Suppr超能文献

使用用于MinION测序的数字微流控平台在3小时内扩增飞克级细菌DNA

Amplification of Femtograms of Bacterial DNA Within 3 h Using a Digital Microfluidics Platform for MinION Sequencing.

作者信息

Liu Yuguang, Jeraldo Patricio, Mendes-Soares Helena, Masters Thao, Asangba Abigail E, Nelson Heidi, Patel Robin, Chia Nicholas, Walther-Antonio Marina

机构信息

Department of Surgery, Division of Surgical Research, Mayo Clinic, Rochester, Minnesota 55905-0002, United States.

Microbiome Program, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota 55905-0002, United States.

出版信息

ACS Omega. 2021 Sep 23;6(39):25642-25651. doi: 10.1021/acsomega.1c03683. eCollection 2021 Oct 5.

Abstract

Whole genome sequencing is emerging as a promising tool for the untargeted detection of a broad range of microbial species for diagnosis and analysis. However, it is logistically challenging to perform the multistep process from sample preparation to DNA amplification to sequencing and analysis within a short turnaround time. To address this challenge, we developed a digital microfluidic device for rapid whole genome amplification of low-abundance bacterial DNA and compared results with conventional in-tube DNA amplification. In this work, we chose DNA as a bacterial target for method development and optimization, as it is not a common contaminant. Sequencing was performed in a hand-held Oxford Nanopore Technologies MinION sequencer. Our results show that using an in-tube amplification approach, at least 1 pg starting DNA is needed to reach the amount required for successful sequencing within 2 h. While using a digital microfluidic device, it is possible to amplify as low as 10 fg of DNA (equivalent to the amount of DNA within a single bacterial cell) within 2 h and to identify the target bacterium within 30 min of MinION sequencing-100× lower than the detection limit of an in-tube amplification approach. We demonstrate the detection of DNA in a mock community DNA sample and characterize the limit of bacterial detection in the presence of human cells. This approach can be used to identify microbes with minute amounts of genetic material in samples depleted of human cells within 3 h.

摘要

全基因组测序正成为一种有前景的工具,可用于无靶向检测多种微生物物种以进行诊断和分析。然而,要在短时间内完成从样品制备到DNA扩增再到测序和分析的多步骤过程,在后勤方面具有挑战性。为应对这一挑战,我们开发了一种数字微流控装置,用于对低丰度细菌DNA进行快速全基因组扩增,并将结果与传统的管内DNA扩增进行比较。在这项工作中,我们选择DNA作为方法开发和优化的细菌靶标,因为它不是常见的污染物。测序在手持式牛津纳米孔技术公司的MinION测序仪中进行。我们的结果表明,使用管内扩增方法,至少需要1 pg起始DNA才能在2小时内达到成功测序所需的量。而使用数字微流控装置时,有可能在2小时内扩增低至10 fg的DNA(相当于单个细菌细胞内的DNA量),并在MinION测序30分钟内鉴定出目标细菌——比管内扩增方法的检测限低100倍。我们展示了在模拟群落DNA样品中对DNA的检测,并表征了在存在人类细胞的情况下细菌检测的极限。这种方法可用于在3小时内从不含人类细胞的样品中鉴定出含有微量遗传物质的微生物。

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