Abstract

Trypanosoma congolense, the causative agent of the most important livestock disease in Africa, expresses specific surface proteins involved in its parasitic lifestyle. Unfortunately, the complete repertoire of such molecules is far from being deciphered. As these membrane components are exposed to the host environment, they could be used as therapeutic or diagnostic targets. By mining the T. congolense genome database, we identified a novel family of lectin-like glycoproteins (TcoClecs). These molecules are predicted to have a transmembrane domain, a tandem repeat amino acid motif, a signal peptide and a C-type lectin-like domain (CTLD). This paper depicts several experimental arguments in favor of a surface localization in bloodstream forms of T. congolense. A TcoClec gene was heterologously expressed in U-2 OS cells and the product could be partially found at the plasma membrane. TcoClecs were also localized at the surface of T. congolense bloodstream forms. The signal was suppressed when the cells were treated with a detergent to remove the plasma membrane or with trypsin to « shave » the parasites and remove their external proteins. This suggests that TcoClecs could be potential diagnostic or therapeutic antigens of African animal trypanosomiasis. The potential role of these proteins in T. congolense as well as in other trypanosomatids is discussed.

Highlights

  • Trypanosomes are eukaryotic microbes found in different parts of the world

  • In silico identification of new putative T. congolense lectins Our first goal was to identify in silico new genes that could code for surface proteins of T. congolense Bloodstream forms (BSF)

  • In order to minimize the number of potential candidates, we focused our search on lectins

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Summary

Introduction

Trypanosomes are eukaryotic microbes found in different parts of the world. The development of trypanosomes follows a complex lifecycle. Bloodstream forms (BSF) proliferate in the blood of the infected mammalian host and are ingested by an insect (called tsetse fly, Glossina spp) during the meal. They differentiate into procyclic forms (PCF) in the midgut and migrate to the salivary glands and proboscis where they attach as epimastigote forms (EMF). They differentiate into infective metacyclic forms (MCF) that are transmitted to a new mammalian host during the blood meal

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