Protection of swine by live and inactivated vaccines prepared from a leader proteinase-deficient serotype A12 foot-and-mouth disease virus

被引:82
作者
Chinsangaram, J [1 ]
Mason, PW [1 ]
Grubman, MJ [1 ]
机构
[1] ARS, USDA, NAA, Plum Isl Anim Dis Ctr, Greenport, NY 11944 USA
关键词
foot-and-mouth disease; attenuated vaccine; swine;
D O I
10.1016/S0264-410X(98)00029-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previously, we demonstrated that a genetically engineered variant of foot-and-mouth disease virus (FMDV) serotype A12 lacking the leader proteinase-coding region (A12-LLV2) was attenuated and induced an immune response that partially protected cattle from FMD. In this study A12-LLV2 was tested in swine as a live or chemically inactivated vaccine. Animals vaccinated with chemically inactivated A12-LLV2 or wild-type (WT) virus in oil adjuvant developed high levels of neutralizing antibodies and were protected from FMD upon challenge. Animals vaccinated with live A12-LLV2 did not exhibit signs of FMD, did not spread virus to other animals, developed a neutralizing antibody response and antibodies to nonstructural protein 3D, and were partially protected from FMD. Animals given a similar dose of chemically inactivated A12-LLV2 in the absence of adjuvant developed a poor immune response and were not protected from FMD, indicating that limited replication was responsible for the improved immune response found in animals vaccinated with live A12-LLV2. The results demonstrate the potential of A12-LLV2 as a live-attenuated vaccine as well as a safe source of antigen for chemically inactivated vaccines. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1516 / 1522
页数:7
相关论文
共 28 条
[1]  
Bachrach H. L., 1978, Viruses and environment, P299
[2]   FOOT-AND-MOUTH DISEASE [J].
BACHRACH, HL .
ANNUAL REVIEW OF MICROBIOLOGY, 1968, 22 :201-+
[3]   INACTIVATION OF VIRAL-ANTIGENS FOR VACCINE PREPARATION WITH PARTICULAR REFERENCE TO THE APPLICATION OF BINARY ETHYLENIMINE [J].
BAHNEMANN, HG .
VACCINE, 1990, 8 (04) :299-303
[4]   DEVELOPMENTS IN FOOT-AND-MOUTH-DISEASE VACCINES [J].
BARTELING, SJ ;
VREESWIJK, J .
VACCINE, 1991, 9 (02) :75-88
[5]   SUBTYPING OF EUROPEAN FOOT-AND-MOUTH-DISEASE VIRUS-STRAINS BY NUCLEOTIDE-SEQUENCE DETERMINATION [J].
BECK, E ;
STROHMAIER, K .
JOURNAL OF VIROLOGY, 1987, 61 (05) :1621-1629
[6]   PORTRAITS OF VIRUSES - FOOT-AND-MOUTH-DISEASE VIRUS .8. [J].
BROOKSBY, JB .
INTERVIROLOGY, 1982, 18 (1-2) :1-23
[7]   Pathogenesis of wild-type and leaderless foot-and-mouth disease virus in cattle [J].
Brown, CC ;
Piccone, ME ;
Mason, PW ;
McKenna, TSC ;
Grubman, MJ .
JOURNAL OF VIROLOGY, 1996, 70 (08) :5638-5641
[8]   NEW APPROACHES TO VACCINATION AGAINST FOOT-AND-MOUTH-DISEASE [J].
BROWN, F .
VACCINE, 1992, 10 (14) :1022-1026
[9]  
Cottral G E, 1965, Bull Off Int Epizoot, V63, P1607
[10]   LEADER PROTEIN OF FOOT-AND-MOUTH-DISEASE VIRUS IS REQUIRED FOR CLEAVAGE OF THE P220 COMPONENT OF THE CAP-BINDING PROTEIN COMPLEX [J].
DEVANEY, MA ;
VAKHARIA, VN ;
LLOYD, RE ;
EHRENFELD, E ;
GRUBMAN, MJ .
JOURNAL OF VIROLOGY, 1988, 62 (11) :4407-4409