Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2013 Apr 4;1(2):e00126-13. doi: 10.1128/genomeA.00126-13

Complete Genome Sequence of Serratia marcescens WW4

Wan-Chia Chung a, Ling-Ling Chen a, Wen-Sui Lo a,b,c, Pei-An Kuo a,d, Jenn Tu a, Chih-Horng Kuo a,b,e,
PMCID: PMC3622982  PMID: 23558532

Abstract

Serratia marcescens WW4 is a biofilm-forming bacterium isolated from paper machine aggregates. Under conditions of phosphate limitation, this bacterium exhibits intergeneric inhibition of Pseudomonas aeruginosa. Here, the complete genome sequence of S. marcescens WW4, which consists of one circular chromosome (5,241,455 bp) and one plasmid (pSmWW4; 3,248 bp), was determined.

GENOME ANNOUNCEMENT

The bacterial strain Serratia marcescens WW4 was isolated from a paper machine in Taiwan (1). Phenotypic characterization of this bacterium revealed that it is capable of forming biofilms individually or with Pseudomonas aeruginosa. Intriguingly, while the two bacteria may coexist in LB medium or M9 minimal medium, phosphate limitation can induce intergeneric inhibition of P. aeruginosa by S. marcescens WW4 (1).

To determine the complete genome sequence of S. marcescens WW4, we performed whole-genome shotgun sequencing using one Illumina paired-end library with an average insert size of ~325 bp. With the 150-bp paired-end reads generated using the Genome Analyzer IIx platform (Illumina), we obtained ~8 Gb of raw reads. These reads were trimmed using a quality score cutoff of 20 and a length cutoff of 70 bp. The initial de novo genome assembly was performed using Velvet (2). The resulting chromosomal contigs were oriented and assembled into one circular scaffold based on a physical map generated from optical mapping of HindIII-digested DNA fragments (OpGen). The sequence gaps were closed by primer walking and Sanger sequencing. In addition to the chromosome, we found one plasmid in the initial assembly and confirmed its circularity by PCR.

The procedure for genome annotation was largely based on that described in one of our previous studies (3). Briefly, the protein-coding genes were predicted using Prodigal (4) and annotated according to the orthologous gene in the Escherichia coli K-12 MG1655 genome (5), the KEGG Automatic Annotation System (KAAS) tool (6) provided by the Kyoto Encyclopedia of Genes and Genomes (KEGG) database (7, 8), and the BLASTp (9, 10) hits in the NCBI nonredundant protein database (11). The gene names and product descriptions were manually curated to incorporate information from these different sources. The rRNA and tRNA genes were predicted and annotated using RNAmmer (12) and tRNAscan-SE (13), respectively.

The genome of S. marcescens WW4 consists of one circular chromosome (5,241,455 bp; 59.6% G+C content) and one circular plasmid, pSmWW4 (3,248 bp; 47.8% G+C content). The first version of annotation includes 4,809 protein-coding genes (4,806 on the chromosome and three on the plasmid), 79 tRNA genes, and 22 rRNA genes, in seven operons. Our preliminary examination of the gene content identified one complete pig gene cluster for the biosynthesis of prodigiosin (i.e., a red pigment with antibiotic activities), which shares the same gene organization with S. marcescens ATCC 274 (14). Additionally, several putative bacteriocin genes exist in the S. marcescens WW4 genome, which are likely to be responsible for the intergeneric inhibition phenotype of this bacterium (1).

Nucleotide sequence accession numbers.

The complete genome sequence of S. marcescens WW4 has been included in the GenBank Whole-Genome Shotgun (WGS) database under accession no. CP003959 (chromosome) and CP003960 (plasmid pSmWW4).

ACKNOWLEDGMENTS

This work was supported by funding from the Institute of Plant and Microbial Biology, Academia Sinica to C.-H.K.

We thank the DNA Analysis Core Laboratory (Institute of Plant and Microbial Biology, Academia Sinica) for providing Sanger sequencing service. The Illumina sequencing and optical mapping services were provided by Yourgene BioScience (Taipei, Taiwan).

Footnotes

Citation Chung W-C, Chen L-L, Lo W-S, Kuo P-A, Tu J, Kuo C-H. 2013. Complete genome sequence of Serratia marcescens WW4. Genome Announc. 1(2):e00126-13. doi:10.1128/genomeA.00126-13.

REFERENCES

  • 1. Kuo PA, Kuo CH, Lai YK, Graumann PL, Tu J. 7 February 2013. Phosphate limitation induces the intergeneric inhibition of Pseudomonas aeruginosa by Serratia marcescens isolated from paper machines. FEMS Microbiol. Ecol. [Epub ahead of print.] http://dx.doi.org/10.1111/1574-6941.12086 [DOI] [PMC free article] [PubMed]
  • 2. Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res. 18:821–829 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Lo WS, Chen LL, Chung WC, Gasparich GE, Kuo CH. 2013. Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium. BMC Genomics 14:22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Hyatt D, Chen GL, LoCascio PF, Land ML, Larimer FW, Hauser LJ. 2010. Prodigal: prokaryotic gene recognition and translation initiation site identification. BMC Bioinformatics 11:119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Blattner FR, Plunkett G, Bloch CA, Perna NT, Burland V, Riley M, Collado-Vides J, Glasner JD, Rode CK, Mayhew GF, Gregor J, Davis NW, Kirkpatrick HA, Goeden MA, Rose DJ, Mau B, Shao Y. 1997. The complete genome sequence of Escherichia coli K-12. Science 277:1453–1462 [DOI] [PubMed] [Google Scholar]
  • 6. Moriya Y, Itoh M, Okuda S, Yoshizawa AC, Kanehisa M. 2007. KAAS: an automatic genome annotation and pathway reconstruction server. Nucleic Acids Res. 35:W182–W185 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Kanehisa M, Goto S. 2000. KEGG: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 28:27–30 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Kanehisa M, Goto S, Furumichi M, Tanabe M, Hirakawa M. 2010. KEGG for representation and analysis of molecular networks involving diseases and drugs. Nucleic Acids Res. 38:D355–D360 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. 1990. Basic local alignment search tool. J. Mol. Biol. 215:403–410 [DOI] [PubMed] [Google Scholar]
  • 10. Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, Madden TL. 2009. BLAST +: architecture and applications. BMC Bioinformatics 10:421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Benson DA, Karsch-Mizrachi I, Clark K, Lipman DJ, Ostell J, Sayers EW. 2012. GenBank. Nucleic Acids Res. 40:D48–D53 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Lagesen K, Hallin P, Rødland EA, Staerfeldt HH, Rognes T, Ussery DW. 2007. RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res. 35:3100–3108 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Lowe TM, Eddy SR. 1997. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 25:955–964 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Harris AKP, Williamson NR, Slater H, Cox A, Abbasi S, Foulds I, Simonsen HT, Leeper FJ, Salmond GPC. 2004. The Serratia gene cluster encoding biosynthesis of the red antibiotic, prodigiosin, shows species- and strain-dependent genome context variation. Microbiology 150:3547–3560 [DOI] [PubMed] [Google Scholar]

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES