Literature DB >> 26184948

Complete Genome Sequence of Noninvasive Streptococcus pyogenes M/emm28 Strain STAB10015, Isolated from a Child with Perianal Dermatitis in French Brittany.

Suzane de Andrade Barboza, Alexandra Meygret, Pascal Vincent, Séverine Moullec, Nicolas Soriano1, Vincent Lagente2, Jacques Minet3, Samer Kayal4, Ahmad Faili5.   

Abstract

We report here the complete genome sequence of a noninvasive strain of Streptococcus pyogenes M/emm28, isolated from perianal dermatitis in a child. The genome is composed of 1,950,454 bp, with a G+C content of 38.2%, and it has 1,925 identified coding sequences and harbors two intact prophages and a new integrating conjugative element (ICE).
Copyright © 2015 de Andrade Barboza et al.

Entities:  

Year:  2015        PMID: 26184948      PMCID: PMC4505136          DOI: 10.1128/genomeA.00806-15

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Streptococcus pyogenes, or group A streptococcus (GAS), is a Gram-positive human-specific pathogen that causes a broad range of invasive and noninvasive diseases. Although the throat and skin are the primary ecological niches, the genotype M/emm28 of GAS has been described as a disease specializing in perineal infections (1). Streptococcal perianal dermatitis (SPD) caused by GAS is a noninvasive infection that occurs mainly in children between 6 months and 5 years of age, affecting boys more often than girls (2). In an effort to gain new insights into invasive M/emm28 GAS infections, we sequenced and annotated the whole genome of one strain, named STAB10015, isolated in 2010 from a child (a young boy) with SPD and compared it with that of the sequenced strain MGAS6180 isolated from a patient with puerperal sepsis (1). The strain STAB10015 was grown in Todd-Hewitt medium supplemented with 0.2% yeast extract (THY), and DNA for sequencing was extracted and purified using the phenol-chloroform technique. Genomic DNA was sequenced using HiSeq 2000 technology (Illumina, Inc., San Diego, CA), and the paired-end library was built at the MGX facility of the CNRS in Montpellier, France. There is a total of 36,785,510 high-quality reads, giving an average of 1,933-fold coverage of the genome, which was assembled using the CLC Genomics Workbench version 6 software. The resulting assembly consisted of 56 contigs, which were oriented and connected with the module Microbial Genome Finishing Tools based on the MGAS6180 sequence. After reassembling, 11 gaps persisted, which were filled by PCR, followed by Sanger sequencing. Genome annotation was performed in parallel by using the RAST server (3) and NCBI PGAP (http://ncbi.nlm.nih.gov/genome/annotation_prok). Prophages were identified using the PHAge Search Tool (PHAST) (4). Finally, strain STAB10015 was found to harbor a single circular genome of 1,950,454 bp, with a G+C content of 38.2%. We identified 1,925 coding sequences (CDSs), 65 tRNA genes, 18 rRNA genes, and two intact integrated prophages. The multilocus sequence type (ST) (5) was determined to be ST52. In comparison with MGAS6180, all known virulence factors (6, 7) (proteinases, gene regulators, and adhesion proteins) were also identified in STAB10015. It contains genes encoding the secreted superantigens SpeC, SpeG, SpeJ, SmeZ, and SpeK. Nonsynonymous single-nucleotide polymorphisms (SNPs) were present in several genes coding for proteases (speB), exoenzymes (hylP), immunoreactive antigens (isp1), and adhesion proteins (sof, enn, and spr28 from the region-deleted 2 [RD2] region). Many genes encoding adhesins (emm, mrp-emm-like, sclA, sclB, and sbfx) or proteases (scp) presented significant deletions. We also identified a new integrating conjugative element (ICE) with a length of 54.2 kb, not encoding apparent virulence factors or antibiotic resistance genes, and it is inserted in the 3′ end of the tRNA uracil-5-methyltransferase gene, described as a hot spot for ICE (8). Sequence comparisons indicated significant homology with other intestinal bacterial ICEs (Streptococcus dysgalactiae RE378 [9] and Clostridium difficile 630 [10]). These bacterial interactions might result in antibiotic resistance gene [erm(TR)-tet(O)] acquisition, as described for ICESp2905 in the IB21 GAS strain (11). Before deciphering the bacterial phenotype and invasive potential, it is necessary to compare the STAB10015 sequence with that of strains isolated in the same geographical and temporal context.

Nucleotide sequence accession numbers.

The complete genome sequence of S. pyogenes strain STAB10015 has been deposited in the NCBI under the accession no. CP011068, part of BioProject PRJNA278400.
  11 in total

1.  Multilocus sequence typing of Streptococcus pyogenes and the relationships between emm type and clone.

Authors:  M C Enright; B G Spratt; A Kalia; J H Cross; D E Bessen
Journal:  Infect Immun       Date:  2001-04       Impact factor: 3.441

2.  Genome sequence of an M3 strain of Streptococcus pyogenes reveals a large-scale genomic rearrangement in invasive strains and new insights into phage evolution.

Authors:  Ichiro Nakagawa; Ken Kurokawa; Atsushi Yamashita; Masanobu Nakata; Yusuke Tomiyasu; Nobuo Okahashi; Shigetada Kawabata; Kiyoshi Yamazaki; Tadayoshi Shiba; Teruo Yasunaga; Hideo Hayashi; Masahira Hattori; Shigeyuki Hamada
Journal:  Genome Res       Date:  2003-06       Impact factor: 9.043

3.  ICESp2905, the erm(TR)-tet(O) element of Streptococcus pyogenes, is formed by two independent integrative and conjugative elements.

Authors:  Eleonora Giovanetti; Andrea Brenciani; Erika Tiberi; Alessandro Bacciaglia; Pietro Emanuele Varaldo
Journal:  Antimicrob Agents Chemother       Date:  2011-10-10       Impact factor: 5.191

4.  The multidrug-resistant human pathogen Clostridium difficile has a highly mobile, mosaic genome.

Authors:  Mohammed Sebaihia; Brendan W Wren; Peter Mullany; Neil F Fairweather; Nigel Minton; Richard Stabler; Nicholas R Thomson; Adam P Roberts; Ana M Cerdeño-Tárraga; Hongmei Wang; Matthew T G Holden; Anne Wright; Carol Churcher; Michael A Quail; Stephen Baker; Nathalie Bason; Karen Brooks; Tracey Chillingworth; Ann Cronin; Paul Davis; Linda Dowd; Audrey Fraser; Theresa Feltwell; Zahra Hance; Simon Holroyd; Kay Jagels; Sharon Moule; Karen Mungall; Claire Price; Ester Rabbinowitsch; Sarah Sharp; Mark Simmonds; Kim Stevens; Louise Unwin; Sally Whithead; Bruno Dupuy; Gordon Dougan; Bart Barrell; Julian Parkhill
Journal:  Nat Genet       Date:  2006-06-25       Impact factor: 38.330

5.  Genome sequence of a serotype M28 strain of group a streptococcus: potential new insights into puerperal sepsis and bacterial disease specificity.

Authors:  Nicole M Green; Shizhen Zhang; Stephen F Porcella; Michal J Nagiec; Kent D Barbian; Stephen B Beres; Rance B LeFebvre; James M Musser
Journal:  J Infect Dis       Date:  2005-07-29       Impact factor: 5.226

6.  Two distinct genetic elements are responsible for erm(TR)-mediated erythromycin resistance in tetracycline-susceptible and tetracycline-resistant strains of Streptococcus pyogenes.

Authors:  Andrea Brenciani; Erika Tiberi; Alessandro Bacciaglia; Dezemona Petrelli; Pietro E Varaldo; Eleonora Giovanetti
Journal:  Antimicrob Agents Chemother       Date:  2011-02-22       Impact factor: 5.191

7.  Perianal cellulitis associated with group A streptococci.

Authors:  D P Amren; A S Anderson; L W Wannamaker
Journal:  Am J Dis Child       Date:  1966-12

8.  PHAST: a fast phage search tool.

Authors:  You Zhou; Yongjie Liang; Karlene H Lynch; Jonathan J Dennis; David S Wishart
Journal:  Nucleic Acids Res       Date:  2011-06-14       Impact factor: 16.971

9.  Evolutionary paths of streptococcal and staphylococcal superantigens.

Authors:  Kayo Okumura; Yumi Shimomura; Somay Yamagata Murayama; Junji Yagi; Kimiko Ubukata; Teruo Kirikae; Tohru Miyoshi-Akiyama
Journal:  BMC Genomics       Date:  2012-08-17       Impact factor: 3.969

10.  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

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  3 in total

1.  Capsule-Negative emm Types Are an Increasing Cause of Pediatric Group A Streptococcal Infections at a Large Pediatric Hospital in Texas.

Authors:  Anthony R Flores; J Chase McNeil; Brittany Shah; Chris Van Beneden; Samuel A Shelburne
Journal:  J Pediatric Infect Dis Soc       Date:  2019-07-01       Impact factor: 3.164

2.  Genome Sequence of the Uncommon Streptococcus pyogenes M/emm66 Strain STAB13021, Isolated from Clonal Clustered Cases in French Brittany.

Authors:  Alexandra Meygret; Pascal Vincent; Séverine Moullec; Jessica Nacazume; Yahia Adnani; Dominique Lavenier; Samer Kayal; Ahmad Faili
Journal:  Genome Announc       Date:  2016-07-21

3.  The Emergence of Successful Streptococcus pyogenes Lineages through Convergent Pathways of Capsule Loss and Recombination Directing High Toxin Expression.

Authors:  Claire E Turner; Matthew T G Holden; Beth Blane; Carolyne Horner; Sharon J Peacock; Shiranee Sriskandan
Journal:  mBio       Date:  2019-12-10       Impact factor: 7.867

  3 in total

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