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Brazilian Plasmodium falciparum isolates: investigation of candidate polymorphisms for artemisinin resistance before introduction of artemisinin-based combination therapy

BACKGROUND: This study was performed to better understand the genetic diversity of known polymorphisms in pfatpase6 and pfmdr1 genes before the introduction of ACT in Brazil, in order to get a genotypic snapshot of Plasmodium falciparum parasites that may be used as baseline reference for future stu...

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Autores principales: Gama, Bianca E, de Oliveira, Natália K Almeida, de Souza, José M, Santos, Fátima, de Carvalho, Leonardo JM, Melo, Yonne FC, Rosenthal, Philip J, Daniel-Ribeiro, Cláudio T, Ferreira-da-Cruz, Maria de Fátima
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017535/
https://www.ncbi.nlm.nih.gov/pubmed/21143867
http://dx.doi.org/10.1186/1475-2875-9-355
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author Gama, Bianca E
de Oliveira, Natália K Almeida
de Souza, José M
Santos, Fátima
de Carvalho, Leonardo JM
Melo, Yonne FC
Rosenthal, Philip J
Daniel-Ribeiro, Cláudio T
Ferreira-da-Cruz, Maria de Fátima
author_facet Gama, Bianca E
de Oliveira, Natália K Almeida
de Souza, José M
Santos, Fátima
de Carvalho, Leonardo JM
Melo, Yonne FC
Rosenthal, Philip J
Daniel-Ribeiro, Cláudio T
Ferreira-da-Cruz, Maria de Fátima
author_sort Gama, Bianca E
collection PubMed
description BACKGROUND: This study was performed to better understand the genetic diversity of known polymorphisms in pfatpase6 and pfmdr1 genes before the introduction of ACT in Brazil, in order to get a genotypic snapshot of Plasmodium falciparum parasites that may be used as baseline reference for future studies. METHODS: Parasites from P. falciparum samples collected in 2002, 2004 and 2006-2007 were genotyped using PCR and DNA sequencing at codons 86, 130, 184, 1034, 1042, 1109 and 1246 for pfmdr1 gene, and 243, 263, 402, 431, 623, 630, 639, 683, 716, 776, 769 and 771 for pfatpase6 gene. RESULTS: A pfmdr1 haplotype NEF/CDVY was found in 97% of the samples. In the case of pfatpase6, four haplotypes, wild-type (37%), 630 S (35%), 402 V (5%) and double-mutant 630 S + 402 V (23%), were detected. CONCLUSION: Although some polymorphism in pfmdr1 and pfatpase6 were verified, no reported haplotypes in both genes that may mediate altered response to ACT was detected before the introduction of this therapy in Brazil. Thus, the haplotypes herein described can be very useful as a baseline reference of P. falciparum populations without ACT drug pressure.
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spelling pubmed-30175352011-01-08 Brazilian Plasmodium falciparum isolates: investigation of candidate polymorphisms for artemisinin resistance before introduction of artemisinin-based combination therapy Gama, Bianca E de Oliveira, Natália K Almeida de Souza, José M Santos, Fátima de Carvalho, Leonardo JM Melo, Yonne FC Rosenthal, Philip J Daniel-Ribeiro, Cláudio T Ferreira-da-Cruz, Maria de Fátima Malar J Research BACKGROUND: This study was performed to better understand the genetic diversity of known polymorphisms in pfatpase6 and pfmdr1 genes before the introduction of ACT in Brazil, in order to get a genotypic snapshot of Plasmodium falciparum parasites that may be used as baseline reference for future studies. METHODS: Parasites from P. falciparum samples collected in 2002, 2004 and 2006-2007 were genotyped using PCR and DNA sequencing at codons 86, 130, 184, 1034, 1042, 1109 and 1246 for pfmdr1 gene, and 243, 263, 402, 431, 623, 630, 639, 683, 716, 776, 769 and 771 for pfatpase6 gene. RESULTS: A pfmdr1 haplotype NEF/CDVY was found in 97% of the samples. In the case of pfatpase6, four haplotypes, wild-type (37%), 630 S (35%), 402 V (5%) and double-mutant 630 S + 402 V (23%), were detected. CONCLUSION: Although some polymorphism in pfmdr1 and pfatpase6 were verified, no reported haplotypes in both genes that may mediate altered response to ACT was detected before the introduction of this therapy in Brazil. Thus, the haplotypes herein described can be very useful as a baseline reference of P. falciparum populations without ACT drug pressure. BioMed Central 2010-12-08 /pmc/articles/PMC3017535/ /pubmed/21143867 http://dx.doi.org/10.1186/1475-2875-9-355 Text en Copyright ©2010 Gama et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Gama, Bianca E
de Oliveira, Natália K Almeida
de Souza, José M
Santos, Fátima
de Carvalho, Leonardo JM
Melo, Yonne FC
Rosenthal, Philip J
Daniel-Ribeiro, Cláudio T
Ferreira-da-Cruz, Maria de Fátima
Brazilian Plasmodium falciparum isolates: investigation of candidate polymorphisms for artemisinin resistance before introduction of artemisinin-based combination therapy
title Brazilian Plasmodium falciparum isolates: investigation of candidate polymorphisms for artemisinin resistance before introduction of artemisinin-based combination therapy
title_full Brazilian Plasmodium falciparum isolates: investigation of candidate polymorphisms for artemisinin resistance before introduction of artemisinin-based combination therapy
title_fullStr Brazilian Plasmodium falciparum isolates: investigation of candidate polymorphisms for artemisinin resistance before introduction of artemisinin-based combination therapy
title_full_unstemmed Brazilian Plasmodium falciparum isolates: investigation of candidate polymorphisms for artemisinin resistance before introduction of artemisinin-based combination therapy
title_short Brazilian Plasmodium falciparum isolates: investigation of candidate polymorphisms for artemisinin resistance before introduction of artemisinin-based combination therapy
title_sort brazilian plasmodium falciparum isolates: investigation of candidate polymorphisms for artemisinin resistance before introduction of artemisinin-based combination therapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017535/
https://www.ncbi.nlm.nih.gov/pubmed/21143867
http://dx.doi.org/10.1186/1475-2875-9-355
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