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噬菌体末端和包装机制的快速准确确定工具:基于下一代测序数据的噬菌体末端和包装机制的快速准确确定工具。

PhageTerm: a tool for fast and accurate determination of phage termini and packaging mechanism using next-generation sequencing data.

机构信息

Département de Microbiologie, Institut Pasteur, Laboratoire Pathogenèse des bactéries anaérobies, Paris, France.

Département de Microbiologie et d'infectiologie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.

出版信息

Sci Rep. 2017 Aug 15;7(1):8292. doi: 10.1038/s41598-017-07910-5.

Abstract

The worrying rise of antibiotic resistance in pathogenic bacteria is leading to a renewed interest in bacteriophages as a treatment option. Novel sequencing technologies enable description of an increasing number of phage genomes, a critical piece of information to understand their life cycle, phage-host interactions, and evolution. In this work, we demonstrate how it is possible to recover more information from sequencing data than just the phage genome. We developed a theoretical and statistical framework to determine DNA termini and phage packaging mechanisms using NGS data. Our method relies on the detection of biases in the number of reads, which are observable at natural DNA termini compared with the rest of the phage genome. We implemented our method with the creation of the software PhageTerm and validated it using a set of phages with well-established packaging mechanisms representative of the termini diversity, i.e. 5'cos (Lambda), 3'cos (HK97), pac (P1), headful without a pac site (T4), DTR (T7) and host fragment (Mu). In addition, we determined the termini of nine Clostridium difficile phages and six phages whose sequences were retrieved from the Sequence Read Archive. PhageTerm is freely available (https://sourceforge.net/projects/phageterm), as a Galaxy ToolShed and on a Galaxy-based server (https://galaxy.pasteur.fr).

摘要

病原菌对抗生素耐药性的令人担忧的上升趋势,促使人们重新关注噬菌体作为一种治疗选择。新型测序技术使人们能够描述越来越多的噬菌体基因组,这是了解其生命周期、噬菌体-宿主相互作用和进化的关键信息。在这项工作中,我们展示了如何从测序数据中获得比噬菌体基因组更多的信息。我们开发了一个理论和统计框架,利用 NGS 数据来确定 DNA 末端和噬菌体包装机制。我们的方法依赖于检测读取数量的偏差,与噬菌体基因组的其余部分相比,在自然 DNA 末端可以观察到这种偏差。我们使用 PhageTerm 软件创建并验证了我们的方法,该软件使用了一组具有既定包装机制的噬菌体,这些噬菌体代表了末端多样性,即 5'cos(Lambda)、3'cos(HK97)、pac(P1)、无头但无 pac 位点(T4)、DTR(T7)和宿主片段(Mu)。此外,我们还确定了 9 株艰难梭菌噬菌体和 6 株从 Sequence Read Archive 中检索到的噬菌体的末端。PhageTerm 可免费获得(https://sourceforge.net/projects/phageterm),也可作为 Galaxy Toolshed 和基于 Galaxy 的服务器(https://galaxy.pasteur.fr)使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3176/5557969/f9ab5464fd88/41598_2017_7910_Fig1_HTML.jpg

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