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直接从感染组织中提取微生物 DNA 的 DNA 提取:用于纳米孔测序的优化方案。

DNA extraction of microbial DNA directly from infected tissue: an optimized protocol for use in nanopore sequencing.

机构信息

Akershus University Hospital, Department of Microbiology and Infection Control, Lørenskog, 1478, Norway.

Akershus University Hospital and University of Oslo, Department of Clinical Molecular Biology (Epigen), Lørenskog, 1478, Norway.

出版信息

Sci Rep. 2020 Feb 19;10(1):2985. doi: 10.1038/s41598-020-59957-6.

Abstract

Identification of bacteria causing tissue infections can be comprehensive and, in the cases of non- or slow-growing bacteria, near impossible with conventional methods. Performing shotgun metagenomic sequencing on bacterial DNA extracted directly from the infected tissue may improve time to diagnosis and targeted treatment considerably. However, infected tissue consists mainly of human DNA (hDNA) which hampers bacterial identification. In this proof of concept study, we present a modified version of the Ultra-Deep Microbiome Prep kit for DNA extraction procedure, removing additional human DNA. Tissue biopsies from 3 patients with orthopedic implant-related infections containing varying degrees of Staphylococcus aureus were included. Subsequent DNA shotgun metagenomic sequencing using Oxford Nanopore Technologies' (ONT) MinION platform and ONTs EPI2ME WIMP and ARMA bioinformatic workflows for microbe and antibiotic resistance genes identification, respectively. The modified DNA extraction protocol led to an additional ~10-fold reduction of human DNA while preserving S. aureus DNA. Including the DNA sequencing and bioinformatics analyses, the presented protocol has the potential of identifying the infection-causing pathogen in infected tissue within 7 hours after biopsy. However, due to low number of S. aureus reads, positive identification of antibiotic resistance genes was not possible.

摘要

鉴定引起组织感染的细菌可以全面进行,而对于非生长缓慢或生长缓慢的细菌,传统方法几乎不可能。对从感染组织中直接提取的细菌 DNA 进行鸟枪法宏基因组测序可以大大提高诊断和靶向治疗的速度。然而,感染组织主要由人类 DNA (hDNA)组成,这阻碍了细菌的鉴定。在这项概念验证研究中,我们提出了一种改良的 Ultra-Deep Microbiome Prep 试剂盒 DNA 提取方法,去除了额外的人类 DNA。研究纳入了 3 名患有骨科植入物相关感染的患者的组织活检样本,其中包含不同程度的金黄色葡萄球菌。随后,使用 Oxford Nanopore Technologies (ONT) MinION 平台和 ONTs EPI2ME WIMP 和 ARMA 生物信息学工作流程进行 DNA 鸟枪法宏基因组测序,分别用于微生物和抗生素耐药基因的鉴定。改良的 DNA 提取方案导致人类 DNA 额外减少了约 10 倍,同时保留了金黄色葡萄球菌 DNA。包括 DNA 测序和生物信息学分析,该方案有可能在活检后 7 小时内确定感染组织中的病原体。然而,由于金黄色葡萄球菌读数较少,无法确定抗生素耐药基因的阳性鉴定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec20/7031281/20e68e181f3e/41598_2020_59957_Fig1_HTML.jpg

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