Publications des scientifiques de l'IRD

Gazanion Elodie, Garcia Deborah, Silvestre R., Gérard C., Guichou J. F., Labesse G., Seveno Martial, Cordeiro-Da-Silva A., Ouaissi A., Sereno Denis, Vergnes Baptiste. (2011). The Leishmania nicotinamidase is essential for NAD(+) production and parasite proliferation. Molecular Microbiology, 82 (1), p. 21-38. ISSN 0950-382X.

Titre du document
The Leishmania nicotinamidase is essential for NAD(+) production and parasite proliferation
Année de publication
2011
Type de document
Article référencé dans le Web of Science WOS:000295226700004
Auteurs
Gazanion Elodie, Garcia Deborah, Silvestre R., Gérard C., Guichou J. F., Labesse G., Seveno Martial, Cordeiro-Da-Silva A., Ouaissi A., Sereno Denis, Vergnes Baptiste
Source
Molecular Microbiology, 2011, 82 (1), p. 21-38 ISSN 0950-382X
NAD(+) is a central cofactor that plays important roles in cellular metabolism and energy production in all living cells. Genomics-based reconstruction of NAD(+) metabolism revealed that Leishmania protozoan parasites are NAD(+) auxotrophs. Consequently, these parasites require assimilating NAD(+) precursors (nicotinamide, nicotinic acid, nicotinamide riboside) from their host environment to synthesize NAD(+) by a salvage pathway. Nicotinamidase is a key enzyme of this salvage pathway that catalyses conversion of nicotinamide (NAm) to nicotinic acid (Na), and that is absent in higher eukaryotes. We present here the biochemical and functional characterizations of the Leishmania infantum nicotinamidase (LiPNC1). Generation of Lipnc1 null mutants leads to a decrease in NAD(+) content, associated with a metabolic shutdown-like phenotype with an extensive lag phase of growth. Both phenotypes could be rescued by an add-back construct or by addition of exogenous Na. In addition, Lipnc1 null mutants were unable to establish a sustained infection in a murine experimental model. Altogether, these results illustrate that NAD(+) homeostasis is a fundamental component of Leishmania biology and virulence, and that NAm constitutes its main NAD(+) source in the mammalian host. The crystal structure of LiPNC1 we solved allows now the design of rational inhibitors against this new promising therapeutic target.
Plan de classement
Entomologie médicale / Parasitologie / Virologie [052]
Localisation
Fonds IRD [F B010053856]
Identifiant IRD
fdi:010053856
Contact