Molecular characterization of the Plasmodium falciparum k13 gene helix domain in samples from native communities of Condorcanqui, Amazonas, Perú

Julio Sandoval-Bances, Milagros Saavedra-Samillán, Sonia Huyhua-Gutiérrez, Luis M Rojas, Sonia Tejada-Muñoz, Rafael Tapia-Limonchi, Stella M Chenet
{"title":"Molecular characterization of the Plasmodium falciparum k13 gene helix domain in samples from native communities of Condorcanqui, Amazonas, Perú","authors":"Julio Sandoval-Bances,&nbsp;Milagros Saavedra-Samillán,&nbsp;Sonia Huyhua-Gutiérrez,&nbsp;Luis M Rojas,&nbsp;Sonia Tejada-Muñoz,&nbsp;Rafael Tapia-Limonchi,&nbsp;Stella M Chenet","doi":"10.7705/biomedica.6849","DOIUrl":null,"url":null,"abstract":"<p><p>Introduction. Resistance of Plasmodium falciparum to different antimalarial drugs is an obstacle to disease elimination. The artemisinin-resistant genotype of P. falciparum can be assessed by examining polymorphisms in the helix domain of the Pfk13 gene. The World Health Organization recommends these mutations as molecular markers to detect artemisinin-resistant in countries where P. falciparum malaria is endemic.\nObjective. To identify artemisinin resistance-related mutations present in the helix domain of the P. falciparum k13 gene.\nMaterials and methods. We collected a total of 51 samples through passive case detection, positive for Plasmodium by microscopy, from six communities in the district of Río Santiago in Condorcanqui, Amazonas. Molecular species confirmation was performed by real-time PCR and Pfk13 helix domain was amplified and sequenced by capillary electrophoresis. The obtained sequences were compared with the wild type 3D7 reference strain.\nResults. A total of 51 positive samples were confirmed for P. falciparum from the communities of Ayambis, Chapiza, Palometa, Muchinguis, Alianza Progreso and Caterpiza. DNA sequences alignment showed the absence of resistance-associated mutations in the k13 gene of the collected samples.\nDiscussion. The obtained results are consistent with similar studies conducted in other South American countries, including Perú, so these data provide a baseline for artemisinin-resistance molecular surveillance in the Amazon region and reinforce the efficacy of artemisinin-based combination therapy in this area.</p>","PeriodicalId":101322,"journal":{"name":"Biomedica : revista del Instituto Nacional de Salud","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10624420/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedica : revista del Instituto Nacional de Salud","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7705/biomedica.6849","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction. Resistance of Plasmodium falciparum to different antimalarial drugs is an obstacle to disease elimination. The artemisinin-resistant genotype of P. falciparum can be assessed by examining polymorphisms in the helix domain of the Pfk13 gene. The World Health Organization recommends these mutations as molecular markers to detect artemisinin-resistant in countries where P. falciparum malaria is endemic. Objective. To identify artemisinin resistance-related mutations present in the helix domain of the P. falciparum k13 gene. Materials and methods. We collected a total of 51 samples through passive case detection, positive for Plasmodium by microscopy, from six communities in the district of Río Santiago in Condorcanqui, Amazonas. Molecular species confirmation was performed by real-time PCR and Pfk13 helix domain was amplified and sequenced by capillary electrophoresis. The obtained sequences were compared with the wild type 3D7 reference strain. Results. A total of 51 positive samples were confirmed for P. falciparum from the communities of Ayambis, Chapiza, Palometa, Muchinguis, Alianza Progreso and Caterpiza. DNA sequences alignment showed the absence of resistance-associated mutations in the k13 gene of the collected samples. Discussion. The obtained results are consistent with similar studies conducted in other South American countries, including Perú, so these data provide a baseline for artemisinin-resistance molecular surveillance in the Amazon region and reinforce the efficacy of artemisinin-based combination therapy in this area.

Abstract Image

秘鲁亚马逊康多尔坎基土著社区样本中恶性疟原虫K13基因螺旋结构域的分子特征。
介绍。恶性疟原虫对不同抗疟药物的耐药性是消除该疾病的障碍。恶性疟原虫对青蒿素的抗性基因型可以通过检测PFK13基因螺旋结构域的多态性来评估。世界卫生组织建议将这些突变用作分子标记,以检测疟疾流行的国家对青蒿素的耐药性。恶性疟。目标。确定恶性疟原虫K13基因螺旋结构域中存在的与青蒿素耐药性相关的突变。材料和方法。通过被动检测病例,从亚马孙州康多尔坎基的圣地亚哥河地区的六个社区收集了51份疟原虫显微镜阳性样本。通过实时PCR对该物种进行了分子确认,并通过毛细管电泳扩增和测序了PFK13基因的螺旋结构域。获得的序列与野生型参考菌株3D7进行了比较。结果。共确认了来自阿亚姆比斯、查皮萨、帕洛梅塔、穆钦吉、阿连扎·普罗格罗索和卡特皮萨社区的51例恶性疟原虫阳性样本。在DNA序列对齐后,确定样本中没有与K13基因抗性相关的突变。讨论。所得结果与包括秘鲁在内的南美其他国家进行的类似研究一致。这些数据为亚马逊地区青蒿素耐药性的分子监测提供了基线,并加强了该地区青蒿素联合疗法的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信