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Jianshun Chen 2 Articles
Catabolite Control Protein A of Streptococcus suis Type 2 Contributes to Sugar Metabolism and Virulence
Yulong Tang , Wei Wu , Xiaoyan Zhang , Zhongyan Lu , Jianshun Chen , Weihuan Fang
J. Microbiol. 2012;50(6):994-1002.   Published online December 30, 2012
DOI: https://doi.org/10.1007/s12275-012-2035-3
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  • 25 Crossref
AbstractAbstract PDF
Catabolite control protein A (CcpA) is the major transcriptional regulator in carbon catabolite repression in several Gram-positive bacteria. We attempted to characterize the role of a CcpA homologue of Streptococcus suis type 2 in sugar metabolism and virulence. Addition of glucose or sucrose to the defined medium significantly reduced the activity of raffinose-inducible α-galactosidase, cellobiose-inducible β-glucosidase, and maltose-inducible α-glucosidase of the wildtype strain by about 9, 4, and 2-3 fold, respectively. Deletion of ccpA substantially derepressed the effects of repressing sugars on α-galactosidase or β-glucosidase activity. The ccpA deletion mutant showed reduced expression of virulence genes sly and eno (P<0.05), decreased adhesion to and invasion into endothelial cells (P<0.05), and attenuated virulence to mice with significant reduction of death rate and bacterial burden in organs, as compared to the wild-type strain. Both the in vitro and in vivo defect phenotypes were reversible by ccpA complementation. Thus, this study shows that CcpA of S. suis type 2 plays an important role in carbon catabolite repression and virulence.

Citations

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    Microbiology Spectrum.2026;[Epub]     CrossRef
  • Clinically relevant genomic and phenotypic differences in virulence, antimicrobial resistance, and biofilm-associated tolerance between Streptococcus suis lineages ST1 and ST123
    Cristina Uruén, Clara M. Marín, Luis Daniel González-Vázquez, Marcelo Gottschalk, Miguel Arenas, Jesús Arenas
    Veterinary Research.2026;[Epub]     CrossRef
  • Thioredoxin C of Streptococcus suis serotype 2 contributes to virulence by inducing antioxidative stress and inhibiting autophagy via the MSR1/PI3K-Akt-mTOR pathway in macrophages
    Chunxiao Ji, Yanying Pan, Bocheng Liu, Jianying Liu, Chijun Zhao, Zhuyuan Nie, Simeng Liao, Guangwei Kuang, Xin Wu, Quan Liu, Jie Ning, Yulong Tang, Lihua Fang
    Veterinary Microbiology.2024; 298: 110263.     CrossRef
  • Ultrasound-assisted extraction of emodin from Rheum officinale Baill and its antibacterial mechanism against Streptococcus suis based on CcpA
    Jingwen Bai, Yu Xie, Miao Li, Xianjun Huang, Yujia Guo, Jingwen Sun, Yang Tang, Xuantong Liu, Chi Wei, Jianqiang Li, Yu Yang
    Ultrasonics Sonochemistry.2024; 102: 106733.     CrossRef
  • Thioredoxin A of Streptococcus suis Serotype 2 Contributes to Virulence by Inhibiting the Expression of Pentraxin 3 to Promote Survival Within Macrophages
    Chijun Zhao, Xinglin Jia, Yanying Pan, Simeng Liao, Shuo Zhang, Chunxiao Ji, Guangwei Kuang, Xin Wu, Quan Liu, Yulong Tang, Lihua Fang
    Journal of Microbiology.2023; 61(4): 433.     CrossRef
  • Role of Metabolic Adaptation of Streptococcus suis to Host Niches in Bacterial Fitness and Virulence
    Muriel Dresen, Peter Valentin-Weigand, Yenehiwot Berhanu Weldearegay
    Pathogens.2023; 12(4): 541.     CrossRef
  • The biological role of MutT in the pathogenesis of the zoonotic pathogen Streptococcus suis serotype 2
    Quan Li, Xia Fei, Yuhang Zhang, Genglin Guo, Huoying Shi, Wei Zhang
    Virulence.2021; 12(1): 1538.     CrossRef
  • Identification of conditionally essential genes for Streptococcus suis infection in pigs
    Jesús Arenas, Aldert Zomer, Jose Harders-Westerveen, Hester J. Bootsma, Marien I. De Jonge, Norbert Stockhofe-Zurwieden, Hilde E. Smith, Astrid De Greeff
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  • ICESsuHN105, a Novel Multiple Antibiotic Resistant ICE in Streptococcus suis Serotype 5 Strain HN105
    Yinchu Zhu, Yue Zhang, Jiale Ma, Wenyang Dong, Xiaojun Zhong, Zihao Pan, Huochun Yao
    Frontiers in Microbiology.2019;[Epub]     CrossRef
  • Design and development of a “Y-shaped” microbial consortium capable of simultaneously utilizing biomass sugars for efficient production of butanol
    Chunhua Zhao, Jean Paul Sinumvayo, Yanping Zhang, Yin Li
    Metabolic Engineering.2019; 55: 111.     CrossRef
  • The VraSR regulatory system contributes to virulence in Streptococcus suis via resistance to innate immune defenses
    Peixi Chang, Weitian Li, Guolin Shi, Huan Li, Xiaoqing Yang, Zechen Xia, Yuan Ren, Zhiwei Li, Huanchun Chen, Weicheng Bei
    Virulence.2018; 9(1): 771.     CrossRef
  • Streptococcus suis DivIVA Protein Is a Substrate of Ser/Thr Kinase STK and Involved in Cell Division Regulation
    Hua Ni, Weiwei Fan, Chaolong Li, Qianqian Wu, Hongfen Hou, Dan Hu, Feng Zheng, Xuhui Zhu, Changjun Wang, Xiangrong Cao, Zhu-Qing Shao, Xiuzhen Pan
    Frontiers in Cellular and Infection Microbiology.2018;[Epub]     CrossRef
  • Regulation of the β-hemolysin gene cluster of Streptococcus anginosus by CcpA
    Richard Bauer, Stefanie Mauerer, Barbara Spellerberg
    Scientific Reports.2018;[Epub]     CrossRef
  • Enhanced Production of Polymyxin E in Paenibacillus polymyxa by Replacement of Glucose by Starch
    Zhiliang Yu, Zhongqi Sun, Jianhua Yin, Juanping Qiu
    BioMed Research International.2018; 2018: 1.     CrossRef
  • Role of two-component regulatory systems in the virulence of Streptococcus suis
    Chengkun Zheng, Lingzhi Li, Haojie Ge, Hongmei Meng, Yang Li, Weicheng Bei, Xiaohui Zhou
    Microbiological Research.2018; 214: 123.     CrossRef
  • Streptococcus suis small RNA rss04 contributes to the induction of meningitis by regulating capsule synthesis and by inducing biofilm formation in a mouse infection model
    Genhui Xiao, Huanyu Tang, Shouming Zhang, Haiyan Ren, Jiao Dai, Liying Lai, Chengping Lu, Huochun Yao, Hongjie Fan, Zongfu Wu
    Veterinary Microbiology.2017; 199: 111.     CrossRef
  • Stress Physiology of Lactic Acid Bacteria
    Konstantinos Papadimitriou, Ángel Alegría, Peter A. Bron, Maria de Angelis, Marco Gobbetti, Michiel Kleerebezem, José A. Lemos, Daniel M. Linares, Paul Ross, Catherine Stanton, Francesca Turroni, Douwe van Sinderen, Pekka Varmanen, Marco Ventura, Manuel Z
    Microbiology and Molecular Biology Reviews.2016; 80(3): 837.     CrossRef
  • Superoxide dismutase of Streptococcus suis serotype 2 plays a role in anti-autophagic response by scavenging reactive oxygen species in infected macrophages
    Lihua Fang, Hongxia Shen, Yulong Tang, Weihuan Fang
    Veterinary Microbiology.2015; 176(3-4): 328.     CrossRef
  • Investigation into the role of catabolite control protein A in the metabolic regulation of Streptococcus suis serotype 2 using gene expression profile analysis
    XULONG LANG, ZHONGHAI WAN, YING PAN, XIURAN WANG, XIAOXU WANG, ZHAOYANG BU, JING QIAN, HUAZONG ZENG, XINGLONG WANG
    Experimental and Therapeutic Medicine.2015; 10(1): 127.     CrossRef
  • Two Spx Regulators Modulate Stress Tolerance and Virulence in Streptococcus suis Serotype 2
    Chengkun Zheng, Jiali Xu, Jinquan Li, Luohong Hu, Jiandong Xia, Jingyan Fan, Weina Guo, Huanchun Chen, Weicheng Bei, José A. Lemos
    PLoS ONE.2014; 9(9): e108197.     CrossRef
  • Streptococcus suisinfection
    Youjun Feng, Huimin Zhang, Zuowei Wu, Shihua Wang, Min Cao, Dan Hu, Changjun Wang
    Virulence.2014; 5(4): 477.     CrossRef
  • CcpA Is Important for Growth and Virulence of Enterococcus faecium
    Sudha R. Somarajan, Jung H. Roh, Kavindra V. Singh, George M. Weinstock, Barbara E. Murray, L. Pirofski
    Infection and Immunity.2014; 82(9): 3580.     CrossRef
  • RNA-seq analysis of the influence of anaerobiosis and FNR on Shigella flexneri
    Marta Vergara-Irigaray, Maria C Fookes, Nicholas R Thomson, Christoph M Tang
    BMC Genomics.2014;[Epub]     CrossRef
  • Streptococcus suis Type 2 SSU0587 Protein is a Beta-Galactosidase That Contributes to Bacterial Adhesion but Not to Virulence in Mice
    Yulong TANG, Xiaoyan ZHANG, Yulong YIN, Philip R. HARDWIDGE, Weihuan FANG
    Journal of Veterinary Medical Science.2014; 76(7): 1055.     CrossRef
  • Catabolite control protein A is an important regulator of metabolism in Streptococcus suis type 2
    XULONG LANG, ZHONGHAI WAN, ZHAOYANG BU, XIURAN WANG, XIAOXU WANG, LINGWEI ZHU, JIAYU WAN, YANG SUN, XINGLONG WANG
    Biomedical Reports.2014; 2(5): 709.     CrossRef
Deciphering the Biodiversity of Listeria monocytogenes Lineage III Strains by Polyphasic Approaches
Hanxin Zhao , Jianshun Chen , Chun Fang , Ye Xia , Changyong Cheng , Lingli Jiang , Weihuan Fang
J. Microbiol. 2011;49(5):759-767.   Published online November 9, 2011
DOI: https://doi.org/10.1007/s12275-011-1006-4
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  • 1 Download
  • 6 Crossref
AbstractAbstract PDF
Listeria monocytogenes is a foodborne pathogen of humans and animals. The majority of human listeriosis cases are caused by strains of lineages I and II, while lineage III strains are rare and seldom implicated in human listeriosis. We revealed by 16S rRNA sequencing the special evolutionary status of L. monocytogenes lineage III, which falls between lineages I and II strains of L. monocytogenes and the non-pathogenic species L. innocua and L. marthii in the dendrogram. Thirteen lineage III strains were then characterized by polyphasic approaches. Biochemical reactions demonstrated 8 biotypes, internalin profiling identified 10 internalin types clustered in 4 groups, and multilocus sequence typing differentiated 12 sequence types. These typing schemes show that lineage III strains represent the most diverse population of L. monocytogenes, and comprise at least four subpopulations IIIA-1, IIIA-2, IIIB, and IIIC. The in vitro and in vivo virulence assessments showed that two lineage IIIA-2 strains had reduced pathogenicity, while the other lineage III strains had comparable virulence to lineages I and II. The IIIB strains are phylogenetically distinct from other subpopulations, providing additional evidence that this sublineage represents a novel lineage. The two biochemical reactions L-rhamnose and L-lactate alkalinization, and 10 internalins were identified as potential markers for lineage III subpopulations. This study provides new insights into the biodiversity and population structure of lineage III strains, which are important for understanding the evolution of the L. monocytogenes-L. innocua clade.

Citations

Citations to this article as recorded by  
  • Proposal to validate Listeria swaminathanii sp. nov. and reassign the type strain to UTK S2-0008
    Catharine R. Carlin, Lauren K. Hudson, Harleen K. Chaggar, Claire N. Schamp, Ahmed Gaballa, Renato H. Orsi, Martin Wiedmann, Thomas G. Denes, Jeffrey A. Gralnick
    Microbiology Spectrum.2026;[Epub]     CrossRef
  • Listeria monocytogenes, Salmonella spp., and Staphylococcus aureus: Threats to the Food Industry and Public Health
    Vinicius B. Mantovam, David F. dos Santos, Luis C. Giola Junior, Mariza Landgraf, Uelinton M. Pinto, Svetoslav D. Todorov
    Foodborne Pathogens and Disease.2025; 22(12): 809.     CrossRef
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    Phillip Brown, Sangmi Lee, Driss Elhanafi, Wilhelm Tham, Marie-Louise Danielsson-Tham, Gloria Lopez-Valladares, Yi Chen, Mirena Ivanova, Pimlapas Leekitcharoenphon, Sophia Kathariou
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    Dongyou Liu
    Microbiology Insights.2013;[Epub]     CrossRef
  • Genetic diversity of internalin genes in the ascB‐dapE locus among Listeria monocytogenes lineages III and IV strains
    Jianshun Chen, Changyong Cheng, Yonghui Lv, Weihuan Fang
    Journal of Basic Microbiology.2013; 53(9): 778.     CrossRef
  • Genomic Presence of Gadd1 Glutamate Decarboxylase Correlates with the Organization ofAscb-DapeInternalin Cluster inListeria monocytogenes
    Jianshun Chen, Chun Fang, Tianlun Zheng, Ningyu Zhu, Yijiang Bei, Weihuan Fang
    Foodborne Pathogens and Disease.2012; 9(2): 175.     CrossRef

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