Molecular evaluation of pvdhfr and pvmdr-1 mutants in Plasmodium vivax isolates after treatment with sulfadoxine/pyrimethamine and chloroquine in Iran during 2015–2016

Molecular evaluation of pvdhfr and pvmdr-1 mutants in Plasmodium vivax isolates after treatment with sulfadoxine/pyrimethamine and chloroquine in Iran during 2015–2016


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اطلاعات تفضیلی
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نویسندگان: تیمور حضرتیان , عادل اسپوتین , محمود محامی اسکوئی , عباس شهبازی سیاه اسطلخی , مهدی پارسائی , احد بازمانی , نازیلا سرافراز

عنوان کنگره / همایش: 4 th International & 11 th National Congress on Parasitology and Parasitic Diseases of Iran ( NICOPA 11) 10-14 Dec 2016 , , ارومیه , 2019

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نویسنده ثبت کننده مقاله تیمور حضرتیان
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده پزشکی
کد مقاله 69491
عنوان فارسی مقاله Molecular evaluation of pvdhfr and pvmdr-1 mutants in Plasmodium vivax isolates after treatment with sulfadoxine/pyrimethamine and chloroquine in Iran during 2015–2016
عنوان لاتین مقاله Molecular evaluation of pvdhfr and pvmdr-1 mutants in Plasmodium vivax isolates after treatment with sulfadoxine/pyrimethamine and chloroquine in Iran during 2015–2016
نوع ارائه پوستر
عنوان کنگره / همایش 4 th International & 11 th National Congress on Parasitology and Parasitic Diseases of Iran ( NICOPA 11) 10-14 Dec 2016
نوع کنگره / همایش بین المللی
کشور محل برگزاری کنگره/ همایش
شهر محل برگزاری کنگره/ همایش ارومیه
سال انتشار/ ارائه شمسی 1398
سال انتشار/ارائه میلادی 2019
تاریخ شمسی شروع و خاتمه کنگره/همایش 1398/07/17 الی 1398/07/19
آدرس لینک مقاله/ همایش در شبکه اینترنت
آدرس علمی (Affiliation) نویسنده متقاضی Departmemt of Parasitology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran

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نویسنده نفر چندم مقاله
تیمور حضرتیانششم
عادل اسپوتینسوم
محمود محامی اسکوئیپنجم
عباس شهبازی سیاه اسطلخیچهارم
مهدی پارسائیاول
احد بازمانینهم
نازیلا سرافرازدهم

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عنوان متن
خلاصه مقالهIntroduction The rising use of sulfadoxine/pyrimethamine (SP) in the treatment of chloroquine (CQ)-resistant Plasmodium falciparum has resulted in increased exposure to P. vivaxisolates in Iran, where both species are being circulated. In this investigation, the frequency of pvdhfr and pvmdr-1 mutants was assessed in P. vivax strains during 2015-2016 after the introduction of SP/CQ in malarious areas of Iran. Material and Method The P. vivax isolates (n, 52) were obtained from autochthonous samples in Southeast Iran during 2015–2016. The genomic DNA was extracted and examined using nested polymerase chain reaction and sequencing. Result Mutations were detected in pvdhfr codons P33L (21.2%), T61 M (25%), S93H (3.9%), and S117 T (1.9%) and 5 isolates showed double mutations (33 L/61 M, 7.7%; 33 L/117 T, 1.9%). No mutation was identified in pvdhfr codons F57 and S58. The pvmdr-1 1076 L mutation was detected in 93.3% of P. vivax isolates. Discussion The findings indicated that the frequency of three codons of pvdhfr F57/S58/S117 has decreased from 2001 (1.05%/7.0%/16.9%) to 2016 (0%/0%/1.9%). Genomic analysis of pvmdr-1 showed that the frequency of 1076 L has gradually increased from 2013 (93%) to 2016 (93.3%) (P > .05). The results demonstrated that P. vivax isolates are probably being exited under SP pressure, which reflects the appropriate level of training for field microscopists, as established by Iranian policymakers. Emergent pvdhfr codons 33L, 61M, and 93H should be noticed in plausible drug tolerance and treatment plans. The high prevalence of pvmdr-1 1076L mutation shows that efficacy of CQ combination with primaquine may be in danger of being compromised.
کلمات کلیدیPlasmodium vivax, Drug resistance markers, Polymorphism, Iran

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