Expression of tetanus toxin Fragment C in tobacco chloroplasts

被引:167
作者
Tregoning, JS
Nixon, P
Kuroda, H
Svab, Z
Clare, S
Bowe, F
Fairweather, N
Ytterberg, J
van Wijk, KJ
Dougan, G
Maliga, P
机构
[1] Rutgers State Univ, Waksman Inst, Piscataway, NJ 08854 USA
[2] Univ London Imperial Coll Sci Technol & Med, Dept Biol Sci, London SW7 2AY, England
[3] Univ London Imperial Coll Sci Technol & Med, Ctr Mol Microbiol & Infect, London SW7 2AY, England
[4] Cornell Univ, Dept Plant Biol, Ithaca, NY 14853 USA
基金
英国惠康基金;
关键词
D O I
10.1093/nar/gkg221
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fragment C (TetC) is a non-toxic 47 kDa polypeptide fragment of tetanus toxin that can be used as a subunit vaccine against tetanus. Expression of TetC in Escherichia coli and yeast was dependent on the availability of synthetic genes that were required to improve translation efficiency and stabilize the mRNA. To explore the feasibility of producing TetC in tobacco leaves, we attempted expression of both the bacterial high-AT (72.3% AT) and the synthetic higher-GC genes (52.5% AT) in tobacco chloroplasts. We report here that the bacterial high-AT mRNA is stable in tobacco chloroplasts. Significant TetC accumulation was obtained from both genes, 25 and 10% of total soluble cellular protein, respectively, proving the versatility of plastids for expression of unmodified high-AT and high-GC genes. Mucosal immunization of mice with the plastid- produced TetC induced protective levels of TetC antibodies. Thus, expression of TetC in chloroplasts provides a potential route towards the development of a safe, plant-based tetanus vaccine for nasal and oral applications.
引用
收藏
页码:1174 / 1179
页数:6
相关论文
共 33 条
[1]   Immune response in mice following immunization with DNA encoding fragment C of tetanus toxin [J].
Anderson, R ;
Gao, XM ;
Papakonstantinopoulou, A ;
Roberts, M ;
Dougan, G .
INFECTION AND IMMUNITY, 1996, 64 (08) :3168-3173
[2]   Analysis of the N-glycosylation of recombinant glycoproteins produced in transgenic plants [J].
Bardor, M ;
Faye, L ;
Lerouge, P .
TRENDS IN PLANT SCIENCE, 1999, 4 (09) :376-380
[3]   Transgenic plastids in basic research and plant biotechnology [J].
Bock, R .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 312 (03) :425-438
[4]   KANAMYCIN RESISTANCE AS A SELECTABLE MARKER FOR PLASTID TRANSFORMATION IN TOBACCO [J].
CARRER, H ;
HOCKENBERRY, TN ;
SVAB, Z ;
MALIGA, P .
MOLECULAR AND GENERAL GENETICS, 1993, 241 (1-2) :49-56
[5]   SYNTHESIS OF TETANUS TOXIN FRAGMENT-C IN INSECT CELLS BY USE OF A BACULOVIRUS EXPRESSION SYSTEM [J].
CHARLES, IG ;
RODGERS, BC ;
MAKOFF, AJ ;
CHATFIELD, SN ;
SLATER, DE ;
FAIRWEATHER, NF .
INFECTION AND IMMUNITY, 1991, 59 (05) :1627-1632
[6]   Intranasal immunogenicity and adjuvanticity of site-directed mutant derivatives of cholera toxin [J].
Douce, G ;
Fontana, M ;
Pizza, M ;
Rappuoli, R ;
Dougan, G .
INFECTION AND IMMUNITY, 1997, 65 (07) :2821-2828
[7]   CHARACTERIZATION OF RECOMBINANT TETANUS TOXIN DERIVATIVES SUITABLE FOR VACCINE DEVELOPMENT [J].
FIGUEIREDO, D ;
TURCOTTE, C ;
FRANKEL, G ;
LI, Y ;
DOLLY, O ;
WILKIN, G ;
MARRIOTT, D ;
FAIRWEATHER, N ;
DOUGAN, G .
INFECTION AND IMMUNITY, 1995, 63 (08) :3218-3221
[8]   Development of a GFP reporter gene for Chlamydomonas reinhardtii chloroplast [J].
Franklin, S ;
Ngo, B ;
Efuet, E ;
Mayfield, SP .
PLANT JOURNAL, 2002, 30 (06) :733-744
[9]   Transgenic plants as factories for biopharmaceuticals [J].
Giddings, G ;
Allison, G ;
Brooks, D ;
Carter, A .
NATURE BIOTECHNOLOGY, 2000, 18 (11) :1151-1155
[10]   Degrading chloroplast mRNA: the role of polyadenylation [J].
Hayes, R ;
Kudla, J ;
Gruissem, W .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (05) :199-202