PT  - JOURNAL ARTICLE
AU  - Ibrahim A. Teka
AU  - Anne J. N. Kazibwe
AU  - Nasser El-Sabbagh
AU  - Mohammed I. Al-Salabi
AU  - Christopher P. Ward
AU  - Anthonius A. Eze
AU  - Jane C. Munday
AU  - Pascal Mäser
AU  - Enock Matovu
AU  - Michael P. Barrett
AU  - Harry P. de Koning
TI  - The Diamidine Diminazene Aceturate Is a Substrate for the High-Affinity Pentamidine Transporter: Implications for the Development of High Resistance Levels in Trypanosomes
AID  - 10.1124/mol.111.071555
DP  - 2011 Jul 01
TA  - Molecular Pharmacology
PG  - 110--116
VI  - 80
IP  - 1
4099  - http://molpharm.aspetjournals.org/content/80/1/110.short
4100  - http://molpharm.aspetjournals.org/content/80/1/110.full
SO  - Mol Pharmacol2011 Jul 01; 80
AB  - African trypanosomiasis is a disease of humans and livestock in many areas south of the Sahara. Resistance to the few existing drugs is a major impediment to the control of these diseases, and we investigated how resistance to the main veterinary drug diminazene aceturate correlates with changes in drug transport in resistant strains. The strain tbat1(−/−), lacking the TbAT1/P2 aminopurine transporter implicated previously in diminazene transport, was adapted to higher levels of diminazene resistance. The resulting cell line was designated ABR and was highly cross-resistant to other diamidines and moderately resistant to cymelarsan. Procyclic trypanosomes were shown to be a convenient model to study diamidine uptake in Trypanosoma brucei brucei given the lack of TbAT1/P2 and a 10-fold higher activity of the high-affinity pentamidine transporter (HAPT1). Diminazene could be transported by HAPT1 in procyclic trypanosomes. This drug transport activity was lacking in the ABR line, as reported previously for the pentamidine-adapted line B48. The Km for diminazene transport in bloodstream tbat1(−/−) trypanosomes was consistent with uptake by HAPT1. Diminazene transport in ABR and B48 cells was reduced compared with tbat1(−/−), but their resistance phenotype was different: B48 displayed higher levels of resistance to pentamidine and the melaminophenyl arsenicals, whereas ABR displayed higher resistance to diminazene. These results establish a loss of HAPT1 function as a contributing factor to diminazene resistance but equally demonstrate for the first time that adaptations other than those determining the initial rates of drug uptake contribute to diamidine and arsenical resistance in African trypanosomes.