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Please select the False statement regarding antibiotic resistance.


A) Modifications in the penicillin-binding proteins (PBPs) prevent β-lactam antibiotics from binding to them.
B) Some antibiotic-inactivating enzymes have an extended spectrum and confer resistance to a wide variety of antibiotics.
C) Changes in the porin proteins can prevent certain antimicrobials from entering a cell's periplasm or cytoplasm.
D) The bacterial enzyme chloramphenicol acetyltransferase confers resistance to the penicillins.
E) Bacteria that produce efflux pumps sometimes become resistant to several different antimicrobials simultaneously.

F) B) and C)
G) C) and D)

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Which of the following drugs does NOT target peptidoglycan?


A) Penicillin
B) Cephalosporin
C) Vancomycin
D) Bacitracin
E) Doxycycline

F) A) and C)
G) B) and E)

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Acyclovir interferes with viral DNA replication. Other mechanisms of antiviral medications include all of the following EXCEPT


A) preventing fusion and inhibiting viral entry into a host cell.
B) interfering with viral uncoating and release of viral nucleic acid in a host cell.
C) preventing the assembly viral proteins to form capsids.
D) inhibition of viral particle release from host cells.
E) destroying viral ribosomes and preventing protein synthesis.

F) A) and B)
G) B) and D)

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Inhibitors of protein synthesis typically act on


A) peptidoglycan precursors.
B) penicillin-binding proteins.
C) ribosomes.
D) porin proteins.
E) transfer RNA.

F) A) and C)
G) B) and E)

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What is the minimum inhibitory concentration (MIC) ?


A) It is the lowest concentration of a specific antimicrobial medication needed to prevent the visible growth of a given bacterial strain in vitro.
B) It is the highest concentration of a specific antimicrobial medication needed to prevent the visible growth of a given bacterial strain in vitro.
C) It is the lowest concentration of a specific antimicrobial medication needed to prevent the visible growth of a given bacterial strain in vivo.
D) It is the highest concentration of a specific antimicrobial medication needed to prevent the visible growth of a given bacterial strain in vivo.
E) It is the lowest concentration of a specific antimicrobial medication that kills 99.9% of cells of a given bacterial strain in vitro.

F) A) and C)
G) A) and B)

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The MBC may be determined by an extension of the MIC.

A) True
B) False

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Why would antimicrobials that have toxic side effects be used at all? (select the BEST reason)


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 from a time when we didn't have as many drug options.
E) These are all reasons to use antimicrobials that have a low therapeutic index.

F) A) and D)
G) B) and E)

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The lowest concentration of a drug that prevents growth of a microorganism is the


A) infectious effective dose.
B) minimum inhibitory concentration.
C) lethal dose.
D) most effective concentration.
E) minimal death dose.

F) B) and C)
G) A) and B)

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The situation in which the effect of two antimcrobials given together is more effective than the effect of either medication given individually is referred to as 


A) synergism.
B) antagonism.
C) nihilism.
D) symbiosis.
E) dysbiosis.

F) B) and C)
G) A) and C)

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The target of most antifungal drugs is


A) the ribosome AND the cytoplasmic membrane.
B) the nucleus AND mitochondria.
C) cholesterol.
D) ergosterol.
E) cholesterol AND ergosterol.

F) A) and D)
G) D) and E)

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Several diseases caused by herpesviruses are treated with a medication called acyclovir. This medication is a nucleoside analog, meaning


A) it contains a nucleotide analog and a phosphate.
B) it contains a nucleotide analog, a phosphate, and a sugar.
C) it contains a nucleotide analog and a sugar.
D) it is composed of NAG, NAM, and tetrapeptides.
E) it is composed of NAG, NAM, and a sugar.

F) B) and E)
G) B) and D)

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Explain how using a combination of two antimicrobial drugs helps prevent the development of spontaneously resistant mutants.


A) All drugs work synergistically with each other. Their combined effects are far greater than either could achieve individually. Two drugs together helps to eliminate microbes, even if they have developed spontaneous mutations that would make them resistant to the drugs.
B) It is highly unlikely that the microbe might spontaneously develop two specific mutations to resist the effects of a pair of drugs. As such, even if one drug is resisted by the microbe, the second drug will eliminate the mutated microbe, thus preventing the development of spontaneously resistant mutants overall.
C) All drugs work antagonistically with each other. Their combined effects are far greater than either could achieve individually. Two drugs together helps to eliminate microbes, even if they have developed spontaneous mutations that would make them resistant to the drugs.
D) Drugs can also select for mutations that will enhance the activity of another drug. Therefore, each of the paired drugs will help to select for spontaneous mutations that enhance the activity of the other drug in the pair.
E) Bacteria can only ever develop resistance to a single antibiotic. If more than one drug is used, the organisms will definitely become resistant to one of them but it will not become resistant to both of them. The second antibiotic will kill the organism.

F) All of the above
G) D) and E)

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Please select the True statement regarding bacterial resistance to antimicrobials.


A) Gram-positive bacteria are intrinsically resistant to certain medications because the lipid bilayer of their outer membrane prevents the molecules from entering.
B) Intrinsic resistance  generally occurs through spontaneous mutation or horizontal gene transfer.
C) The genes for antimicrobial resistance are often carried on fertility plasmids (F plasmids) .
D) Mycoplasma species lack a cell wall, so they are resistant to penicillin that interferes with peptidoglycan synthesis. This is an example of intrinsic resistance.
E) Acquired resistance is very limited because microorganisms cannot evolve, so are incapable of developing mechanisms to avoid the effects of medications. 

F) None of the above
G) A) and E)

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The arsenic compound that proved highly effective in treating syphilis was called


A) penicillin.
B) sulfa.
C) erythromycin.
D) Salvarsan.
E) erlichsan.

F) A) and C)
G) A) and E)

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The minimum bactericidal concentration is the lowest concentration of a specific antimicrobial drug that kills ________ of a specific type of bacteria.


A) 10%
B) 50%
C) 99.9%
D) 100%
E) 25%

F) A) and E)
G) A) and D)

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Spontaneous development of resistance to a particular antimicrobial is difficult if the drug


A) targets a single type of molecule AND binds to a single site on that target molecule.
B) targets several different molecules AND affects the cytoplasmic membrane.
C) affects only one molecule.
D) affects the cytoplasmic membrane.
E) binds to several sites on the target molecule AND targets several different molecules.

F) A) and C)
G) C) and D)

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The major class(es) of antibiotics that inhibit protein synthesis include all of the following EXCEPT


A) bacitracins.
B) aminoglycosides.
C) tetracyclines.
D) macrolides.
E) streptogramins.

F) A) and E)
G) A) and B)

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Compliance problems are leading to a large increase in antibiotic resistant strains of


A) Mycobacterium.
B) Streptococcus.
C) Staphylococcus.
D) Pseudomonas.
E) Mycoplasma.

F) C) and D)
G) B) and C)

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Why would co-administration of a bacteriostatic drug interfere with the effects of penicillin?


A) Since most bacteriostatic drugs are produced from bacteria but penicillin is produced from mold, the two drugs are incompatible with each other.
B) A bacteriostatic drug interferes with the ability of a bacterial cell to take in compounds from the outside environment. Penicillin must be taken in by the cell in order to have its effect, so this would directly inhibit it.
C) The bacteriostatic drugs would bind directly to the penicillin, preventing both its uptake by the cell and its ability to perform its duty within the bacterial cell.
D) Penicillin interferes with cell wall production so it only works when the cells are actively replicating and MAKING new peptidoglycan. A bacteriostatic drug works by shutting down replication, holding the cells "static." This would interfere with the mode of action required by the penicillin.
E) Nothing interferes with the effects of penicillin. It is the most effective medication that we have, so is never used with the addition of a second drug when treating a person.

F) C) and E)
G) All of the above

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The most effective form of penicillin is


A) penicillin A.
B) penicillin B.
C) penicillin E.
D) penicillin G.
E) penicillium.

F) C) and D)
G) B) and E)

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