Vitamin and cofactor acquisition in apicomplexans: Synthesis versus salvage

J Biol Chem. 2020 Jan 17;295(3):701-714. doi: 10.1074/jbc.AW119.008150. Epub 2019 Nov 25.

Abstract

The Apicomplexa phylum comprises diverse parasitic organisms that have evolved from a free-living ancestor. These obligate intracellular parasites exhibit versatile metabolic capabilities reflecting their capacity to survive and grow in different hosts and varying niches. Determined by nutrient availability, they either use their biosynthesis machineries or largely depend on their host for metabolite acquisition. Because vitamins cannot be synthesized by the mammalian host, the enzymes required for their synthesis in apicomplexan parasites represent a large repertoire of potential therapeutic targets. Here, we review recent advances in metabolic reconstruction and functional studies coupled to metabolomics that unravel the interplay between biosynthesis and salvage of vitamins and cofactors in apicomplexans. A particular emphasis is placed on Toxoplasma gondii, during both its acute and latent stages of infection.

Keywords: Apicomplexa; Cryptosporidium; Plasmodium; Toxoplasma gondii; cofactor; metabolic pathway; metabolomics; nutrient acquisition; parasite metabolism; parasitology; vitamin.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Apicomplexa / genetics
  • Apicomplexa / metabolism*
  • Coenzymes / genetics
  • Coenzymes / metabolism*
  • Host-Parasite Interactions / genetics
  • Humans
  • Metabolic Networks and Pathways / genetics
  • Protein Biosynthesis / genetics
  • Toxoplasma / genetics
  • Toxoplasma / metabolism
  • Toxoplasma / pathogenicity
  • Toxoplasmosis / metabolism*
  • Toxoplasmosis / parasitology
  • Vitamins / genetics
  • Vitamins / metabolism*

Substances

  • Coenzymes
  • Vitamins