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C H A P T E R<br />

16<br />

Drug resistance in parasites<br />

Marc Ouellette 1 and Steve A. Ward 2<br />

1 Centre de Recherche en Infectiologie, Université Laval and Centre<br />

Hospitalier Universitaire de Québec, Québec, Canada; and<br />

2 Liverpool School of Tropical Medicine, Liverpool, UK<br />

INTRODUCTION<br />

Parasitic protozoa and helminths are responsible<br />

for some of the most devastating and prevalent<br />

diseases of humans and domestic animals.<br />

Protozoan parasites threaten the lives of nearly<br />

one-third of the worldwide human population,<br />

and are responsible for the loss of more than<br />

50 million disability-adjusted life years (DALYs)<br />

and more than 2 million deaths a year (www.<br />

who.int). The parasites responsible for malaria<br />

(Plasmodium spp.) contribute most to DALYs<br />

and death, but the parasites responsible for<br />

the various forms of leishmaniasis (Leishmania<br />

spp.), African sleeping sickness (Trypanosoma<br />

brucei gambiense, Trypanosoma brucei rhodesiense),<br />

and Chagas disease (Trypanosoma<br />

cruzi) are also important contributors to global<br />

morbidity and mortality figures. Anaerobic parasitic<br />

diseases such as Entamoeba histolytica,<br />

Trichomonas vaginalis (vaginitis, urethritis) and<br />

Giardia duodenalis (diarrhea) as well as worms<br />

responsible for lymphatic filariasis, schistosomiasis<br />

and onchocerciasis also contribute<br />

significantly to the world’s disease burden.<br />

Parasitic protozoa and helminths result in<br />

considerable losses of life and productivity in<br />

humans and domesticated animals. Ideally,<br />

prevention would be the most efficient way to<br />

control infectious agents but despite considerable<br />

efforts, there are no effective vaccines<br />

against any of the clinically important parasites.<br />

For the moment, drugs are therefore the mainstay<br />

in our control of parasitic protozoa when<br />

simple prevention measures fail or prove<br />

impractical. Protozoa share with their hosts a<br />

number of cellular organelles and metabolic<br />

pathways, but they nonetheless have a number<br />

of unique and exotic biochemical pathways<br />

that should provide many exploitable targets<br />

for the development of parasite-specific drugs.<br />

Proof of this concept includes the effective use<br />

Molecular Medical Parasitology<br />

ISBN 0–12–473346–8<br />

397<br />

Copyright © 2003 Elsevier Science Ltd.<br />

All rights of reproduction in any form reserved.

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