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. 2013 Jul 11;1(4):e00444-13. doi: 10.1128/genomeA.00444-13

Draft Genome Sequences of Elizabethkingia meningoseptica

Stephanie A Matyi a, Peter R Hoyt a, Akira Hosoyama b, Atsushi Yamazoe b, Nobuyuki Fujita b, John E Gustafson a,
PMCID: PMC3709143  PMID: 23846266

Abstract

Elizabethkingia meningoseptica is ubiquitous in nature, exhibits a multiple-antibiotic resistance phenotype, and causes rare opportunistic infections. We now report two draft genome sequences of E. meningoseptica type strains that were sequenced independently in two laboratories.

GENOME ANNOUNCEMENT

The genus Elizabethkingia was derived in 2005 following a series of systematic investigations that led to the reclassification of members previously found within the genera Flavobacterium and Chryseobacterium (14). Currently, Elizabethkingia is represented by the three species Elizabethkingia miricola (5), Elizabethkingia meningoseptica (6, 7), and Elizabethkingia anophelis (8).

E. meningoseptica expresses a multiple-antibiotic resistance phenotype and causes infections primarily within immunocompromised individuals (911). The type strain of E. meningoseptica was isolated in 1958 in a case of neonatal meningitis (6, 7). We now report the draft genome sequences of two E. meningoseptica type strains, NBRC 12535T and ATCC 13253T. Both of these culture collection strains are representatives of the original E. meningoseptica strain isolated by Elizabeth King and colleagues (6).

The draft genome sequences of NBRC 12535T and ATCC 13253T were prepared at the National Institute of Technology and Evaluation, Tokyo, Japan, using Illumina HiSeq 1000 technology and at Oklahoma State University using the Roche 454 GS Junior platform, respectively. Genomic DNA to be sequenced was isolated from overnight cultures (30°C) of NBRC 12535T grown on nutrient agar containing 75% artificial seawater and ATCC 13253T grown in nutrient broth. Sequencing of NBRC 12535T generated 3,974,452 reads (103× coverage; average read length, 99.4 bp) that were assembled with the Newbler assembler (v2.6). ATCC 13253T sequencing produced 223,447 reads (29.7× coverage; average read length, 504.9 bp) that were assembled with the Roche GS de novo assembler (v2.7). Both draft genome sequences were uploaded to the Rapid Annotations using Subsystems Technology (RAST) server for annotation (12).

The NBRC 12535T draft genome sequence is 3,840,286 bp in length (36.2% G+C content) and includes 3,519 protein-coding regions distributed in 34 contigs (>500 bp). The ATCC 13253T draft genome sequence is 3,797,222 bp (35.2% G+C content) in length and includes 3,486 protein-coding regions distributed in 115 contigs (>200 bp). One hundred eleven contigs (representing 3,795,245 bp) of the ATCC 13253T sequence demonstrated 99 to 100% nucleotide identity with the 34 contigs of the NBRC 12535T sequence, which indicates that these draft genome sequences are essentially the same.

The nucleotide alignment of several highly conserved genes from the E. meningoseptica draft genome sequences and E. anophelis R26T (gene and nucleotide identities are as follows: gln, 86%; gyrB, 87%; recA, 88%; atpD, 92%; and dnaK, 92%) strongly supports previous findings that E. anophelis is at least a separate species (8). The 16S rRNA sequences of these two species are 98% identical, which is not very definitive for speciation (13). E. meningoseptica is resistant to β-lactam antibiotics due to the production of metallo-β-lactamases (MBLs) and extended-spectrum β-lactamases (ESBLs) (1416). Two MBL variants (blaGOB-17 and blaB3) and one ESBL gene (blaACME-1) were found in both E. meningoseptica draft genome sequences and were aligned with similar E. anophelis genes. A comparison of the β-lactamase orthologs from these two species revealed only 74% to 85% amino acid identity. This finding confirms that Elizabethkingia species, which are ubiquitous in nature (17), may act as potential reservoirs of novel β-lactamase genes.

Nucleotide sequence accession numbers.

These whole-genome shotgun projects have been deposited at DDBJ/EMBL/GenBank under the accession no. BARD00000000 for NBRC 12535T and ASAN00000000 for ATCC 13253T.

ACKNOWLEDGEMENTS

We thank the Japanese Ministry of Economy, Trade and Industry for their support sequencing NBRC 12535T. We acknowledge prior support from the National Institutes of Health for the sequencing of ATCC 13253T: SC1GM083882-01 (J.E.G.), R25 GM07667-30 (NMSU-MARC program), S06-GM61222-05 (NMSU-MBRS-RISE program), the National Center for Research Resources (5P20RR016480-12), and the National Institute of General Medical Sciences (8P20GM103451) (NM-INBRE program).

Footnotes

Citation Matyi SA, Hoyt PR, Hosoyama A, Yamazoe A, Fujita N, Gustafson JE. 2013. Draft genome sequences of Elizabethkingia meningoseptica. Genome Announc. 1(4):e00444-13. doi:10.1128/genomeA.00444-13.

REFERENCES

  • 1. Ursing J, Bruun B. 1987. Genetic heterogeneity of Flavobacterium meningosepticum demonstrated by DNA-DNA hybridization. Acta Pathol. Microbiol. Immunol. Scand. B 95:33–39 [DOI] [PubMed] [Google Scholar]
  • 2. Bruun B, Ursing J. 1987. Phenotypic characterization of Flavobacterium meningosepticum strains identified by DNA-DNA hybridization. Acta Pathol. Microbiol. Immunol. Scand. B 95:41–47 [DOI] [PubMed] [Google Scholar]
  • 3. Vandamme P, Bernardet J-F, Segers P, Kersters K, Holmes B. 1994. New perspectives in the classification of the Flavobacteria: description of Chryseobacterium gen. nov., Bergeyella gen. nov., and Empedobacter nom. rev. Int. J. Syst. Bacteriol. 44:827–831 [Google Scholar]
  • 4. Kim KK, Kim MK, Lim JH, Park HY, Lee ST. 2005. Transfer of Chryseobacterium meningosepticum and Chryseobacterium miricola to Elizabethkingia gen. nov. as Elizabethkingia meningoseptica comb. nov. and Elizabethkingia miricola comb. nov. Int. J. Syst. Evol. Microbiol. 55:1287–1293 [DOI] [PubMed] [Google Scholar]
  • 5. Li Y, Kawamura Y, Fujiwara N, Naka T, Liu H, Huang X, Kobayashi K, Ezaki T. 2003. Chryseobacterium miricola sp. nov., a novel species isolated from condensation water of space station Mir. Syst. Appl. Microbiol. 26:523–528 [DOI] [PubMed] [Google Scholar]
  • 6. Brody JA, Moore H, King EO. 1958. Meningitis caused by an unclassified Gram-negative bacterium in newborn infants. AMA J. Dis. Child. 96:1–5 [DOI] [PubMed] [Google Scholar]
  • 7. King EO. 1959. Studies on a group of previously unclassified bacteria associated with meningitis in infants. Am. J. Clin. Pathol. 31:241–247 [DOI] [PubMed] [Google Scholar]
  • 8. Kämpfer P, Matthews H, Glaeser SP, Martin K, Lodders N, Faye I. 2011. Elizabethkingia anophelis sp. nov., isolated from the midgut of the mosquito Anopheles gambiae. Int. J. Syst. Evol. Microbiol. 61:2670–2675 [DOI] [PubMed] [Google Scholar]
  • 9. Yang YS, Chun JW, Koh JW. 2013. Keratitis with Elizabethkingia meningoseptica occurring after contact lens wear: a case report. Korean J. Ophthalmol. 27:133–136 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Issack MI, Neetoo Y. 2011. An outbreak of Elizabethkingia meningoseptica neonatal meningitis in Mauritius. J. Infect. Dev. Ctries. 5:834–839 [DOI] [PubMed] [Google Scholar]
  • 11. Cartwright EJ, Prabhu RM, Zinderman CE, Schobert WE, Jensen B, Noble-Wang J, Church K, Welsh C, Kuehnert M, Burke TL, Srinivasan A. 2010. Transmission of Elizabethkingia meningoseptica (formerly Chryseobacterium meningosepticum) to tissue-allograft recipients: a report of two cases. J. Bone Joint Surg. Am. 92:1501–1506 [DOI] [PubMed] [Google Scholar]
  • 12. Aziz RK, Bartels A, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O. 2008. The RAST server: rapid annotations using subsystems technology. BMC Genomics 9:75. 10.1186/1471-2164-9-75 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Gevers D, Cohan FM, Lawrence JG, Spratt BG, Coenye T, Feil EJ, Stackerbrandt E, Van de Peer Y, Vandamme P, Thompson FL, Swings J. 2005. Re-evaluating prokaryotic species. Nat. Rev. Microbiol. 3:733–739 [DOI] [PubMed] [Google Scholar]
  • 14. Yum JH, Lee EY, Hur S-H, Jeong SH, Lee HL, Yong D, Chong Y, Lee E-W, Nordmann P, Lee K. 2010. Genetic diversity of chromosomal metallo-β-lactamase genes in clinical isolates of Elizabethkingia meningoseptica from Korea. J. Microbiol. 48:358–364 [DOI] [PubMed] [Google Scholar]
  • 15. Woodford N, Palepou M-F, Babini GS, Holmes B, Livermore DM. 2000. Carbapenemases of Chryseobacterium (Flavobacterium) meningosepticum: distribution of blaB and characterization of a novel metallo-β-lactamase gene, blaB3, in the type strain, NCTC 10016. Antimicrob. Agents Chemother. 44:1448–1452 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Rossolini GM, Franceschini N, Lauretti L, Caravelli B, Riccio ML, Galleni M, Frère JM, Amicosante G. 1999. Cloning of a Chryseobacterium (Flavobacterium) meningosepticum chromosomal gene (blaACME) encoding an extended-spectrum class A beta-lactamase related to the Bacteroides cephalosporinases and the VEB-1 and PER beta-lactamases. Antimicrob. Agents Chemother. 43:2193–2199 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Bernardet JF, Hugo C, Bruun B. 2006. The genera Chryseobacterium and Elizabethkingia. Prokaryotes 7:638–676 [Google Scholar]

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