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The early UL3 gene of equine herpesvirus-1 encodes a tegument protein not essential for replication or virulence in the mouse
被引:8
作者:
Ahn, Byung Chul
[1
]
Kim, Seongman
[1
]
Zhang, Yunfei
[1
]
Charvat, Robert A.
[1
]
O'Callaghan, Dennis J.
[1
]
机构:
[1] Louisiana State Univ, Ctr Mol & Tumor Virol, Hlth Sci Ctr, Dept Microbiol & Immunol, Shreveport, LA 71130 USA
来源:
基金:
美国国家卫生研究院;
关键词:
Equine herpesvirus 1;
UL3 gene of EHV-1;
Tegument protein of EHV-1;
UL3;
not essential for EHV-1 virulence;
DEFECTIVE INTERFERING PARTICLES;
IMMEDIATE-EARLY GENE;
ICP22/ICP27 HYBRID PROTEIN;
VARICELLA-ZOSTER VIRUS;
BOVINE HERPESVIRUS-1;
PERSISTENT INFECTION;
ICP22;
PROTEIN;
DNA-SEQUENCE;
IE PROTEIN;
REGULATORY FUNCTION;
D O I:
10.1016/j.virol.2011.08.016
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
The UL3 gene of equine herpesvirus-1 (EHV-1) is retained in the genome of defective interfering particles and encodes a similar to 33 kDa myristylated protein. Further characterization showed that the UL3 gene is trans-activated only by the sole immediate early (IE) protein and encodes an early protein that is dispensable for EHV-1 replication and localizes in the tegument of purified virions. UL3-deleted EHV-1 (vL11 Delta UL3) exhibits properties of host cell tropism, plaque size, and growth kinetics similar to those of the parental virus. Expression levels of EHV-1 proteins representative of all three gene classes in vL11 Delta UL3-infected cells were identical to those in cells infected with parental virus. Mice intranasally infected with vL11 Delta UL3 and parental virus showed no significant difference in mortality or virus lung titers. These findings suggest that the UL3 protein does not play a major role in the biology of EHV-1 in cell culture or virulence in the mouse. (C) 2011 Elsevier Inc. All rights reserved.
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页码:20 / 31
页数:12
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