Suppr超能文献

通用数字高分辨率熔解:一种用于广泛分析异质生物样本的新方法。

Universal digital high-resolution melt: a novel approach to broad-based profiling of heterogeneous biological samples.

机构信息

Department of Biomedical Engineering, The Johns Hopkins University, Baltimore, MD 21218, USA, Department of Emergency Medicine, The Johns Hopkins University, Baltimore, MD 21218, USA, Division of Infectious Disease, Department of Medicine, The Johns Hopkins University, Baltimore, MD 21218, USA, Division of Medical Microbiology, Department of Pathology, The Johns Hopkins University, Baltimore, MD 21218, USA, The Johns Hopkins Hospital, Baltimore, MD 21287, USA and Department of Mechanical Engineering, The Johns Hopkins University, Baltimore, MD 21218, USA.

出版信息

Nucleic Acids Res. 2013 Oct;41(18):e175. doi: 10.1093/nar/gkt684. Epub 2013 Aug 9.

Abstract

Comprehensive profiling of nucleic acids in genetically heterogeneous samples is important for clinical and basic research applications. Universal digital high-resolution melt (U-dHRM) is a new approach to broad-based PCR diagnostics and profiling technologies that can overcome issues of poor sensitivity due to contaminating nucleic acids and poor specificity due to primer or probe hybridization inaccuracies for single nucleotide variations. The U-dHRM approach uses broad-based primers or ligated adapter sequences to universally amplify all nucleic acid molecules in a heterogeneous sample, which have been partitioned, as in digital PCR. Extensive assay optimization enables direct sequence identification by algorithm-based matching of melt curve shape and Tm to a database of known sequence-specific melt curves. We show that single-molecule detection and single nucleotide sensitivity is possible. The feasibility and utility of U-dHRM is demonstrated through detection of bacteria associated with polymicrobial blood infection and microRNAs (miRNAs) associated with host response to infection. U-dHRM using broad-based 16S rRNA gene primers demonstrates universal single cell detection of bacterial pathogens, even in the presence of larger amounts of contaminating bacteria; U-dHRM using universally adapted Lethal-7 miRNAs in a heterogeneous mixture showcases the single copy sensitivity and single nucleotide specificity of this approach.

摘要

对遗传异质性样本中的核酸进行全面分析对于临床和基础研究应用非常重要。通用数字高分辨率熔解曲线(U-dHRM)是一种新的基于 PCR 的诊断和分析技术方法,可克服因污染核酸导致的灵敏度差以及因单核苷酸变异的引物或探针杂交不准确导致的特异性差的问题。U-dHRM 方法使用广泛的引物或连接的接头序列,以数字 PCR 中的分区方式,普遍扩增异质样本中的所有核酸分子。广泛的试验优化可通过基于算法的熔解曲线形状和 Tm 与已知序列特异性熔解曲线数据库的匹配,直接进行序列鉴定。我们表明,单分子检测和单核苷酸灵敏度是可行的。通过检测与多微生物血液感染相关的细菌和与宿主对感染反应相关的 microRNAs(miRNAs),证明了 U-dHRM 的可行性和实用性。使用广泛的 16S rRNA 基因引物的 U-dHRM 可普遍检测细菌病原体,即使存在大量污染细菌;在异质混合物中使用普遍适应的 Lethal-7 miRNAs 的 U-dHRM 展示了该方法的单拷贝灵敏度和单核苷酸特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea96/3794612/be888509a8c3/gkt684f2p.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验