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新型多重高清聚合酶链反应检测全血标本中蜱传病原体的评估。

Evaluation of a Novel Multiplex High-Definition PCR Assay for Detection of Tick-Borne Pathogens in Whole-Blood Specimens.

机构信息

Department of Pathology, The Medical College of Wisconsin, Milwaukee, Wisconsin, USA

Microbiology Research and Molecular Diagnostics Laboratories, Gundersen Medical Foundation, La Crosse, Wisconsin, USA.

出版信息

J Clin Microbiol. 2019 Oct 23;57(11). doi: 10.1128/JCM.00513-19. Print 2019 Nov.

Abstract

The prevalence of tick-borne infections has been steadily increasing in both number and geographic distribution in the United States and abroad. This increase, in conjunction with the continued recognition of novel pathogens transmitted by ticks, has made accurate diagnosis of these infections challenging. Mainstay serologic tests are insensitive during the acute phase of infection and are often cross-reactive with similar pathogenic and nonpathogenic organisms. Further, they are unable to reliably differentiate active versus past infection which can lead to misdiagnosis and incorrect understanding of the epidemiology and incidence of specific tick-borne pathogens. We evaluated a novel multiplexed high-definition PCR (HDPCR) Tickborne Panel (TBP) assay (ChromaCode, Carlsbad, CA) for the detection of nine tick-borne pathogens or groups associated with human illness. The HDPCR technology enables multiplex identification of multiple targets in a single fluorometric channel based on fluorescent signal modulation using a limiting probe design. A collection of 530 whole-blood specimens collected from patients being evaluated for tick-borne infections, in addition to a panel of 93 simulated specimens, were used to challenge the HDPCR TBP. The results were compared to a clinically validated traditional multiplexed PCR test with additional sequence analysis and clinical history collected to aid in resolving discrepancies. Among clinical specimens the TBP demonstrated 100% sensitivity for the identification of , , , and The sensitivity for identification of was 44.4% compared to a composite gold standard. Among simulated specimens containing single or multiple targets present at 10 to 10 copies/PCR, the sensitivity of TBP was 100% for all targets, with a combined specificity of 99.5%. Of note, an increased rate of false-positive results was observed among simulated specimens that contained multiple targets. Based on these data, we find the HDPCR TBP to be a useful adjunct for the diagnosis of tick-borne infections in patients with suspected tick-borne illness.

摘要

蜱传感染的流行率在美国和国外都在数量和地理分布上稳步上升。这种增加,加上对蜱传播的新型病原体的持续认识,使得这些感染的准确诊断具有挑战性。主要的血清学检测在感染的急性期不敏感,并且经常与类似的致病性和非致病性生物发生交叉反应。此外,它们不能可靠地区分活跃感染与既往感染,这可能导致误诊和对特定蜱传病原体的流行病学和发病率的不正确理解。我们评估了一种新的高通量高清聚合酶链反应(HDPCR)蜱传面板(TBP)检测试剂盒(ChromaCode,卡尔斯巴德,加利福尼亚州),用于检测与人类疾病相关的九种蜱传病原体或病原体组。HDPCR 技术基于使用限制探针设计的荧光信号调制,能够在单个荧光通道中对多个靶标进行多重识别。我们使用了 530 份来自正在接受蜱传感染评估的患者的全血样本和 93 份模拟样本的集合来对 HDPCR TBP 进行挑战。将结果与经过临床验证的传统多重 PCR 检测进行比较,并收集了额外的序列分析和临床病史,以帮助解决差异。在临床标本中,TBP 对鉴定、、、和的敏感性为 100%。与复合金标准相比,对鉴定的敏感性为 44.4%。在含有 10 至 10 拷贝/PCR 的单个或多个靶标存在的模拟标本中,TBP 的敏感性为所有靶标的 100%,综合特异性为 99.5%。值得注意的是,在含有多个靶标的模拟标本中观察到假阳性结果的发生率增加。基于这些数据,我们发现 HDPCR TBP 是一种有用的辅助手段,可用于诊断疑似蜱传疾病患者的蜱传感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b62/6812998/ed57a91f0d24/JCM.00513-19-f0001.jpg

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