共 4 条
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
来源:
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.
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页码:172 / 181
页数:10
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