GENETIC-VARIATION OF FOOT-AND-MOUTH-DISEASE VIRUS FROM FIELD OUTBREAKS TO LABORATORY ISOLATION

被引:30
作者
MEYER, RF
PACCIARINI, M
HILYARD, EJ
FERRARI, S
VAKHARIA, VN
DONINI, G
BROCCHI, E
MOLITOR, TW
机构
[1] INST ZOOPROFILATT SPERIMENTALE,DEPT BIOTECHNOL,BRESCIA,ITALY
[2] UNIV MARYLAND,CTR AGR BIOTECHNOL,COLL PK,MD 20742
[3] COLL VET MED,COLL PK,MD
[4] UNIV MINNESOTA,DEPT CLIN & POPULAT SCI,ST PAUL,MN 55108
关键词
FOOT-AND-MOUTH DISEASE VIRUS; POLYMERASE CHAIN REACTION; GENETIC VARIATION;
D O I
10.1016/0168-1702(94)90079-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Foot-and-mouth disease virus (FMDV), by nature of its RNA genome, possesses a high rate of mutation during replication. This results in extensive genetic polymorphism of virus populations in nature. The emergence of FMDV variants during replication has been reported. Genetic changes in the viral capsid protein (VP1) gene can result in amino acid changes affecting the immunodominant epitopes of FMDV. The genetic heterogeneity of FMDV in the field and the antigenic variants observed after cell culture isolation has been investigated by PCR sequencing and reactivity with monoclonal antibodies. These methods were applied to viruses causing two different outbreaks of FMD before and after replication in cell culture and in the animal host. The VP1 region of the genome was amplified by PCR and sequenced to reveal variant sequences identified after passage and to determine their presence in the original field tissue. In one case, reactivity with monoclonal antibodies was lost after passage as a result of an amino acid change in the subpopulation. These findings suggest that host cells can select specific virus genetic and antigenic subpopulations during virus isolation and propagation.
引用
收藏
页码:299 / 312
页数:14
相关论文
共 38 条
[31]   CONSERVATION OF THE PUTATIVE RECEPTOR ATTACHMENT SITE IN PICORNAVIRUSES [J].
ROSSMANN, MG ;
PALMENBERG, AC .
VIROLOGY, 1988, 164 (02) :373-382
[32]   CHEMICAL BASIS OF ANTIGENIC VARIATION IN FOOT-AND-MOUTH-DISEASE VIRUS [J].
ROWLANDS, DJ ;
CLARKE, BE ;
CARROLL, AR ;
BROWN, F ;
NICHOLSON, BH ;
BITTLE, JL ;
HOUGHTEN, RA ;
LERNER, RA .
NATURE, 1983, 306 (5944) :694-697
[33]   EVALUATION OF A TRAPPING ELISA FOR THE DIFFERENTIATION OF FOOT-AND-MOUTH-DISEASE VIRUS-STRAINS USING MONOCLONAL-ANTIBODIES [J].
SAMUEL, AR ;
KNOWLES, NJ ;
SAMUEL, GD ;
CROWTHER, JR .
BIOLOGICALS, 1991, 19 (04) :299-310
[34]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467
[35]   FIXATION OF MUTATIONS IN THE VIRAL GENOME DURING AN OUTBREAK OF FOOT-AND-MOUTH-DISEASE - HETEROGENEITY AND RATE VARIATIONS [J].
SOBRINO, F ;
PALMA, EL ;
BECK, E ;
DAVILA, M ;
DELATORRE, JC ;
NEGRO, P ;
VILLANUEVA, N ;
ORTIN, J ;
DOMINGO, E .
GENE, 1986, 50 (1-3) :149-159
[36]   MULTIPLE GENETIC-VARIANTS ARISE IN THE COURSE OF REPLICATION OF FOOT-AND-MOUTH-DISEASE VIRUS IN CELL-CULTURE [J].
SOBRINO, F ;
DAVILA, M ;
ORTIN, J ;
DOMINGO, E .
VIROLOGY, 1983, 128 (02) :310-318
[37]  
STOHMAIER K, 1982, J GEN VIROL, V59, P295
[38]   SEQUENCE VARIATION IN THE GENE FOR THE IMMUNOGENIC CAPSID PROTEIN VP1 OF FOOT-AND-MOUTH-DISEASE VIRUS TYPE-A [J].
WEDDELL, GN ;
YANSURA, DG ;
DOWBENKO, DJ ;
HOATLIN, ME ;
GRUBMAN, MJ ;
MOORE, DM ;
KLEID, DG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) :2618-2622