| Literature DB >> 30348825 |
Ying-Xia He1, Cheng-Lin Ye1, Pei Zhang1, Qiao Li1, Chae Gyu Park2, Kun Yang3, Ling-Yu Jiang1, Yin Lv1, Xiao-Ling Ying1, Hong-Hui Ding1, Hong-Ping Huang1, John Mambwe Tembo1,4, An-Yi Li1, Bing Cheng1, Shu-Sheng Zhang5, Guo-Xing Zheng5, Shi-Yun Chen6, Wei Li7, Lian-Xu Xia7, Biao Kan7, Xin Wang7, Huai-Qi Jing7, Rui-Fu Yang8, Hua Peng9, Yang-Xin Fu10, John D Klena11, Mikael Skurnik12, Tie Chen13.
Abstract
Yersinia pseudotuberculosis is a Gram-negative enteropathogen and causes gastrointestinal infections. It disseminates from gut to mesenteric lymph nodes (MLNs), spleen, and liver of infected humans and animals. Although the molecular mechanisms for dissemination and infection are unclear, many Gram-negative enteropathogens presumably invade the small intestine via Peyer's patches to initiate dissemination. In this study, we demonstrate that Y. pseudotuberculosis utilizes its lipopolysaccharide (LPS) core to interact with CD209 receptors, leading to invasion of human dendritic cells (DCs) and murine macrophages. These Y. pseudotuberculosis-CD209 interactions result in bacterial dissemination to MLNs, spleens, and livers of both wild-type and Peyer's patch-deficient mice. The blocking of the Y. pseudotuberculosis-CD209 interactions by expression of O-antigen and with oligosaccharides reduces infectivity. Based on the well-documented studies in which HIV-CD209 interaction leads to viral dissemination, we therefore propose an infection route for Y. pseudotuberculosis where this pathogen, after penetrating the intestinal mucosal membrane, hijacks the Y. pseudotuberculosis-CD209 interaction antigen-presenting cells to reach their target destinations, MLNs, spleens, and livers.Entities:
Keywords: CD209a; CD209b; DC-SIGN; DCs; LPS core; SIGN-R1; Yersinia pseudotuberculosis; dendritic cells; dissemination; lipopolysaccharide core
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Year: 2018 PMID: 30348825 PMCID: PMC6300620 DOI: 10.1128/IAI.00654-18
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441