Innovating Works

PoEMM

Financiado
Plasmodium Exploitation of Liver-specific Methionine Metabolism
Malaria remains the most serious parasitic infectious disease, killing one child every two minutes. Plasmodium infection starts when the female Anopheles mosquito injects sporozoites into the skin of the vertebrate host. All Plasm... Malaria remains the most serious parasitic infectious disease, killing one child every two minutes. Plasmodium infection starts when the female Anopheles mosquito injects sporozoites into the skin of the vertebrate host. All Plasmodium species go through a phase of replication inside nucleated cells prior to infecting red blood cells and causing malaria, however, only mammalian-infectious parasites target the liver and replicate inside hepatocytes at an extraordinary rate to generate tens of thousands of erythrocyte-infectious merozoites. Avian and reptile malaria parasites, in contrast, infect macrophages near the bite site and differentiate into only dozens of erythrocyte-infectious merozoites. The reason behind the high replication rate achieved by mammalian-infectious parasites inside hepatocytes, key to guarantee the establishment of infection by overcoming the bottleneck of malaria transmission caused by a low sporozoite inoculum, remains utterly unexplored. The hypothesizes of this proposal is that the explanation for this lies in the uniqueness of the mammalian hepatic methionine metabolism bestowed by the mammalian liver-specific methionine adenosyltransferase (MAT1) enzyme and its capacity for generating unlimited amounts of S-adenosylmethionine. In agreement with this hypothesis, preliminary data show that Plasmodium’s high replication rate inside hepatocytes relies on the host liver-specific MAT1. By using a combination of genetic, cellular and molecular approaches I will decipher how the liver-specific methionine metabolism present in hepatocytes is hijacked and used by the parasite to achieve such high replication rates and assess the competence of the liver-specific MAT1 in sustaining Plasmodium replication. This proposal has the potential to establish a novel paradigm on how the environment and the resources provided by the host have evolutionarily influenced Plasmodium’s life cycle and will pave the way for new therapeutic targets against malaria. ver más
31/08/2026
iMM
173K€
Perfil tecnológico estimado
Duración del proyecto: 27 meses Fecha Inicio: 2024-05-22
Fecha Fin: 2026-08-31

Línea de financiación: concedida

El organismo HORIZON EUROPE notifico la concesión del proyecto el día 2024-05-22
Línea de financiación objetivo El proyecto se financió a través de la siguiente ayuda:
HORIZON-MSCA-2023-PF-01-01: MSCA Postdoctoral Fellowships 2023
Cerrada hace 1 año
Presupuesto El presupuesto total del proyecto asciende a 173K€
Líder del proyecto
INSTITUTO DE MEDICINA MOLECULAR JOAO LOBO ANT... No se ha especificado una descripción o un objeto social para esta compañía.
Perfil tecnológico TRL 4-5