Molecular mechanisms of poliovirus persistence:: key role of capsid determinants during the establishment phase

被引:18
作者
Pelletier, I [1 ]
Duncan, G [1 ]
Pavio, N [1 ]
Colbère-Garapin, F [1 ]
机构
[1] Inst Pasteur, Unite Neurovirol & Regenerat Syst Nerveux, Grp Genet Virale, F-75724 Paris 15, France
关键词
virus; poliovirus; picornavirus; mutations; capsid; persistence; receptor;
D O I
10.1007/s000180050261
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As viral persistence is of major medical importance, well-characterized, simple models are needed to improve our understanding of persistent infections. We have chosen to study the molecular mechanisms of viral persistence with the poliovirus (PV), because this picornavirus is one of the best characterized animal viruses, it infects the central nervous system which is a target organ for viral persistence, and it belongs to the Picornaviridae family of viruses, which includes several naturally persisting viruses. We have developed models of PV persistence in neuronal and epidermoid cells, and the present review will focus on the latter one because both lytic and persistent PV strains can be used to study the PV-HEp-2 cell interactions. The viral determinants of persistence have been investigated with this model, and PV determinants have proven to be of crucial importance for the establishment of persistence in HEp-2 cells. Precise determinants of PV persistence have been identified for PV serotypes 1 and 3, in capsid proteins VP1 and VP2. These determinants modify the early steps of the PV cycle, and in particular, the conformational modifications of the capsid following virus adsorption onto its receptor. These results permit us to propose several hypotheses concerning PV persistence and the early steps of the PV cycle.
引用
收藏
页码:1385 / 1402
页数:18
相关论文
共 107 条
[1]   EVOLUTION OF MOUSE HEPATITIS-VIRUS (MHV) DURING CHRONIC INFECTION - QUASI-SPECIES NATURE OF THE PERSISTING MHV RNA [J].
ADAMI, C ;
POOLEY, J ;
GLOMB, J ;
STECKER, E ;
FAZAL, F ;
FLEMING, JO ;
BAKER, SC .
VIROLOGY, 1995, 209 (02) :337-346
[2]  
AHMED R, 1996, VIROLOGY, P219
[3]  
Ansardi DC, 1996, ADV VIRUS RES, V46, P1, DOI 10.1016/S0065-3527(08)60069-X
[4]   K562 CELL STRAINS DIFFER IN THEIR RESPONSE TO POLIOVIRUS INFECTION [J].
BENTON, PA ;
MURPHY, JW ;
LLOYD, RE .
VIROLOGY, 1995, 213 (01) :7-18
[5]   MOLECULAR CHARACTERIZATION OF THE CELLULAR RECEPTOR FOR POLIOVIRUS [J].
BERNHARDT, G ;
BIBB, JA ;
BRADLEY, J ;
WIMMER, E .
VIROLOGY, 1994, 199 (01) :105-113
[6]  
BIENZ K, 1994, ARCH VIROL, P147
[7]   Molecular aspects of poliovirus biology with a special focus on the interactions with nerve cells [J].
Blondel, B ;
Duncan, G ;
Couderc, T ;
Delpeyroux, F ;
Pavio, N ;
Colbère-Garapin, F .
JOURNAL OF NEUROVIROLOGY, 1998, 4 (01) :1-26
[8]   PERSISTENT POLIOVIRUS INFECTION - ESTABLISHMENT AND MAINTENANCE INVOLVE DISTINCT MECHANISMS [J].
BORZAKIAN, S ;
COUDERC, T ;
BARBIER, Y ;
ATTAL, G ;
PELLETIER, I ;
COLBEREGARAPIN, F .
VIROLOGY, 1992, 186 (02) :398-408
[9]   PRECISE MISSENSE AND SILENT POINT MUTATIONS ARE FIXED IN THE GENOMES OF POLIOVIRUS MUTANTS FROM PERSISTENTLY INFECTED-CELLS [J].
BORZAKIAN, S ;
PELLETIER, I ;
CALVEZ, V ;
COLBEREGARAPIN, F .
JOURNAL OF VIROLOGY, 1993, 67 (05) :2914-2917
[10]   THEILERS VIRUS PERSISTS IN GLIAL-CELLS DURING DEMYELINATING DISEASE [J].
BRAHIC, M ;
STROOP, WG ;
BARINGER, JR .
CELL, 1981, 26 (01) :123-128