Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Digital do Instituto Evandro Chagas (Patuá) |
Texto Completo: | https://patua.iec.gov.br/handle/iec/1062 |
Resumo: | Objective To evaluate the in vitro efficacy of artesunate (ATN) and artemether (ATH) against Plasmodium falciparum isolates from the Brazilian Amazon state of Pará and to search for mutations and ⁄ or altered copy numbers in the putative resistance-associated pfcrt, pfmdr1 and pfATPase6 genes. methods In vitro efficacy of ATN and ATH was successfully measured in 56 freshly collected P. falciparum isolates, using a conventional WHO microtest with minor modifications. Single nucleotide polymorphisms (SNPs) in the same isolates were inspected using DNA sequencing and ⁄ or PCR-RFLP. We used real-time quantitative PCR to assess gene copy numbers. results ATN and ATH geometric mean IC50s were 0.85 nm, 95% CI (0.55–1.15) and 3.0 nm, 95% CI (1.5–4.5), respectively. There was extremely limited diversity of pfcrt and pfmdr1 genotypes and three SNPs were identified in the pfATPase6 gene: one T to A synonymous mutation at nucleotide 2694 and two non-synonymous (both G to A) mutations at nucleotides 110 and 1916, causing predicted aminoacid shifts of arginine to lysine and of glycine to aspartate, respectively. The previously reported S769N mutation was not detected in any of the isolates inspected. In addition, no gene amplifications were detected in a subset of eight isolates. conclusion Artemisinin derivatives display satisfactory in vitro activity locally and the pfATPase6 gene is distinct from that reported in French Guiana, suggesting that those haplotypes have not been introduced regionally. |
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Ferreira, Isabel DMartinelli, AxelRodrigues, Louise ACarmo, Ediclei Lima doRosário, Virgílio E doPóvoa, Marinete MarinsCravo, Pedro2016-01-26T11:43:21Z2016-01-26T11:43:21Z2008FERREIRA, Isabel D. et al. Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6. Tropical Medicine and International Health, v. 13, n. 1, p. 199-207, Feb. 20081360-2276https://patua.iec.gov.br/handle/iec/106210.1111/j.1365-3156.2007.01991.xObjective To evaluate the in vitro efficacy of artesunate (ATN) and artemether (ATH) against Plasmodium falciparum isolates from the Brazilian Amazon state of Pará and to search for mutations and ⁄ or altered copy numbers in the putative resistance-associated pfcrt, pfmdr1 and pfATPase6 genes. methods In vitro efficacy of ATN and ATH was successfully measured in 56 freshly collected P. falciparum isolates, using a conventional WHO microtest with minor modifications. Single nucleotide polymorphisms (SNPs) in the same isolates were inspected using DNA sequencing and ⁄ or PCR-RFLP. We used real-time quantitative PCR to assess gene copy numbers. results ATN and ATH geometric mean IC50s were 0.85 nm, 95% CI (0.55–1.15) and 3.0 nm, 95% CI (1.5–4.5), respectively. There was extremely limited diversity of pfcrt and pfmdr1 genotypes and three SNPs were identified in the pfATPase6 gene: one T to A synonymous mutation at nucleotide 2694 and two non-synonymous (both G to A) mutations at nucleotides 110 and 1916, causing predicted aminoacid shifts of arginine to lysine and of glycine to aspartate, respectively. The previously reported S769N mutation was not detected in any of the isolates inspected. In addition, no gene amplifications were detected in a subset of eight isolates. conclusion Artemisinin derivatives display satisfactory in vitro activity locally and the pfATPase6 gene is distinct from that reported in French Guiana, suggesting that those haplotypes have not been introduced regionally.Instituto de Higiene e Medicina Tropical. Centro de Malária e Outras Doenças Tropicais. UEI Biologia Molecular. UEI Malária. Lisbon, Portugal.Instituto de Higiene e Medicina Tropical. Centro de Malária e Outras Doenças Tropicais. UEI Biologia Molecular. UEI Malária. Lisbon, Portugal.Instituto de Higiene e Medicina Tropical. Centro de Malária e Outras Doenças Tropicais. UEI Biologia Molecular. UEI Malária. Lisbon, Portugal.Ministério da Saúde. Secretaria de Vigilância em Saúde . Instituto Evandro Chagas. Belém, PA, Brasil.Instituto de Higiene e Medicina Tropical. Centro de Malária e Outras Doenças Tropicais. UEI Biologia Molecular. UEI Malária. Lisbon, Portugal.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Belém, PA, Brasil.Instituto de Higiene e Medicina Tropical. Centro de Malária e Outras Doenças Tropicais. UEI Biologia Molecular. UEI Malária. Lisbon, Portugal.application/pdfengWileyPlasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleArtemisininas / administração & dosagemArtemisininas / análisePlasmodium falciparum / efeitos de drogasMalária / prevenção & controleBiomarcadoresinfo:eu-repo/semantics/openAccessreponame:Repositório Digital do Instituto Evandro Chagas (Patuá)instname:Instituto Evandro Chagas (IEC)instacron:IECORIGINALPlasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 .pdfapplication/pdf293948https://patua.iec.gov.br/bitstreams/bdb90e9e-d0d6-4a24-b7be-dbac6bf7a435/downloada510f436594b20157ff43abb89de2aa3MD51TEXTfile_1.pdf.txtfile_1.pdf.txtExtracted texttext/plain41196https://patua.iec.gov.br/bitstreams/56a8507b-ddd3-4b1b-9a97-876c5d9436db/download197dabb041acb61ecc0487823b3cd261MD52Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 .pdf.txtPlasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 .pdf.txtExtracted texttext/plain42154https://patua.iec.gov.br/bitstreams/afe5fcb5-e71b-4cdb-86be-d9dedd4a06f1/download1ebf8ae51911d972b92355c808fbc854MD56THUMBNAILPlasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 .pdf.jpgPlasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 .pdf.jpgGenerated Thumbnailimage/jpeg5604https://patua.iec.gov.br/bitstreams/f7ffafbb-3e94-4051-907e-dc98fcee5026/download3690356e85423c36262938770ac88ce9MD57LICENSElicense.txtlicense.txttext/plain; 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dc.title.pt_BR.fl_str_mv |
Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 |
title |
Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 |
spellingShingle |
Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 Ferreira, Isabel D Artemisininas / administração & dosagem Artemisininas / análise Plasmodium falciparum / efeitos de drogas Malária / prevenção & controle Biomarcadores |
title_short |
Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 |
title_full |
Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 |
title_fullStr |
Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 |
title_full_unstemmed |
Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 |
title_sort |
Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6 |
author |
Ferreira, Isabel D |
author_facet |
Ferreira, Isabel D Martinelli, Axel Rodrigues, Louise A Carmo, Ediclei Lima do Rosário, Virgílio E do Póvoa, Marinete Marins Cravo, Pedro |
author_role |
author |
author2 |
Martinelli, Axel Rodrigues, Louise A Carmo, Ediclei Lima do Rosário, Virgílio E do Póvoa, Marinete Marins Cravo, Pedro |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Ferreira, Isabel D Martinelli, Axel Rodrigues, Louise A Carmo, Ediclei Lima do Rosário, Virgílio E do Póvoa, Marinete Marins Cravo, Pedro |
dc.subject.decsPrimary.pt_BR.fl_str_mv |
Artemisininas / administração & dosagem Artemisininas / análise Plasmodium falciparum / efeitos de drogas Malária / prevenção & controle Biomarcadores |
topic |
Artemisininas / administração & dosagem Artemisininas / análise Plasmodium falciparum / efeitos de drogas Malária / prevenção & controle Biomarcadores |
description |
Objective To evaluate the in vitro efficacy of artesunate (ATN) and artemether (ATH) against Plasmodium falciparum isolates from the Brazilian Amazon state of Pará and to search for mutations and ⁄ or altered copy numbers in the putative resistance-associated pfcrt, pfmdr1 and pfATPase6 genes. methods In vitro efficacy of ATN and ATH was successfully measured in 56 freshly collected P. falciparum isolates, using a conventional WHO microtest with minor modifications. Single nucleotide polymorphisms (SNPs) in the same isolates were inspected using DNA sequencing and ⁄ or PCR-RFLP. We used real-time quantitative PCR to assess gene copy numbers. results ATN and ATH geometric mean IC50s were 0.85 nm, 95% CI (0.55–1.15) and 3.0 nm, 95% CI (1.5–4.5), respectively. There was extremely limited diversity of pfcrt and pfmdr1 genotypes and three SNPs were identified in the pfATPase6 gene: one T to A synonymous mutation at nucleotide 2694 and two non-synonymous (both G to A) mutations at nucleotides 110 and 1916, causing predicted aminoacid shifts of arginine to lysine and of glycine to aspartate, respectively. The previously reported S769N mutation was not detected in any of the isolates inspected. In addition, no gene amplifications were detected in a subset of eight isolates. conclusion Artemisinin derivatives display satisfactory in vitro activity locally and the pfATPase6 gene is distinct from that reported in French Guiana, suggesting that those haplotypes have not been introduced regionally. |
publishDate |
2008 |
dc.date.issued.fl_str_mv |
2008 |
dc.date.accessioned.fl_str_mv |
2016-01-26T11:43:21Z |
dc.date.available.fl_str_mv |
2016-01-26T11:43:21Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
FERREIRA, Isabel D. et al. Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6. Tropical Medicine and International Health, v. 13, n. 1, p. 199-207, Feb. 2008 |
dc.identifier.uri.fl_str_mv |
https://patua.iec.gov.br/handle/iec/1062 |
dc.identifier.issn.-.fl_str_mv |
1360-2276 |
dc.identifier.doi.-.fl_str_mv |
10.1111/j.1365-3156.2007.01991.x |
identifier_str_mv |
FERREIRA, Isabel D. et al. Plasmodium falciparum from Pará state (Brazil) shows satisfactory in vitro response to artemisinin derivatives and absence of the S769N mutation in the SERCA-type PfATPase6. Tropical Medicine and International Health, v. 13, n. 1, p. 199-207, Feb. 2008 1360-2276 10.1111/j.1365-3156.2007.01991.x |
url |
https://patua.iec.gov.br/handle/iec/1062 |
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