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使用分子信标实时PCR从血液中检测和区分莱姆螺旋体及其他蜱传病原体

Detection and Differentiation of Lyme Spirochetes and Other Tick-Borne Pathogens from Blood Using Real-Time PCR with Molecular Beacons.

作者信息

Schlachter Samantha, Chan Kamfai, Marras Salvatore A E, Parveen Nikhat

机构信息

Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers-New Jersey Medical School, 225 Warren Street, Newark, NJ, 07103-3535, USA.

AI Biosciences, Inc., 1902 Pinon Drive, Suite C, College Station, TX, 77845-5816, USA.

出版信息

Methods Mol Biol. 2017;1616:155-170. doi: 10.1007/978-1-4939-7037-7_10.

Abstract

Real-time PCR assays have recently been implemented in diagnostics for many bacterial pathogens, allowing rapid and accurate detection, which ultimately results in improved clinical intervention. Here, we describe a sensitive method of detection for three common tick-borne pathogens Borrelia burgdorferi, Anaplasma phagocytophilum, and Babesia microti since coinfections with these pathogens have started occurring with increasing frequency over the last several years in both North America and Europe. A shared geographic region, the same tick vectors, and similar transmission cycle all favor simultaneous transmission of these three tick-borne pathogens. Furthermore, early symptoms of the diseases are often similar and somewhat nonspecific leading to poor clinical identification. The multiplex real-time PCR assay we describe here utilizes gene-specific primers, molecular beacon probes tagged with different fluorophores, and optimized PCR conditions to detect even small amounts of specific pathogen DNA without interference. Application of this detection method will offer better diagnostics for acute and persistent infection compared to the two-tier serological tests that are currently approved in North America and Europe, which do not necessarily detect active infection.

摘要

实时荧光定量PCR检测方法最近已应用于多种细菌病原体的诊断,能够实现快速准确的检测,最终改善临床干预效果。在此,我们描述一种针对三种常见蜱传病原体——伯氏疏螺旋体、嗜吞噬细胞无形体和微小巴贝斯虫的灵敏检测方法,因为在过去几年中,北美和欧洲这三种病原体的合并感染发生率都在不断上升。相同的地理区域、相同的蜱虫媒介以及相似的传播周期都有利于这三种蜱传病原体同时传播。此外,这些疾病的早期症状往往相似且缺乏特异性,导致临床识别困难。我们在此描述的多重实时荧光定量PCR检测方法利用基因特异性引物、标记有不同荧光团的分子信标探针以及优化的PCR条件,能够检测到极少量的特定病原体DNA且不受干扰。与目前北美和欧洲批准的两级血清学检测相比,这种检测方法在诊断急性和持续性感染方面具有更好的效果,因为两级血清学检测不一定能检测到活动性感染。

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