Publication: Practical PCR genotyping protocols for Plasmodium vivax using Pvcs and Pvmsp1
Issued Date
2005-04-27
Resource Type
ISSN
14752875
14752875
14752875
Other identifier(s)
2-s2.0-21444453280
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Malaria Journal. Vol.4, (2005)
Suggested Citation
Mallika Imwong, Sasithon Pukrittayakamee, Anne Charlotte Grüner, Laurent Rénia, Frank Letourneur, Sornchai Looareesuwan, Nicholas J. White, Georges Snounou Practical PCR genotyping protocols for Plasmodium vivax using Pvcs and Pvmsp1. Malaria Journal. Vol.4, (2005). doi:10.1186/1475-2875-4-20 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/16594
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Practical PCR genotyping protocols for Plasmodium vivax using Pvcs and Pvmsp1
Abstract
Background: Plasmodium vivax is the second most prevalent malaria parasite affecting more than 75 million people each year, mostly in South America and Asia. In addition to major morbidity this parasite is associated with relapses and a reduction in birthweight. The emergence and spread of drug resistance in Plasmodium falciparum is a major factor in the resurgence of this parasite. P. vivax resistance to drugs has more recently emerged and monitoring the situation would be helped, as for P. falciparum, by molecular methods that can be used to characterize parasites in field studies and drug efficacy trials. Methods: Practical PCR genotyping protocols based on polymorphic loci present in two P. vivax genetic markers, Pvcs and Pvmsp1, were developed. The methodology was evaluated using 100 P. vivax isolates collected in Thailand. Results and Discussion: Analysis revealed that P. vivax populations in Thailand are highly diverse genetically, with mixed genotype infections found in 26 % of the samples (average multiplicity of infection = 1.29). A large number of distinguishable alleles were found for the two markers, 23 for Pvcs and 36 for Pvmsp1. These were generally randomly distributed amongst the isolates. A total of 68 distinct genotypes could be enumerated in the 74 isolates with a multiplicity of infection of 1. Conclusion: These results indicate that the genotyping protocols presented can be useful in the assessment of in vivo drug efficacy clinical trials conducted in endemic areas and for epidemiological studies of P. vivax infections. © 2005 Imwong et al; licensee BioMed Central Ltd.