Pseudorabies virus US3-and UL49.5-dependent and -independent downregulation of MHC I cell surface expression in different cell types

被引:27
|
作者
Deruelle, Matthias J. [1 ]
Van den Broeke, Celine [1 ]
Nauwynck, Hans J. [1 ]
Mettenleiter, Thomas C. [2 ]
Favoreel, Herman W. [1 ]
机构
[1] Univ Ghent, Dept Virol Parasitol & Immunol, Fac Vet Med, B-9820 Merelbeke, Belgium
[2] Fed Res Inst Anim Hlth, Friedrich Loeffler Inst, Inst Mol Biol, D-17493 Greifswald, Germany
关键词
Pseudorabies virus; MHC I; Downregulation; US3 protein kinase; UL49.5; Alphaherpesvirus; Varicellovirus; VARICELLA-ZOSTER-VIRUS; HERPES-SIMPLEX-VIRUS; ANTIGEN-PROCESSING TAP; EQUINE HERPESVIRUS-1; DENDRITIC CELLS; PROTEIN; COMPLEX; KINASE; US3; TRANSPORT;
D O I
10.1016/j.virol.2009.09.019
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Many herpesviruses interfere with the MHC I antigen-processing pathway in order to limit elimination by cytotoxic T-lymphocytes. For varicelloviruses, the largest subgroup of alphaherpesviruses, two viral proteins have been reported to downregulate MHC I cell surface expression: UL49.5 for BoHV-1 PRV and EHV-1 and the US3 orthologue for VZV. Here, we report that PRV reduces MHC I cell surface expression during infection in a cell-type-dependent manner. In ST cells, a kinase-active US3 was necessary but not sufficient to downregulate cell surface MHC I expression, whereas US3 was not required in PK-15 cells and porcine alveolar macrophages (PAM). MHC I downregulation was not (PAM, ST) or only partly (PK-15) dependent on UL49.5. In Conclusion, we show that the mechanism(s) of PRV-mediated cell surface MHC I downregulation are cell-type-dependent, with variable roles for US3, UL49.5, and additional, yet unidentified early viral proteins. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:172 / 181
页数:10
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