We describe here a rapid procedure to predict the resistance of Plasmo
dium falciparum to pyrimethamine or cycloguanil. The method consists o
f amplification by PCR of the DHFR gene followed by restriction enzyme
digestion of codons 16 and 108. Three different enzymes are used to c
ut the wild-type, 108-threonine mutant, and 108-asparagine mutant gene
. Since every natural antifolate-resistant isolate identified until no
w carries a mutation in codon 108, determination of the nature of this
codon can predict the sensitivity of any P. falciparum isolate. (C) 1
995 Academic Press, Inc.