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Complete genome sequence of the Clostridium difficile laboratory strain 630Δerm reveals differences from strain 630, including translocation of the mobile element CTn5

BACKGROUND: Clostridium difficile strain 630Δerm is a spontaneous erythromycin sensitive derivative of the reference strain 630 obtained by serial passaging in antibiotic-free media. It is widely used as a defined and tractable C. difficile strain. Though largely similar to the ancestral strain, it...

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Autores principales: van Eijk, Erika, Anvar, Seyed Yahya, Browne, Hilary P, Leung, Wai Yi, Frank, Jeroen, Schmitz, Arnoud M, Roberts, Adam P, Smits, Wiep Klaas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320837/
https://www.ncbi.nlm.nih.gov/pubmed/25636331
http://dx.doi.org/10.1186/s12864-015-1252-7
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author van Eijk, Erika
Anvar, Seyed Yahya
Browne, Hilary P
Leung, Wai Yi
Frank, Jeroen
Schmitz, Arnoud M
Roberts, Adam P
Smits, Wiep Klaas
author_facet van Eijk, Erika
Anvar, Seyed Yahya
Browne, Hilary P
Leung, Wai Yi
Frank, Jeroen
Schmitz, Arnoud M
Roberts, Adam P
Smits, Wiep Klaas
author_sort van Eijk, Erika
collection PubMed
description BACKGROUND: Clostridium difficile strain 630Δerm is a spontaneous erythromycin sensitive derivative of the reference strain 630 obtained by serial passaging in antibiotic-free media. It is widely used as a defined and tractable C. difficile strain. Though largely similar to the ancestral strain, it demonstrates phenotypic differences that might be the result of underlying genetic changes. Here, we performed a de novo assembly based on single-molecule real-time sequencing and an analysis of major methylation patterns. RESULTS: In addition to single nucleotide polymorphisms and various indels, we found that the mobile element CTn5 is present in the gene encoding the methyltransferase rumA rather than adhesin CD1844 where it is located in the reference strain. CONCLUSIONS: Together, the genetic features identified in this study may help to explain at least part of the phenotypic differences. The annotated genome sequence of this lab strain, including the first analysis of major methylation patterns, will be a valuable resource for genetic research on C. difficile. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1252-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-43208372015-02-09 Complete genome sequence of the Clostridium difficile laboratory strain 630Δerm reveals differences from strain 630, including translocation of the mobile element CTn5 van Eijk, Erika Anvar, Seyed Yahya Browne, Hilary P Leung, Wai Yi Frank, Jeroen Schmitz, Arnoud M Roberts, Adam P Smits, Wiep Klaas BMC Genomics Research Article BACKGROUND: Clostridium difficile strain 630Δerm is a spontaneous erythromycin sensitive derivative of the reference strain 630 obtained by serial passaging in antibiotic-free media. It is widely used as a defined and tractable C. difficile strain. Though largely similar to the ancestral strain, it demonstrates phenotypic differences that might be the result of underlying genetic changes. Here, we performed a de novo assembly based on single-molecule real-time sequencing and an analysis of major methylation patterns. RESULTS: In addition to single nucleotide polymorphisms and various indels, we found that the mobile element CTn5 is present in the gene encoding the methyltransferase rumA rather than adhesin CD1844 where it is located in the reference strain. CONCLUSIONS: Together, the genetic features identified in this study may help to explain at least part of the phenotypic differences. The annotated genome sequence of this lab strain, including the first analysis of major methylation patterns, will be a valuable resource for genetic research on C. difficile. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1252-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-31 /pmc/articles/PMC4320837/ /pubmed/25636331 http://dx.doi.org/10.1186/s12864-015-1252-7 Text en © van Eijk et al.; licensee BioMed Central. 2015 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, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
van Eijk, Erika
Anvar, Seyed Yahya
Browne, Hilary P
Leung, Wai Yi
Frank, Jeroen
Schmitz, Arnoud M
Roberts, Adam P
Smits, Wiep Klaas
Complete genome sequence of the Clostridium difficile laboratory strain 630Δerm reveals differences from strain 630, including translocation of the mobile element CTn5
title Complete genome sequence of the Clostridium difficile laboratory strain 630Δerm reveals differences from strain 630, including translocation of the mobile element CTn5
title_full Complete genome sequence of the Clostridium difficile laboratory strain 630Δerm reveals differences from strain 630, including translocation of the mobile element CTn5
title_fullStr Complete genome sequence of the Clostridium difficile laboratory strain 630Δerm reveals differences from strain 630, including translocation of the mobile element CTn5
title_full_unstemmed Complete genome sequence of the Clostridium difficile laboratory strain 630Δerm reveals differences from strain 630, including translocation of the mobile element CTn5
title_short Complete genome sequence of the Clostridium difficile laboratory strain 630Δerm reveals differences from strain 630, including translocation of the mobile element CTn5
title_sort complete genome sequence of the clostridium difficile laboratory strain 630δerm reveals differences from strain 630, including translocation of the mobile element ctn5
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320837/
https://www.ncbi.nlm.nih.gov/pubmed/25636331
http://dx.doi.org/10.1186/s12864-015-1252-7
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