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Microbiology · Parasitology: chloroquine resistance mechanism
Sample itemChloroquine-resistant Plasmodium falciparum accumulates much less drug in its digestive vacuole than sensitive strains. Which change mainly explains this?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. Mutant PfCRT transporter that pumps the drug out
Chloroquine concentrates in the parasite food vacuole and blocks haem polymerisation. Resistant parasites carry mutant PfCRT, which effluxes the drug from the vacuole so it no longer reaches toxic concentrations.
Option by option
A. Increased dihydrofolate reductase production by the parasite
Extra dihydrofolate reductase relates to antifolate resistance, not chloroquine.
B. Mutant PfCRT transporter that pumps the drug out (correct)
Correct. Mutant PfCRT-mediated efflux lowers vacuolar chloroquine.
C. Faster haemozoin crystal growth that traps the drug
Enhanced haemozoin formation would remove toxic haem, but the main resistance mechanism is drug efflux.
D. Altered cytochrome b drug-binding site in the mitochondrion
Cytochrome b changes relate to atovaquone resistance.
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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