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IMP dehydrogenase deficiency in Leishmania donovani causes a restrictive growth phenotype in promastigotes but is not essential for infection in mice.

Abstract
Leishmania cannot synthesize purines de novo and therefore must scavenge purines from its host for survival and growth. Biochemical and genomic analyses have indicated that Leishmania species express three potential routes for the synthesis of guanylate nucleotides: (1) a two-step pathway that converts IMP to GMP; (2) a three-step pathway that starts with the deamination of guanine to xanthine, followed by phosphoribosylation to XMP and then conversion to GMP; or (3) direct guanine phosphoribosylation by HGPRT. To determine the role of the first of these pathways to guanylate nucleotide synthesis, an L. donovani line deficient in IMP dehydrogenase (IMPDH), the first step in the IMP to GMP pathway, was constructed by targeted gene replacement. The Δimpdh lesion triggered a highly restrictive growth phenotype in promastigotes in culture but did not impact parasitemias in mice. The dispensability of IMPDH in vivo is the first definitive demonstration that intracellular L. donovani amastigotes have access to a sufficient pool of guanine, xanthine, or guanylate precursors from the host.
AuthorsAudrey L Fulwiler, Jan M Boitz, Caslin Gilroy, Phillip A Yates, Armando Jardim, Buddy Ullman
JournalMolecular and biochemical parasitology (Mol Biochem Parasitol) Vol. 180 Issue 2 Pg. 123-6 (Dec 2011) ISSN: 1872-9428 [Electronic] Netherlands
PMID21907738 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
CopyrightCopyright © 2011 Elsevier B.V. All rights reserved.
Chemical References
  • Protozoan Proteins
  • Ribonucleotides
  • Xanthine
  • xanthosine monophosphate
  • Guanosine Monophosphate
  • IMP Dehydrogenase
Topics
  • Animals
  • Guanosine Monophosphate (metabolism)
  • Humans
  • IMP Dehydrogenase (deficiency, genetics)
  • Leishmania donovani (enzymology, genetics, growth & development, physiology)
  • Leishmania infantum (parasitology)
  • Mice
  • Mice, Inbred BALB C
  • Phenotype
  • Protozoan Proteins (genetics, metabolism)
  • Ribonucleotides (metabolism)
  • Xanthine

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