Biochemical and genetic analysis of methylenetetrahydrofolate reductase in Leishmania metabolism and virulence

Tim J. Vickers, Giuseppe Orsomando, Rocío Díaz De La Garza, David A. Scott, Song O. Kang, Andrew D. Hanson, Stephen M. Beverley

Research output: Contribution to journalArticlepeer-review

19 Scopus citations


Methylenetetrahydrofolate reductase (MTHFR; EC is the sole enzyme responsible for generation of 5-methyltetrahydrofolate, which is required for methionine synthesis and provision of methyl groups via S-adenosylmethionine. Genome analysis showed that Leishmania species, unlike Trypanosoma brucei and Trypanosoma cruzi, contain genes encoding MTHFR and two distinct methionine synthases. Leishmania MTHFR differed from those in other eukaryotes by the absence of a C-terminal regulatory domain. L. major MTHFR was expressed in yeast and recombinant enzyme was produced in Escherichia coli. MTHFR was not inhibited by S-adenosylmethionine and, uniquely among folate-metabolizing enzymes, showed dual-cofactor specificity with NADH and NADPH under physiological conditions. MTHFR null mutants (mthfr-) lacked 5-methyltetrahydrofolate, the most abundant intracellular folate, and could not utilize exogenous homocysteine for growth. Under conditions of methionine limitation mthfr- mutant cells grew poorly, whereas their growth was normal in standard culture media. Neither in vitro MTHFR activity nor the growth of mthfr- mutants or MTHFR overexpressors were differentially affected by antifolates known to inhibit parasite growth via targets beyond dihydrofolate reductase and pteridine reductase 1. In a mouse model of infection mthfr- mutants showed good infectivity and virulence, indicating that sufficient methionine is available within the parasitophorous vacuole to meet the needs of the parasite.

Original languageEnglish
Pages (from-to)38150-38158
Number of pages9
JournalJournal of Biological Chemistry
Issue number50
StatePublished - Dec 15 2006


Dive into the research topics of 'Biochemical and genetic analysis of methylenetetrahydrofolate reductase in Leishmania metabolism and virulence'. Together they form a unique fingerprint.

Cite this