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Detection of Trypanosoma brucei Variant Surface Glycoprotein Switching by Magnetic Activated Cell Sorting and Flow Cytometry
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Published on: October 19, 2016

An update on antigenic variation in African trypanosomes.

L Vanhamme1, E Pays, R McCulloch

  • 1Laboratory of Molecular Parasitology, IBMM, Free University of Brussels, Rue des Professeurs Jeener et Brachet 12, B-6041, Gosselies, Belgium. Ivanham@dbm.ulb.ac.be

Trends in Parasitology
|June 26, 2001
PubMed
Summary

African trypanosomes evade immune detection by switching their major surface protein, the variant surface glycoprotein (VSG). This study investigates the mechanisms controlling single VSG gene expression and switching in trypanosomes.

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Area of Science:

  • Parasitology
  • Molecular Biology
  • Immunology

Background:

  • African trypanosomes, the causative agents of sleeping sickness, persist in mammalian hosts by evading the immune system.
  • The variant surface glycoprotein (VSG) is the primary target of the host immune response.
  • Trypanosomes possess a large repertoire of VSG genes, enabling them to switch their surface coat periodically.

Purpose of the Study:

  • To elucidate the regulatory mechanisms governing the exclusive expression of a single VSG gene.
  • To understand the process by which trypanosomes switch between different VSG genes.

Main Methods:

  • Analysis of VSG gene expression patterns.
  • Investigating the role of specialized telomeric expression sites.
  • Exploring the molecular machinery involved in VSG gene switching.

Main Results:

  • Identification of regulatory elements controlling VSG gene transcription.
  • Characterization of the dynamic changes in VSG gene expression during infection.
  • Insights into the coordination of VSG gene selection and silencing.

Conclusions:

  • The exclusive expression of a single VSG is tightly regulated at the transcriptional level.
  • VSG switching is a complex process essential for trypanosome survival and immune evasion.
  • Understanding these mechanisms offers potential targets for therapeutic intervention.