Literature DB >> 28572323

Complete Genome Sequence of Staphylococcus epidermidis 1457.

Madeline R Galac1, Jason Stam1, Rosslyn Maybank1, Mary Hinkle1, Dietrich Mack2, Holger Rohde3, Amanda L Roth1, Paul D Fey4.   

Abstract

Staphylococcus epidermidis 1457 is a frequently utilized strain that is amenable to genetic manipulation and has been widely used for biofilm-related research. We report here the whole-genome sequence of this strain, which encodes 2,277 protein-coding genes and 81 RNAs within its 2.4-Mb genome and plasmid.
Copyright © 2017 Galac et al.

Entities:  

Year:  2017        PMID: 28572323      PMCID: PMC5454206          DOI: 10.1128/genomeA.00450-17

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Staphylococcus epidermidis is a commensal bacterium that colonizes human skin and mucous membranes (1, 2). Its commensal function is not well understood but clearly involves inhibition of pathogen colonization (3). However, due to its proximity to the insertion sites of catheters or other foreign bodies, S. epidermidis frequently colonizes these devices and forms biofilms that are inherently resistant to the host immune system (4) and antibiotics (5). Most infected foreign devices require removal from the body for effective treatment, resulting in significant morbidity. S. epidermidis strain 1457 (6) is often used as the model organism for molecular studies investigating biofilm formation for multiple reasons. First, strain 1457 is pansusceptible to antibiotics, including erythromycin, the most common antibiotic used as a marker in staphylococcal genetics. Second, in contrast to many S. epidermidis strains, including RP62A (7), strain 1457 is amenable to genetic manipulation, including transduction with Φ71 (8), A6C (9), and Φ187 (10). Third, strain 1457 produces a significant amount of polysaccharide intercellular adhesin-dependent biofilm (11, 12) and thus is an excellent model strain to understand icaADBC transcriptional regulation. Additionally, accumulation associated protein-dependent biofilm formation has also been studied in this strain using icaADBC allelic replacement mutants (13, 14). Finally, multiple allelic replacement mutants already exist for strain 1457 (15–28). Sequencing was performed as previously described (29). RS II (Pacific Biosciences, USA) single-molecule real-time sequencing (SMRT) produced 81,634 reads with an average length of 15,543 bp. The reads were assembled using HGAP2 in the SMRT Analysis Portal into two polished contigs, one for the chromosome and one for the plasmid, p1457. MiSeq (Illumina, Inc., USA) short-read sequencing produced 1,526,588 reads with an average length of 350 bp and insert size of 500 bp. These reads were mapped to the SMRT sequences using the mapper within Geneious (Biomatters, New Zealand), resulting in an average depth of coverage of 199×. Genes were predicted using the NCBI Prokaryotic Genome Annotation Pipeline version 4.1. The genome of strain 1457 is 2,454,929 bp long containing 2,260 protein-coding sequences (CDSs) and 81 RNAs with a 32.3% GC content. The plasmid, p1457, comprises 15,142 bp coding for 17 CDSs. A previous draft genome for this strain, which was sequenced by another group and comprises 2,417,500 bp in 74 contigs, is available in GenBank (accession no. JMID00000000.1). We found that 73 draft contigs aligned to the finished genome, while the remaining one aligned to the plasmid. This alignment demonstrates the challenges of short-read assembly, with the draft contigs ending in genes known for being highly variable or typically present with multiple copies. Additionally, there are genes that appear to be missing between the draft contigs. We identified minimal differences between the two versions, which we were confident were not the result of assembly errors: two intragenic amino acid substitution single nucleotide polymorphisms (SNPs), one intergenic SNP, and one intragenic insertion in the draft relative to the finished genome.

Accession number(s).

The complete genome sequence of S. epidermidis 1457 has been deposited in GenBank under the accession numbers CP020462 to CP020463.
  29 in total

1.  Genetic and biochemical analysis of Staphylococcus epidermidis biofilm accumulation.

Authors:  D Mack; K Bartscht; C Fischer; H Rohde; C de Grahl; S Dobinsky; M A Horstkotte; K Kiel; J K Knobloch
Journal:  Methods Enzymol       Date:  2001       Impact factor: 1.600

2.  Genetic engineering of untransformable coagulase-negative staphylococcal pathogens.

Authors:  Volker Winstel; Petra Kühner; Holger Rohde; Andreas Peschel
Journal:  Nat Protoc       Date:  2016-04-21       Impact factor: 13.491

Review 3.  Current concepts in biofilm formation of Staphylococcus epidermidis.

Authors:  Paul D Fey; Michael E Olson
Journal:  Future Microbiol       Date:  2010-06       Impact factor: 3.165

4.  CcpA coordinates central metabolism and biofilm formation in Staphylococcus epidermidis.

Authors:  Marat R Sadykov; Torsten Hartmann; Theodoric A Mattes; Megan Hiatt; Naja J Jann; Yefei Zhu; Nagender Ledala; Regine Landmann; Mathias Herrmann; Holger Rohde; Markus Bischoff; Greg A Somerville
Journal:  Microbiology (Reading)       Date:  2011-09-29       Impact factor: 2.777

5.  Generalized transduction for genetic linkage analysis and transfer of transposon insertions in different Staphylococcus epidermidis strains.

Authors:  M Nedelmann; A Sabottke; R Laufs; D Mack
Journal:  Zentralbl Bakteriol       Date:  1998-01

6.  Impact of the Staphylococcus epidermidis LytSR two-component regulatory system on murein hydrolase activity, pyruvate utilization and global transcriptional profile.

Authors:  Tao Zhu; Qiang Lou; Yang Wu; Jian Hu; Fangyou Yu; Di Qu
Journal:  BMC Microbiol       Date:  2010-11-12       Impact factor: 3.605

7.  Quorum-sensing control of biofilm factors in Staphylococcus epidermidis.

Authors:  Cuong Vuong; Christiane Gerke; Greg A Somerville; Elizabeth R Fischer; Michael Otto
Journal:  J Infect Dis       Date:  2003-08-11       Impact factor: 5.226

8.  RsbU-dependent regulation of Staphylococcus epidermidis biofilm formation is mediated via the alternative sigma factor sigmaB by repression of the negative regulator gene icaR.

Authors:  Johannes K-M Knobloch; Sebastian Jäger; Matthias A Horstkotte; Holger Rohde; Dietrich Mack
Journal:  Infect Immun       Date:  2004-07       Impact factor: 3.441

9.  Analysis of Serial Isolates of mcr-1-Positive Escherichia coli Reveals a Highly Active ISApl1 Transposon.

Authors:  Erik Snesrud; Ana C Ong; Brendan Corey; Yoon I Kwak; Robert Clifford; Todd Gleeson; Shannon Wood; Timothy J Whitman; Emil P Lesho; Mary Hinkle; Patrick McGann
Journal:  Antimicrob Agents Chemother       Date:  2017-04-24       Impact factor: 5.191

10.  Antimicrobials from human skin commensal bacteria protect against Staphylococcus aureus and are deficient in atopic dermatitis.

Authors:  Teruaki Nakatsuji; Tiffany H Chen; Saisindhu Narala; Kimberly A Chun; Aimee M Two; Tong Yun; Faiza Shafiq; Paul F Kotol; Amina Bouslimani; Alexey V Melnik; Haythem Latif; Ji-Nu Kim; Alexandre Lockhart; Keli Artis; Gloria David; Patricia Taylor; Joanne Streib; Pieter C Dorrestein; Alex Grier; Steven R Gill; Karsten Zengler; Tissa R Hata; Donald Y M Leung; Richard L Gallo
Journal:  Sci Transl Med       Date:  2017-02-22       Impact factor: 17.956

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5.  Mining the Methylome Reveals Extensive Diversity in Staphylococcus epidermidis Restriction Modification.

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6.  Short chain fatty acids produced by Cutibacterium acnes inhibit biofilm formation by Staphylococcus epidermidis.

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8.  codY and pdhA Expression Is Induced in Staphylococcus epidermidis Biofilm and Planktonic Populations With Higher Proportions of Viable but Non-Culturable Cells.

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9.  Development of an artificial synovial fluid useful for studying Staphylococcus epidermidis joint infections.

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10.  Complete Genome Sequence of Staphylococcus epidermidis ATCC 12228 Chromosome and Plasmids, Generated by Long-Read Sequencing.

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