EXPRESSION OF AN ANIMAL VIRUS ANTIGENIC SITE ON THE SURFACE OF A PLANT-VIRUS PARTICLE

被引:151
作者
USHA, R
ROHLL, JB
SPALL, VE
SHANKS, M
MAULE, AJ
JOHNSON, JE
LOMONOSSOFF, GP
机构
[1] JOHN INNES INST,JOHN INNES CTR,DEPT VIRUS RES,COLNEY LANE,NORWICH NR4 7UH,NORFOLK,ENGLAND
[2] PURDUE UNIV,DEPT BIOL,W LAFAYETTE,IN 47907
关键词
D O I
10.1006/viro.1993.1598
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
To investigate if cowpea mosaic virus (CPMV) particles can be used to express foreign protein sequences, oligonucleotides encoding an epitope derived from VP1 of foot-and-mouth disease virus (FMDV) were cloned into the region of the CPMV genome encoding the small (S) coat protein. The chimeras were designed so that the foreign sequence was expressed either as an insertion or as a replacement for part of the wild-type sequence. While RNA from both chimeras was able to replicate in cowpea protoplasts only the construct containing the FMDV sequence as an insertion was able to direct capsid formation and infect whole cowpea plants. The modified S protein produced in plants infected with the insertion derivative reacted with FMDV-specific antiserum. These results show that CPMV can be used as an antigen presentation system and raises the possibility of producing vaccines in plants using a RNA virus-based vector. © 1993 Academic Press, Inc.
引用
收藏
页码:366 / 374
页数:9
相关论文
共 38 条
[1]   THE EXPRESSION OF HYBRID HIV-TY VIRUS-LIKE PARTICLES IN YEAST [J].
ADAMS, SE ;
DAWSON, KM ;
GULL, K ;
KINGSMAN, SM ;
KINGSMAN, AJ .
NATURE, 1987, 329 (6134) :68-70
[2]   PROTECTION AGAINST FOOT-AND-MOUTH-DISEASE BY IMMUNIZATION WITH A CHEMICALLY SYNTHESIZED PEPTIDE PREDICTED FROM THE VIRAL NUCLEOTIDE-SEQUENCE [J].
BITTLE, JL ;
HOUGHTEN, RA ;
ALEXANDER, H ;
SHINNICK, TM ;
SUTCLIFFE, JG ;
LERNER, RA ;
ROWLANDS, DJ ;
BROWN, F .
NATURE, 1982, 298 (5869) :30-33
[3]   A RAPID, SENSITIVE METHOD FOR DETECTION OF ALKALINE-PHOSPHATASE CONJUGATED ANTI-ANTIBODY ON WESTERN BLOTS [J].
BLAKE, MS ;
JOHNSTON, KH ;
RUSSELLJONES, GJ ;
GOTSCHLICH, EC .
ANALYTICAL BIOCHEMISTRY, 1984, 136 (01) :175-179
[4]   ANTIGEN CHIMERAS OF POLIOVIRUS AS POTENTIAL NEW VACCINES [J].
BURKE, KL ;
DUNN, G ;
FERGUSON, M ;
MINOR, PD ;
ALMOND, JW .
NATURE, 1988, 332 (6159) :81-82
[5]   IMPROVED IMMUNOGENICITY OF A PEPTIDE EPITOPE AFTER FUSION TO HEPATITIS-B CORE PROTEIN [J].
CLARKE, BE ;
NEWTON, SE ;
CARROLL, AR ;
FRANCIS, MJ ;
APPLEYARD, G ;
SYRED, AD ;
HIGHFIELD, PE ;
ROWLANDS, DJ ;
BROWN, F .
NATURE, 1987, 330 (6146) :381-384
[6]   POLIOVIRUS CHIMERAS EXPRESSING SEQUENCES FROM THE PRINCIPAL NEUTRALIZATION DOMAIN OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 [J].
DEDIEU, JF ;
RONCO, J ;
VANDERWERF, S ;
HOGLE, JM ;
HENIN, Y ;
GIRARD, M .
JOURNAL OF VIROLOGY, 1992, 66 (05) :3161-3167
[7]   A POLIOVIRUS NEUTRALIZATION EPITOPE EXPRESSED ON HYBRID HEPATITIS-B SURFACE-ANTIGEN PARTICLES [J].
DELPEYROUX, F ;
CHENCINER, N ;
LIM, A ;
MALPIECE, Y ;
BLONDEL, B ;
CRAINIC, R ;
VANDERWERF, S ;
STREECK, RE .
SCIENCE, 1986, 233 (4762) :472-475
[8]   MUTATIONAL ANALYSIS OF THE PUTATIVE CATALYTIC TRIAD OF THE COWPEA MOSAIC-VIRUS 24K PROTEASE [J].
DESSENS, JT ;
LOMONOSSOFF, GP .
VIROLOGY, 1991, 184 (02) :738-746
[9]   IMPROVEMENTS OF THE INFECTIVITY OF INVITRO TRANSCRIPTS FROM CLONED COWPEA MOSAIC-VIRUS CDNA - IMPACT OF TERMINAL NUCLEOTIDE-SEQUENCES [J].
EGGEN, R ;
VERVER, J ;
WELLINK, J ;
DEJONG, A ;
GOLDBACH, R ;
VANKAMMEN, A .
VIROLOGY, 1989, 173 (02) :447-455
[10]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13