SARS coronavirus accessory proteins

被引:132
作者
Narayanan, Krishna [1 ]
Huang, Cheng [1 ]
Makino, Shinji [1 ]
机构
[1] Univ Texas Galveston, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA
关键词
RNA viruses; SARS coronavirus; SARS-CoV; accessory proteins;
D O I
10.1016/j.virusres.2007.10.009
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The emergence of the severe acute respiratory syndrome coronavirus (SARS-CoV) has led to a renewed interest in studying the role of accessory proteins in regulating coronavirus infections in the natural host. A significant body of evidence has accumulated in the area of SARS-CoV and host interactions that indicate that the accessory proteins might play an important role in modulating the host response to virus infection and thereby, contribute to pathogenesis. In this review, we have compiled the current knowledge about SARS-CoV accessory proteins, obtained from studies in cell culture systems, reverse genetics and animal models, to shed some light into the possible role of these proteins in the propagation and virulence of SARS-CoV in its natural host. We conclude by providing some questions for future studies that will greatly advance our knowledge about the biological significance and contributions of the accessory proteins in the development of SARS in humans. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:113 / 121
页数:9
相关论文
共 70 条
[1]   Amino acids 15-28 in the ectodomain of SARS coronavirus 3a protein induces neutralizing antibodies [J].
Akerstrom, Sara ;
Tan, Yee-Joo ;
Mirazimi, Ali .
FEBS LETTERS, 2006, 580 (16) :3799-3803
[2]   Construction of a severe acute respiratory syndrome coronavirus infectious cDNA clone and a replicon to study coronavirus RNA synthesis [J].
Almazan, Fernando ;
DeDiego, Marta L. ;
Galan, Carmen ;
Escors, David ;
Alvarez, Enrique ;
Ortego, Javier ;
Sola, Isabel ;
Zuniga, Sonia ;
Alonso, Sara ;
Moreno, Jose L. ;
Nogales, Aitor ;
Capiscol, Carmen ;
Enjuanes, Luis .
JOURNAL OF VIROLOGY, 2006, 80 (21) :10900-10906
[3]   Coronaviral hypothetical and structural proteins were found in the intestinal surface enterocytes and pneumocytes of severe acute respiratory syndrome (SARS) [J].
Chan, WS ;
Wu, C ;
Chow, SCS ;
Cheung, T ;
To, KF ;
Leung, WK ;
Chan, PKS ;
Lee, KC ;
Ng, HK ;
Au, DMY ;
Lo, AWI .
MODERN PATHOLOGY, 2005, 18 (11) :1432-1439
[4]   Heterologous gene expression from transmissible gastroenteritis virus replicon particles [J].
Curtis, KM ;
Yount, B ;
Baric, RS .
JOURNAL OF VIROLOGY, 2002, 76 (03) :1422-1434
[5]   The group-specific murine coronavirus genes are not essential, but their deletion, by reverse genetics, is attenuating in the natural host [J].
de Haan, CAM ;
Masters, PS ;
Shen, XL ;
Weiss, S ;
Rottier, PJM .
VIROLOGY, 2002, 296 (01) :177-189
[6]   Severe acute respiratory syndrome coronavirus protein 7a interacts with hSGT [J].
Fielding, BC ;
Gunalan, V ;
Tan, THP ;
Chou, CF ;
Shen, S ;
Khan, S ;
Lim, SG ;
Hong, W ;
Tan, YJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 343 (04) :1201-1208
[7]   Characterization of a unique group-specific protein (U122) of the severe acute respiratory syndrome coronavirus [J].
Fielding, BC ;
Tan, YJ ;
Shuo, S ;
Tan, THP ;
Ooi, EE ;
Lim, SG ;
Hong, WJ ;
Goh, PY .
JOURNAL OF VIROLOGY, 2004, 78 (14) :7311-7318
[8]  
FRIEMAN M, 2007, J VIROL
[9]  
FRIEMAN M, 2007, VIRUS RES
[10]   The putative protein 6 of the severe acute respiratory syndrome-aassociated coronavirus: Expression and functional characterization [J].
Geng, H ;
Liu, YM ;
Chan, WS ;
Lo, AWI ;
Au, DMY ;
Waye, MMY ;
Ho, YY .
FEBS LETTERS, 2005, 579 (30) :6763-6768