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用于三种猫科动物病原体检测与特征分析的靶向富集

Targeted Enrichment for Pathogen Detection and Characterization in Three Felid Species.

作者信息

Lee Justin S, Mackie Ryan S, Harrison Thomas, Shariat Basir, Kind Trey, Kehl Timo, Löchelt Martin, Boucher Christina, VandeWoude Sue

机构信息

Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, USA

Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, USA.

出版信息

J Clin Microbiol. 2017 Jun;55(6):1658-1670. doi: 10.1128/JCM.01463-16. Epub 2017 Mar 22.

Abstract

Traditional diagnostic assays often lack sensitivity and can be difficult to multiplex across many pathogens. Next-generation sequencing (NGS) can overcome some of these problems but has limited application in the detection of low-copy-number pathogens in complex samples. Targeted genome capture (TGC) utilizes oligonucleotide probes to enrich specific nucleic acids in heterogeneous extracts and can therefore increase the proportion of NGS reads for low-abundance targets. While earlier studies have demonstrated the utility of this technology for detection of novel pathogens in human clinical samples, the capacity and practicality of TGC-NGS in a veterinary diagnostic setting have not yet been evaluated. Here we report the use of TGC-NGS assays for the detection and characterization of diverse feline pathogen taxa. We detected 31 pathogens comprising nine pathogen taxa in 28 felid samples analyzed. This included 20 pathogens detected via traditional PCR and 11 additional pathogens that had not been previously detected in the same samples. Most of the pathogens detected were sequenced at sufficient breadth and depth to confidently classify them at the species or subspecies level. Target nucleic acids were enriched from a low of 58-fold to 56 million-fold relative to host nucleic acids. Despite the promising performance of these assays, a number of pathogens detected by conventional PCR or serology were not isolated by TGC-NGS, suggesting that further validation is required before this technology can be used in lieu of quality-controlled standard assays. We conclude that TGC-NGS offers great potential as a broad multiplex pathogen characterization assay in veterinary diagnostic and research settings.

摘要

传统的诊断检测方法往往缺乏敏感性,并且难以对多种病原体进行多重检测。下一代测序(NGS)可以克服其中一些问题,但在复杂样本中检测低拷贝数病原体方面应用有限。靶向基因组捕获(TGC)利用寡核苷酸探针在异质提取物中富集特定核酸,因此可以增加低丰度靶标的NGS读数比例。虽然早期研究已经证明了该技术在检测人类临床样本中的新型病原体方面的实用性,但TGC-NGS在兽医诊断环境中的能力和实用性尚未得到评估。在此,我们报告了使用TGC-NGS检测方法对多种猫科病原体分类群进行检测和鉴定。我们在分析的28份猫科动物样本中检测到31种病原体,包括9个病原体分类群。这包括通过传统PCR检测到的20种病原体,以及在同一样本中先前未检测到的另外11种病原体。检测到的大多数病原体的测序深度和广度足以在物种或亚种水平上可靠地对其进行分类。相对于宿主核酸,靶标核酸的富集倍数低至58倍至5600万倍。尽管这些检测方法表现出了良好的性能,但一些通过传统PCR或血清学检测到的病原体并未通过TGC-NGS分离出来,这表明在该技术可用于替代质量控制的标准检测方法之前,还需要进一步验证。我们得出结论,TGC-NGS作为一种广泛的多重病原体鉴定检测方法,在兽医诊断和研究环境中具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53c4/5442522/3ae3f8b6439d/zjm9990955050001.jpg

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