Dorado Erika Jimena, Okoth Sheila Akinyi, Montenegro Lidia Madeline, Diaz Gustavo, Barnwell John W, Udhayakumar Venkatachalam, Murillo Solano Claribel
Malaria Research Group, Centro Internacional de Entrenamiento e Investigaciones Medicas (CIDEIM), Cali, Valle, Colombia.
Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, United States of America.
PLoS One. 2016 Sep 16;11(9):e0163137. doi: 10.1371/journal.pone.0163137. eCollection 2016.
Most Plasmodium falciparum-detecting rapid diagnostic tests (RDTs) target histidine-rich protein 2 (PfHRP2). However, P. falciparum isolates with deletion of the pfhrp2 gene and its homolog gene, pfhrp3, have been detected. We carried out an extensive investigation on 365 P. falciparum dried blood samples collected from seven P. falciparum endemic sites in Colombia between 2003 and 2012 to genetically characterise and geographically map pfhrp2- and/or pfhrp3-negative P. falciparum parasites in the country. We found a high proportion of pfhrp2-negative parasites only in Amazonas (15/39; 38.5%), and these parasites were also pfhrp3-negative. These parasites were collected between 2008 and 2009 in Amazonas, while pfhrp3-negative parasites (157/365, 43%) were found in all the sites and from each of the sample collection years evaluated (2003 to 2012). We also found that all pfhrp2- and/or pfhrp3-negative parasites were also negative for one or both flanking genes. Six sub-population clusters were established with 93.3% (14/15) of the pfhrp2-negative parasites grouped in the same cluster and sharing the same haplotype. This haplotype corresponded with the genetic lineage BV1, a multidrug resistant strain that caused two outbreaks reported in Peru between 2010 and 2013. We found this BV1 lineage in the Colombian Amazon as early as 2006. Two new clonal lineages were identified in these parasites from Colombia: the genetic lineages EV1 and F. PfHRP2 sequence analysis revealed high genetic diversity at the amino acid level, with 17 unique sequences identified among 53 PfHRP2 sequences analysed. The use of PfHRP2-based RDTs is not recommended in Amazonas because of the high proportion of parasites with pfhrp2 deletion (38.5%), and implementation of new strategies for malaria diagnosis and control in Amazonas must be prioritised. Moreover, studies to monitor and genetically characterise pfhrp2-negative P. falciparum parasites in the Americas are warranted, given the extensive human migration occurring in the region.
大多数检测恶性疟原虫的快速诊断检测(RDT)都以富含组氨酸的蛋白2(PfHRP2)为靶点。然而,已检测到缺失pfhrp2基因及其同源基因pfhrp3的恶性疟原虫分离株。我们对2003年至2012年间从哥伦比亚7个恶性疟原虫流行地区采集的365份恶性疟原虫干血样本进行了广泛调查,以对该国pfhrp2和/或pfhrp3阴性的恶性疟原虫进行基因特征分析和地理定位。我们发现仅在亚马孙地区有高比例的pfhrp2阴性寄生虫(15/39;38.5%),并且这些寄生虫也是pfhrp3阴性。这些寄生虫于2008年至2009年在亚马孙地区采集,而pfhrp3阴性寄生虫(157/365,43%)在所有地点以及评估的每个样本采集年份(2003年至2012年)均有发现。我们还发现所有pfhrp2和/或pfhrp3阴性的寄生虫对一个或两个侧翼基因也呈阴性。建立了6个亚种群簇,93.3%(14/15)的pfhrp2阴性寄生虫聚集在同一簇中并共享相同的单倍型。这个单倍型与遗传谱系BV1相对应,BV1是一种多重耐药菌株,在2010年至2013年间在秘鲁引发了两次疫情。我们早在2006年就在哥伦比亚亚马孙地区发现了这种BV1谱系。在来自哥伦比亚的这些寄生虫中鉴定出了两个新的克隆谱系:遗传谱系EV1和F。PfHRP2序列分析显示在氨基酸水平上有很高的遗传多样性,在分析的53个PfHRP2序列中鉴定出17个独特序列。由于pfhrp2缺失的寄生虫比例很高(38.5%),不建议在亚马孙地区使用基于PfHRP2的RDT,并且必须优先实施亚马孙地区疟疾诊断和控制的新策略。此外,鉴于该地区发生的广泛人口迁移,有必要开展监测和基因特征分析美洲pfhrp2阴性恶性疟原虫的研究。