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

被引:47
作者
van Eijk, Erika [1 ]
Anvar, Seyed Yahya [2 ,3 ]
Browne, Hilary P. [4 ]
Leung, Wai Yi [5 ]
Frank, Jeroen [3 ]
Schmitz, Arnoud M. [3 ]
Roberts, Adam P. [6 ]
Smits, Wiep Klaas [1 ]
机构
[1] Leiden Univ, Dept Med Microbiol, Med Ctr, Leiden, Netherlands
[2] Leiden Univ, Dept Human Genet, Med Ctr, NL-2300 RA Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Leiden Genome Technol Ctr, Leiden, Netherlands
[4] Wellcome Trust Sanger Inst, Cambridge, Hinxton, England
[5] Leiden Univ, Sequence Anal Support Core, Med Ctr, Leiden, Netherlands
[6] UCL Eastman Dent Inst, Dept Microbial Dis, London, England
来源
BMC GENOMICS | 2015年 / 16卷
关键词
Genome sequence; Conjugative transposon; Integrative and conjugative element; Single-molecule real-time sequencing; HORIZONTAL GENE-TRANSFER; ESCHERICHIA-COLI; METHYLATION; M(5)U1939; VISUALIZATION; VIRULENCE; ARTEMIS;
D O I
10.1186/s12864-015-1252-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Clostridium difficile strain 630 Delta erm 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.
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页数:14
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