Literature DB >> 27013051

Draft Genome Sequence of Streptococcus gordonii Type Strain CCUG 33482T.

Francisco Salvà-Serra1, Hedvig E Jakobsson2, Kaisa Thorell3, Lucia Gonzales-Siles2, Erika T Hallbäck2, Daniel Jaén-Luchoro4, Fredrik Boulund5, Per Sikora6, Roger Karlsson7, Liselott Svensson8, Antoni Bennasar4, Lars Engstrand3, Erik Kristiansson5, Edward R B Moore9.   

Abstract

Streptococcus gordoniitype strain CCUG 33482(T)is a member of theStreptococcus mitisgroup, isolated from a case of subacute bacterial endocarditis. Here, we report the draft genome sequence ofS. gordoniiCCUG 33482(T), composed of 41 contigs of a total size of 2.15 Mb with 2,061 annotated coding sequences.
Copyright © 2016 Salvà-Serra et al.

Entities:  

Year:  2016        PMID: 27013051      PMCID: PMC4807240          DOI: 10.1128/genomeA.00175-16

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Streptococcus gordonii is a commensal bacterium commonly found in human oral cavities and pharynges (1) and has been implicated in the formation of dental biofilms (2). S. gordonii also has been isolated from samples of bacterial endocarditis (3). S. gordonii was described as a novel species in 1989 after analyses of viridans streptococci (4). In those studies, Streptococcus sanguis type I-II, strain SK3T (=CCUG 33482T ←NCTC 7865T ←ATCC 10558T), isolated from a patient with subacute bacterial endocarditis (5), was reclassified as a distinct species, S. gordonii, with strain SK3T designated the type strain. S. gordonii is one of 14 species within the Streptococcus mitis group (6). S. gordonii CCUG 33482T was cultivated with 5% CO2, at 37°C, on Columbia agar base plus 5% horse blood. A fresh, pure-culture biomass was lysed in low-TE buffer (1 mM Tris, 0.1 mM EDTA, pH 8.0) supplemented with Triton 1.2% (wt/vol), lysozyme (20 mg/ml), and proteinase K (1 mg/ml), at 56°C overnight. Genomic DNA was isolated, using a MagNA pure compact nucleic acid isolation kit version I (Roche Diagnostics, Mannheim, Germany). DNA was sequenced with an Illumina MiSeq instrument (SciLifeLab, Stockholm, Sweden), generating 633,858 paired-end reads of 300 bp, yielding a total of 190.2 Mb. Sequence reads were trimmed and assembled de novo with CLC Genomic Workbench version 8 (CLC bio, Aarhus, Denmark) and default settings. Assembly quality was assessed using Quast version 3.1 (7). Trimming of the sequence reads left 632,358 paired-end reads (80.2% of initial sequence data) with an average of 241 bp, producing an assembly length of 2,166,763 bp, consisting of 41 contigs; the longest contig measures 632,335 bp. The N50 is 233,538 bp, and the average genome coverage of the assembly is 71×. The G+C content of the genome sequence is 40.5%, which is consistent with the 41% reported when the species was described (4). The genome sequence was annotated using the NCBI Prokaryotic Genome Annotation Pipeline (PGAP) (8). Annotation identified 2,061 coding sequences, 46 tRNAs, and 3 repeat regions. Comparative analyses of the sequence, by average nucleotide identity based on BLAST (ANIb) (9), using JSpecies version 1.2.1 (10), with the genome sequences of the type strains of species of the S. mitis group ranged from 73.1% to 81.8%. The analysis of the genome sequence for the presence of CRISPR-Cas systems (11) with CRISPRFinder (12) confirmed the presence of 4 CRISPR regions. Analyses against the Comprehensive Antibiotic Resistance Database (CARD) (13) and against the virulence factor database (VFDB) (14) identified 8 putative antibiotic resistance genes and 72 putative virulence factors. At the beginning of this project, the genome sequence of the type strains of all species included within the S. mitis group were available, except for that of S. gordonii. The genome sequence of S. gordonii CCUG 33482T represents essential data for the characterization of metabolic features of Streptococcus and phylogenomic studies of the S. mitis group.

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited at DDBJ/ENA/GenBank under the accession number LQWV00000000. The version described in this paper is the first version, LQWV01000000.
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1.  Streptococcus S.B.E.: A Streptococcus Associated with Subacute Bacterial Endocarditis.

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3.  CRISPR provides acquired resistance against viruses in prokaryotes.

Authors:  Rodolphe Barrangou; Christophe Fremaux; Hélène Deveau; Melissa Richards; Patrick Boyaval; Sylvain Moineau; Dennis A Romero; Philippe Horvath
Journal:  Science       Date:  2007-03-23       Impact factor: 47.728

4.  QUAST: quality assessment tool for genome assemblies.

Authors:  Alexey Gurevich; Vladislav Saveliev; Nikolay Vyahhi; Glenn Tesler
Journal:  Bioinformatics       Date:  2013-02-19       Impact factor: 6.937

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Journal:  Antimicrob Agents Chemother       Date:  2013-05-06       Impact factor: 5.191

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7.  Update on RefSeq microbial genomes resources.

Authors:  Tatiana Tatusova; Stacy Ciufo; Scott Federhen; Boris Fedorov; Richard McVeigh; Kathleen O'Neill; Igor Tolstoy; Leonid Zaslavsky
Journal:  Nucleic Acids Res       Date:  2014-12-15       Impact factor: 16.971

8.  Identity of viridans streptococci isolated from cases of infective endocarditis.

Authors:  C W Douglas; J Heath; K K Hampton; F E Preston
Journal:  J Med Microbiol       Date:  1993-09       Impact factor: 2.472

9.  Determination of 16S rRNA sequences of Streptococcus mitis and Streptococcus gordonii and phylogenetic relationships among members of the genus Streptococcus.

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Journal:  Int J Syst Bacteriol       Date:  1995-04

10.  CRISPRFinder: a web tool to identify clustered regularly interspaced short palindromic repeats.

Authors:  Ibtissem Grissa; Gilles Vergnaud; Christine Pourcel
Journal:  Nucleic Acids Res       Date:  2007-05-30       Impact factor: 16.971

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  1 in total

1.  Draft Genome Sequences of Six Strains of Streptococcus pneumoniae from Serotypes 5, 6A, 6B, 18C, 19A, and 23F.

Authors:  Hedvig E Jakobsson; Francisco Salvà-Serra; Kaisa Thorell; Roger Karlsson; Lucia Gonzales-Silès; Fredrik Boulund; Lars Engstrand; Erik Kristiansson; Edward R B Moore
Journal:  Genome Announc       Date:  2017-04-06
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