Development and evaluation of an RPA-CRISPR/Cas12a molecular assay for rapid diagnosis of Theileria annulata infection in bovines

IF 2.6 3区 医学 Q2 PARASITOLOGY
Acta tropica Pub Date : 2026-11-01 Epub Date: 2026-10-16 DOI:10.1016/j.actatropica.2026.108371
Aditi Mondal, B.C. Saravanan, Prachand Pratap Singh, P. Madhankumar, M. Sankar, Sonalika Mahajan, S. Dey, Rajveer Singh Pawaiya
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引用次数: 0

Abstract

Tropical theileriosis, caused by Theileria annulata, continues to be the most significant tick-borne disease affecting cattle, particularly in endemic regions where it leads to significant production losses. Prompt and reliable diagnosis is critically important for timely treatment and disease control; however, conventional diagnostic methods have important limitations. Microscopic examination lacks sensitivity, particularly in carrier animals, while PCR requires specialized laboratory infrastructure. To overcome these limitations, a fluorescence-based RPA-CRISPR/Cas12a assay targeting the multicopy mitochondrial cytb gene was developed for rapid detection of T. annulata. Five RPA primer pairs were designed and evaluated, and primer set-5, generating a 324-bp amplicon, exhibited the best amplification performance. A CRISPR RNA (crRNA) was designed within the selected amplicon to enable specific Cas12a-mediated target recognition. The assay was completed within 50 min and demonstrated no cross-reactivity with DNA from Theileria orientalis, Babesia bigemina, Babesia bovis, Anaplasma marginale, and bovine host DNA, confirming excellent analytical specificity. Sensitivity analysis using recombinant plasmid DNA demonstrated a detection limit of approximately ten copies per reaction. The field evaluation of the assay was done by testing 206 bovine field samples showed that the developed assay identified 163 positive samples, exceeding the detection rates obtained by PCR (151 positives) and microscopy (116 positives). On comparison with PCR, the assay achieved 100% diagnostic sensitivity, 78.18% specificity, 92.64% positive predictive value, 100% negative predictive value, with an overall agreement of 94.17%. These findings indicate that the RPA-CRISPR/Cas12a platform is a rapid, sensitive, and accurate molecular diagnostic approach with strong potential for field application and point-of-care diagnosis of bovine tropical theileriosis, particularly in resource-constrained settings.
快速诊断牛环状杆菌感染的RPA-CRISPR/Cas12a分子检测方法的建立与评价
由环纹伊勒菌引起的热带伊勒菌病仍然是影响牛的最严重的蜱传疾病,特别是在流行地区,它导致重大的生产损失。迅速和可靠的诊断对于及时治疗和疾病控制至关重要;然而,传统的诊断方法有重要的局限性。显微镜检查缺乏灵敏度,特别是在携带动物中,而PCR需要专门的实验室基础设施。为了克服这些局限性,我们开发了一种基于荧光的靶向多拷贝线粒体cytb基因的RPA-CRISPR/Cas12a检测方法,用于快速检测环状绦虫。设计并评价了5对RPA引物,引物set-5扩增效果最佳,扩增量为324bp。在选择的扩增子内设计CRISPR RNA (crRNA)以实现特定的cas12a介导的靶标识别。该检测在50分钟内完成,与东方伊氏菌、双双巴贝斯虫、牛巴贝斯虫、边缘无原体和牛宿主DNA无交叉反应,证实了良好的分析特异性。利用重组质粒DNA进行敏感性分析表明,每个反应的检测限约为10个拷贝。该方法的现场评价是通过测试206个牛的现场样品来完成的。结果表明,该方法鉴定出163份阳性样本,超过PCR(151份阳性)和镜检(116份阳性)的检出率。与PCR比较,诊断敏感性100%,特异性78.18%,阳性预测值92.64%,阴性预测值100%,总体一致性为94.17%。这些发现表明,RPA-CRISPR/Cas12a平台是一种快速、敏感和准确的分子诊断方法,具有很强的现场应用和护理点诊断潜力,特别是在资源有限的环境中。
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来源期刊
Acta tropica
Acta tropica 医学-寄生虫学
CiteScore
5.40
自引率
11.10%
发文量
383
审稿时长
37 days
期刊介绍: Acta Tropica, is an international journal on infectious diseases that covers public health sciences and biomedical research with particular emphasis on topics relevant to human and animal health in the tropics and the subtropics.
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