用于调查人类非洲锥虫病耐药性的下一代 CRISPR 诊断工具。

Elena Perez Anton, Annick Dujeancourt-Henry, Brice Rotureau, Lucy Glover
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摘要

世界卫生组织的目标是到 2030 年消灭冈比亚型非洲锥虫病(HAT)。随着新报告病例的减少,保持高效的流行病学监测至关重要,包括耐药菌株的出现。我们利用特异性高灵敏度报告酶解锁(SHERLOCK)技术开发了新的高特异性诊断工具,用于监测以下耐药基因型的存在:(1) 已在流行的耐药基因型,如对喷他脒和美拉索洛尔产生耐药性的 AQP2/3(814)嵌合体;或 (2) 可能出现的耐药基因型,如在实验室条件下与阿喹唑啉耐药性相关的 TbCPSF3 (N232H)。美拉索波罗-喷他脒 AQP2/3(814)SHERLOCK检测法可从培养的寄生虫和治疗后复发的 gHAT 患者的野外分离菌株中检测到 RNA。阿考唑硼酸 CPSF3(SNV) SHERLOCK 检测法可区分野生型 CPSF3 RNA 和具有单一 A-C 突变的 CPSF3,后者在体外对阿考唑硼酸产生抗性。
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A next generation CRISPR diagnostic tool to survey drug resistance in Human African Trypanosomiasis.
The WHO aims to eliminate the gambiense form of human African trypanosomiasis (HAT) by 2030. With the decrease of new reported cases, maintaining an efficient epidemiological surveillance is essential, including the emergence of drug-resistant strains. We have developed new highly specific diagnostic tools using Specific High-Sensitivity Reporter Enzymatic UnLOCKing (SHERLOCK) technology for monitoring the presence of drug-resistant genotypes that (1) are already circulating, such as the AQP2/3(814) chimera providing resistance to pentamidine and melarsoprol, or (2) could emerge, such as TbCPSF3 (N232H), associated to acoziborole resistance in lab conditions. The melarsoprol - pentamidine AQP2/3(814) SHERLOCK assay detected RNA from both cultured parasites and field isolated strains from gHAT patients in relapse following treatment. The acoziborole CPSF3(SNV) SHERLOCK assay discriminated between wild-type CPSF3 RNA and CPSF3 with a single A-C mutation that confers resistance to acoziborole in vitro.
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