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Streptococcus suis sequence type 7 outbreak, Sichuan, China.

Changyun Ye | Xiaoping Zhu | Huaiqi Jing | Huamao Du | Mariela Segura | Han Zheng | Biao Kan | Lili Wang | Xuemei Bai | Yongyun Zhou | Zhigang Cui | Shouying Zhang | Dong Jin | Na Sun | Xia Luo | Ji Zhang | Zhaolong Gong | Xin Wang | Lei Wang | Hui Sun | Zhenjun Li | Qiangzheng Sun | Honglu Liu | Boqing Dong | Changwen Ke | Hui Yuan | Hua Wang | Kecheng Tian | Yu Wang | Marcelo Gottschalk | Jianguo Xu
Emerging infectious diseases | 2006

An outbreak of Streptococcus suis serotype 2 emerged in the summer of 2005 in Sichuan Province, and sporadic infections occurred in 4 additional provinces of China. In total, 99 S. suis strains were isolated and analyzed in this study: 88 isolates from human patients and 11 from diseased pigs. We defined 98 of 99 isolates as pulse type I by using pulsed-field gel electrophoresis analysis of SmaI-digested chromosomal DNA. Furthermore, multilocus sequence typing classified 97 of 98 members of the pulse type I in the same sequence type (ST), ST-7. Isolates of ST-7 were more toxic to peripheral blood mononuclear cells than ST-1 strains. S. suis ST-7, the causative agent, was a single-locus variant of ST-1 with increased virulence. These findings strongly suggest that ST-7 is an emerging, highly virulent S. suis clone that caused the largest S. suis outbreak ever described.

Pubmed ID: 16965698

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MLST (tool)

RRID:SCR_010245

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on March 17, 2022. A nucleotide sequence based approach for the unambiguous characterisation of isolates of bacteria and other organisms via the internet. The aim of MLST is to provide a portable, accurate, and highly discriminating typing system that can be used for most bacteria and some other organisms. It is envisaged that this approach will be particularly helpful for the typing of bacterial pathogens. To achieve this aim we have taken the proven concepts of multilocus enzyme electrophoresis (MLEE) and have adapted them so that alleles at each locus are defined directly, by nucleotide sequencing, rather than indirectly from the electrophoretic moblity of their gene products. MLST was developed in the laboratories of Martin Maiden, Dominique Caugant, Ian Feavers, Mark Achtman and Brian Spratt. This site is hosted at Imperial College with funding from the Wellcome Trust. The location of the subsites for the individual species are shown on their respective front pages.

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