Currently, the mechanism of metronidazole resistance is not understood
in Helicobacter pylori. We have looked at uptake of metronidazole int
o a sensitive and a resistant strain of H. pylori. Both strains displa
yed rapid uptake of [C-14]metronidazole, although the resistant strain
accumulated the drug at a slower rate and to a lesser amount than the
sensitive strain. Uptake was inhibited by KCN and carbonyl cyanide m-
chlorophenyl-hydrazone (CCCP) but not by sodium arsenate. Thin-layer c
hromatography analysis of lysed cell supernatants showed that metronid
azole was metabolized in both strains. A variety of related imidazole
compounds inhibited metronidazole uptake, consistent with a common tra
nsport system for this group of antibiotics. Our data do not support a
n absence of uptake or metabolism as a cause of resistance in the stra
in examined.