Assume a bacterium makes beta-lactamase. Could you still use a glycopeptide drug to treat an infection caused by this bacterium? Explain your reasoning.
Why is it challenging to obtain selectively toxic drugs against fungi, protozoans, and viruses?
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Key Concepts
Selective Toxicity
Similarity Between Pathogens and Host Cells
Challenges in Targeting Viruses
If a gene encoding a bacterial transpeptidase enzyme undergoes mutation, which of the following antimicrobials may no longer be effective against the mutated bacterium?
a. Macrolides
b. Polypeptide drugs
c. Tetracyclines
d. Penicillins
e. Quinolones
Mark the following as true or false, and then correct the false statements so they are true.
a. Human cells make drug efflux pumps.
b. The minimum bactericidal concentration is the minimum concentration of the drug that kills at least 50 percent of the bacteria present.
c. The E-test can reveal if a drug is bactericidal or bacteriostatic.
d. A drug that is bactericidal at one dose may be bacteriostatic at another dose.
e. The antifolate combination therapy trimethoprim-sulfamethoxazole may be used to treat protozoan infections.
Choose the false statement(s). Select all that apply.
a. Antifungal drugs may target cholesterol in fungal cell membranes.
b. Azole and polyene drugs promote cell lysis by impacting fungal cell plasma membranes.
c. Echinocandin drugs inhibit fungal cell wall synthesis.
d. Antifungal drugs may target DNA replication.
e. Antifungal drugs may target protein synthesis.
Match the antimicrobial drug to its feature. Some features may be used more than once, and some may not be used at all.
Which sensitivity test is best for determining the minimum bactericidal concentration and the minimum inhibitory concentration of a drug?
