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Project Description
  Flow Diagrams
Contact Information
  Consortium Members
Diseases Under Investigation
  * Chagas' Disease
    [American Trypanosomiasis]
  * African Sleeping Sickness
    [African Trypanosomiasis]
  * Leishmaniasis
  * Malaria
Target Organisms
  * Trypanosoma cruzi
  * Trypanosoma brucei
  * Leishmania spp.
  * Plasmodium falciparum
  * (Plasmodium vivax)
Genome Status
SGPP Progress
Papers by SGPP
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DISEASES UNDER INVESTIGATION

Trypanosomatids and Plasmodia

These protozoa afflict approximately 500 million people per year, mostly in the tropics and subtropics. The resulting diseases cause disability, disfigurement, and in some cases death. Vaccines against these single cell organisms seem unlikely due to antigenic variation. Additionally, these protozoa promote drug resistance via multiple pathways. The drugs currently available to destroy these parasites are toxic to humans themselves. Overall, our problem with pathogenic protozoa is understudied; however, these issues are pertinent given the human toll.


Predicted Number of Parasite Genes

Organism Chromosome(s)
Completed
Genes
identified
Gene density
(gene/Mb)
Genome
size
P. falciparum Chr2, Chr3 425 211 25 Mb
T. brucei Chr1 325 305 35 Mb
L. major Chr1, Chr3, Chr4 301 249 33 Mb
T. cruzi Chr3a 150 417 80 Mb
  • Antigenic variation and variability of surface proteins
  • Proteins of protozoa that modify host cells and immune response
  • Many surface proteins are attached by GPI anchors
  • Rhoptry organelles, unique to apicoplasts, in Plasmodia
  • Plastid organelles, related to plant chloroplasts, in Plasmodia
  • Flagellar pocket of trypanosomatids, distinct function in secretion and importation
  • Parasitophorous vacuoles surrounding intracellular forms
  • Glycosomes of trypanosomatids
  • Food vacuoles of Plasmodia
  • Trans-splicing of mRNA and lack of introns in trypanosomatids
  • Extensive RNA editing in mitochondria of trypanosomatids
  • Unique transcriptional control of trypanosomatids
  • Plasmodium falciparum sporozoites travel through hepatocytes