Literature DB >> 23766409

Draft Genome Sequence of Streptococcus agalactiae PR06.

Irma Syakina Mz1, L K Teh, M Z Salleh.   

Abstract

Streptococcus agalactiae (group B streptococcus [GBS]) is a Gram-positive bacterium that was first recognized as a causative agent of bovine mastitis. S. agalactiae has subsequently emerged as a significant cause of human diseases. Here, we report the draft genome sequence of S. agalactiae PR06, which was isolated from a septicemic patient in a local hospital in Malaysia.

Entities:  

Year:  2013        PMID: 23766409      PMCID: PMC3707580          DOI: 10.1128/genomeA.00351-13

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Streptococcus agalactiae is well-adapted to asymptomatic colonization in the gastrointestinal and genitourinary tracts of healthy individuals (1). However, under certain circumstances, it may turn into a life-threatening pathogen causing septicemia, meningitis, and pneumonia in neonates (2). It is also a serious cause of mortality and morbidity in nonpregnant adults, particurly in elderly persons and those with underlying diseases (3). Here, we report the draft genome sequence of the S. agalactiae PR06 isolate from a local hospital in Malaysia. S. agalactiae PR06 was grown in Todd-Hewitt broth under optimal growth conditions. Gram stain and biochemical tests were performed to determine the purity of the bacterium. The genomic DNA of S. agalactiae PR06 was isolated using the Wizard genomic DNA purification kit (Promega). The draft genome of local S. agalactiae PR06 was determined using the Genome Analyzer IIx platform (Illumina). This genome was sequenced to produce ultra-deep coverage of 1,000×, and the quality was checked using FastQC. The reads were trimmed using the CLC bio Genomic Workbench 5.1 and assembled by mapping against the genome of the closest reference strain, S. agalactiae A909. A total of 67 contigs were produced, and these contigs were ordered with respect to the best-aligned positions compared to the reference genome of S. agalactiae A909 using Optimal Syntenic Layout of Unfinished Assemblies (OSLay) (4). The genome was annotated using the Rapid Annotations using Subsystems Technology (RAST) server (5), and putative coding sequences (CDSs) and annotated genes were identified by comparing outputs from the Bacterial Annotation System (BASys) (6). The draft genome of S. agalactiae contains a circular chromosome of 2,120,750 bp with a G+C content of 37% and 2,143 protein-coding sequences. The genome revealed >37 RNA genes and several virulence genes, including the cyl locus, which is responsible for pulmonary epithelial cell damage; the cfb gene, which codes for CAMP factor (7); the scp gene, which codes for C5a peptidase (8); and gene loci involved in capsule synthesis. These observations and comparative genomic studies would be useful in providing better knowledge of the genetic and molecular elements that might reveal drug-resistance profiles and vulnerabilities. The genome offers targets for the development of diagnostic tests, as well as new antimicrobial drugs and vaccines.

Nucleotide sequence accession number.

The genome sequence of S. agalactiae PR06 has been deposited at DDBJ/EMBL/GenBank under the accession no. AOSD00000000.
  8 in total

1.  Identification of novel adhesins from Group B streptococci by use of phage display reveals that C5a peptidase mediates fibronectin binding.

Authors:  Christiane Beckmann; Joshua D Waggoner; Theresa O Harris; Glen S Tamura; Craig E Rubens
Journal:  Infect Immun       Date:  2002-06       Impact factor: 3.441

2.  OSLay: optimal syntenic layout of unfinished assemblies.

Authors:  Daniel C Richter; Stephan C Schuster; Daniel H Huson
Journal:  Bioinformatics       Date:  2007-04-26       Impact factor: 6.937

Review 3.  Neonatal group B streptococcal disease: from pathogenesis to preventive strategies.

Authors:  P Melin
Journal:  Clin Microbiol Infect       Date:  2011-06-14       Impact factor: 8.067

4.  Group B streptococcal disease in the era of intrapartum antibiotic prophylaxis.

Authors:  S J Schrag; S Zywicki; M M Farley; A L Reingold; L H Harrison; L B Lefkowitz; J L Hadler; R Danila; P R Cieslak; A Schuchat
Journal:  N Engl J Med       Date:  2000-01-06       Impact factor: 91.245

Review 5.  Group B streptococcus and early-onset sepsis in the era of maternal prophylaxis.

Authors:  Joyce M Koenig; William J Keenan
Journal:  Pediatr Clin North Am       Date:  2009-06       Impact factor: 3.278

6.  BASys: a web server for automated bacterial genome annotation.

Authors:  Gary H Van Domselaar; Paul Stothard; Savita Shrivastava; Joseph A Cruz; AnChi Guo; Xiaoli Dong; Paul Lu; Duane Szafron; Russ Greiner; David S Wishart
Journal:  Nucleic Acids Res       Date:  2005-07-01       Impact factor: 16.971

7.  Characterization of a new CAMP factor carried by an integrative and conjugative element in Streptococcus agalactiae and spreading in Streptococci.

Authors:  Sarah Chuzeville; Aurore Puymège; Jean-Yves Madec; Marisa Haenni; Sophie Payot
Journal:  PLoS One       Date:  2012-11-09       Impact factor: 3.240

8.  The RAST Server: rapid annotations using subsystems technology.

Authors:  Ramy K Aziz; Daniela Bartels; Aaron A Best; Matthew DeJongh; Terrence Disz; Robert A Edwards; Kevin Formsma; Svetlana Gerdes; Elizabeth M Glass; Michael Kubal; Folker Meyer; Gary J Olsen; Robert Olson; Andrei L Osterman; Ross A Overbeek; Leslie K McNeil; Daniel Paarmann; Tobias Paczian; Bruce Parrello; Gordon D Pusch; Claudia Reich; Rick Stevens; Olga Vassieva; Veronika Vonstein; Andreas Wilke; Olga Zagnitko
Journal:  BMC Genomics       Date:  2008-02-08       Impact factor: 3.969

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.