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Department of - Instituut voor Tropische Geneeskunde

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Unit <strong>of</strong> Molecular Parasitology<br />

In the course <strong>of</strong> 2007, the Unit <strong>of</strong> Molecular Parasitology<br />

Unit has made considerable progress in its two main,<br />

closely related research lines on leishmaniasis, i.e.<br />

treatment failure and drug resistance, and parasite<br />

genotyping.<br />

Our studies on drug resistance were highlighted in the<br />

PhD thesis <strong>of</strong> Saskia Decuypere “Antimony treatment<br />

failure in anthroponotic visceral leishmaniasis: towards<br />

improved tools and strategies for epidemiological<br />

surveillance and disease control”, which provides<br />

a synthesis <strong>of</strong> five years work on drug resistance<br />

leishmaniasis. Saskia joined the University <strong>of</strong> Strathclyde<br />

(Pr<strong>of</strong>. G. Coombs) with a Marie-Curie scholarship, where<br />

she will pursue the biochemical characterisation <strong>of</strong> drugresistant<br />

strains for two years before continuing her<br />

postdoctoral work at the ITM. By the end <strong>of</strong> 2007, Meriem<br />

Ouakad joined the unit for postdoctoral studies on drug<br />

resistance.<br />

Our research on parasite genotyping consists <strong>of</strong> three<br />

main activities and PhD projects:<br />

• dissemination, standardisation and quality control <strong>of</strong><br />

existing typing methods<br />

• new and simple methods for species identification<br />

• the application <strong>of</strong> molecular methods to specific<br />

epidemiological questions<br />

The composition <strong>of</strong> our team, with PhD and postdoctoral<br />

fellows from Cuba, Peru, Algeria, Kenya and Nepal<br />

illustrate the success <strong>of</strong> our intercontinental networking.<br />

Among the major findings <strong>of</strong> 2007, we quote the first<br />

extensive description <strong>of</strong> the L. donovani population<br />

structure among healthy carriers in Nepal.<br />

The Euro-Mediterranean consortium “Leishmed”,<br />

which we coordinated, concluded its activities with<br />

two workshops on immunological and environmental<br />

control <strong>of</strong> leishmaniasis, both in Tunisia. A main<br />

deliverable <strong>of</strong> this project was the digital compendium<br />

on geo-referenced publications on the epidemiology<br />

<strong>of</strong> leishmaniasis in the Mediterranean, developed<br />

in close collaboration with the Leishmed partners<br />

and WHO. Another networking milestone was the<br />

“Leishrisk” conference in November 2007 in Antwerp<br />

(see highlights) which brought together 150 world class<br />

leishmaniacs.<br />

The unit pursued its contribution simplified molecular<br />

diagnosis <strong>of</strong> Leishmania and genotyping <strong>of</strong> Plasmodium<br />

by the other units in the <strong>Department</strong>.<br />

Unit <strong>of</strong> Parasite Diagnostics<br />

The Unit <strong>of</strong> Parasite Diagnostics conducts research<br />

on parasitological, serological, bioclinical and genetic<br />

markers for the diagnosis, stage determination and<br />

follow-up <strong>of</strong> trypanosomiasis (African and South-<br />

American) and leishmaniaisis. We collaborate with<br />

partners in DR Congo, Uganda, Kenya, Sudan, Malawi,<br />

Ethiopia, South Africa, Mozambique, Zambia, Burkina<br />

Faso, Venezuela, Chile and Spain, and are a partner in<br />

WHO and FIND-Diagnostics consortia aiming to develop<br />

new diagnostics for sleeping sickness.<br />

The results <strong>of</strong> the first randomised clinical trial on<br />

combination therapy for sleeping sickness were<br />

published. This pioneer study was conducted in<br />

Bwamanda (DR Congo), in collaboration with national<br />

partners and the Drugs for Neglected Diseases Initiative<br />

(DNDi). It allowed the identification <strong>of</strong> biological markers<br />

in cerebrospinal fluid (CSF) as risk factors for relapse<br />

and provided a rationale for shortening post-treatment<br />

follow-up. These results should be confirmed in a new<br />

study conducted in Mbuji-Mayi (DR Congo), where rates<br />

<strong>of</strong> treatment failure are uncommonly high. The first in<br />

vitro drug sensitivity tests on parasite strains isolated<br />

from such patients seem to reject the hypothesis that the<br />

high relapse rates are caused by parasite drug resistance.<br />

The unit is partner in the NEUROTRYP consortium, which<br />

intends to unravel the mechanisms by which African<br />

trypanosomes invade the brain. We have constructed<br />

recombinant Trypanosoma brucei strains that express<br />

Renilla luciferase enabling in vivo tracking <strong>of</strong> the parasites<br />

in mice (see highlight). Within the same project, an<br />

RESEARCH | 51

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