Abstract

BackgroundMSP-1 is one of the potential malarial vaccine candidate antigens. However, extensive genetic polymorphism of this antigen in the field isolates of Plasmodium falciparum represents a major hindrance for the development of an effective vaccine. Therefore, this study aimed to establish the prevalence and genetic polymorphisms of K1, MAD20 and RO33 allelic types of msp-1 block 2 among P. falciparum clinical isolates from Lao PDR.MethodsPlasmodium falciparum isolates were collected from 230 P. falciparum-infected blood samples from three regions of Lao PDR. K1, MAD20 and RO33 were detected by nested PCR; SSCP was used for polymorphism screening. The nested PCR products of each K1, MAD20 and RO33 allelic types that had different banding patterns by SSCP, were sequenced.ResultsThe overall prevalence of K1, MAD20 and RO33 allelic types in P. falciparum isolates from Lao PDR were 66.95%, 46.52% and 31.30%, respectively, of samples under study. Single infections with K1, MAD20 and RO33 allelic types were 27.83%, 11.74% and 5.22%, respectively; the remainders were multiple clonal infections. Neither parasite density nor age was related to MOI. Sequence analysis revealed that there were 11 different types of K1, eight different types of MAD20, and 7 different types of RO33. Most of them were regional specific, except type 1 of each allelic type was common found in 3 regions under study.ConclusionsGenetic polymorphism with diverse allele types was identified in msp-1 block 2 among P. falciparum clinical isolates in Lao PDR. A rather high level of multiple clonal infections was also observed but the multiplicity of infection was rather low as not exceed 2.0. This basic data are useful for treatment and malaria control program in Lao PDR.

Highlights

  • merozoite surface protein-1 (MSP-1) is one of the potential malarial vaccine candidate antigens

  • The distribution of msp-1 block 2 allelic types in P. falciparum field isolates from Lao PDR was determined, based on microscopic diagnosis, from a total of 230 blood samples randomly collected from P. falciparum-infected patients who attended regional malarial clinics in three geographic areas of Lao PDR from July 2008 to May 2009: in Oudomxay province, Savannakhet province, and Xekong province

  • All blood samples were typed for msp-1 block 2 K1, MAD20 and RO33 allelic types by nested PCR

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Summary

Introduction

Extensive genetic polymorphism of this antigen in the field isolates of Plasmodium falciparum represents a major hindrance for the development of an effective vaccine. This study aimed to establish the prevalence and genetic polymorphisms of K1, MAD20 and RO33 allelic types of msp-1 block 2 among P. falciparum clinical isolates from Lao PDR. Malaria remains one of the most important health-threatening parasitic diseases in tropical and subtropical areas, such as Lao PDR and other countries in Southeast Asia. Extensive genetic polymorphisms of the MSP-1 gene have been identified in P. falciparum isolates worldwide; this has caused extensive antigenic polymorphism [10,11]. It is important to investigate the diversity of msp-1 gene, in different geographic areas for the further development of effective malaria prevention and control

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