Author/Authors :
Sharifi, K Dept. of Parasitology and Mycology - School of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Haghighi,A Dept. of Parasitology and Mycology - School of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Gachkar, L Infectious Disease and Tropical Medicine Research Center - School of Medicine - Shahid Beheshti Universityof Medical Sciences, Tehran, Iran , Kazemi, B Dept. of Parasitology and Mycology - School of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Taghipour, N Dept. of Parasitology and Mycology - School of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Hosseinzadeh, N Dept. of Parasitology and Mycology - School of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Background: The recently reported resistance to antimalarials contributesto making the control of malaria more difficult. There is a need to evaluate the current antimalaria regimens to prevent this emerging problem. The aim of this study was to determine dihydrofolate reductase-thymidylate synthase gene mutation (pvdhfr) regarding antifulate resistance in Plasmodium vivax. Methods: From 2007 to 2009, 117 P. vivax infected blood samples collected from two regions of Hormozgan Province, south of Iran were analyzed using PCR, semi-nested-PCR and RFLP methods. Results: Eighty four isolates (71.8 %) showed no mutation in pvdhfr gene of P. vivax known as wild type and 33 (28.2%) of the samples revealed nine single (7.7%), twenty two double (18.8%) and two (1.7%) triple mutations. Conclusion: Genetic diversity was observed by molecular methods in pvdhfr gene of p. vivax in Hormozgan Province suggests that the antifolate falciparum malaria drug (fansidar) is proportionally affecting P. vivax dhfr mutation. Therefore, more studies to evaluate antimalarial drugs that should preferably be effective against both P. vivax and P. falciparum are recommended.
Keywords :
Dihydrofolate reductase-thymidylate synthase , PCR-RFLP , Plasmodium vivax , Mutation