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Culture independent analysis using gnd as a target gene to assess Escherichia coli diversity and community structure

Current culture methods to investigate changes in Escherichia coli community structure are often slow and laborious. Genes such as gnd (6-phosphogluconate dehydrogenase) have a highly variable nucleotide sequence and may provide a target for E. coli microbiome analysis using culture-independent meth...

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Autores principales: Cookson, Adrian L., Biggs, Patrick J., Marshall, Jonathan C., Reynolds, Angela, Collis, Rose M., French, Nigel P., Brightwell, Gale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429811/
https://www.ncbi.nlm.nih.gov/pubmed/28404985
http://dx.doi.org/10.1038/s41598-017-00890-6
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author Cookson, Adrian L.
Biggs, Patrick J.
Marshall, Jonathan C.
Reynolds, Angela
Collis, Rose M.
French, Nigel P.
Brightwell, Gale
author_facet Cookson, Adrian L.
Biggs, Patrick J.
Marshall, Jonathan C.
Reynolds, Angela
Collis, Rose M.
French, Nigel P.
Brightwell, Gale
author_sort Cookson, Adrian L.
collection PubMed
description Current culture methods to investigate changes in Escherichia coli community structure are often slow and laborious. Genes such as gnd (6-phosphogluconate dehydrogenase) have a highly variable nucleotide sequence and may provide a target for E. coli microbiome analysis using culture-independent methods. Metabarcoded PCR primers were used to generate separate libraries from calf faecal samples for high throughput sequencing. Although a total of 348 separate gnd sequence types (gSTs) were identified, 188 were likely to be due to sequencing errors. Of the remaining 160 gSTs, 92 did not match those in a database of 319 separate gnd sequences. ‘Animal’ was the main determinant of E. coli diversity with limited impact of sample type or DNA extraction method on intra-host E. coli community variation from faeces and recto-anal mucosal swab samples. This culture-independent study has addressed the difficulties of quantifying bacterial intra-species diversity and revealed that, whilst individual animals may harbour >50 separate E. coli strains, communities are dominated by <10 strains alongside a large pool of subdominant strains present at low abundances. This method will be useful for characterising the diversity and population structure of E. coli in experimental studies designed to assess the impact of interventions on the gut microbiome.
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spelling pubmed-54298112017-05-15 Culture independent analysis using gnd as a target gene to assess Escherichia coli diversity and community structure Cookson, Adrian L. Biggs, Patrick J. Marshall, Jonathan C. Reynolds, Angela Collis, Rose M. French, Nigel P. Brightwell, Gale Sci Rep Article Current culture methods to investigate changes in Escherichia coli community structure are often slow and laborious. Genes such as gnd (6-phosphogluconate dehydrogenase) have a highly variable nucleotide sequence and may provide a target for E. coli microbiome analysis using culture-independent methods. Metabarcoded PCR primers were used to generate separate libraries from calf faecal samples for high throughput sequencing. Although a total of 348 separate gnd sequence types (gSTs) were identified, 188 were likely to be due to sequencing errors. Of the remaining 160 gSTs, 92 did not match those in a database of 319 separate gnd sequences. ‘Animal’ was the main determinant of E. coli diversity with limited impact of sample type or DNA extraction method on intra-host E. coli community variation from faeces and recto-anal mucosal swab samples. This culture-independent study has addressed the difficulties of quantifying bacterial intra-species diversity and revealed that, whilst individual animals may harbour >50 separate E. coli strains, communities are dominated by <10 strains alongside a large pool of subdominant strains present at low abundances. This method will be useful for characterising the diversity and population structure of E. coli in experimental studies designed to assess the impact of interventions on the gut microbiome. Nature Publishing Group UK 2017-04-12 /pmc/articles/PMC5429811/ /pubmed/28404985 http://dx.doi.org/10.1038/s41598-017-00890-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cookson, Adrian L.
Biggs, Patrick J.
Marshall, Jonathan C.
Reynolds, Angela
Collis, Rose M.
French, Nigel P.
Brightwell, Gale
Culture independent analysis using gnd as a target gene to assess Escherichia coli diversity and community structure
title Culture independent analysis using gnd as a target gene to assess Escherichia coli diversity and community structure
title_full Culture independent analysis using gnd as a target gene to assess Escherichia coli diversity and community structure
title_fullStr Culture independent analysis using gnd as a target gene to assess Escherichia coli diversity and community structure
title_full_unstemmed Culture independent analysis using gnd as a target gene to assess Escherichia coli diversity and community structure
title_short Culture independent analysis using gnd as a target gene to assess Escherichia coli diversity and community structure
title_sort culture independent analysis using gnd as a target gene to assess escherichia coli diversity and community structure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429811/
https://www.ncbi.nlm.nih.gov/pubmed/28404985
http://dx.doi.org/10.1038/s41598-017-00890-6
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