Deck 20: Antimicrobial Drugs

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سؤال
A drug that inhibits mitosis, such as griseofulvin, would be more effective against

A) fungi.
B) gram-positive bacteria.
C) mycobacteria.
D) wall-less bacteria.
E) gram-negative bacteria.
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سؤال
Figure 20.1 <strong>Figure 20.1   The antibiotic tetracycline binds to the 30S subunit of the ribosome, as shown by the dark black bar on the right portion of the diagram in Figure 20.1. The effect is to</strong> A) prevent peptide bond formation. B) stop the ribosome from moving along the mRNA. C) prevent transcription. D) interfere with the attachment of the tRNA to mRNA-ribosome complex. E) prevent attachment of DNA. <div style=padding-top: 35px> The antibiotic tetracycline binds to the 30S subunit of the ribosome, as shown by the dark black bar on the right portion of the diagram in Figure 20.1. The effect is to

A) prevent peptide bond formation.
B) stop the ribosome from moving along the mRNA.
C) prevent transcription.
D) interfere with the attachment of the tRNA to mRNA-ribosome complex.
E) prevent attachment of DNA.
سؤال
In what way are semisynthetic penicillins and natural penicillins alike?

A) Both are resistant to stomach acids.
B) Both are bactericidal.
C) Both are broad spectrum.
D) Both are based on β-lactam.
E) Both are resistant to penicillinase.
سؤال
Figure 20.2 <strong>Figure 20.2   The antibiotic chloramphenicol binds to the 50S subunit of the ribosome, as shown in Figure 20.2. The effect is to</strong> A) prevent peptide bond formation in prokaryotes. B) prevent transcription in prokaryotes. C) prevent polypeptide elongation in eukaryotes. D) prevent ribosome formation in bacteria. E) prevent mRNA-ribosome binding in eukaryotes. <div style=padding-top: 35px> The antibiotic chloramphenicol binds to the 50S subunit of the ribosome, as shown in Figure 20.2. The effect is to

A) prevent peptide bond formation in prokaryotes.
B) prevent transcription in prokaryotes.
C) prevent polypeptide elongation in eukaryotes.
D) prevent ribosome formation in bacteria.
E) prevent mRNA-ribosome binding in eukaryotes.
سؤال
Which compound would be the most useful to treat candidiasis?

A) thymine
B) flucytosine
C) penicillin
D) uracil
E) guanine
سؤال
Table 20.1
The following data were obtained from a broth dilution test.  Concentration of AntibioticX  Growth  Growth in  Subculture 2μg/ml++10μg/ml+15μg/ml25μg/ml\begin{array}{|l|l|l|}\hline\text { Concentration of AntibioticX } & \text { Growth } & \frac{\text { Growth in }}{\text { Subculture }} \\\hline 2 \mu \mathrm{g} / \mathrm{ml} & + & + \\\hline 10 \mu \mathrm{g} / \mathrm{ml} & - & + \\\hline 15 \mu \mathrm{g} / \mathrm{ml} & - & - \\\hline 25 \mu \mathrm{g} / \mathrm{ml} & - & - \\ \hline\end{array}

-5) In Table 20.1, as illustrated by the data shown, the minimal bactericidal concentration of antibiotic X is

A) 10 ?g/ml.
B) 2 ?g/ml.
C) 25 ?g/ml.
D) 15 ?g/ml.
E) The answer cannot be determined based on the information provided.
سؤال
More than half of our antibiotics are

A) synthesized in laboratories.
B) produced by Fleming.
C) produced by eukaryotic organisms.
D) produced by fungi.
E) produced by bacteria.
سؤال
Antimicrobial peptides (AMPs) frequently work by

A) disrupting the plasma membrane.
B) hydrolyzing peptidoglycan.
C) complementary base pairing with DNA.
D) inhibiting cell-wall synthesis.
E) inhibiting protein synthesis.
سؤال
Which of the following antibiotics is recommended for use against gram -negative bacteria?

A) polymyxin
B) penicillin
C) bacitracin
D) cephalosporin
E) polyenes
سؤال
Which of the following methods of action would be bacteriostatic?

A) competitive inhibition with folic acid synthesis
B) competitive inhibition with DNA gyrase
C) injury to plasma membrane
D) inhibition of protein synthesis
E) inhibition of cell wall synthesis
سؤال
Which of the following is mismatched?

A) Fleming  initial identification of penicillinʹs effect on gram-positive microbial growth
B) Florey and Chain  identification of Penicillium as the producer of penicillin
C) Kirby and Bauer  disc-diffusion method
D) Ehrlich  ʺmagic bulletʺ theory
E) None of these is mismatched.
سؤال
Which of the following antimicrobial agents has the fewest side effects?

A) streptomycin
B) chloramphenicol
C) erythromycin
D) penicillin
E) tetracycline
سؤال
Which one of the following does NOT belong with the others?

A) cephalosporin
B) monobactam
C) penicillin
D) bacitracin
E) streptomycin
سؤال
To date, most of our natural antibiotics have been found to be produced by members of what genus?

A) Bacillus
B) Paenibacillus
C) Streptomyces
D) Penicillium
E) Cephalosporium
سؤال
Most of the available antimicrobial agents are effective against

A) bacteria.
B) viruses.
C) protozoa.
D) fungi.
E) All of the answers are correct.
سؤال
Which of the following drugs does NOT act by competitive inhibition?

A) trimethoprim
B) ethambutol
C) sulfonamide
D) streptomycin
E) isoniazid
سؤال
Penicillin was considered a ʺmiracle drugʺ for all of the following reasons EXCEPT

A) it was the first antibiotic.
B) it has selective toxicity.
C) it does not affect eukaryotic cells.
D) it kills bacteria.
E) it inhibits gram-positive cell wall synthesis.
سؤال
Which of the following antimicrobial agents is recommended for use against fungal infections?

A) polymyxin
B) bacitracin
C) amphotericin B
D) cephalosporin
E) penicillin
سؤال
Which of the following antibiotics is NOT bactericidal?

A) polyenes
B) cephalosporins
C) penicillin
D) aminoglycosides
E) rifampins
سؤال
Table 20.1
The following data were obtained from a broth dilution test.  Concentration of AntibioticX  Growth  Growth in  Subculture 2μg/ml++10μg/ml+15μg/ml25μg/ml\begin{array}{|l|l|l|}\hline\text { Concentration of AntibioticX } & \text { Growth } & \frac{\text { Growth in }}{\text { Subculture }} \\\hline 2 \mu \mathrm{g} / \mathrm{ml} & + & + \\\hline 10 \mu \mathrm{g} / \mathrm{ml} & - & + \\\hline 15 \mu \mathrm{g} / \mathrm{ml} & - & - \\\hline 25 \mu \mathrm{g} / \mathrm{ml} & - & - \\ \hline\end{array}

-In Table 20.1, the minimal inhibitory concentration of antibiotic X is

A) 25 ?g/ml.
B) 15 ?g/ml.
C) 2 ?g/ml.
D) 10 ?g/ml.
E) The answer cannot be determined based on the information provided.
سؤال
Drug resistance occurs

A) when antibiotics are taken after the symptoms disappear.
B) against antibiotics and not against synthetic chemotherapeutic agents.
C) because bacteria are normal microbiota.
D) when antibiotics are used indiscriminately.
E) All of the answers are correct.
سؤال
Which of the following statements about drug resistance is FALSE?

A) It may be transferred from one bacterium to another during conjugation.
B) It may be carried on a plasmid.
C) It may be due to enzymes that degrade some antibiotics.
D) It is found only in gram-negative bacteria.
E) It may be due to increased uptake of a drug.
سؤال
Table 20.2
The following results were obtained from a disk-diffusion test for microbial susceptibility to antibiotics. Staphylococcus aureus was the test organism.  Antibiotic  Zone of Inhibition A3 mmB7 mmC0 mmD10 mm\begin{array} { | l | l | } \hline { \text { Antibiotic } } & \text { Zone of Inhibition } \\\hline \mathrm { A } & 3 \mathrm {~mm} \\\hline \mathrm { B } & 7 \mathrm {~mm} \\\hline \mathrm { C } & 0 \mathrm {~mm} \\\hline \mathrm { D } & 10 \mathrm {~mm} \\\hline\end{array}

-In Table 20.2, the antibiotic that exhibited bactericidal action was

A) A.
B) B.
C) C.
D) D.
E) The answer cannot be determined based on the information provided.
سؤال
Lamisil is an allylamine used to treat dermatomycoses. Lamisilʹs method of action is similar to that of

A) polymyxin B.
B) echinocandins.
C) bacitracin.
D) azole antibiotics.
E) griseofulvin.
سؤال
Figure 20.3 <strong>Figure 20.3   The substrate for transpeptidase used to synthesize peptidoglycan is shown in Figure 20.3. Which of the drugs shown would inhibit peptidoglycan synthesis?</strong> A) a B) b C) c D) d E) e <div style=padding-top: 35px> The substrate for transpeptidase used to synthesize peptidoglycan is shown in Figure 20.3. Which of the drugs shown would inhibit peptidoglycan synthesis?

A) a
B) b
C) c
D) d
E) e
سؤال
Niclosamide prevents ATP generation in mitochondria. You would expect this drug to be effective against

A) helminths.
B) gram-positive bacteria.
C) Mycobacterium tuberculosis.
D) viruses.
E) gram-negative bacteria.
سؤال
Table 20.3 The following data were obtained from a broth dilution test:  Concentration  of Antibiotic X Growth 2.0μg/ml1.0μml0.5μml/ml0.25μg/ml+0.125μg/ml+0+\begin{array} { | c | c | } \hline \begin{array} { c } \text { Concentration } \\\text { of Antibiotic } \\X\end{array} & \text { Growth } \\\hline 2.0 \mu \mathrm { g } / \mathrm { ml } & - \\\hline 1.0 \mu \mathrm { ml } & - \\\hline 0.5 \mu \mathrm { ml } / \mathrm { ml } & - \\\hline 0.25 \mu \mathrm { g } / \mathrm { ml } & + \\\hline 0.125 \mu \mathrm { g } / \mathrm { ml } & + \\\hline 0 & + \\\hline\end{array} Bacteria from the 0.25 ?g/ml tube were transferred to new growth media containing antibiotic X with the following results:  Concentration  of Antibiotic X Growth 2.0μg/ml1.0μml+0.5μml/ml+0.25μg/ml+\begin{array} { | c | c | } \hline \begin{array} { c } \text { Concentration } \\\text { of Antibiotic } \\X\end{array} & \text { Growth } \\\hline 2.0 \mu \mathrm { g } / \mathrm { ml } & - \\\hline 1.0 \mu \mathrm { ml } & + \\\hline 0.5 \mu \mathrm { ml } / \mathrm { ml } & + \\\hline 0.25 \mu \mathrm { g } / \mathrm { ml } & + \\\hline\end{array} The data in Table 20.3 show that these bacteria

A) were resistant to 1.0 ?g/ml at the start of the experiment.
B) were killed by 0.5 ?g/ml of antibiotic X.
C) are pathogenic.
D) were killed by 0.125 ?g/ml of antibiotic X.
E) developed resistance to antibiotics.
سؤال
The antimicrobial drugs with the broadest spectrum of activity are

A) chloramphenicol.
B) tetracyclines.
C) penicillin G.
D) macrolides.
E) aminoglycosides.
سؤال
Which of the following does NOT constitute an advantage of using two antibiotics together?

A) It lessens the toxicity of individual drugs.
B) It allows treatment to be provided prior to diagnosis.
C) It can prevent drug resistance.
D) Two are always twice as effective as one.
E) All of these are advantages of using two antibiotics together.
سؤال
Which of the following organisms would MOST likely be sensitive to natural penicillin?

A) penicillinase-producing Neisseria gonorrhoeae
B) helminths
C) Penicillium
D) Mycoplasma
E) Streptococcus pyogenes
سؤال
Table 20.2
The following results were obtained from a disk-diffusion test for microbial susceptibility to antibiotics. Staphylococcus aureus was the test organism.  Antibiotic  Zone of Inhibition A3 mmB7 mmC0 mmD10 mm\begin{array} { | l | l | } \hline { \text { Antibiotic } } & \text { Zone of Inhibition } \\\hline \mathrm { A } & 3 \mathrm {~mm} \\\hline \mathrm { B } & 7 \mathrm {~mm} \\\hline \mathrm { C } & 0 \mathrm {~mm} \\\hline \mathrm { D } & 10 \mathrm {~mm} \\\hline\end{array}

-In Table 20.2, the most effective antibiotic tested was

A) A.
B) B.
C) C.
D) D.
E) The answer cannot be determined based on the information provided.
سؤال
Table 20.2
The following results were obtained from a disk-diffusion test for microbial susceptibility to antibiotics. Staphylococcus aureus was the test organism.  Antibiotic  Zone of Inhibition A3 mmB7 mmC0 mmD10 mm\begin{array} { | l | l | } \hline { \text { Antibiotic } } & \text { Zone of Inhibition } \\\hline \mathrm { A } & 3 \mathrm {~mm} \\\hline \mathrm { B } & 7 \mathrm {~mm} \\\hline \mathrm { C } & 0 \mathrm {~mm} \\\hline \mathrm { D } & 10 \mathrm {~mm} \\\hline\end{array}

-In Table 20.2, which antibiotic would be most useful for treating a Salmonella infection?

A) A
B) B
C) C
D) D
E) The answer cannot be determined based on the information provided.
سؤال
In the presence of penicillin, a cell dies because

A) it lacks a cell membrane.
B) it undergoes lysis.
C) its contents leak out.
D) it lacks a cell wall.
E) it plasmolyzes.
سؤال
Which of the following statements is FALSE?

A) Interferon inhibits glycolysis.
B) Acyclovir inhibits DNA synthesis.
C) Azoles inhibit plasma membrane synthesis.
D) Amantadine inhibits the release of viral nucleic acid.
E) Fluoroquinolone inhibits DNA synthesis.
سؤال
Protozoan and helminthic diseases are difficult to treat because

A) their cells are structurally and functionally similar to human cells.
B) they replicate inside human cells.
C) they do not reproduce.
D) they have more genes than bacteria.
E) they do not have ribosomes.
سؤال
Which of the following antibiotics does NOT interfere with cell wall synthesis?

A) natural penicillins
B) semisynthetic penicillins
C) cephalosporins
D) vancomycin
E) macrolides
سؤال
Figure 20.4 <strong>Figure 20.4   The structures of the influenza drug Tamiflu and sialic acid, the substrate for influenza virusʹs neuramidase, are shown in Figure 20.4. What is the method of action of Tamiflu?</strong> A) inhibits plasma membrane synthesis B) competitive inhibition C) inhibits synthesis of neuramidase D) inhibits cell wall synthesis E) prevents synthesis of virus spikes <div style=padding-top: 35px> The structures of the influenza drug Tamiflu and sialic acid, the substrate for influenza virusʹs neuramidase, are shown in Figure 20.4. What is the method of action of Tamiflu?

A) inhibits plasma membrane synthesis
B) competitive inhibition
C) inhibits synthesis of neuramidase
D) inhibits cell wall synthesis
E) prevents synthesis of virus spikes
سؤال
Which of the following statements about drugs that competitively inhibit DNA polymerase or RNA polymerase is FALSE?

A) They are used against viral infections.
B) They cause cellular plasmolysis.
C) They can affect host cell DNA synthesis.
D) They interfere with protein synthesis.
E) They can potentially cause mutations.
سؤال
Which of the following would be selective against the tubercle bacillus?

A) streptogramin  inhibits protein synthesis
B) ethambutol  inhibits mycolic acid synthesis
C) vancomycin  inhibits peptidoglycan synthesis
D) bacitracin  inhibits peptidoglycan synthesis
E) streptomycin  inhibits protein synthesis
سؤال
Which of the following antibiotics are used to treat fungal infections? 1. aminoglycosides
2) cephalosporins
3) griseofulvin
4) polyenes
5) bacitracin

A) 1, 2, and 3
B) 3, 4, and 5
C) 3 and 4
D) 4 and 5
E) All of these antibiotics are used to treat fungal infections.
سؤال
Explain why penicillin was called the ʺmiracle drugʺ when it was first used in the 1940s.
سؤال
PABA serves as the competitive inhibitor in the action of sulfanilamides.
سؤال
Both trimethoprim and sulfamethoxazole inhibit reactions along the same metabolic pathway.
سؤال
Penicillin and streptomycin are commonly used in synergism because they display the same mode of action.
سؤال
Use of antibiotics in animal feed leads to antibiotic-resistant bacteria because

A) the antibiotics kill susceptible bacteria, but the few that are naturally resistant live and reproduce, and their progeny repopulate the host animal.
B) bacteria from other animals replace those killed by the antibiotics.
C) the antibiotics persist in soil and water.
D) the antibiotics cause new mutations to occur in the surviving bacteria, which results in resistance to antibiotics.
E) the few surviving bacteria that are affected by the antibiotics develop immunity to the antibiotics, which they pass on to their progeny.
سؤال
The antibiotic actinomycin D binds between adjacent G-C pairs, thus interfering with

A) translation.
B) peptide bond formation.
C) cellular respiration.
D) plasma membrane function.
E) transcription.
سؤال
Antiviral drugs target viral processes that occur during viral infection.
سؤال
Undergrowth of fungi after antibiotic use is commonly referred to as a superinfection.
سؤال
An antibiotic that attacks the LPS layer would be expected to have a narrow spectrum of activity.
سؤال
Community-acquired MRSA is typically more virulent than health care-associated MRSA.
سؤال
Explain the difficulties in developing antiviral drugs against DNA viruses, when compared to RNA viruses.
سؤال
Penicillin does not directly kill bacteria. Why, then, is it considered to be bacteriocidal?
سؤال
Phage therapy has been used in the past as an antiviral treatment.
سؤال
Which of the following antibiotics causes misreading of mRNA?

A) tetracyclines  bind with 30S subunit
B) aminoglycoside  changes shape of 30S units
C) chloramphenicol  inhibits peptide bonds at 50S subunit
D) oxazolidinone  prevents formation of 70S ribosome
E) streptogamin  prevents release of peptide from 70S ribosome
سؤال
Can you determine both MIC and MBC from an E-test? Explain.
سؤال
An official from an international health agency predicts that if all countries enacted legislation to only sell antibiotics with a prescription, then the rate of antibiotic resistant would ʺgrind to a halt.ʺ Do you agree? Explain.
سؤال
Which of the following does NOT affect eukaryotic cells?

A) antifungal drugs
B) semisynthetic penicillins
C) antiprotozoan drugs
D) antihelminthic drugs
E) nucleotide analogs
سؤال
Due to its target, rifamycins can be effective over a broad spectrum.
سؤال
Mebendazole is used to treat cestode infections. It interferes with microtubule formation; therefore, it would NOT affect

A) protozoa.
B) helminths.
C) human cells.
D) bacteria.
E) fungi.
سؤال
Only microbes produce antimicrobial peptides.
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Deck 20: Antimicrobial Drugs
1
A drug that inhibits mitosis, such as griseofulvin, would be more effective against

A) fungi.
B) gram-positive bacteria.
C) mycobacteria.
D) wall-less bacteria.
E) gram-negative bacteria.
A
2
Figure 20.1 <strong>Figure 20.1   The antibiotic tetracycline binds to the 30S subunit of the ribosome, as shown by the dark black bar on the right portion of the diagram in Figure 20.1. The effect is to</strong> A) prevent peptide bond formation. B) stop the ribosome from moving along the mRNA. C) prevent transcription. D) interfere with the attachment of the tRNA to mRNA-ribosome complex. E) prevent attachment of DNA. The antibiotic tetracycline binds to the 30S subunit of the ribosome, as shown by the dark black bar on the right portion of the diagram in Figure 20.1. The effect is to

A) prevent peptide bond formation.
B) stop the ribosome from moving along the mRNA.
C) prevent transcription.
D) interfere with the attachment of the tRNA to mRNA-ribosome complex.
E) prevent attachment of DNA.
D
3
In what way are semisynthetic penicillins and natural penicillins alike?

A) Both are resistant to stomach acids.
B) Both are bactericidal.
C) Both are broad spectrum.
D) Both are based on β-lactam.
E) Both are resistant to penicillinase.
D
4
Figure 20.2 <strong>Figure 20.2   The antibiotic chloramphenicol binds to the 50S subunit of the ribosome, as shown in Figure 20.2. The effect is to</strong> A) prevent peptide bond formation in prokaryotes. B) prevent transcription in prokaryotes. C) prevent polypeptide elongation in eukaryotes. D) prevent ribosome formation in bacteria. E) prevent mRNA-ribosome binding in eukaryotes. The antibiotic chloramphenicol binds to the 50S subunit of the ribosome, as shown in Figure 20.2. The effect is to

A) prevent peptide bond formation in prokaryotes.
B) prevent transcription in prokaryotes.
C) prevent polypeptide elongation in eukaryotes.
D) prevent ribosome formation in bacteria.
E) prevent mRNA-ribosome binding in eukaryotes.
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5
Which compound would be the most useful to treat candidiasis?

A) thymine
B) flucytosine
C) penicillin
D) uracil
E) guanine
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6
Table 20.1
The following data were obtained from a broth dilution test.  Concentration of AntibioticX  Growth  Growth in  Subculture 2μg/ml++10μg/ml+15μg/ml25μg/ml\begin{array}{|l|l|l|}\hline\text { Concentration of AntibioticX } & \text { Growth } & \frac{\text { Growth in }}{\text { Subculture }} \\\hline 2 \mu \mathrm{g} / \mathrm{ml} & + & + \\\hline 10 \mu \mathrm{g} / \mathrm{ml} & - & + \\\hline 15 \mu \mathrm{g} / \mathrm{ml} & - & - \\\hline 25 \mu \mathrm{g} / \mathrm{ml} & - & - \\ \hline\end{array}

-5) In Table 20.1, as illustrated by the data shown, the minimal bactericidal concentration of antibiotic X is

A) 10 ?g/ml.
B) 2 ?g/ml.
C) 25 ?g/ml.
D) 15 ?g/ml.
E) The answer cannot be determined based on the information provided.
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7
More than half of our antibiotics are

A) synthesized in laboratories.
B) produced by Fleming.
C) produced by eukaryotic organisms.
D) produced by fungi.
E) produced by bacteria.
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8
Antimicrobial peptides (AMPs) frequently work by

A) disrupting the plasma membrane.
B) hydrolyzing peptidoglycan.
C) complementary base pairing with DNA.
D) inhibiting cell-wall synthesis.
E) inhibiting protein synthesis.
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9
Which of the following antibiotics is recommended for use against gram -negative bacteria?

A) polymyxin
B) penicillin
C) bacitracin
D) cephalosporin
E) polyenes
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10
Which of the following methods of action would be bacteriostatic?

A) competitive inhibition with folic acid synthesis
B) competitive inhibition with DNA gyrase
C) injury to plasma membrane
D) inhibition of protein synthesis
E) inhibition of cell wall synthesis
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11
Which of the following is mismatched?

A) Fleming  initial identification of penicillinʹs effect on gram-positive microbial growth
B) Florey and Chain  identification of Penicillium as the producer of penicillin
C) Kirby and Bauer  disc-diffusion method
D) Ehrlich  ʺmagic bulletʺ theory
E) None of these is mismatched.
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12
Which of the following antimicrobial agents has the fewest side effects?

A) streptomycin
B) chloramphenicol
C) erythromycin
D) penicillin
E) tetracycline
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13
Which one of the following does NOT belong with the others?

A) cephalosporin
B) monobactam
C) penicillin
D) bacitracin
E) streptomycin
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14
To date, most of our natural antibiotics have been found to be produced by members of what genus?

A) Bacillus
B) Paenibacillus
C) Streptomyces
D) Penicillium
E) Cephalosporium
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15
Most of the available antimicrobial agents are effective against

A) bacteria.
B) viruses.
C) protozoa.
D) fungi.
E) All of the answers are correct.
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16
Which of the following drugs does NOT act by competitive inhibition?

A) trimethoprim
B) ethambutol
C) sulfonamide
D) streptomycin
E) isoniazid
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17
Penicillin was considered a ʺmiracle drugʺ for all of the following reasons EXCEPT

A) it was the first antibiotic.
B) it has selective toxicity.
C) it does not affect eukaryotic cells.
D) it kills bacteria.
E) it inhibits gram-positive cell wall synthesis.
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18
Which of the following antimicrobial agents is recommended for use against fungal infections?

A) polymyxin
B) bacitracin
C) amphotericin B
D) cephalosporin
E) penicillin
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19
Which of the following antibiotics is NOT bactericidal?

A) polyenes
B) cephalosporins
C) penicillin
D) aminoglycosides
E) rifampins
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20
Table 20.1
The following data were obtained from a broth dilution test.  Concentration of AntibioticX  Growth  Growth in  Subculture 2μg/ml++10μg/ml+15μg/ml25μg/ml\begin{array}{|l|l|l|}\hline\text { Concentration of AntibioticX } & \text { Growth } & \frac{\text { Growth in }}{\text { Subculture }} \\\hline 2 \mu \mathrm{g} / \mathrm{ml} & + & + \\\hline 10 \mu \mathrm{g} / \mathrm{ml} & - & + \\\hline 15 \mu \mathrm{g} / \mathrm{ml} & - & - \\\hline 25 \mu \mathrm{g} / \mathrm{ml} & - & - \\ \hline\end{array}

-In Table 20.1, the minimal inhibitory concentration of antibiotic X is

A) 25 ?g/ml.
B) 15 ?g/ml.
C) 2 ?g/ml.
D) 10 ?g/ml.
E) The answer cannot be determined based on the information provided.
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21
Drug resistance occurs

A) when antibiotics are taken after the symptoms disappear.
B) against antibiotics and not against synthetic chemotherapeutic agents.
C) because bacteria are normal microbiota.
D) when antibiotics are used indiscriminately.
E) All of the answers are correct.
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22
Which of the following statements about drug resistance is FALSE?

A) It may be transferred from one bacterium to another during conjugation.
B) It may be carried on a plasmid.
C) It may be due to enzymes that degrade some antibiotics.
D) It is found only in gram-negative bacteria.
E) It may be due to increased uptake of a drug.
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23
Table 20.2
The following results were obtained from a disk-diffusion test for microbial susceptibility to antibiotics. Staphylococcus aureus was the test organism.  Antibiotic  Zone of Inhibition A3 mmB7 mmC0 mmD10 mm\begin{array} { | l | l | } \hline { \text { Antibiotic } } & \text { Zone of Inhibition } \\\hline \mathrm { A } & 3 \mathrm {~mm} \\\hline \mathrm { B } & 7 \mathrm {~mm} \\\hline \mathrm { C } & 0 \mathrm {~mm} \\\hline \mathrm { D } & 10 \mathrm {~mm} \\\hline\end{array}

-In Table 20.2, the antibiotic that exhibited bactericidal action was

A) A.
B) B.
C) C.
D) D.
E) The answer cannot be determined based on the information provided.
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24
Lamisil is an allylamine used to treat dermatomycoses. Lamisilʹs method of action is similar to that of

A) polymyxin B.
B) echinocandins.
C) bacitracin.
D) azole antibiotics.
E) griseofulvin.
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25
Figure 20.3 <strong>Figure 20.3   The substrate for transpeptidase used to synthesize peptidoglycan is shown in Figure 20.3. Which of the drugs shown would inhibit peptidoglycan synthesis?</strong> A) a B) b C) c D) d E) e The substrate for transpeptidase used to synthesize peptidoglycan is shown in Figure 20.3. Which of the drugs shown would inhibit peptidoglycan synthesis?

A) a
B) b
C) c
D) d
E) e
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26
Niclosamide prevents ATP generation in mitochondria. You would expect this drug to be effective against

A) helminths.
B) gram-positive bacteria.
C) Mycobacterium tuberculosis.
D) viruses.
E) gram-negative bacteria.
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27
Table 20.3 The following data were obtained from a broth dilution test:  Concentration  of Antibiotic X Growth 2.0μg/ml1.0μml0.5μml/ml0.25μg/ml+0.125μg/ml+0+\begin{array} { | c | c | } \hline \begin{array} { c } \text { Concentration } \\\text { of Antibiotic } \\X\end{array} & \text { Growth } \\\hline 2.0 \mu \mathrm { g } / \mathrm { ml } & - \\\hline 1.0 \mu \mathrm { ml } & - \\\hline 0.5 \mu \mathrm { ml } / \mathrm { ml } & - \\\hline 0.25 \mu \mathrm { g } / \mathrm { ml } & + \\\hline 0.125 \mu \mathrm { g } / \mathrm { ml } & + \\\hline 0 & + \\\hline\end{array} Bacteria from the 0.25 ?g/ml tube were transferred to new growth media containing antibiotic X with the following results:  Concentration  of Antibiotic X Growth 2.0μg/ml1.0μml+0.5μml/ml+0.25μg/ml+\begin{array} { | c | c | } \hline \begin{array} { c } \text { Concentration } \\\text { of Antibiotic } \\X\end{array} & \text { Growth } \\\hline 2.0 \mu \mathrm { g } / \mathrm { ml } & - \\\hline 1.0 \mu \mathrm { ml } & + \\\hline 0.5 \mu \mathrm { ml } / \mathrm { ml } & + \\\hline 0.25 \mu \mathrm { g } / \mathrm { ml } & + \\\hline\end{array} The data in Table 20.3 show that these bacteria

A) were resistant to 1.0 ?g/ml at the start of the experiment.
B) were killed by 0.5 ?g/ml of antibiotic X.
C) are pathogenic.
D) were killed by 0.125 ?g/ml of antibiotic X.
E) developed resistance to antibiotics.
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28
The antimicrobial drugs with the broadest spectrum of activity are

A) chloramphenicol.
B) tetracyclines.
C) penicillin G.
D) macrolides.
E) aminoglycosides.
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29
Which of the following does NOT constitute an advantage of using two antibiotics together?

A) It lessens the toxicity of individual drugs.
B) It allows treatment to be provided prior to diagnosis.
C) It can prevent drug resistance.
D) Two are always twice as effective as one.
E) All of these are advantages of using two antibiotics together.
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30
Which of the following organisms would MOST likely be sensitive to natural penicillin?

A) penicillinase-producing Neisseria gonorrhoeae
B) helminths
C) Penicillium
D) Mycoplasma
E) Streptococcus pyogenes
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31
Table 20.2
The following results were obtained from a disk-diffusion test for microbial susceptibility to antibiotics. Staphylococcus aureus was the test organism.  Antibiotic  Zone of Inhibition A3 mmB7 mmC0 mmD10 mm\begin{array} { | l | l | } \hline { \text { Antibiotic } } & \text { Zone of Inhibition } \\\hline \mathrm { A } & 3 \mathrm {~mm} \\\hline \mathrm { B } & 7 \mathrm {~mm} \\\hline \mathrm { C } & 0 \mathrm {~mm} \\\hline \mathrm { D } & 10 \mathrm {~mm} \\\hline\end{array}

-In Table 20.2, the most effective antibiotic tested was

A) A.
B) B.
C) C.
D) D.
E) The answer cannot be determined based on the information provided.
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32
Table 20.2
The following results were obtained from a disk-diffusion test for microbial susceptibility to antibiotics. Staphylococcus aureus was the test organism.  Antibiotic  Zone of Inhibition A3 mmB7 mmC0 mmD10 mm\begin{array} { | l | l | } \hline { \text { Antibiotic } } & \text { Zone of Inhibition } \\\hline \mathrm { A } & 3 \mathrm {~mm} \\\hline \mathrm { B } & 7 \mathrm {~mm} \\\hline \mathrm { C } & 0 \mathrm {~mm} \\\hline \mathrm { D } & 10 \mathrm {~mm} \\\hline\end{array}

-In Table 20.2, which antibiotic would be most useful for treating a Salmonella infection?

A) A
B) B
C) C
D) D
E) The answer cannot be determined based on the information provided.
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33
In the presence of penicillin, a cell dies because

A) it lacks a cell membrane.
B) it undergoes lysis.
C) its contents leak out.
D) it lacks a cell wall.
E) it plasmolyzes.
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34
Which of the following statements is FALSE?

A) Interferon inhibits glycolysis.
B) Acyclovir inhibits DNA synthesis.
C) Azoles inhibit plasma membrane synthesis.
D) Amantadine inhibits the release of viral nucleic acid.
E) Fluoroquinolone inhibits DNA synthesis.
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35
Protozoan and helminthic diseases are difficult to treat because

A) their cells are structurally and functionally similar to human cells.
B) they replicate inside human cells.
C) they do not reproduce.
D) they have more genes than bacteria.
E) they do not have ribosomes.
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36
Which of the following antibiotics does NOT interfere with cell wall synthesis?

A) natural penicillins
B) semisynthetic penicillins
C) cephalosporins
D) vancomycin
E) macrolides
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37
Figure 20.4 <strong>Figure 20.4   The structures of the influenza drug Tamiflu and sialic acid, the substrate for influenza virusʹs neuramidase, are shown in Figure 20.4. What is the method of action of Tamiflu?</strong> A) inhibits plasma membrane synthesis B) competitive inhibition C) inhibits synthesis of neuramidase D) inhibits cell wall synthesis E) prevents synthesis of virus spikes The structures of the influenza drug Tamiflu and sialic acid, the substrate for influenza virusʹs neuramidase, are shown in Figure 20.4. What is the method of action of Tamiflu?

A) inhibits plasma membrane synthesis
B) competitive inhibition
C) inhibits synthesis of neuramidase
D) inhibits cell wall synthesis
E) prevents synthesis of virus spikes
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38
Which of the following statements about drugs that competitively inhibit DNA polymerase or RNA polymerase is FALSE?

A) They are used against viral infections.
B) They cause cellular plasmolysis.
C) They can affect host cell DNA synthesis.
D) They interfere with protein synthesis.
E) They can potentially cause mutations.
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39
Which of the following would be selective against the tubercle bacillus?

A) streptogramin  inhibits protein synthesis
B) ethambutol  inhibits mycolic acid synthesis
C) vancomycin  inhibits peptidoglycan synthesis
D) bacitracin  inhibits peptidoglycan synthesis
E) streptomycin  inhibits protein synthesis
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40
Which of the following antibiotics are used to treat fungal infections? 1. aminoglycosides
2) cephalosporins
3) griseofulvin
4) polyenes
5) bacitracin

A) 1, 2, and 3
B) 3, 4, and 5
C) 3 and 4
D) 4 and 5
E) All of these antibiotics are used to treat fungal infections.
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41
Explain why penicillin was called the ʺmiracle drugʺ when it was first used in the 1940s.
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42
PABA serves as the competitive inhibitor in the action of sulfanilamides.
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43
Both trimethoprim and sulfamethoxazole inhibit reactions along the same metabolic pathway.
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44
Penicillin and streptomycin are commonly used in synergism because they display the same mode of action.
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45
Use of antibiotics in animal feed leads to antibiotic-resistant bacteria because

A) the antibiotics kill susceptible bacteria, but the few that are naturally resistant live and reproduce, and their progeny repopulate the host animal.
B) bacteria from other animals replace those killed by the antibiotics.
C) the antibiotics persist in soil and water.
D) the antibiotics cause new mutations to occur in the surviving bacteria, which results in resistance to antibiotics.
E) the few surviving bacteria that are affected by the antibiotics develop immunity to the antibiotics, which they pass on to their progeny.
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46
The antibiotic actinomycin D binds between adjacent G-C pairs, thus interfering with

A) translation.
B) peptide bond formation.
C) cellular respiration.
D) plasma membrane function.
E) transcription.
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47
Antiviral drugs target viral processes that occur during viral infection.
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48
Undergrowth of fungi after antibiotic use is commonly referred to as a superinfection.
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49
An antibiotic that attacks the LPS layer would be expected to have a narrow spectrum of activity.
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50
Community-acquired MRSA is typically more virulent than health care-associated MRSA.
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51
Explain the difficulties in developing antiviral drugs against DNA viruses, when compared to RNA viruses.
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52
Penicillin does not directly kill bacteria. Why, then, is it considered to be bacteriocidal?
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53
Phage therapy has been used in the past as an antiviral treatment.
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54
Which of the following antibiotics causes misreading of mRNA?

A) tetracyclines  bind with 30S subunit
B) aminoglycoside  changes shape of 30S units
C) chloramphenicol  inhibits peptide bonds at 50S subunit
D) oxazolidinone  prevents formation of 70S ribosome
E) streptogamin  prevents release of peptide from 70S ribosome
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55
Can you determine both MIC and MBC from an E-test? Explain.
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56
An official from an international health agency predicts that if all countries enacted legislation to only sell antibiotics with a prescription, then the rate of antibiotic resistant would ʺgrind to a halt.ʺ Do you agree? Explain.
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57
Which of the following does NOT affect eukaryotic cells?

A) antifungal drugs
B) semisynthetic penicillins
C) antiprotozoan drugs
D) antihelminthic drugs
E) nucleotide analogs
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58
Due to its target, rifamycins can be effective over a broad spectrum.
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59
Mebendazole is used to treat cestode infections. It interferes with microtubule formation; therefore, it would NOT affect

A) protozoa.
B) helminths.
C) human cells.
D) bacteria.
E) fungi.
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60
Only microbes produce antimicrobial peptides.
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