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Multiple Choice
A) anti-metabolic.
B) catabolic.
C) synthetic.
D) semi-synthetic.
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Multiple Choice
A) examples of metabolic inhibitors.
B) folate inhibitors.
C) protein synthesis inhibitors.
D) inhibitors of cell wall synthesis.
E) examples of metabolic inhibitors AND folate inhibitors.
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Multiple Choice
A) Koch.
B) Hooke.
C) Fleming.
D) Ehrlich.
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True/False
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True/False
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Multiple Choice
A) penicillin
B) cephalosporin
C) vancomycin
D) bacitracin
E) All of the choices are correct.
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Multiple Choice
A) We want the largest possible number of choices of drugs in case a microbe shows resistance. With more possible weapons (even toxic ones) , we have greater ability to eliminate infections.
B) Every person is different. What is toxic to one person may not be toxic to another person. To eliminate a useful drug because it's toxic to 1% of people treated is a waste.
C) Depending on the location of the infection, we may have no choice but to utilize a drug that has some toxic side effects to the patient.
D) They shouldn't be used. We have enough of a selection of drugs that we can always select a drug with no toxicity. Drugs with toxicity are simply leftovers-relics from a time when we didn't have as many drug options.
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Multiple Choice
A) S. aureus
B) S. epidermidis
C) M. luteus
D) Mycoplasma
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Multiple Choice
A) uncoating.
B) nucleic acid synthesis.
C) viral assembly.
D) viral ribosomes.
E) uncoating, nucleic acid synthesis AND viral assembly.
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Multiple Choice
A) Antibiotics only work within a narrow range of cell concentrations. If you use a concentration that is too low or too high, you will get inaccurate measurements of the zone of inhibition.
B) Antibiotic resistance is usually only manifested by bacteria that have achieved a very high concentration (i.e. they are in the very end of the stationary phase of the growth curve) . It's important to use bacteria specifically at this particular point for disc diffusion testing.
C) If you were to use 1 strain that was in stationary phase (high concentration, replicating very slowly or not at all) , and another strain that was just beginning log phase (low concentration but replicating quickly) , you could see dramatically different results in the disc diffusion test. This could skew your interpretations of resistance/susceptibility.
D) Growth on the Mueller-Hinton agar plates utilized is very sensitive to the phase of the growth curve the bacteria are in when they are placed on the plate. If they are not in the log phase when they are placed on the plate, they will not grow and the test will be worthless.
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Multiple Choice
A) They are bacteriostatic.
B) They irreversibly bind to the 30S ribosomal subunit.
C) They block peptidoglycan synthesis.
D) They are bactericidal.
E) They irreversibly bind to the 30S ribosomal subunit AND they are bactericidal.
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Multiple Choice
A) penicillin.
B) sulfa.
C) erythromycin.
D) Salvarsan.
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Multiple Choice
A) metabolic destructive rate.
B) half-life.
C) effective time.
D) dosage rate.
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Multiple Choice
A) MIC
B) MIB
C) MLB
D) Kirby-Bauer test
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Multiple Choice
A) energetic.
B) antagonistic.
C) additive.
D) synergistic.
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Multiple Choice
A) Koch.
B) Hooke.
C) Fleming.
D) Ehrlich.
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Multiple Choice
A) drug-inactivating enzymes.
B) alteration in the target molecule.
C) decreased uptake of the drug.
D) increased elimination of the drug.
E) All of the choices are correct.
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True/False
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True/False
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