Kattoor Jobin J, Nikolai Emma, Qurollo Barbara, Wilkes Rebecca P
Animal Disease Diagnostic Laboratory, Department of Comparative Pathobiology, College of Veterinary Medicine, Purdue University, West Lafayette, IN 47907, USA.
Vector Borne Disease Diagnostic Laboratory, Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27606, USA.
Pathogens. 2022 Aug 24;11(9):964. doi: 10.3390/pathogens11090964.
The standard for detecting vector-borne pathogens is real-time PCR (rtPCR). However, this requires many individual tests to obtain an accurate diagnosis. The purpose of this study was to develop and validate a targeted next-generation sequencing (NGS) assay for vector-borne pathogens. Pathogen target regions were amplified via PCR using two primer pools that were developed in conjunction with ThermoFisher Scientific, and barcoded DNA libraries were prepared and sequenced with the Ion Torrent S5 system. Data were assembled using SPAdes and mapped to a reference file containing sequences from the pathogens. The raw reads were analyzed to confirm the results. Test feasibility and analytical specificity were evaluated with type strains or validated positive clinical samples from dogs. The analytical sensitivity of the method was compared to Ct values obtained by rtPCR testing. Diagnostic sensitivity and specificity were assessed with a set of known positive and negative clinical samples based on rtPCR testing. Positive and negative percent agreements and Cohen's kappa were calculated. The primer sets were specific for the intended targets, based on sequence analysis of the amplified products, and the method detected 17 different pathogens. Analytical sensitivity was equivalent to an rtPCR Ct value of approximately 35-36. The positive percent agreement was 92%, and the negative percent agreement was 88%. Cohen's kappa was 0.804, which indicates almost perfect agreement between the rtPCR assays and the targeted NGS assay. Using a targeted method reduces the costs associated with NGS sequencing and allows for a 2-3 day turn-around time, making this a viable method for detection of vector-borne pathogens in canine whole blood samples.
检测媒介传播病原体的标准方法是实时聚合酶链反应(rtPCR)。然而,这需要进行许多单独检测才能获得准确诊断。本研究的目的是开发并验证一种针对媒介传播病原体的靶向新一代测序(NGS)检测方法。通过PCR使用与赛默飞世尔科技联合开发的两个引物池扩增病原体靶区域,制备带条形码的DNA文库,并使用Ion Torrent S5系统进行测序。使用SPAdes组装数据并将其映射到包含病原体序列的参考文件。对原始读数进行分析以确认结果。用标准菌株或经验证的犬类阳性临床样本评估检测可行性和分析特异性。将该方法的分析灵敏度与rtPCR检测获得的Ct值进行比较。基于rtPCR检测,用一组已知的阳性和阴性临床样本评估诊断灵敏度和特异性。计算阳性和阴性百分比一致性以及科恩kappa系数。根据扩增产物的序列分析,引物组对预期靶标具有特异性,该方法检测到17种不同病原体。分析灵敏度相当于rtPCR Ct值约为35 - 36。阳性百分比一致性为92%,阴性百分比一致性为88%。科恩kappa系数为0.804,这表明rtPCR检测与靶向NGS检测之间几乎完全一致。使用靶向方法可降低与NGS测序相关的成本,并实现2 - 3天的周转时间,使其成为检测犬全血样本中媒介传播病原体的可行方法。