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Pharmacology · Antiviral drugs
Sample itemWhy is acyclovir selectively toxic to herpes-infected cells?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. It is first phosphorylated by viral thymidine kinase
Acyclovir is a guanosine analogue converted to its monophosphate only by herpesvirus thymidine kinase, then to the triphosphate by host kinases. The triphosphate inhibits viral DNA polymerase and terminates the chain, so uninfected cells are largely spared.
Option by option
A. It inhibits reverse transcriptase
Reverse transcriptase inhibition is the action of anti-HIV nucleoside analogues.
B. It is first phosphorylated by viral thymidine kinase (correct)
Initial activation depends on the viral enzyme, concentrating the drug in infected cells.
C. It inhibits viral neuraminidase
Neuraminidase inhibition is how oseltamivir acts on influenza.
D. It blocks the M2 ion channel and uncoating
M2 channel blockade and uncoating inhibition is the action of amantadine.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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