Dengue virus infection induces passive release of high mobility group box 1 protein by epithelial cells

被引:35
作者
Chen, Lien-Cheng [2 ]
Yeh, Trai-Ming [3 ]
Wu, Huey-Nan [4 ]
Lin, Yi-Ying [1 ,5 ]
Shyu, Huey-Wen [1 ]
机构
[1] Fooyin Univ, Dept Med Technol, Kaohsiung Hsien 831, Taiwan
[2] Natl Cheng Kung Univ, Inst Basic Med Sci, Tainan 70101, Taiwan
[3] Natl Cheng Kung Univ, Dept Med Technol, Tainan 70101, Taiwan
[4] Acad Sinica, Inst Mol Biol, Taipei 115, Taiwan
[5] Ctr Dis Control, Dept Hlth, Branch Off 5, Kaohsiung, Taiwan
关键词
DV-2; necrosis; HMGB1; interferon-beta;
D O I
10.1016/j.jinf.2007.10.008
中图分类号
R51 [传染病];
学科分类号
100401 [流行病与卫生统计学];
摘要
Objectives: Dengue hemorrhagic fever and dengue shock syndrome (DHF/DSS) are severe complications of secondary dengue virus (DV) infection. In the current study, we provide the first evidence of induction of cellular necrosis by DV type 2 (DV-2). Methods and Results: The epithelial cell line A549 can support replication of dengue virus as demonstrated by expression of viral NS1 antigen and virus plaque assay. DV-2 infection of cells induced cell death in approximately half of the cells that were actively infected. Using sodium 3'-[1-(phenylaminocarbonyl)-3, 4-tetrazolium]-bis(4-methoxy-6-nitro) benzene sulfonic acid hydrate [XTT]-based cell viability assays, we found that DV-2 infection at a multiplicity of infection (MOI) of 10 resulted in significant death of cells as well as high extracellular lactate dehydrogenase (LDH) activity and leakage of the high mobility group 1 (HMGB1) protein into the extracellular space. Conclusions: These results suggest that HMGB1 may be a signal of tissue or cellular injury by DV-2, which in turn is likely to induce and/or enhance an immune reaction. (C) 2007 The British Infection Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:143 / 150
页数:8
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