scholarly journals Streptococcal Toxic Shock Syndrome Caused by Streptococcus suis Serotype 2

PLoS Medicine ◽  
2006 ◽  
Vol 3 (5) ◽  
pp. e151 ◽  
Author(s):  
Jiaqi Tang ◽  
Changjun Wang ◽  
Youjun Feng ◽  
Weizhong Yang ◽  
Huaidong Song ◽  
...  
PLoS Medicine ◽  
2006 ◽  
Vol 3 (8) ◽  
pp. e377 ◽  
Author(s):  
Jiaqi Tang ◽  
Changjun Wang ◽  
Youjun Feng ◽  
Weizhong Yang ◽  
Huaidong Song ◽  
...  

2008 ◽  
Vol 22 (5) ◽  
pp. 313-316 ◽  
Author(s):  
Yefei Zhu ◽  
Zhongmin Tan ◽  
Lingyang Zhu ◽  
Hongxing Pan ◽  
Xuejun Zhang ◽  
...  

2008 ◽  
Vol 190 (22) ◽  
pp. 7567-7578 ◽  
Author(s):  
Youjun Feng ◽  
Ming Li ◽  
Huimin Zhang ◽  
Beiwen Zheng ◽  
Huiming Han ◽  
...  

ABSTRACT Zinc is an essential trace element for all living organisms and plays pivotal roles in various cellular processes. However, an excess of zinc is extremely deleterious to cells. Bacteria have evolved complex machineries (such as efflux/influx systems) to control the concentration at levels appropriate for the maintenance of zinc homeostasis in cells and adaptation to the environment. The Zur (zinc uptake regulator) protein is one of these functional members involved in the precise control of zinc homeostasis. Here we identified a zur homologue designated 310 from Streptococcus suis serotype 2, strain 05ZYH33, a highly invasive isolate causing streptococcal toxic shock syndrome. Biochemical analysis revealed that the protein product of gene 310 exists as a dimer form and carries zinc ions. An isogenic gene replacement mutant of gene 310, the Δ310 mutant, was obtained by homologous recombination. Physiological tests demonstrated that the Δ310 mutant is specifically sensitive to Zn2+, while functional complementation of the Δ310 mutant can restore its duration capability, suggesting that 310 is a functional member of the Zur family. Two-dimensional electrophoresis indicated that nine proteins in the Δ310 mutant are overexpressed in comparison with those in the wild type. DNA microarray analyses suggested that 121 genes in the Δ310 mutant are affected, of which 72 genes are upregulated and 49 are downregulated. The transcriptome of S. suis serotype 2 with high Zn2+ concentrations also showed 117 differentially expressed genes, with 71 upregulated and 46 downregulated. Surprisingly, more than 70% of the genes differentially expressed in the Δ310 mutant were the same as those in S. suis serotype 2 that were differentially expressed in response to high Zn2+ concentration, consistent with the notion that 310 is involved in zinc homeostasis. We thus report for the first time a novel zinc-responsive regulator, Zur, from Streptococcus suis serotype 2.


AMB Express ◽  
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Xiaomeng Pei ◽  
Junchi Liu ◽  
Mingxing Liu ◽  
Hong Zhou ◽  
Xiaomin Wang ◽  
...  

Abstract Streptococcus suis serotype 2 (SS2) is a serious zoonotic pathogen; it can lead to symptoms of streptococcal toxic shock syndrome (STSS) in humans and sepsis in pigs, and poses a great threat to public health. The SS2 MetQ gene deletion strain has attenuated antiphagocytosis, although the mechanism of antiphagocytosis and pathogenesis of MetQ in SS2 has remained unclear. In this study, stable isotope labeling by amino acids in cell culture (SILAC) based liquid chromatography–mass spectrometry (LC–MS) and subsequent bioinformatics analysis was used to determine differentially expressed proteins of RAW264.7 cells infected with △MetQ and ZY05719. Proteomic results were verified by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blotting for selected proteins. Further research was focused mainly on immune system processes related to downregulated proteins, such as Src and Ccl9, and actin cytoskeleton and endocytosis related upregulated proteins, like Pstpip1 and Ppp1r9b. The proteomic results in this study shed light on the mechanism of antiphagocytosis and innate immunity of macrophages infected with △MetQ and ZY05719, which might provide novel targets to prevent or control the infection of SS2.


2009 ◽  
Vol 191 (8) ◽  
pp. 2601-2612 ◽  
Author(s):  
Xiuzhen Pan ◽  
Junchao Ge ◽  
Ming Li ◽  
Bo Wu ◽  
Changjun Wang ◽  
...  

ABSTRACT Streptococcus suis serotype 2 is an emerging zoonotic pathogen responsible for a wide range of life-threatening diseases in pigs and humans. However, the pathogenesis of S. suis serotype 2 infection is not well understood. In this study, we report that an orphan response regulator, CovR, globally regulates gene expression and negatively controls the virulence of S. suis 05ZYH33, a streptococcal toxic shock syndrome (STSS)-causing strain. A covR-defective (ΔcovR) mutant of 05ZYH33 displayed dramatic phenotypic changes, such as formation of longer chains, production of thicker capsules, and increased hemolytic activity. Adherence of the ΔcovR mutant to epithelial cells was greatly increased, and its resistance to phagocytosis and killing by neutrophils and monocytes was also significantly enhanced. More importantly, inactivation of covR increased the lethality of S. suis serotype 2 in experimental infection of piglets, and this phenotype was restored by covR complementation. Colonization experiments also showed that the ΔcovR mutant exhibited an increased ability to colonize susceptible tissues of piglets. The pleiotropic phenotype of the ΔcovR mutant is in full agreement with the large number of genes controlled by CovR as revealed by transcription profile analysis: 2 genes are positively regulated, and 193 are repressed, including many that encode known or putative virulence factors. These findings suggested that CovR is a global repressor in virulence regulation of STSS-causing S. suis serotype 2.


2016 ◽  
Vol 22 (11) ◽  
pp. 774-776 ◽  
Author(s):  
Fabiola Mancini ◽  
Francesco Adamo ◽  
Roberta Creti ◽  
Monica Monaco ◽  
Giovanna Alfarone ◽  
...  

Author(s):  
Roel M. van Harten ◽  
Johanna L.M. Tjeerdsma-van Bokhoven ◽  
Astrid de Greeff ◽  
Melanie D. Balhuizen ◽  
Albert van Dijk ◽  
...  

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