell wall cross-linking, inhibiting
transpeptidation and cell wall synthesis

A

Beta-lactams

26
Q

types of Beta-lactams

A

penicillins, cephalosporins, carbapenems,
and monobactams

27
Q

These antibiotics bind to the 30s subunit resulting in the misreading of mRNA and thus interfering with
aminoacyl-tRNA binding

A

Protein-synthesis inhibitors

28
Q

It also binds with the 50S subunit resulting in the
inhibition of peptidyl-transferase and peptide chain
elongation

A

Protein-synthesis inhibitors

29
Q

Drugs that bind to the 30S ribosomal subunit —

A

aminoglycosides, tetracyclines, and
spectinomycin

30
Q

Drugs that bind to the 50s ribosomal subunit—

A

chloramphenicol, erythromycin, lincomycin,
clindamycin, and streptogramins

31
Q

Blocks the initial step in protein synthesis

A

linezolid

32
Q

antimicrobial agents that target DNA
metabolism

A

Nucleic acid synthesis inhibitors

33
Q

The primary antimicrobial agents that target DNA
metabolism are the _________________________________

A

fluoroquinolones and
metronidazole

34
Q

derivatives of nalidixic acid; interfere with DNA gyrase
and topoisomerase IV and are highly effective for
enteric bacteria like E. Coli:

A

Quinolones/fluoroquinolones

35
Q

disrupts DNA and is effective against anaerobic
bacteria

A

Metronidazole

36
Q

most potent against anaerobic
microaerophilic organisms, notably those
that are gram-negative

A

Metronidazole

37
Q

inhibits RNA polymerase; inhibits RNA synthesis
○ Does not effectively penetrate the outer
member membrane of most gram-negative
bacteria

A

Rifampicin

38
Q

competitively
inhibits the binding of the structural analog
aminobenzoic acid with dihydropteroate
synthase, blocks the formation of
7,8-dihydropteroate

A

Sulfamethoxazole (SMZ)

39
Q

prevents the dihydrofolate
reductase—mediated recycling of folate
coenzymes, blocks the formation of THF

A

Trimethoprim

40
Q

cord factor inhibitor; cord factor is found in
the cell wall of TMP

A

Isoniazid

41
Q

● Bind to the terminal D-Ala-D-Ala of the
pentapeptide-glycosyl peptidoglycan intermediates

A

Glycopeptides

42
Q

The clinical spectrum is limited to gram-positive
microorganisms

A

Glycopeptides

43
Q

types of Glycopeptides

A

Vancomycin, dalbavancin, teicoplanin