Salmonella enterica Serovar Typhimurium Interacts with CD209 Receptors To Promote Host Dissemination and Infection

serovar Typhimurium, a Gram-negative bacterium, can cause infectious diseases ranging from gastroenteritis to systemic dissemination and infection. However, the molecular mechanisms underlying this bacterial dissemination have yet to be elucidated. A study indicated that using the lipopolysaccharide...

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Veröffentlicht in:Infection and immunity 2019-08, Vol.87 (8)
Hauptverfasser: Ye, Chenglin, Li, Qiao, Li, Xinyi, Park, Chae Gyu, He, Yingxia, Zhang, Yingmiao, Wu, Bicong, Xue, Ying, Yang, Kun, Lv, Yin, Ying, Xiao-Ling, Ding, Hong-Hui, Cai, Huahua, Alkraiem, Ayman Ahmad, Njiri, Olivia, Tembo, John, Huang, Hong-Ping, Li, An-Yi, Gong, Jianping, Qin, Jichao, Cheng, Bing, Wei, Xiang, Sun, Ziyong, Zhang, Shu-Sheng, Zhang, Pei, Zheng, Guo-Xing, Li, Wei, Kan, Biao, Yan, Meiying, Xiding, Xiamu, Huo, Xixiang, Zeng, Yingchun, Peng, Hua, Fu, Yangxin, Klena, John D, Skurnik, Mikael, Jiang, Ling-Yu, Chen, Tie
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Sprache:eng
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Zusammenfassung:serovar Typhimurium, a Gram-negative bacterium, can cause infectious diseases ranging from gastroenteritis to systemic dissemination and infection. However, the molecular mechanisms underlying this bacterial dissemination have yet to be elucidated. A study indicated that using the lipopolysaccharide (LPS) core as a ligand, Typhimurium was able to bind human dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (hCD209a), an HIV receptor that promotes viral dissemination by hijacking antigen-presenting cells (APCs). In this study, we showed that Typhimurium interacted with CD209s, leading to the invasion of APCs and potentially the dissemination to regional lymph nodes, spleen, and liver in mice. Shielding of the exposed LPS core through the expression of O-antigen reduces dissemination and infection. Thus, we propose that similar to HIV, Typhimurium may also utilize APCs via interactions with CD209s as a way to disseminate to the lymph nodes, spleen, and liver to initiate host infection.
ISSN:0019-9567
1098-5522
DOI:10.1128/IAI.00100-19