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宏基因组测序背景下污水中病毒浓缩与提取方法的评估

Evaluation of Methods for the Concentration and Extraction of Viruses from Sewage in the Context of Metagenomic Sequencing.

作者信息

Hjelmsø Mathis Hjort, Hellmér Maria, Fernandez-Cassi Xavier, Timoneda Natàlia, Lukjancenko Oksana, Seidel Michael, Elsässer Dennis, Aarestrup Frank M, Löfström Charlotta, Bofill-Mas Sílvia, Abril Josep F, Girones Rosina, Schultz Anna Charlotte

机构信息

Research Group for Genomic Epidemiology, The National Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark.

Division of Microbiology and Production, The National Food Institute, Technical University of Denmark, Søborg, Denmark.

出版信息

PLoS One. 2017 Jan 18;12(1):e0170199. doi: 10.1371/journal.pone.0170199. eCollection 2017.

Abstract

Viral sewage metagenomics is a novel field of study used for surveillance, epidemiological studies, and evaluation of waste water treatment efficiency. In raw sewage human waste is mixed with household, industrial and drainage water, and virus particles are, therefore, only found in low concentrations. This necessitates a step of sample concentration to allow for sensitive virus detection. Additionally, viruses harbor a large diversity of both surface and genome structures, which makes universal viral genomic extraction difficult. Current studies have tackled these challenges in many different ways employing a wide range of viral concentration and extraction procedures. However, there is limited knowledge of the efficacy and inherent biases associated with these methods in respect to viral sewage metagenomics, hampering the development of this field. By the use of next generation sequencing this study aimed to evaluate the efficiency of four commonly applied viral concentrations techniques (precipitation with polyethylene glycol, organic flocculation with skim milk, monolithic adsorption filtration and glass wool filtration) and extraction methods (Nucleospin RNA XS, QIAamp Viral RNA Mini Kit, NucliSENS® miniMAG®, or PowerViral® Environmental RNA/DNA Isolation Kit) to determine the viriome in a sewage sample. We found a significant influence of concentration and extraction protocols on the detected viriome. The viral richness was largest in samples extracted with QIAamp Viral RNA Mini Kit or PowerViral® Environmental RNA/DNA Isolation Kit. Highest viral specificity were found in samples concentrated by precipitation with polyethylene glycol or extracted with Nucleospin RNA XS. Detection of viral pathogens depended on the method used. These results contribute to the understanding of method associated biases, within the field of viral sewage metagenomics, making evaluation of the current literature easier and helping with the design of future studies.

摘要

病毒污水宏基因组学是一个用于监测、流行病学研究和评估废水处理效率的新兴研究领域。在未经处理的污水中,人类排泄物与生活污水、工业废水和排水混合在一起,因此病毒颗粒的浓度很低。这就需要进行样本浓缩步骤,以便能够灵敏地检测病毒。此外,病毒具有多种多样的表面结构和基因组结构,这使得通用的病毒基因组提取变得困难。目前的研究采用了多种病毒浓缩和提取程序,以多种不同方式应对这些挑战。然而,对于这些方法在病毒污水宏基因组学方面的功效和内在偏差了解有限,这阻碍了该领域的发展。本研究通过使用下一代测序技术,旨在评估四种常用的病毒浓缩技术(聚乙二醇沉淀、脱脂牛奶有机絮凝、整体吸附过滤和玻璃棉过滤)和提取方法(Nucleospin RNA XS、QIAamp Viral RNA Mini试剂盒、NucliSENS® miniMAG® 或PowerViral® 环境RNA/DNA分离试剂盒)的效率,以确定污水样本中的病毒群落。我们发现浓缩和提取方案对检测到的病毒群落有显著影响。用QIAamp Viral RNA Mini试剂盒或PowerViral® 环境RNA/DNA分离试剂盒提取的样本中病毒丰富度最高。在通过聚乙二醇沉淀浓缩或用Nucleospin RNA XS提取的样本中发现病毒特异性最高。病毒病原体的检测取决于所使用的方法。这些结果有助于理解病毒污水宏基因组学领域中与方法相关的偏差,使对现有文献的评估更加容易,并有助于未来研究的设计。

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