Trypanosoma cruzi: role of δ-amastin on extracellular amastigote cell invasion and differentiation

PLoS One. 2012;7(12):e51804. doi: 10.1371/journal.pone.0051804. Epub 2012 Dec 18.

Abstract

Trypanosoma cruzi is a protozoan parasite that comprises different phylogenetic groups and is the causative agent of Chagas' disease. Different T. cruzi strains present differences in infectivity in in vitro and in vivo experimental models, which are likely related to the expression of different virulence factors. Amastin is a surface glycoprotein abundantly expressed on the intracellular mammalian amastigote form of the parasite. In this study, we showed that a highly infective strain (G strain) of extracellular amastigote (EA) invasive forms expressed reduced RNA levels of amastin compared to a less infective strain (CL). The treatment of HeLa cells with recombinant δ-amastin reduced infectivity of EA forms. However, the ectopic expression of δ-amastin accelerated amastigote differentiation into trypomastigotes. Corroborating the virulence behavior in association with amastin expression, the EAs overexpressing amastin were precociously and robustly observed in the liver of susceptible mouse strains (A/JUnib), whereas parasitemia was never detected in in vivo assays. This is the first report on the regulatory role of amastin in the course of both in vitro and in vivo T. cruzi infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Line
  • Chagas Disease / parasitology
  • Gene Expression
  • Host-Parasite Interactions
  • Humans
  • Liver / parasitology
  • Membrane Glycoproteins / chemistry
  • Membrane Glycoproteins / genetics*
  • Membrane Glycoproteins / metabolism
  • Mice
  • Molecular Sequence Data
  • Protozoan Proteins / chemistry
  • Protozoan Proteins / genetics*
  • Protozoan Proteins / metabolism
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Transcription, Genetic
  • Trypanosoma cruzi / genetics*
  • Trypanosoma cruzi / pathogenicity*

Substances

  • Membrane Glycoproteins
  • Protozoan Proteins
  • Recombinant Fusion Proteins
  • amastin protein, Trypanosoma cruzi

Grants and funding

This study was supported by FAPESP (grants 2006/61450-0 and 2011/51475-3); RAM and ST are recipients of CNPq fellowships; DB is supported by FAPESP (07/50551-2) and is a CNPq fellow. WDDR and NSM were supported by Fundação Araucária, CAPES/Reuni, PPSUS/MS and CNPq and had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.