Cargando…

Biases during DNA extraction of activated sludge samples revealed by high throughput sequencing

Standardization of DNA extraction is a fundamental issue of fidelity and comparability in investigations of environmental microbial communities. Commercial kits for soil or feces are often adopted for studies of activated sludge because of a lack of specific kits, but they have never been evaluated...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Feng, Zhang, Tong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647099/
https://www.ncbi.nlm.nih.gov/pubmed/22760785
http://dx.doi.org/10.1007/s00253-012-4244-4
_version_ 1782268686829092864
author Guo, Feng
Zhang, Tong
author_facet Guo, Feng
Zhang, Tong
author_sort Guo, Feng
collection PubMed
description Standardization of DNA extraction is a fundamental issue of fidelity and comparability in investigations of environmental microbial communities. Commercial kits for soil or feces are often adopted for studies of activated sludge because of a lack of specific kits, but they have never been evaluated regarding their effectiveness and potential biases based on high throughput sequencing. In this study, seven common DNA extraction kits were evaluated, based on not only yield/purity but also sequencing results, using two activated sludge samples (two sub-samples each, i.e. ethanol-fixed and fresh, as-is). The results indicate that the bead-beating step is necessary for DNA extraction from activated sludge. The two kits without the bead-beating step yielded very low amounts of DNA, and the least abundant operational taxonomic units (OTUs), and significantly underestimated the Gram-positive Actinobacteria, Nitrospirae, Chloroflexi, and Alphaproteobacteria and overestimated Gammaproteobacteria, Deltaproteobacteria, Bacteroidetes, and the rare phyla whose cell walls might have been readily broken. Among the other five kits, FastDNA(@) SPIN Kit for Soil extracted the most and the purest DNA. Although the number of total OTUs obtained using this kit was not the highest, the abundant OTUs and abundance of Actinobacteria demonstrated its efficiency. The three MoBio kits and one ZR kit produced fair results, but had a relatively low DNA yield and/or less Actinobacteria-related sequences. Moreover, the 50 % ethanol fixation increased the DNA yield, but did not change the sequenced microbial community in a significant way. Based on the present study, the FastDNA SPIN kit for Soil is recommended for DNA extraction of activated sludge samples. More importantly, the selection of the DNA extraction kit must be done carefully if the samples contain dominant lysing-resistant groups, such as Actinobacteria and Nitrospirae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-012-4244-4) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-3647099
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Springer-Verlag
record_format MEDLINE/PubMed
spelling pubmed-36470992013-05-08 Biases during DNA extraction of activated sludge samples revealed by high throughput sequencing Guo, Feng Zhang, Tong Appl Microbiol Biotechnol Environmental Biotechnology Standardization of DNA extraction is a fundamental issue of fidelity and comparability in investigations of environmental microbial communities. Commercial kits for soil or feces are often adopted for studies of activated sludge because of a lack of specific kits, but they have never been evaluated regarding their effectiveness and potential biases based on high throughput sequencing. In this study, seven common DNA extraction kits were evaluated, based on not only yield/purity but also sequencing results, using two activated sludge samples (two sub-samples each, i.e. ethanol-fixed and fresh, as-is). The results indicate that the bead-beating step is necessary for DNA extraction from activated sludge. The two kits without the bead-beating step yielded very low amounts of DNA, and the least abundant operational taxonomic units (OTUs), and significantly underestimated the Gram-positive Actinobacteria, Nitrospirae, Chloroflexi, and Alphaproteobacteria and overestimated Gammaproteobacteria, Deltaproteobacteria, Bacteroidetes, and the rare phyla whose cell walls might have been readily broken. Among the other five kits, FastDNA(@) SPIN Kit for Soil extracted the most and the purest DNA. Although the number of total OTUs obtained using this kit was not the highest, the abundant OTUs and abundance of Actinobacteria demonstrated its efficiency. The three MoBio kits and one ZR kit produced fair results, but had a relatively low DNA yield and/or less Actinobacteria-related sequences. Moreover, the 50 % ethanol fixation increased the DNA yield, but did not change the sequenced microbial community in a significant way. Based on the present study, the FastDNA SPIN kit for Soil is recommended for DNA extraction of activated sludge samples. More importantly, the selection of the DNA extraction kit must be done carefully if the samples contain dominant lysing-resistant groups, such as Actinobacteria and Nitrospirae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-012-4244-4) contains supplementary material, which is available to authorized users. Springer-Verlag 2012-07-04 2013 /pmc/articles/PMC3647099/ /pubmed/22760785 http://dx.doi.org/10.1007/s00253-012-4244-4 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Environmental Biotechnology
Guo, Feng
Zhang, Tong
Biases during DNA extraction of activated sludge samples revealed by high throughput sequencing
title Biases during DNA extraction of activated sludge samples revealed by high throughput sequencing
title_full Biases during DNA extraction of activated sludge samples revealed by high throughput sequencing
title_fullStr Biases during DNA extraction of activated sludge samples revealed by high throughput sequencing
title_full_unstemmed Biases during DNA extraction of activated sludge samples revealed by high throughput sequencing
title_short Biases during DNA extraction of activated sludge samples revealed by high throughput sequencing
title_sort biases during dna extraction of activated sludge samples revealed by high throughput sequencing
topic Environmental Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647099/
https://www.ncbi.nlm.nih.gov/pubmed/22760785
http://dx.doi.org/10.1007/s00253-012-4244-4
work_keys_str_mv AT guofeng biasesduringdnaextractionofactivatedsludgesamplesrevealedbyhighthroughputsequencing
AT zhangtong biasesduringdnaextractionofactivatedsludgesamplesrevealedbyhighthroughputsequencing