Viral security proteins: counteracting host defences

被引:62
作者
Agol, Vadim I. [1 ,2 ]
Gmyl, Anatoly P. [1 ]
机构
[1] Russian Acad Med Sci, MP Chumakov Inst Poliomyelitis & Viral Encephalit, Moscow 142782, Russia
[2] Moscow MV Lomonosov State Univ, Moscow 119899, Russia
基金
俄罗斯基础研究基金会;
关键词
MOUTH-DISEASE VIRUS; MURINE ENCEPHALOMYELITIS VIRUS; HEPATITIS-A VIRUS; APOPTOTIC CELL-DEATH; ALPHA/BETA INTERFERON-PRODUCTION; MEDIATED DEMYELINATING DISEASE; POLYMERASE-II TRANSCRIPTION; TRANSLATION INITIATION SITE; STRANDED RNA VIRUSES; L-ASTERISK PROTEIN;
D O I
10.1038/nrmicro2452
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Interactions with host defences are key aspects of viral infection. Various viral proteins perform counter-defensive functions, but a distinct class, called security proteins, is dedicated specifically to counteracting host defences. Here, the properties of the picornavirus security proteins L and 2A are discussed. These proteins have well-defined positions in the viral polyprotein, flanking the capsid precursor, but they are structurally and biochemically unrelated. Here, we consider the impact of these two proteins, as well as that of a third security protein, L*, on viral reproduction, pathogenicity and evolution. The concept of security proteins could serve as a paradigm for the dedicated counter-defensive proteins of other viruses.
引用
收藏
页码:867 / 878
页数:12
相关论文
共 134 条
[1]  
Agol VI., 2010, PICORNAVIRUSES MOL B, P239
[2]   Inhibition of U snRNP assembly by a virus-encoded proteinase [J].
Almstead, Laura L. ;
Sarnow, Peter .
GENES & DEVELOPMENT, 2007, 21 (09) :1086-1097
[3]   Encephalomyocarditis virus (EMCV) proteins 2A and 3BCD localize to nuclei and inhibit cellular mRNA transcription but not rRNA transcription [J].
Aminev, AG ;
Amineva, SP ;
Palmenberg, AC .
VIRUS RESEARCH, 2003, 95 (1-2) :59-73
[4]   Encephalomyocarditis viral protein 2A localizes to nucleoli and inhibits cap-dependent mRNA translation [J].
Aminev, AG ;
Amineva, SP ;
Palmenberg, AC .
VIRUS RESEARCH, 2003, 95 (1-2) :45-57
[5]   MORPHOGENESIS OF HEPATITIS-A VIRUS - ISOLATION AND CHARACTERIZATION OF SUBVIRAL PARTICLES [J].
ANDERSON, DA ;
ROSS, BC .
JOURNAL OF VIROLOGY, 1990, 64 (11) :5284-5289
[6]   A case for "StopGo'': Reprogramming translation to augment codon meaning of GGN by promoting unconventional termination (Stop) after addition of glycine and then allowing continued translation (Go) [J].
Atkins, John F. ;
Wills, Norma M. ;
Loughran, Gary ;
Wu, Chih-Yu ;
Parsawar, Krishna ;
Ryan, Martin D. ;
Wang, Chung-Hsiung ;
Nelson, Chad C. .
RNA, 2007, 13 (06) :803-810
[7]   Early phosphatidylinositol 3-kinase/Akt pathway activation limits poliovirus-induced JNK-mediated cell death [J].
Autret, Arnaud ;
Martin-Latil, Sandra ;
Brisac, Cynthia ;
Mousson, Laurence ;
Colbere-Garapin, Florence ;
Blondel, Bruno .
JOURNAL OF VIROLOGY, 2008, 82 (07) :3796-3802
[8]   Enteroviral protease 2A cleaves dystrophin: Evidence of cytoskeletal disruption in an acquired cardiomyopathy [J].
Badorff, C ;
Lee, GH ;
Lamphear, BJ ;
Martone, ME ;
Campbell, KP ;
Rhoads, RE ;
Knowlton, KU .
NATURE MEDICINE, 1999, 5 (03) :320-326
[9]   Mengovirus-Induced Rearrangement of the Nuclear Pore Complex: Hijacking Cellular Phosphorylation Machinery [J].
Bardina, Maryana V. ;
Lidsky, Peter V. ;
Sheval, Eugene V. ;
Fominykh, Ksenia V. ;
van Kuppeveld, Frank J. M. ;
Polyakov, Vladimir Y. ;
Agol, Vadim I. .
JOURNAL OF VIROLOGY, 2009, 83 (07) :3150-3161
[10]   RIG-I is cleaved during picornavirus infection [J].
Barral, Paola M. ;
Sarkar, Devanand ;
Fisher, Paul B. ;
Racaniello, Vincent R. .
VIROLOGY, 2009, 391 (02) :171-176