Rapid Dissemination of Plasmodium falciparum Drug Resistance Despite Strictly Controlled Antimalarial Use

• Published in: PloS one Vol. 2; no. 1
• Main Authors: Noranate, Nitchakarn, Durand, Remy, Tall, Adama, Marrama, Laurence, Spiegel, Andre, Sokhna, Cheikh, Pradines, Bruno, Cojean, Sandrine, Guillotte, Micheline, Bischoff, Emmanuel, Ekala, Marie-Therese, Bouchier, Christiane, Fandeur, Thierry, Ariey, Frederic, Patarapotikul, Jintana, Le Bras, Jacques, Trape, Jean Francois, Rogier, Christophe, Mercereau-Puijalon, Odile
• Format: Journal Article
• Language: English
• Published: 01.01.2007
• Subjects: Plasmodium falciparum
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0000139.

Inadequate treatment practices with antimalarials are considered major contributors to Plasmodium falciparum resistance to chloroquine, pyrimethamine and sulfadoxine. The longitudinal survey conducted in Dielmo, a rural Senegalese community, offers a unique frame to explore the impact of strictly controlled and quantified antimalarial use for diagnosed malaria on drug resistance. Methodology/Principal Findings We conducted on a yearly basis a retrospective survey over a ten-year period that included two successive treatment policies, namely quinine during 1990-1994, and chloroquine x28; CQx29; and sulfadoxine/pyrimethamine x28; SPx29; as first and second line treatments, respectively, during 1995-1999. Molecular beacon-based genotyping, gene sequencing and microsatellite analysis showed a low prevalence of Pfcrt and Pfdhfr-ts resistance alleles of Southeast Asian origin by the end of 1994 and their effective dissemination within one year of CQ and SP implementation. The Pfcrt resistant allele rose from 9x25; to 46x25; prevalence during the first year of CQ reintroduction, i.e., after a mean of 1.66 CQ treatment courses/person/year. The Pfdhfr-ts triple mutant rose from 0x25; to 20x25; by end 1996, after a mean of 0.35 SP treatment courses/person in a 16-month period. Both resistance alleles were observed at a younger age than all other alleles. Their spreading was associated with enhanced in vitro resistance and rapidly translated in an increased incidence of clinical malaria episodes during the early post-treatment period. Conclusion/Significance In such a highly endemic setting, selection of drug-resistant parasites took a single year after drug implementation, resulting in a rapid progression of the incidence of clinical malaria during the early post-treatment period. Controlled antimalarial use at the community level did not prevent dissemination of resistance haplotypes. This data pleads against reintroduction of CQ in places where resistant allele frequency has dropped to a very low level after CQ use has been discontinued, unless drastic measures are put in place to prevent selection and spreading of mutants during the post-treatment period.