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Profiling soil microbial communities with next-generation sequencing: the influence of DNA kit selection and technician technical expertise

Structure and diversity of microbial communities are an important research topic in biology, since microbes play essential roles in the ecology of various environments. Different DNA isolation protocols can lead to data bias and can affect results of next-generation sequencing. To evaluate the impac...

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Autores principales: Soliman, Taha, Yang, Sung-Yin, Yamazaki, Tomoko, Jenke-Kodama, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740954/
https://www.ncbi.nlm.nih.gov/pubmed/29302394
http://dx.doi.org/10.7717/peerj.4178
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author Soliman, Taha
Yang, Sung-Yin
Yamazaki, Tomoko
Jenke-Kodama, Holger
author_facet Soliman, Taha
Yang, Sung-Yin
Yamazaki, Tomoko
Jenke-Kodama, Holger
author_sort Soliman, Taha
collection PubMed
description Structure and diversity of microbial communities are an important research topic in biology, since microbes play essential roles in the ecology of various environments. Different DNA isolation protocols can lead to data bias and can affect results of next-generation sequencing. To evaluate the impact of protocols for DNA isolation from soil samples and also the influence of individual handling of samples, we compared results obtained by two researchers (R and T) using two different DNA extraction kits: (1) MO BIO PowerSoil(®) DNA Isolation kit (MO_R and MO_T) and (2) NucleoSpin(®) Soil kit (MN_R and MN_T). Samples were collected from six different sites on Okinawa Island, Japan. For all sites, differences in the results of microbial composition analyses (bacteria, archaea, fungi, and other eukaryotes), obtained by the two researchers using the two kits, were analyzed. For both researchers, the MN kit gave significantly higher yields of genomic DNA at all sites compared to the MO kit (ANOVA; P < 0.006). In addition, operational taxonomic units for some phyla and classes were missed in some cases: Micrarchaea were detected only in the MN_T and MO_R analyses; the bacterial phylum Armatimonadetes was detected only in MO_R and MO_T; and WIM5 of the phylum Amoebozoa of eukaryotes was found only in the MO_T analysis. Our results suggest the possibility of handling bias; therefore, it is crucial that replicated DNA extraction be performed by at least two technicians for thorough microbial analyses and to obtain accurate estimates of microbial diversity.
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spelling pubmed-57409542018-01-04 Profiling soil microbial communities with next-generation sequencing: the influence of DNA kit selection and technician technical expertise Soliman, Taha Yang, Sung-Yin Yamazaki, Tomoko Jenke-Kodama, Holger PeerJ Genetics Structure and diversity of microbial communities are an important research topic in biology, since microbes play essential roles in the ecology of various environments. Different DNA isolation protocols can lead to data bias and can affect results of next-generation sequencing. To evaluate the impact of protocols for DNA isolation from soil samples and also the influence of individual handling of samples, we compared results obtained by two researchers (R and T) using two different DNA extraction kits: (1) MO BIO PowerSoil(®) DNA Isolation kit (MO_R and MO_T) and (2) NucleoSpin(®) Soil kit (MN_R and MN_T). Samples were collected from six different sites on Okinawa Island, Japan. For all sites, differences in the results of microbial composition analyses (bacteria, archaea, fungi, and other eukaryotes), obtained by the two researchers using the two kits, were analyzed. For both researchers, the MN kit gave significantly higher yields of genomic DNA at all sites compared to the MO kit (ANOVA; P < 0.006). In addition, operational taxonomic units for some phyla and classes were missed in some cases: Micrarchaea were detected only in the MN_T and MO_R analyses; the bacterial phylum Armatimonadetes was detected only in MO_R and MO_T; and WIM5 of the phylum Amoebozoa of eukaryotes was found only in the MO_T analysis. Our results suggest the possibility of handling bias; therefore, it is crucial that replicated DNA extraction be performed by at least two technicians for thorough microbial analyses and to obtain accurate estimates of microbial diversity. PeerJ Inc. 2017-12-19 /pmc/articles/PMC5740954/ /pubmed/29302394 http://dx.doi.org/10.7717/peerj.4178 Text en ©2017 Soliman et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Genetics
Soliman, Taha
Yang, Sung-Yin
Yamazaki, Tomoko
Jenke-Kodama, Holger
Profiling soil microbial communities with next-generation sequencing: the influence of DNA kit selection and technician technical expertise
title Profiling soil microbial communities with next-generation sequencing: the influence of DNA kit selection and technician technical expertise
title_full Profiling soil microbial communities with next-generation sequencing: the influence of DNA kit selection and technician technical expertise
title_fullStr Profiling soil microbial communities with next-generation sequencing: the influence of DNA kit selection and technician technical expertise
title_full_unstemmed Profiling soil microbial communities with next-generation sequencing: the influence of DNA kit selection and technician technical expertise
title_short Profiling soil microbial communities with next-generation sequencing: the influence of DNA kit selection and technician technical expertise
title_sort profiling soil microbial communities with next-generation sequencing: the influence of dna kit selection and technician technical expertise
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740954/
https://www.ncbi.nlm.nih.gov/pubmed/29302394
http://dx.doi.org/10.7717/peerj.4178
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