AI Article Synopsis

  • Leishmania spp. are protozoan parasites transmitted by sandflies, causing various diseases in humans.
  • They exhibit unique enzymes in their central carbon metabolism that differ from those in mammals, making them potential targets for new drugs.
  • Recent studies reveal that Leishmania can utilize multiple carbon sources throughout its life cycle, indicating adaptations for survival in both insect and mammalian hosts, with metabolomic techniques proving valuable in understanding these processes.

Article Abstract

Leishmania spp. are sandfly-transmitted protozoa parasites that cause a spectrum of diseases in humans. Many enzymes involved in Leishmania central carbon metabolism differ from their equivalents in the mammalian host and are potential drug targets. In this review we summarize recent advances in our understanding of Leishmania central carbon metabolism, focusing on pathways of carbon utilization that are required for growth and pathogenesis in the mammalian host. While Leishmania central carbon metabolism shares many features in common with other pathogenic trypanosomatids, significant differences are also apparent. Leishmania parasites are also unusual in constitutively expressing most core metabolic pathways throughout their life cycle, a feature that may allow these parasites to exploit a range of different carbon sources (primarily sugars and amino acids) rapidly in both the insect vector and vertebrate host. Indeed, recent gene deletion studies suggest that mammal-infective stages are dependent on multiple carbon sources in vivo. The application of metabolomic approaches, outlined here, are likely to be important in defining aspects of central carbon metabolism that are essential at different stages of mammalian host infection.

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Source
http://dx.doi.org/10.1017/S0031182010000077DOI Listing

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