Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/119971
Title: Evaluation of methods for the concentration and extraction of viruses from sewage in the context of metagenomic sequencing
Author: Hjelmso, Mathis Hjort
Hellmér, Maria
Fernández Cassi, Xavier
Timoneda Solé, Natàlia
Lukjancenko, Oksana
Seidel, Michael
Elsässer, Dennis
Aarestrup, Frank M.
Löfström, Charlotta
Bofill Mas, Silvia
Abril Ferrando, Josep Francesc, 1970-
Gironès Llop, Rosina
Schultz, Anna Charlotte
Keywords: Genètica molecular
Aigües residuals
Molecular genetics
Sewage
Issue Date: 18-Jan-2017
Publisher: Public Library of Science (PLoS)
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.
Note: Reproducció del document publicat a: https://doi.org/10.1371/journal.pone.0170199
It is part of: PLoS One, 2017, vol. 12, num. 1, p. e0170199
URI: http://hdl.handle.net/2445/119971
Related resource: https://doi.org/10.1371/journal.pone.0170199
ISSN: 1932-6203
Appears in Collections:Articles publicats en revistes (Institut de Biomedicina (IBUB))
Articles publicats en revistes (Genètica, Microbiologia i Estadística)

Files in This Item:
File Description SizeFormat 
668464.pdf3.25 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons