Application of phage display in selecting Tomato spotted wilt virus-specific single-chain antibodies (scFvs) for sensitive diagnosis in ELISA

被引:24
作者
Griep, RA
Prins, M
van Twisk, C
Keller, HJHG
Kerschbaumer, RJ
Kormelink, R
Goldbach, RW
Schots, A
机构
[1] Wageningen Univ Agr, Lab Monoclonal Antibodies, NL-6700 ES Wageningen, Netherlands
[2] Agr Univ Wageningen, Virol Lab, NL-6709 PD Wageningen, Netherlands
[3] Agr Univ Vienna, Inst Appl Microbiol, A-1190 Vienna, Austria
关键词
D O I
10.1094/PHYTO.2000.90.2.183
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A panel of recombinant single-chain antibodies (scFvs) against structural proteins of Tomato spotted wilt virus (TSWV) was retrieved from a human combinatorial scFv antibody library using the novel phage display technique. After subcloning the encoding DNA sequences in the expression vector pSKAP/S, which allowed the scFvs to be expressed as alkaline phosphatase fusion proteins, 17 different scFv antibodies were obtained. Of these, 12 scFvs were directed against the nucleoprotein (N) and 5, putatively, against the glycoproteins (G1 and G2). Five of the N-specific antibodies cross-reacted with two other tospoviruses (Tomato chlorotic spot virus and Groundnut ringspot virus), but none recognized the more distantly related tospoviruses Impatiens necrotic spot virus, Watermelon silverleaf mottle virus, Iris yellow spot virus, or Physalis severe mottle virus. The successful use of one of the antibodies as coating and detection reagent in a double-antibody sandwich enzyme-linked immunosorbent assay showed the potential of the phage display system in obtaining antibodies for routine TSWV diagnosis.
引用
收藏
页码:183 / 190
页数:8
相关论文
共 37 条
[1]  
Adam G., 1995, Bulletin OEPP, V25, P247, DOI 10.1111/j.1365-2338.1995.tb01465.x
[2]  
Adam G., 1996, Acta Horticulturae, P135
[3]   CHARACTERISTICS OF MICROPLATE METHOD OF ENZYME-LINKED IMMUNOSORBENT ASSAY FOR DETECTION OF PLANT-VIRUSES [J].
CLARK, MF ;
ADAMS, AN .
JOURNAL OF GENERAL VIROLOGY, 1977, 34 (MAR) :475-483
[4]   Molecular and serological characterization of iris yellow spot virus, a new and distinct tospovirus species [J].
Cortês, I ;
Livieratos, IC ;
Derks, A ;
Peters, D ;
Kormelink, R .
PHYTOPATHOLOGY, 1998, 88 (12) :1276-1282
[5]   CLASSIFICATION OF TOSPOVIRUSES BASED ON PHYLOGENY OF NUCLEOPROTEIN GENE-SEQUENCES [J].
DEAVILA, AC ;
DEHAAN, P ;
KORMELINK, R ;
RESENDE, RD ;
GOLDBACH, RW ;
PETERS, D .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :153-159
[6]   SEROLOGICAL DIFFERENTIATION OF 20 ISOLATES OF TOMATO SPOTTED WILT VIRUS [J].
DEAVILA, AC ;
HUGUENOT, C ;
RESENDE, RD ;
KITAJIMA, EW ;
GOLDBACH, RW ;
PETERS, D .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :2801-2807
[7]  
DEHAAN P, 1989, GENETICS AND PATHOGENICITY OF NEGATIVE STRAND VIRUSES, P287
[8]   POSSIBLE CAUSES OF THE EMERGENCE OF TOSPOVIRUS DISEASES [J].
GOLDBACH, R ;
PETERS, D .
SEMINARS IN VIROLOGY, 1994, 5 (02) :113-120
[9]   TOMATO SPOTTED WILT VIRUS IN PAPAYA AND DETECTION OF THE VIRUS BY ELISA [J].
GONSALVES, D ;
TRUJILLO, EE .
PLANT DISEASE, 1986, 70 (06) :501-506
[10]   pSKAP/S: An expression vector for the production of single-chain Fv alkaline phosphatase fusion proteins [J].
Griep, RA ;
van Twisk, C ;
Kerschbaumer, RJ ;
Harper, K ;
Torrance, L ;
Himmler, G ;
van der Wolf, JM ;
Schots, A .
PROTEIN EXPRESSION AND PURIFICATION, 1999, 16 (01) :63-69