RECEPTOR-BINDING SITE-DELETED FOOT-AND-MOUTH-DISEASE (FMD) VIRUS PROTECTS CATTLE FROM FMD

被引:68
作者
MCKENNA, TSC [1 ]
LUBROTH, J [1 ]
RIEDER, E [1 ]
BAXT, B [1 ]
MASON, PW [1 ]
机构
[1] USDA ARS,PLUM ISL ANIM DIS CTR,GREENPORT,NY 11944
关键词
D O I
10.1128/JVI.69.9.5787-5790.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Binding of foot-and-mouth disease virus (FMDV) to cells requires an arginine-glycine-aspartic acid (RGD) sequence in the capsid protein VP1. We have genetically engineered an FMDV in which these three amino acids have been deleted, producing a virus particle which is unable to bind to cells. Cattle vaccinated with these receptor binding site-deleted virions were protected from disease when challenged with a virulent virus, demonstrating that these RGD deleted viruses could serve as the basis for fool-and-mouth disease vaccines safer than those currently in use. This strategy may prove useful in the development of vaccines for other viral diseases.
引用
收藏
页码:5787 / 5790
页数:4
相关论文
共 21 条
[11]   NEW OBSERVATIONS ON ANTIGENIC DIVERSIFICATION OF RNA VIRUSES - ANTIGENIC VARIATION IS NOT DEPENDENT ON IMMUNE SELECTION [J].
DOMINGO, E ;
DIEZ, J ;
MARTINEZ, MA ;
HERNANDEZ, J ;
HOLGUIN, A ;
BORREGO, B ;
MATEU, MG .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :2039-2045
[12]  
Domingo E., 1990, Applied Virology Research, V2, P233
[13]   THE CELL ATTACHMENT SITE ON FOOT-AND-MOUTH-DISEASE VIRUS INCLUDES THE AMINO-ACID SEQUENCE RGD (ARGININE-GLYCINE-ASPARTIC ACID) [J].
FOX, G ;
PARRY, NR ;
BARNETT, PV ;
MCGINN, B ;
ROWLANDS, DJ ;
BROWN, F .
JOURNAL OF GENERAL VIROLOGY, 1989, 70 :625-637
[14]   STRUCTURE OF A MAJOR IMMUNOGENIC SITE ON FOOT-AND-MOUTH-DISEASE VIRUS [J].
LOGAN, D ;
ABUGHAZALEH, R ;
BLAKEMORE, W ;
CURRY, S ;
JACKSON, T ;
KING, A ;
LEA, S ;
LEWIS, R ;
NEWMAN, J ;
PARRY, N ;
ROWLANDS, D ;
STUART, D ;
FRY, E .
NATURE, 1993, 362 (6420) :566-568
[15]  
LUBROTH J, IN PRESS RES VET SCI
[16]   RGD SEQUENCE OF FOOT-AND-MOUTH-DISEASE VIRUS IS ESSENTIAL FOR INFECTING CELLS VIA THE NATURAL RECEPTOR BUT CAN BE BYPASSED BY AN ANTIBODY-DEPENDENT ENHANCEMENT PATHWAY [J].
MASON, PW ;
RIEDER, E ;
BAXT, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (05) :1932-1936
[17]   STRUCTURAL AND SEROLOGICAL EVIDENCE FOR A NOVEL MECHANISM OF ANTIGENIC VARIATION IN FOOT-AND-MOUTH-DISEASE VIRUS [J].
PARRY, N ;
FOX, G ;
ROWLANDS, D ;
BROWN, F ;
FRY, E ;
ACHARYA, R ;
LOGAN, D ;
STUART, D .
NATURE, 1990, 347 (6293) :569-572
[18]  
Pereira H.G., 1981, VIRUS DISEASES FOOD, P333
[19]   VACCINES PREPARED FROM CHIMERAS OF FOOT-AND-MOUTH-DISEASE VIRUS (FMDV) INDUCE NEUTRALIZING ANTIBODIES AND PROTECTIVE IMMUNITY TO MULTIPLE SEROTYPES OF FMDV [J].
RIEDER, E ;
BAXT, B ;
LUBROTH, J ;
MASON, PW .
JOURNAL OF VIROLOGY, 1994, 68 (11) :7092-7098
[20]   GENETICALLY-ENGINEERED FOOT-AND-MOUTH-DISEASE VIRUSES WITH POLY(C) TRACTS OF 2 NUCLEOTIDES ARE VIRULENT IN MICE [J].
RIEDER, E ;
BUNCH, T ;
BROWN, F ;
MASON, PW .
JOURNAL OF VIROLOGY, 1993, 67 (09) :5139-5145