CHARACTERIZATION OF AN ACID-RESISTANT MUTANT OF FOOT-AND-MOUTH-DISEASE VIRUS

Citation
T. Twomey et al., CHARACTERIZATION OF AN ACID-RESISTANT MUTANT OF FOOT-AND-MOUTH-DISEASE VIRUS, Virology, 206(1), 1995, pp. 69-75
Citations number
17
Categorie Soggetti
Virology
Journal title
ISSN journal
00426822
Volume
206
Issue
1
Year of publication
1995
Pages
69 - 75
Database
ISI
SICI code
0042-6822(1995)206:1<69:COAAMO>2.0.ZU;2-Q
Abstract
A foot-and-mouth disease virus mutant which is stable at pH 6.4 has be en isolated from a virus of serotype A. In contrast to the parent (P) virus, which gave a mixture of large and small plaques in BHK21 cells and in a bovine kidney cell line, the acid-resistant (AR) virus gave s mall plaques which did not increase markedly in size after 24 hr. The infectivity titer of the acid-resistant virus was about 100-fold lower in suckling mice than in BHK21 cells, whether the inoculation was mad e intraperitoneally or intracerebrally, whereas the parent virus gave similar titers in both systems. Furthermore, in mice the AR virus reac hed its end point two to three times more slowly. The diameter of the AR virus was almost 20% less than that of the P virus and it had a mor e distinct topography, but the two viruses cosedimented in sucrose gra dients. However, the buoyant density in CsCl of the AR virus was sligh tly lower (1.42 compared with 1.43 g/cc) in coruns. The RNAs and capsi d proteins of the two viruses gave similar profiles in sucrose gradien ts and by SDS-PAGE, respectively. However, isoelectric focusing of the capsid proteins revealed considerable differences between the two vir uses. Whereas the P virus gave four protein bands, corresponding to VP 1-VP4, the AR virus gave one band for VP4, two for VP3, two for VP2, a nd four for VP1. Sequence analysis of the genes coding for the capsid protein regions of the two viruses showed four changes (one silent), r esulting in an Ala-3 --> Ser substitution in VP1 and Glu-131 --> Lys a nd Asp-133 --> Ser substitutions in VP2. (C) 1995 Academic Press, Inc.