Modeling Metabolism and Stage-Specific Growth of Plasmodium falciparum HB3 during the Intraerythrocytic Development Cycle

Abstract

The human malaria parasite Plasmodium falciparum goes through a complex life cycle, including a roughly 48-hour-long intraerythrocytic developmental cycle (IDC) in human red blood cells. A better understanding of the metabolic processes required during the asexual blood-stage reproduction will enhance our basic knowledge of P. falciparum and help identify critical metabolic reactions and pathways associated with blood-stage malaria. We developed a metabolic network model that mechanistically links time-dependent gene expression, metabolism, and stage-specific growth, allowing us to predict the metabolic fluxes, the biomass production rates, and the timing of production of the different biomass components during the IDC. We predicted time- and stage-specific production of precursors and macromolecules for P. falciparum (strain HB3), allowing us to link specific metabolites to specific physiological functions. For example, we hypothesized that coenzyme A might be involved in late-IDC DNA replication and cell division. Moreover, the predicted ATP metabolism indicated that energy was mainly produced from glycolysis and utilized for non-metabolic processes. Finally, we used the model to classify the entire tricarboxylic acid cycle into segments, each with a distinct function, such as superoxide detoxification, glutamate/glutamine processing, and metabolism of fumarate as a byproduct of purine biosynthesis. By capturing the normal metabolic and growth progression in P. falciparum during the IDC, our model provides a starting point for further elucidation of strain-specific metabolic activity, host parasite interactions, stress-induced metabolic responses, and metabolic responses to antimalarial drugs and drug candidates.

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Document Details

Document Type
Technical Report
Publication Date
Jan 01, 2014
Accession Number
ADA610802

Entities

People

  • Anders Wallqvist
  • Jaques Reifman
  • Xing Fang

Organizations

  • United States Army Medical Research and Development Command

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Amines
  • Amino Acids
  • Blood
  • Blood Cells
  • Cell Division
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Computational Biology
  • Experimental Data
  • Gene Expression
  • Macromolecules
  • Malaria
  • Metabolic Pathways
  • Metabolism
  • Proteins
  • Spores

Fields of Study

  • Biology

Readers

  • Molecular and Cellular Biochemistry
  • Molecular and Cellular Biology
  • Parasitology and Pharmacology of Malaria.