Insight into the Early Spread of Chloroquine-Resistant Plasmodium falciparum Infections in Papua New Guinea

• Published in: The Journal of infectious diseases 2005-12, Vol.192 (12), p.2174-2179
• Main Authors: Mehlotra, Rajeev K., Mattera, Gabriel, Bhatia, Kuldeep, Reeder, John C., Stoneking, Mark, Zimmerman, Peter A.
• Format: Article
• Language: English
• Subjects: Alleles; Animals; Antimalarials - pharmacology; Biological and medical sciences; Chloroquine - pharmacology; DNA, Protozoan - analysis; DNA, Protozoan - genetics; Drug Resistance; Female; Fundamental and applied biological sciences. Psychology; Genes, MDR; Genetic loci; Haplotypes; Highlands; Humans; Infections; Infectious diseases; Malaria; Malaria, Falciparum - epidemiology; Malaria, Falciparum - parasitology; Malaria, Falciparum - transmission; Medical sciences; Membrane Proteins - genetics; Membrane Transport Proteins; Microbiology; Microsatellite Repeats - genetics; Papua New Guinea - epidemiology; Parasites; Placenta - parasitology; Placenta Diseases - epidemiology; Placenta Diseases - parasitology; Plasmodium falciparum; Plasmodium falciparum - drug effects; Plasmodium falciparum - genetics; Polymerase Chain Reaction; Polymorphism, Genetic; Population genetics; Pregnancy; Pregnancy Complications, Parasitic - epidemiology; Pregnancy Complications, Parasitic - parasitology; Protozoan Proteins; Selection, Genetic; Tissue samples
• ISSN: 0022-1899; 1537-6613
• DOI: 10.1086/497694

The first report of Plasmodium falciparum chloroquine (CQ) resistance (CQR) in Papua New Guinea (PNG) appeared in 1974. Although the current prevalence of CQR-associated parasite gene polymorphisms has been documented for some regions, the spatial and temporal relationships that characterize CQ-resistant parasites in PNG are unknown. Insight into the evolution of CQ-resistant parasites could be provided by evaluating genetic markers in parasite populations. We compared pfcrt and pfmdr1 polymorphisms and flanking microsatellite (MS) polymorphisms between P. falciparum–infected placental tissue (early 1980s) and blood (late 1990s) samples collected throughout PNG. Consistent with the results of recent studies, pfcrt-SVMNT and pfmdr1-86Y were the only CQR-associated alleles observed in the placental tissue samples, and they were observed together in 79% of the samples. Results of analysis of MS flanking pfcrt (∼40 kb) suggested that there was less diversity in the samples collected during the 1980s than in those collected during the 1990s and that the 1990s parasites were significantly differentiated from the 1980s parasites. On the other hand, for MS flanking pfmdr1 (∼5 kb) and for 1 putatively neutral locus, diversity levels were similar, and the 2 parasite populations were not significantly differentiated. These results suggest that selection for CQR was operating on the pfcrt-SVMNT allele during the early 1980s. Thus, archival samples can provide novel insight into the dynamics of CQR