Grüschow Sabine, Steketee Pieter C, Paxton Edith, Matthews Keith R, Morrison Liam J, White Malcolm F, Grey Finn
School of Biology, University of St Andrews, St Andrews, United Kingdom.
The Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom.
PLoS Negl Trop Dis. 2025 Mar 17;19(3):e0012937. doi: 10.1371/journal.pntd.0012937. eCollection 2025 Mar.
Animal Trypanosomosis (AT) is a significant disease affecting cattle across sub-Saharan Africa, Latin America, and Asia, posing a major threat to economic productivity and animal welfare. The absence of reliable diagnostic tests has led to an over-reliance on widespread pre-emptive drug treatments, which not only compromise animal health but also heighten the risk of drug resistance. The chronic nature of AT, characterized by cyclical low or undetectable parasite levels, and the necessity for field-applicable tests that can distinguish between active infection and prior exposure, present considerable challenges in developing effective diagnostics. In previous work, we identified a parasite-specific small RNA, 7SL-sRNA, which is detectable in the serum of infected cattle, even during the chronic stages of infection. However, existing methods for detecting sRNA require specialized equipment, making them unsuitable for field use. In this study, we have developed both a fluorescence-based and a lateral flow diagnostic test utilizing Cas10 technology for the detection of 7SL-sRNA from Trypanosoma congolense and Trypanosoma brucei. The fluorescence assay detects 10 - 100 fM T. congolense 7SL-sRNA and 1 pM T. brucei 7SL-sRNA, and the lateral flow assay showed a limit of detection of 1 - 10 pM for both species. Either assay can effectively identify active infections in cattle, including during chronic phases (with positive signals observed up to the experimental end point, 63 days post infection). This also highlights the effective use of Cas10 for small RNA detection, paving the way for a cost-effective, user-friendly, and field-deployable diagnostic test for AT, while establishing Cas10 technology for the detection of small RNAs in general.
动物锥虫病(AT)是一种影响撒哈拉以南非洲、拉丁美洲和亚洲牛群的重要疾病,对经济生产力和动物福利构成重大威胁。由于缺乏可靠的诊断测试,人们过度依赖广泛的预防性药物治疗,这不仅损害动物健康,还增加了耐药性风险。AT的慢性性质表现为寄生虫水平周期性低或无法检测到,而且需要能够区分活动性感染和既往暴露的现场适用测试,这在开发有效的诊断方法方面带来了巨大挑战。在之前的工作中,我们鉴定出一种寄生虫特异性小RNA,即7SL-sRNA,即使在感染的慢性阶段,也能在受感染牛的血清中检测到。然而,现有的检测sRNA的方法需要专门设备,因此不适合现场使用。在本研究中,我们开发了一种基于荧光的和一种侧向流动诊断测试,利用Cas10技术检测来自刚果锥虫和布氏锥虫的7SL-sRNA。荧光测定法可检测到10 - 100 fM的刚果锥虫7SL-sRNA和1 pM的布氏锥虫7SL-sRNA,侧向流动测定法对这两种锥虫的检测限均为1 - 10 pM。这两种测定法都能有效识别牛的活动性感染,包括在慢性阶段(在感染后63天的实验终点之前均观察到阳性信号)。这也突出了Cas10在小RNA检测中的有效应用,为开发一种经济高效、用户友好且可现场部署的AT诊断测试铺平了道路,同时也确立了Cas10技术在一般小RNA检测中的应用。