Literature DB >> 25908134

Complete Genome Sequence of Streptococcus iniae YSFST01-82, Isolated from Olive Flounder in Jeju, South Korea.

Sasikumar Rajoo1, Wooyoung Jeon1, Kyungmoon Park2, Sungsik Yoo3, Injung Yoon3, Hongweon Lee, Jungoh Ahn4.   

Abstract

Streptococcus iniae is associated with morbidity in commercial fish species, especially in olive flounders (Paralichthys olivaceus), and was recently identified as an emerging human pathogen. Here, we report the complete 2.09-Mb genome sequence of S. iniae strain YSFST01-82, isolated from an olive flounder with streptococcosis disease in Jeju, South Korea.
Copyright © 2015 Rajoo et al.

Entities:  

Year:  2015        PMID: 25908134      PMCID: PMC4408335          DOI: 10.1128/genomeA.00319-15

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Streptococcus iniae is a hemolytic Gram-positive coccus that was initially isolated in 1976 from skin abrasions on Amazon freshwater dolphins (Inia geoffrensis) in aquariums at San Francisco, CA, and New York, NY (1). The strain has been recognized as the causative agent of a highly contagious and fatal disease characterized by meningitis and panophthalmitis in fish (2). S. iniae–mediated streptococcosis has led to significant economic losses for fish farmers, particularly in the olive flounder (Paralichthys olivaceus), which is a major mariculture species in South Korea (3). Moreover, this strain might cause opportunistic infections in weakened or immunocompromised humans handling contagioned fish; hence, it may be considered an emerging zoonotic agent (4). Whole-genome sequencing of S. iniae strain YSFST01-82, isolated from diseased olive flounder in Jeju, South Korea, was performed with 454 GS-FLX Titanium (Roche Diagnostics, Basel, Switzerland), optical restriction mapping (OpGen, Inc., Madison, WI), and the 3730XL DNA Analyzer (Applied Biosystems, Foster City, CA, USA). Using an initial round of shotgun pyrosequencing, the contigs were assembled by using the Newbler gsAssembler software version 2.5.3 (454 Life Sciences, Branford, CT) and were further combined with 3-kb paired-end reads down to 19 scaffolds. By using the restriction enzyme NheI, an optical map was generated, and the contig orientation was validated using the MapSolver software (OpGen, Inc.). An additional round of Sanger sequencing was necessary for complete gap closure and finishing. The PCR products were subjected to cycle sequencing with ABI BigDye Terminator version 3.1 and were analyzed using the 3730XL DNA Analyzer (Applied Biosystems). The Phred-Phrap-Consed program (5, 6) was used for sequence assembly and editing of the assembled sequences. Gene prediction was carried out using Glimmer version 3.02 (7) and the Clusters of Orthologous Groups (COG) and SEED databases (8); rRNA and tRNA genes were identified by utilizing RNAmmer version 1.2 (9) and tRNAscan-SE version 1.23 (10), respectively. The genome of S. iniae is composed of 2,086,959 bp (36.8% G+C content). A total of 1,897 coding DNA sequences, 58 tRNA genes, and 15 rRNA genes were predicted. The complete genome sequence of the S. iniae found in olive flounder skin lesions will aid in the research of this strain and establish a basis for molecular evolution studies of its systemic invasion, which will lead to a more efficient vaccine and diagnostic methods to establish proper disease control measures.

Nucleotide sequence accession number.

This complete genome sequence of strain YSFST01-82 has been deposited at GenBank under the accession no. CP010783.
  8 in total

1.  Identifying bacterial genes and endosymbiont DNA with Glimmer.

Authors:  Arthur L Delcher; Kirsten A Bratke; Edwin C Powers; Steven L Salzberg
Journal:  Bioinformatics       Date:  2007-01-19       Impact factor: 6.937

2.  Base-calling of automated sequencer traces using phred. I. Accuracy assessment.

Authors:  B Ewing; L Hillier; M C Wendl; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

3.  Base-calling of automated sequencer traces using phred. II. Error probabilities.

Authors:  B Ewing; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

4.  Lactococcus garvieae and Streptococcus iniae infections in rainbow trout Oncorhynchus mykiss: similar, but different diseases.

Authors:  A Eldar; C Ghittino
Journal:  Dis Aquat Organ       Date:  1999-05-31       Impact factor: 1.802

5.  Accessing the SEED genome databases via Web services API: tools for programmers.

Authors:  Terry Disz; Sajia Akhter; Daniel Cuevas; Robert Olson; Ross Overbeek; Veronika Vonstein; Rick Stevens; Robert A Edwards
Journal:  BMC Bioinformatics       Date:  2010-06-14       Impact factor: 3.169

Review 6.  Streptococcus iniae: an aquatic pathogen of global veterinary significance and a challenging candidate for reliable vaccination.

Authors:  Wendy Agnew; Andrew C Barnes
Journal:  Vet Microbiol       Date:  2007-03-12       Impact factor: 3.293

7.  The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs.

Authors:  Peter Schattner; Angela N Brooks; Todd M Lowe
Journal:  Nucleic Acids Res       Date:  2005-07-01       Impact factor: 16.971

8.  RNAmmer: consistent and rapid annotation of ribosomal RNA genes.

Authors:  Karin Lagesen; Peter Hallin; Einar Andreas Rødland; Hans-Henrik Staerfeldt; Torbjørn Rognes; David W Ussery
Journal:  Nucleic Acids Res       Date:  2007-04-22       Impact factor: 16.971

  8 in total
  2 in total

1.  Complete Genome Sequence of Streptococcus iniae 89353, a Virulent Strain Isolated from Diseased Tilapia in Taiwan.

Authors:  Hong-Yi Gong; Sheng-Han Wu; Chun-Yao Chen; Chang-Wen Huang; Jenn-Kan Lu; Hsin-Yiu Chou
Journal:  Genome Announc       Date:  2017-01-26

2.  A high-quality reference genome for the fish pathogen Streptococcus iniae.

Authors:  Areej S Alsheikh-Hussain; Nouri L Ben Zakour; Brian M Forde; Oleksandra Silayeva; Andrew C Barnes; Scott A Beatson
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