Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2015 Jan 8;3(1):e01344-14. doi: 10.1128/genomeA.01344-14

Draft Genome Sequences of Vibrio fluvialis Strains 560 and 539, Isolated from Environmental Samples

Adonney Allan de Oliveira Veras a, Miriam Lopes da Silva b, Jaqueline Conceição Meireles Gomes a, Larissa Maranhão Dias a, Pablo Caracciolo Gomes de Sá a, Jorianne Thyeska Castro Alves a, Wendel Castro a, Fábio Miranda a, Ehilton Kazuo a, Diogo Marinho a, Mateus Rodrigues a, Matheus Freire a, Ramiro Zahlouth a, Wendel Renan a, Thiago Souza Lopes a, Maria Helena Matté b, Cintia Carolina da Silva Mayer b, Suzi de Almeida Vasconcelos Barboni c, Glavur Rogério Matté b, Adriana Ribeiro Carneiro a, Artur Silva a, Rommel Thiago Jucá Ramos a,
PMCID: PMC4290981  PMID: 25573928

Abstract

Vibrio fluvialis is a halophilic bacterium found in many environments and is mainly associated with sporadic cases and outbreaks of gastroenteritis in humans. Here, we describe the genome sequences of environmental strains of V. fluvialis 560 (Vf560) and V. fluvialis 539 (Vf539) possessing a variant of the integrative and conjugative element (ICE) SXT for the first time in Brazil and South America.

GENOME ANNOUNCEMENT

Vibrio fluvialis is a halophilic bacterium normally found in marine and estuarine environments (1). Although reports exist of the occurrence of extra intestinal cases, V. fluvialis is mainly associated with sporadic cases and outbreaks of gastroenteritis in humans, producing diarrhea very similar to cholera (2). Even though only two reports indicating the occurrence of diarrhea caused by V. fluvialis in Brazil are available in the literature, the presence of this species in the environment is well known (3, 4, 5).

The SXT, a member of the integrative and conjugative element (ICE) SXT/R391 family, was first described in clinical strains of Vibrio cholerae O139, the first non-O1 serogroup responsible for epidemics of cholera in the Indian subcontinent (6). Since the emergence of this element in 1992, SXT and its variants were reported among the Gammaproteobacteria, including V. fluvialis (7). Here, we describe the genome sequence of environmental strains of V. fluvialis 560 (Vf560) and V. fluvialis 539 (Vf539) that possess a variant of the ICE SXT element for the first time in Brazil and South America.

These genome sequences might help to characterize the element and enable the comparison of its structure with those already reported. Chromosomal DNA was extracted from each of the V. fluvialis strains by the cetyltrimethylammonium bromide method, as described by Ausubel et al. in 1995 (8).

The genome sequencing of Vf539 and Vf560 was performed using SOLiD 5500xl with a mate-paired library of 60 bp (Life Technologies) and Ion Torrent PGM (Life Technologies) with a fragment library. The SOLiD sequencing generated 267,008,850 reads for Vf539 and 263,712,284 for Vf560. Ion Torrent generated 1,776,055 reads for Vf539 and 5,440,706 reads for Vf560.

The SOLiD data were filtered with Quality Assessment software (9) using PHRED 20, leaving 199,175,010 reads for Vf539 and 188,653,932 reads for Vf560. The assembly of these data was performed with CLC Genomics Workbench software, generating, respectively, 1,336 and 972 contigs. The Ion Torrent PGM data were assembled with MIRA Assembler (10) and produced 361 contigs for Vf539 and 770 contigs for Vf560. The contigs generated by these platforms were merged and submitted to Simplifier software (11) in order to remove redundant sequences. After this step, the SSPACE (12), Gapfiller (13), CISA (14), and SeqMan pro software (DNASTAR, Inc.) were used to generate the scaffold and close gaps. At the end of the whole process, 84 scaffolds were obtained for Vf539 and 152 for Vf560, with 4,992,717 bp and 4,662,925 bp, respectively.

Nucleotide sequence accession numbers.

The V. fluvialis Vf539 and V. fluvialis Vf560 genome sequence data have been deposited at DDBJ/EMBL/GenBank under accession numbers JQHX00000000 and JQHW00000000, respectively. The versions described in this paper are the first versions.

ACKNOWLEDGMENTS

This work was part of the Rede Paraense de Genômica e Proteômica, supported by the Fundação Amazônia Paraense—FAPESPA, Núcleo Amazônico de Excelência em Genômica de Microorganismos—Programa de apoio a Núcleo de Excelência Pronex/CNPq/FAPESPA.

We thank the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (grant 2011/18826-7) for financial support.

Footnotes

Citation de Oliveira Veras AA, da Silva ML, Gomes JCM, Dias LM, de Sá PCG, Alves JTC, Castro W, Miranda F, Kazuo E, Marinho D, Rodrigues M, Freire M, Zahlouth R, Renan W, Lopes TS, Matté MH, da Silva Mayer CC, de Almeida Vasconcelos Barboni S, Matté GR, Carneiro AR, Silva A, Ramos RTJ. 2015. Draft genome sequences of Vibrio fluvialis strains 560 and 539, isolated from environmental samples. Genome Announc. 3(1):e01344-14. doi:10.1128/genomeA.01344-14.

REFERENCES

  • 1.Igbinosa EO, Okoh AI. 2010. Vibrio fluvialis: an unusual enteric pathogen of increasing public health concern. Int J Environ Res Public Health 7:3628–3643. doi: 10.3390/ijerph7103628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Bhattacharjee S, Bhattacharjee S, Bal B, Pal R, Niyogi SK, Sarkar K. 2010. Is Vibrio fluvialis emerging as a pathogen with epidemic potential in coastal region of eastern India following cyclone Aila? J Health Popul Nutr 28:311–317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Magalhães V, Magalhães M, Marques LR. 1993. Vibrios among patients of good socioeconomic conditions during the cholera epidemic in Recife, Brazil. Rev Inst Med Trop Sao Paulo 35:345–346. doi: 10.1590/S0036-46651993000400007. [DOI] [PubMed] [Google Scholar]
  • 4.Magalhães V, Lima RA, Magalhães E, Magalhães M. 1990. Human gastroenteritis associated with Vibrio fluvialis in Recife. Arq Gastroenterol 27:141–143. (In Portuguese.) [PubMed] [Google Scholar]
  • 5.Matté GR, Matté MH, Sato MI, Sanchez PS, Rivera IG, Martins MT. 1994. Potentially pathogenic vibrios associated with mussels from a tropical region on the Atlantic coast of Brazil. J Appl Bacteriol 77:281–287. doi: 10.1111/j.1365-2672.1994.tb03075.x. [DOI] [PubMed] [Google Scholar]
  • 6.Daccord A, Ceccarelli D, Burrus V. 2010. Integrating conjugative elements of the SXT/R391 family trigger the excision and drive the mobilization of a new class of Vibrio genomic islands. Mol Microbiol 78:576–588. doi: 10.1111/j.1365-2958.2010.07364.x. [DOI] [PubMed] [Google Scholar]
  • 7.Ahmed AM, Shinoda S, Shimamoto T. 2005. A variant type of Vibrio cholerae SXT element in a multidrug-resistant strain of Vibrio fluvialis. FEMS Microbiol Lett 242:241–247. doi: 10.1016/j.femsle.2004.11.012. [DOI] [PubMed] [Google Scholar]
  • 8.Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K. 1995. Short protocols in molecular biology, 3rd ed. John Wiley and Sons, New York, NY. [Google Scholar]
  • 9.Ramos RT, Carneiro AR, Baumbach J, Azevedo V, Schneider MP, Silva A. 2011. Analysis of quality raw data of second generation sequencers with Quality Assessment Software. BMC Res Notes 4:130. doi: 10.1186/1756-0500-4-130. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Chevreux B, Pfisterer T, Drescher B, Driesel AJ, Müller WEG, Wetter T, Suhai S. 2004. Using the miraEST assembler for reliable and automated mRNA transcript assembly and SNP detection in sequenced ESTs. Genome Res 14:1147–1159. doi: 10.1101/gr.1917404. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Ramos RTJ, Carneiro AR, Azevedo V, Schneider MP, Barh D, Silva A. 2012. Simplifier: a Web tool to eliminate redundant NGS contigs. Bioinformation 8:996–999. doi: 10.6026/97320630008996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Boetzer M, Henkel CV, Jansen HJ, Butler D, Pirovano W. 2011. Scaffolding pre-assembled contigs using SSPACE. Bioinformatics 27:578–579. doi: 10.1093/bioinformatics/btq683. [DOI] [PubMed] [Google Scholar]
  • 13.Boetzer M, Pirovano W. 2012. Toward almost closed genomes with GapFiller. Genome Biol 13:R56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Lin SH, Liao YC. 2013. CISA: contig integrator for sequence assembly of bacterial genomes. PLoS One 8:e60843–e60843. doi: 10.1371/journal.pone.0060843. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES