Kaddouri Halima, Djimdé Abdoulaye, Dama Souleymane, Kodio Aly, Tekete Mamadou, Hubert Véronique, Koné Aminatou, Maiga Hamma, Yattara Oumar, Fofana Bakary, Sidibe Bakary, Sangaré Cheick P O, Doumbo Ogobara, Le Bras Jacques
Laboratoire de Parasitologie, Centre National de Référence du Paludisme, Assistance Publique-Hôpitaux de Paris & Université Paris Descartes, Hôpital Bichat Claude Bernard, 46 Rue Henri Huchard, Paris Cedex 18, France.
Int J Parasitol. 2008 Jun;38(7):791-8. doi: 10.1016/j.ijpara.2007.12.002. Epub 2008 Jan 3.
In vitro susceptibility to antimalarial drugs of Malian Plasmodium falciparum isolates collected between 2004 and 2006 was studied. Susceptibility to chloroquine and to three artemisinin-based combination therapy (ACT) component drugs was assessed as a first, to our knowledge, in vitro susceptibility study in Mali. Overall 96 Malian isolates (51 from around Bamako and 45 collected from French travellers returning from Mali) were cultivated in a CO(2) incubator. Fifty percent inhibitory concentrations (IC(50)s) were measured by either hypoxanthine incorporation or Plasmodium lactate dehydrogenase (pLDH) ELISA. Although the two sets of data were generated with different methods, the global IC(50) distributions showed parallel trends. A good concordance of resistance phenotype with pfcrt 76T mutant genotype was found within the sets of clinical isolates tested. We confirm a high prevalence of P. falciparum in vitro resistance to chloroquine in Mali (60-69%). While some isolates showed IC(50)s close to the cut-off for resistance to monodesethylamodiaquine, no decreased susceptibility to dihydroartemisinin or lumefantrine was detected. This study provides baseline data for P. falciparum in vitro susceptibility to ACT component drugs in Mali.