Insight into Bacterial Virulence Mechanisms against Host Immune Response via the Yersinia pestis-Human Protein-Protein Interaction Network

• DOI: 10.1128/iai.05622-11
• Publication Date: 2011-09-13T06:31:35Z
• Authors: Huiying Yang; Yuehua Ke; Jian Wang; Yafang Tan; Sebenzile K. Myeni; Dong Li; Qinghai Shi; Yanfeng Yan; Hui Chen; Zhaobiao Guo; Yanzhi Yuan; Xiaoming Yang; Ruifu Yang; Zongmin Du
• Keywords: 0301 basic medicine; Plague; Virulence; Yersinia pestis; Computational Biology; 3. Good health; 03 medical and health sciences; HEK293 Cells; Bacterial Proteins; Gene Expression Regulation; Host-Pathogen Interactions; Humans; Protein Binding

ABSTRACT

A Yersinia pestis -human protein interaction network is reported here to improve our understanding of its pathogenesis. Up to 204 interactions between 66 Y. pestis bait proteins and 109 human proteins were identified by yeast two-hybrid assay and then combined with 23 previously published interactions to construct a protein-protein interaction network. Topological analysis of the interaction network revealed that human proteins targeted by Y. pestis were significantly enriched in the proteins that are central in the human protein-protein interaction network. Analysis of this network showed that signaling pathways important for host immune responses were preferentially targeted by Y. pestis , including the pathways involved in focal adhesion, regulation of cytoskeleton, leukocyte transendoepithelial migration, and Toll-like receptor (TLR) and mitogen-activated protein kinase (MAPK) signaling. Cellular pathways targeted by Y. pestis are highly relevant to its pathogenesis. Interactions with host proteins involved in focal adhesion and cytoskeketon regulation pathways could account for resistance of Y. pestis to phagocytosis. Interference with TLR and MAPK signaling pathways by Y. pestis reflects common characteristics of pathogen-host interaction that bacterial pathogens have evolved to evade host innate immune response by interacting with proteins in those signaling pathways. Interestingly, a large portion of human proteins interacting with Y. pestis (16/109) also interacted with viral proteins (Epstein-Barr virus [EBV] and hepatitis C virus [HCV]), suggesting that viral and bacterial pathogens attack common cellular functions to facilitate infections. In addition, we identified vasodilator-stimulated phosphoprotein (VASP) as a novel interaction partner of YpkA and showed that YpkA could inhibit in vitro actin assembly mediated by VASP.