Literature DB >> 28104658

Draft Genome Sequence of Hypervirulent and Vaccine Candidate Streptococcus suis Strain SC19.

Lin Teng1,2, Xingxing Dong1, Yang Zhou3,4, Zhiwei Li1, Limei Deng5, Huanchun Chen5, Xiaohong Wang1, Jinquan Li6,5,7.   

Abstract

Streptococcus suis, a zoonotic bacterium found primarily in pigs, has been recognized recently as an emerging pathogen of humans. Herein, we describe the genome of Streptococcus suis strain SC19, a hypervirulent and vaccine candidate strain isolated from a pig amid the 2005 outbreak in China.
Copyright © 2017 Teng et al.

Entities:  

Year:  2017        PMID: 28104658      PMCID: PMC5255919          DOI: 10.1128/genomeA.01484-16

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Streptococcus suis is an important pathogen associated with a variety of life-threatening infections, including meningitis, endocarditis, arthritis, septicemia, and even sudden death in pigs (1). S. suis is responsible for significant worldwide economic losses in the pig industry (2). Among the 33 known serotypes, Streptococcus suis serotype 2 is considered to be the most prevalent and virulent. Although only sporadic cases of S. suis infection have been reported in humans (3), two outbreaks (Jiangsu in 1998 and Sichuan in 2005) initiated in China have raised considerable concerns among public health and food safety professionals in recent years (4). S. suis serotype 2 strain SC19 (also known as SC-19, 05ZYS, or ZYS) was isolated from the brain of a diseased piglet during the Chinese S. suis outbreak in 2005. SC19 has been utilized as a prototypic virulent S. suis strain in multiple studies. Foremost, immunoproteomic analysis of strain SC19 identified 34 cell wall-associated proteins, indicating alternative antigens for the further development of S. suis vaccines and diagnostic markers (5). Second, more than 15 virulence factors, such as GlnA, CiaRH, PerR, SsPepO, HP0197, and SspA, were characterized from this strain (6–8). Third, to increase the knowledge of the pathogenesis of meningitis, septicemia, and pneumonia in pigs caused by S. suis 2, gene expression profiles of peripheral blood mononuclear cells (PBMC), porcine monocyte-derived dendritic cells (MoDC), human monocytic cells (THP-1), as well as brain and lung tissues upon infection with strain SC19 were investigated by microarray (9–11). Fourth, several SC19-based live vaccine candidates were developed, among which at least one patent has been authorized in China (our unpublished data). SC19, as a hypervirulent strain, has been broadly used to evaluate the protective efficacy of vaccine candidates. However, in accordance with the scope of this announcement, the genomic composition of SC19 is poorly understood. Therefore, a draft genome sequence of S. suis strain SC19 has been compiled to further support the development of new commercial vaccines and diagnostic markers. The genome was sequenced on the HiSeq platform (Illumina, San Diego, CA, USA) using a paired-end library with a 150-bp read length. The de novo assembly strategy was performed through Edena version 3.131028 (12). The assembly generated 23 contigs with 2,073,313 bp (N50, 223,803 bp), followed by genome annotation using the RAST genome annotation server (version 2.0) (13–15). The genome of SC19 has 2,008 coding sequences, five rRNAs, 45 tRNAs, and a G+C content of 41.0%. The genome encodes the tetracycline resistance protein TetM and presents previously described virulence gene candidates, such as salK, salR, nisK, nisR, sly, ssnA, endA, scpA, epf, fhb, ide, nudp, mrp, ssadS, and igA1, and an 89-kb pathogenicity island (89 K PAI). Since SC19 has a clear origin and significant empirical evidence of hypervirulence (5, 6), it can serve as a prototypic S. suis strain. Genomics Insights of SC19 will support comparative genomics and pathogenicity analyses, therapeutic and vaccine development, and will ultimately help protect the swine industry and human health.

Accession number(s).

This whole-genome shotgun project has been deposited in GenBank under the accession no. MNPY00000000. The version described in this paper is the first version.
  15 in total

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Authors:  Anding Zhang; Chunyan Xie; Huanchun Chen; Meilin Jin
Journal:  Proteomics       Date:  2008-09       Impact factor: 3.984

2.  De novo finished 2.8 Mbp Staphylococcus aureus genome assembly from 100 bp short and long range paired-end reads.

Authors:  David Hernandez; Ryan Tewhey; Jean-Baptiste Veyrieras; Laurent Farinelli; Magne Østerås; Patrice François; Jacques Schrenzel
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Authors:  Yang Zhou; Xingxing Dong; Zhiwei Li; Geng Zou; Li Lin; Xiaohong Wang; Huanchun Chen; Robin B Gasser; Jinquan Li
Journal:  Virulence       Date:  2016-09-30       Impact factor: 5.882

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5.  Microarray analyses of THP-1 cells infected with Streptococcus suis serotype 2.

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Journal:  Vet Microbiol       Date:  2010-12-14       Impact factor: 3.293

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Authors:  Thomas Brettin; James J Davis; Terry Disz; Robert A Edwards; Svetlana Gerdes; Gary J Olsen; Robert Olson; Ross Overbeek; Bruce Parrello; Gordon D Pusch; Maulik Shukla; James A Thomason; Rick Stevens; Veronika Vonstein; Alice R Wattam; Fangfang Xia
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10.  The Role of Porcine Monocyte Derived Dendritic Cells (MoDC) in the Inflammation Storm Caused by Streptococcus suis Serotype 2 Infection.

Authors:  Jin Liu; Zhong-Yuan Tian; Yun-Cai Xiao; Xi-Liang Wang; Mei-Lin Jin; De-Shi Shi
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2.  Complete Genome Sequence of Streptococcus suis Serotype 2 Virulent Strain SS2-1.

Authors:  Haodan Zhu; Yanxiu Ni; Junming Zhou; Zhengyu Yu; Aihua Mao; Dandan Wang; Kongwang He
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3.  PmtA functions as a ferrous iron and cobalt efflux pump in Streptococcus suis.

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4.  Transcriptomic Analysis of Streptococcus suis in Response to Ferrous Iron and Cobalt Toxicity.

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5.  A Markerless Gene Deletion System in Streptococcus suis by Using the Copper-Inducible Vibrio parahaemolyticus YoeB Toxin as a Counterselectable Marker.

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6.  The VraSR regulatory system contributes to virulence in Streptococcus suis via resistance to innate immune defenses.

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7.  Bacitracin resistance and enhanced virulence of Streptococcus suis via a novel efflux pump.

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