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Molecular Monitoring of Plasmodium vivax Infection after Radical Treatment in Southeastern Iran

BACKGROUND: The aim was to evaluate the relapse risk of vivax malaria in patients who received radical treatment in Hormozgan Province, a malarious area located on southeast of Iran. METHODS: A total of 95 symptomatic vivax malaria infected patients were enrolled in urban health centers of Bandar-Ab...

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Autores principales: Nateghpour, M, Mavi, S Ayazian, Keshavarz, H, Rezaei, S, Abedi, F, Edrissian, GH, Raeisi, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385539/
https://www.ncbi.nlm.nih.gov/pubmed/22808385
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author Nateghpour, M
Mavi, S Ayazian
Keshavarz, H
Rezaei, S
Abedi, F
Edrissian, GH
Raeisi, A
author_facet Nateghpour, M
Mavi, S Ayazian
Keshavarz, H
Rezaei, S
Abedi, F
Edrissian, GH
Raeisi, A
author_sort Nateghpour, M
collection PubMed
description BACKGROUND: The aim was to evaluate the relapse risk of vivax malaria in patients who received radical treatment in Hormozgan Province, a malarious area located on southeast of Iran. METHODS: A total of 95 symptomatic vivax malaria infected patients were enrolled in urban health centers of Bandar-Abbas, Minab, Bandar-Jask and Bashagard districts of Hormozgan Province, southeast of Iran from January 2008 to March 2009 for consideration as a case- series study. DNA was extracted from parasite infected whole blood samples. A polymorphic region of Plasmodium vivax merozoite surface protein 1 (pvMSP1) was selected and a PCR method was employed for all the samples to amplify the specific variable gene fragment. The obtained fragments in primary and secondary samples were sequenced. Both nucleotide and amino acid sequences of the samples were investigated for returned patients. RESULTS: 3.2% of the patients experienced a second attack between 83–199 days after the initial episode of infection. Alignment of nucleotide and their deduced amino acid sequences between pair sequences of primary and secondary isolates revealed 8 and 6 dissimilarities respectively for the first case, and 9 and 7 dissimilarities for the second case. Although microscopical examination of recurrent thick blood smear of the third patient confirmed new P. vivax infection, the venous blood sample was accidentally missed. Sequencing results of primary and returned isolates 1P, 1S, 2P, 2S and 3P in this study showed an identity with BP13, T117, BP13, TC28 and Chesson genotypes respectively. CONCLUSION: The returned (secondary) isolates may account to be for the sake of reinfection.
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spelling pubmed-33855392012-07-17 Molecular Monitoring of Plasmodium vivax Infection after Radical Treatment in Southeastern Iran Nateghpour, M Mavi, S Ayazian Keshavarz, H Rezaei, S Abedi, F Edrissian, GH Raeisi, A Iran J Arthropod Borne Dis Original Article BACKGROUND: The aim was to evaluate the relapse risk of vivax malaria in patients who received radical treatment in Hormozgan Province, a malarious area located on southeast of Iran. METHODS: A total of 95 symptomatic vivax malaria infected patients were enrolled in urban health centers of Bandar-Abbas, Minab, Bandar-Jask and Bashagard districts of Hormozgan Province, southeast of Iran from January 2008 to March 2009 for consideration as a case- series study. DNA was extracted from parasite infected whole blood samples. A polymorphic region of Plasmodium vivax merozoite surface protein 1 (pvMSP1) was selected and a PCR method was employed for all the samples to amplify the specific variable gene fragment. The obtained fragments in primary and secondary samples were sequenced. Both nucleotide and amino acid sequences of the samples were investigated for returned patients. RESULTS: 3.2% of the patients experienced a second attack between 83–199 days after the initial episode of infection. Alignment of nucleotide and their deduced amino acid sequences between pair sequences of primary and secondary isolates revealed 8 and 6 dissimilarities respectively for the first case, and 9 and 7 dissimilarities for the second case. Although microscopical examination of recurrent thick blood smear of the third patient confirmed new P. vivax infection, the venous blood sample was accidentally missed. Sequencing results of primary and returned isolates 1P, 1S, 2P, 2S and 3P in this study showed an identity with BP13, T117, BP13, TC28 and Chesson genotypes respectively. CONCLUSION: The returned (secondary) isolates may account to be for the sake of reinfection. Tehran University of Medical Sciences 2010-06-30 /pmc/articles/PMC3385539/ /pubmed/22808385 Text en Copyright © Iranian Society of Medical Entomology & Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Nateghpour, M
Mavi, S Ayazian
Keshavarz, H
Rezaei, S
Abedi, F
Edrissian, GH
Raeisi, A
Molecular Monitoring of Plasmodium vivax Infection after Radical Treatment in Southeastern Iran
title Molecular Monitoring of Plasmodium vivax Infection after Radical Treatment in Southeastern Iran
title_full Molecular Monitoring of Plasmodium vivax Infection after Radical Treatment in Southeastern Iran
title_fullStr Molecular Monitoring of Plasmodium vivax Infection after Radical Treatment in Southeastern Iran
title_full_unstemmed Molecular Monitoring of Plasmodium vivax Infection after Radical Treatment in Southeastern Iran
title_short Molecular Monitoring of Plasmodium vivax Infection after Radical Treatment in Southeastern Iran
title_sort molecular monitoring of plasmodium vivax infection after radical treatment in southeastern iran
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385539/
https://www.ncbi.nlm.nih.gov/pubmed/22808385
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