Unit | Parasite Chemotherapy
The Parasite Chemotherapy Unit (PCU) is a drug discovery centre for protozoan parasites. We have over 20 years of experience in assay development and drug efficacy testing for the causative agents of malaria (Plasmodium spp.), African sleeping sickness (Trypanosoma brucei), Chagas disease (T. cruzi), leishmaniasis (Leishmania spp.) and diarrhoea (Entamoeba and Giardia). Primary and secondary in vitro assays are combined with mouse models of disease (for African trypanosomes and malaria) and molecular approaches to drug action and resistance. The PCU works closely with product development partnerships such as the Medicines for Malaria Venture (MMV), DNDi or GALVmed, with academic partners around the world and with pharmaceutical companies. The PCU has been instrumental in the development of several clinical candidates, including fexinidazole for human African trypanosomiasis (HAT) and artefenomel for malaria.
A substantial part of the research is focused on the development of novel in vitro assays and in vivo models. Drug discovery activities are complemented by preclinical studies on drug absorption and pharmacokinetics. Molecular biology and bioinformatics approaches are also used to investigate mechanisms of drug resistance and mode of drug action. The unit has a screening mandate from the Medicines for Malaria Venture (MMV) Foundation and has become the main WHO/TDR centre for in vitro screening against protozoan parasites.
Eastern African Network for Trypanosomiasis (EANETT)
As well as working on new drugs, the group also collaborates with African partner institutes in the Eastern Africa Network for Trypanosomiasis (EANETT) in the area of sleeping sickness research and control. The Swiss Agency for Development and Cooperation (SDC) has awarded the network a second phase of support for 2004-2006. A key objective for this phase was to involve the network in international activities, with access to additional funding.
Another element of the activities is to study the transmission of trypanosomes by the tsetse fly vector in order to gain more knowledge about the life cycle of the parasite and the function of certain surface proteins.
Latest PublicationsAll Publications
Corbel V et al. A new WHO bottle bioassay method to assess the susceptibility of mosquito vectors to public health insecticides: results from a WHO-coordinated multi-centre study. Parasit Vectors. 2023;16:21. DOI: 10.1186/s13071-022-05554-7
Imlay L.S et al. Fast-killing tyrosine amide ((S)-SW228703) with blood- and liver-stage antimalarial activity associated with the cyclic amine resistance locus (PfCARL). ACS Infect Dis. 2023(in press). DOI: 10.1021/acsinfecdis.2c00527
Kruth S et al. Generation of aurachin derivatives by whole-cell biotransformation and evaluation of their antiprotozoal properties. Molecules. 2023;28:1066. DOI: 10.3390/molecules28031
Nguyen W et al. 7-N-substituted-3-oxadiazole quinolones with potent antimalarial activity target the cytochrome bc1 complex. ACS Infect Dis. 2023(in press). DOI: 10.1021/acsinfecdis.2c00607
Seebacher W, Kaiser M, Mäser P, Saf R, Pferschy-Wenzig E.M, Weis R. Benzyl- and dibenzyl tetrahydropyridinylidene ammonium salts with antiplasmodial and antitrypanosomal activity. Monatsh Chem. 2023;154:105-114. DOI: 10.1007/s00706-022-03003-w