Substances that are naturally produced by certain microorganisms that
can inhibit or destroy other microorganisms are called
A.
antibiotics.
B. narrow-spectrum drugs.
C. semi-synthetic
drugs.
D. synthetic drugs.
E. broad-spectrum drugs.
antibiotics.
Antimicrobials effective against a wide variety of microbial types
are termed
A. antibiotics.
B. narrow-spectrum drugs.
C. semisynthetic drugs.
D. synthetic drugs.
E.
broad-spectrum drugs.
broad-spectrum drugs.
Antibiotics are derived from all of the following except
A.
Penicillium.
B. Bacillus.
C. Staphylococcus.
D.
Streptomyces.
E. Cephalosporium.
Staphylococcus.
Important characteristics of antimicrobial drugs include
A. low
toxicity for human tissues.
B. high toxicity against microbial
cells.
C. do not cause serious side effects in humans.
D.
stable and soluble in body tissues and fluids.
E. All of the
choices are correct.
All of the choices are correct.
The use of a drug to prevent imminent infection is called
A.
competitive inhibition.
B. synergism.
C. prebiotics.
D. prophylaxis.
E. lantibiotics.
prophylaxis.
The use of any chemical in the treatment, relief, or prophylaxis of a
disease is called
A. prophylaxis.
B. chemotherapy.
C.
selective toxicity.
D. nephrotoxicity.
E. synergism.
chemotherapy.
Penicillins and cephalosporins
A. interfere with elongation of
peptidoglycan.
B. block folic acid synthesis.
C. attach to
the 30S ribosomal subunit and disrupt protein synthesis.
D.
damage cell membranes.
E. block peptidases that cross-link glycan molecules.
block peptidases that cross-link glycan molecules.
Selective toxicity refers to
A. damage to pathogenic
organisms.
B. damage to prokaryotic cell membranes.
C.
damage to the target organisms but not host cells.
D. damage to
nucleic acids.
E. None of the choices is correct.
damage to the target organisms but not host cells.
Each of the following effect cell walls except
A.
penicillin.
B. cycloserine.
C. vancomycin.
D.
erythromycin.
E. cephalosporin.
erythromycin.
Aminoglycosides
A. interfere with elongation of
peptidoglycan.
B. block folic acid synthesis.
C. attach to
the 30S ribosomal subunit and disrupt protein synthesis.
D.
damage cell membranes.
E. block peptidases that cross-link glycan molecules.
attach to the 30S ribosomal subunit and disrupt protein synthesis.
Each of the following target prokaryotic ribosomes except
A.
streptomycin.
B. gentamycin.
C. polymyxins.
D.
tetracycline.
E. erythromycin.
polymyxins.
Drugs that insert on the _____ ribosomal subunit prevent peptide bond
formation or inhibit translocation of the subunit during translation.
A. 30S
B. 40S
C. 50S
D. 60S
E. 70S
50S
Sulfonamides
A. interfere with elongation of
peptidoglycan.
B. block folic acid synthesis.
C. attach to
the 30S ribosomal subunit and disrupt protein synthesis.
D.
damage cell membranes.
E. block peptidases that cross-link glycan molecules.
block folic acid synthesis.
Sulfa drugs work on
A. nucleic acid biosynthesis.
B.
ribosome biosynthesis.
C. peptidoglycan biosynthesis.
D.
folic acid biosynthesis.
E. None of the choices is correct.
folic acid biosynthesis.
Sulfonamides are analogs of PABA and, as a result, they inhibit _____
synthesis.
A. protein
B. DNA
C. RNA
D. folic
acid
E. phospholipid
folic acid
Drugs that act by mimicking the normal substrate of an enzyme,
thereby blocking its active
site, are called
A.
inhibitors.
B. blockers.
C. competitive inhibitors.
D.
noncompetitive inhibitors.
E. None of the choices is correct.
competitive inhibitors.
Ampicillin, amoxicillin, mezlocillin, and penicillin G all have
A. a beta-lactam ring.
B. resistance to the action of
penicillinase.
C. a semisynthetic nature.
D. an expanded
spectrum of activity.
E. All of the choices are correct.
a beta-lactam ring.
A chemical that inhibits beta-lactamase enzymes is
A.
synercid.
B. penicillinase.
C. aztreonam.
D.
clavulanic acid.
E. imipenem.
clavulanic acid.
What type of chemical will allow some bacteria to be resistant to
many penicillins?
A. synercid
B. penicillinase
C.
aztreonam
D. clavulanic acid
E. imipenem
penicillinase
All of the following pertain to cephalosporins except
A. have a
beta-lactam ring.
B. greater resistance to
beta-lactamases.
C. newer generations have activity against
gram-negatives.
D. many administered by injection, not
orally.
E. are synthetic drugs.
are synthetic drugs.
Which antimicrobial does not inhibit cell wall synthesis?
A.
gentamicin
B. vancomycin
C. cephalosporins
D.
penicillins
E. clavamox
gentamicin
Which drug is used to treat cases of tuberculosis?
A.
penicillin G
B. vancomycin
C. tetracycline
D.
synercid
E. isoniazid
isoniazid
What drug is used in cases of penicillin and methicillin resistance
and also used to treat endocarditis?
A. penicillin G
B.
vancomycin
C. tetracycline
D. erythromycin
E. isoniazid
vancomycin
Clavulanic acid
A. inhibits B-lactamase activity.
B.
inhibits peptidoglycan synthesis.
C. inhibits formation of
peptidoglycan cross linkages.
D. inhibits cell membrane
synthesis.
E. None of the choices is correct.
inhibits B-lactamase activity.
All _____ consist of a thiazolidine ring, a beta-lactam ring, and an
R group.
A. penicillins
B. tetracyclins
C.
macrolides
D. cephalosporins
E. aminoglycosides
penicillins
The major source of naturally produced penicillin is the mold
A. Penicillium notatum.
B. Penicilium chrysogenum.
C.
Penicilium familiaris.
D. Naturally produced penicillin is no
longer used.
E. None of the choices is correct.
Penicilium chrysogenum.
Gram-negative rods are often treated with
A. penicillin
G.
B. vancomycin.
C. aminoglycosides.
D.
synercid.
E. isoniazid.
aminoglycosides
Which antimicrobial does not interfere with protein synthesis?
A. aminoglycosides
B. tetracyclines
C. erythromycin
D. trimethroprim
E. gentamicin
trimethroprim
Which of these drugs has the most narrow spectrum?
A.
tetracycline
B. isoniazid
C. erythromycin
D.
aminoglycosides
E. cephalosporins
isoniazid
Antimicrobials that are macrolides
A. disrupt cell membrane
function.
B. include tetracyclines.
C. include azithromycin,
clarithromcyin and erythromycin.
D. are very narrow-spectrum
drugs.
E. are hepatotoxic.
include azithromycin, clarithromcyin and erythromycin.
The drug that can cause injury to red blood cells and white blood
cells is
A. chloramphenicol.
B. clindamycin.
C.
ciprofloxacin.
D. bacitracin.
E. gentamicin.
chloramphenicol.
Which of the following antibacterial drug groups does not target
protein synthesis?
A. clindamycin
B. erythromycin
C.
aminoglycosides
D. sulfonamides
E. tetracycline
sulfonamides
Which antibiotic is used to treat MRSA and VRE infections?
A.
synercid
B. clindamycin
C. linezolid
D. azithromycin
E. clarithromycin
linezolid
Which of the following is not true of polymyxins?
A. disrupt
the cell membrane
B. have a narrow-spectrum
C. toxic to
kidneys
D. target cell walls
E. can treat severe urinary
tract infections
target cell walls
The antifungal drug that can be used to treat serious systemic fungal
infections is
A. nystatin.
B. griseofulvin.
C.
amphotericin B.
D. sulfa drugs.
E. metronidazole.
amphotericin B.
Ketoconazole, fluconazole, clotrimazole and miconazole are
broad-spectrum azoles used to treat _____ infections.
A.
bacterial
B. fungal
C. protozoan
D. helminthic
E. viral
fungal
Which of the following is not a drug group used to treat fungal
infections?
A. quinolones
B. macrolide polyene antibiotics
C. griseofulvins
D. synthetic azoles
E. flucytosines
quinolones
The drug used for several protozoan infections is
A.
nystatin.
B. griseofulvin.
C. amphotericin B.
D. sulfa
drugs.
E. metronidazole.
metronidazole.
Mebendazole is a drug used to treat _____ infections.
A.
bacterial
B. fungal
C. protozoan
D. helminthic
E. viral
helminthic
There are fewer antifungal, anti-protozoan, and anti-helminth drugs
compared to antibacterial drugs because fungi, protozoa, and helminths
A. do not cause many human infections.
B. are not affected
by antimicrobials.
C. are so similar to human cells that drug
selective toxicity is difficult.
D. are parasites found inside
human cells.
E. because their cells have fewer target sites
compared to bacteria.
are so similar to human cells that drug selective toxicity is difficult.
Primaquine and chloroquine are drugs used in the treatment of
A. gram-positive infections.
B. gram-negative infections.
C. fungal infections.
D. protozoan infections.
E.
viral infections.
protozoan infections.
Which of the following is not a mode of action of antiviral drugs?
A. block penetration
B. block transcription and
translation
C. inhibit DNA synthesis
D. block
maturation
E. bond to ergosterol in the cell membrane
bond to ergosterol in the cell membrane
An antiviral that is a guanine analog would have an antiviral mode of
action that
A. blocks penetration.
B. blocks transcription
and translation.
C. inhibits DNA synthesis.
D. blocks
maturation.
E. bonds to ergosterol in the cell membrane.
inhibits DNA synthesis.
Antiviral drugs that target reverse transcriptase would be used to
treat
A. influenza A virus.
B. HIV.
C. herpes zoster
virus.
D. respiratory syncytial virus.
E. hepatitis C virus.
HIV.
Acyclovir is used to treat
A. influenza A virus.
B.
HIV.
C. herpes simplex virus.
D. respiratory syncytial
virus.
E. hepatitis C virus.
herpes simplex virus.
Which of the following block HIV binding to host cell receptors?
A. AZT
B. acyclovir
C. nevirapine
D.
fuzeon
E. amantidine
fuzeon
The cellular basis for bacterial resistance to antimicrobials include
A. bacterial chromosomal mutations.
B. synthesis of enzymes
that alter drug structure.
C. prevention of drug entry into the
cell.
D. alteration of drug receptors on cell targets.
E.
All of the choices are correct.
All of the choices are correct.
The multidrug resistant pumps in many bacterial cell membranes
function by
A. bacterial chromosomal mutations.
B.
synthesis of enzymes that alter drug structure.
C. removing the
drug from the cell when it enters.
D. alteration of drug
receptors on cell targets.
E. All of the choices are correct.
removing the drug from the cell when it enters.
Microbial resistance resulting from mutation occurs because
A.
prokaryotic genomes undergo mutation rapidly.
B. prokaryotic
genomes undergo mutation often.
C. short generation times
accumulate mutations in populations.
D. mutations are passed
between organisms.
E. All of the choices are correct.
All of the choices are correct.
Each of the following result in drug resistance except
A. drug
pumped out of the cell.
B. drug used as a nutrient by the
cell.
C. drug binding site altered.
D. drug
inactivated.
E. drug blocked from entering cell.
drug used as a nutrient by the cell.
Each of the following is a mechanism for drug resistance transfer
between microorganisms except
A. transposons.
B.
R-plasmids.
C. conjugation.
D. mutation.
E. All of the
choices provide for transfer of drug resistance.
mutation.
Each of the following contributes to emerging drug resistance except
A. overuse of antibiotics.
B. improper use of
antibiotics.
C. multiple drug therapy.
D. ingestion of
antibiotics with animal feed.
E. addition of antibiotics to
common household products.
multiple drug therapy.
Nutrients that encourage the growth of beneficial microbes in the
intestines are known as
A. prebiotics.
B. probiotics.
C. lantibiotics.
D. phytobiotics.
E. riboswitches.
prebiotics.
The use of vaginal inserts of Lactobacillus to restore a healthy
acidic environment is an example of
A. prebiotics.
B.
probiotics.
C. lantibiotics.
D. phytobiotics.
E. riboswitches.
probiotics.
Broad-spectrum drugs that disrupt the body's normal flora often cause
A. nephrotoxicity.
B. superinfections.
C. allergic
reactions.
D. drug toxicity.
E. All of the choices are correct.
superinfections.
Side effects that occur in patient's tissues while on antimicrobial
drugs include all the following except
A. development of
resistance to the drug.
B. hepatotoxicity.
C.
nephrotoxicity.
D. diarrhea.
E. deafness.
development of resistance to the drug.
A superinfection results from
A. build up of a drug to toxic
levels in the patient.
B. the wrong drug administered to the
patient.
C. an immune system reaction to the drug.
D.
decrease in most normal flora with overgrowth of an unaffected
species.
E. All of the choices are correct.
decrease in most normal flora with overgrowth of an unaffected species.
The _____ are drugs that deposit in developing teeth and cause a
permanent brown discoloration.
A. streptomycins
B.
cephalosporins
C. macrolides
D. tetracyclins
E. penicillins
tetracyclins
Drug susceptibility testing determines
A. the patient's
response to various antimicrobials.
B. the pathogen's response to
various antimicrobials.
C. if normal flora will be affected by
antimicrobials.
D. if the drug is increasing to toxic levels in
a patient.
E. None of the choices is correct.
the pathogen's response to various antimicrobials.
A clinical microbiologist makes serial dilutions of several
antimicrobials in broth, and then incubates each drug dilution series
with a standard amount of a patient's isolated pathogen. What is this
microbiologist setting up?
A. Kirby-Bauer
B.
antibiogram
C. E-test
D. MIC
E. therapeutic index (TI)
MIC
A ratio of the dose of the drug that is toxic to humans versus the
minimum effective dose for that pathogen is assessed to predict the
potential for toxic drug reactions. This is called the
A.
Kirby-Bauer.
B. antibiogram.
C. E-test.
D. MIC.
E.
therapeutic index (TI).
therapeutic index (TI).
If pathogen A is more resistant to an erythromycin disc on a
Kirby-Bauer plate compared to pathogen B, then pathogen A will have
a(n) _____ zone of inhibition compared to pathogen B.
A.
smaller
B. equal
C. larger
D. All of the choices are
correct.
E. None of the choices is correct.
smaller
Which therapeutic index value would be the drug of choice?
A.
20
B. 10
C. 1
D. 0.1
E. Any value would be equally effective.
20
Which two antibiotics affect the DNA and RNA of bacteria?
A.
tetracycline and amphotericin B
B. trimethoprim and
sulfonamides
C. Rifampin and quinolones
D. tetracycline and bacitracin
Rifampin and quinolones