Plasmodium falciparum parasites obtained from symptomatic patients attending clinics in Bindura (altitude 1,100 m), Chiredzi (600 m) and Kariba (< 600 m), previously reported to differ in malaria endemicity were genotyped on the msp-1, msp-2 and glurp loci to examine the extent of parasite genetic diversity. While the parasites were monomorphic for msp-1 allele RO33 from the three locations, the K1 allele was overrepresented in Kariba (p=0.02) and Mad20 alleles occurred at a higher frequency in Bindura. A similar PCR analysis for glurp and the two main allelic families of msp-2, i.e IC/3D7 and FC-27 revealed minimal differences in the parasite population. A total of 8 msp-1 Block 2 and 11 msp-2 genotypes were identified from the three locations combined. On the glurp locus, thirteen different genotypes ranging in size from 660 to 1160 bp were detected in parasites obtained from Bindura and Kariba. To gain further insight into P. falciparum genetic diversity in the three different geographical locations, parasites were examined for neutral microsatellite markers (C4M8, C13M30 and TA81). The number of microsatellite alleles ranged from 8 to 17 and the average expected heterozygosity (HE) for the three areas combined was 0.83 suggesting that the parasite population of Zimbabwe is genetically heterogeneous. These findings have implications in understanding the impact of genetic variation on immunity and possibly emergence of drug resistance.Plasmodium falciparum parasites are highly genetically diverse and studies indicate that at any given time, humans or mosquitoes can harbor a number of different parasite clones (Babiker et al., 1991;Branch et al., 2001). The unique genetic characteristics of each parasite may determine clinical or parasitological outcomes and properties such as cytoadherence, immune evasion, resistance or susceptibility to drugs as well as infectivity to mosquitoes (Snounou et al., 1999). Understanding the distribution of genetically diverse P. falciparum parasites is important in malaria epidemiology as well as in designing vaccines as antigenic diversity continues to pose a big challenge to vaccine development. Additionally, the performance of Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. vaccine candidates employed will need to be monitored by assessing switching of allelic types resulting from either natural or vaccine induced immune selection.
NIH Public AccessMsp-1 and msp-2 are highly polymorphic single copy genes and have been employed to investigate parasite genetic diversity (Anders and Smythe, 1989;Smythe et al., 1990). The examinatio...