塞内加尔一株体外抗青蒿素恶性疟原虫kelch13 R515K突变寄生虫的鉴定

S. Sene, M. Pouye, R. M. Martins, F. Diallo, K. Mangou, A. Bei, Aliou Barry, O. Faye, Oumar Ndiaye, O. Faye, A. Sall, Jose-Juan Lopez-Rubio, A. Mbengue
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引用次数: 1

摘要

恶性疟原虫中青蒿素部分耐药性(ART-r)的出现大大损害了东南亚(东南亚)抗疟治疗的疗效。ART-r在非洲大陆的传播可能会危及过去在减轻全球疟疾负担方面取得的进展。塞内加尔考拉克发现一例临床指标疟疾病例,在接受青蒿琥酯-阿莫地喹(ASAQ)完全治疗后持续发热。达喀尔巴斯德研究所的塞内加尔哨兵监测系统从该指数病例周围的不同医疗中心采集了15份疟疾感染者的血液样本。我们已经鉴定出一种恶性疟原虫临床分离株,该分离株在青蒿素耐药性基因PfKelch13中携带R515K突变。进行CRISPR-Cas9基因组编辑,并对转基因Pf3D7Pfkelch13R515K进行体外标准环期生存测定(RSA 0-3hpi)测试。基因编辑已经证实PfKelch13R515K在体外驱动增加的RSA0-3hpi值。在这篇文章中,我们报道了PfKelch13R515K突变在非洲的功能意义。
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Identification of an in vitro artemisinin-resistant Plasmodium falciparum kelch13 R515K mutant parasite in Senegal
The emergence of artemisinin partial resistance (ART-r) in Plasmodium falciparum malaria parasites has substantially compromised the efficacy of antimalarial treatments across southeast Asia (SE Asia). The spread of ART-r within the African continent could jeopardize past progress made in reducing worldwide malaria burden. A clinical index malaria case was identified in Kaolack, Senegal with persistent fever after complete artesunate-amodiaquine (ASAQ) treatment. Fifteen malaria-infected blood samples were collected by Institut Pasteur Dakar’s Senegalese sentinel surveillance system, from different healthcare centers surrounding the index case. We have identified one Plasmodium falciparum clinical isolate carrying R515K mutation in the artemisinin resistance gene PfKelch13. CRISPR-Cas9 genome editing was carried out and transgenic Pf3D7Pfkelch13R515K was tested for in vitro standard Ring-stage Survival Assay (RSA 0-3hpi). Gene editing has confirmed that PfKelch13R515K drove increased in vitro RSA0-3hpi value. In this article, we report the functional significance of PfKelch13R515K mutation in an African context.
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