Abstract
Fumonisins produced by Fusarium pathogens are mycotoxins present in maize and other grains in the field as well as during storage worldwide and pose a serious threat to humans and domestic animals. Fumonisin B consists of different chemotypes, and fumonisin B1 (FB1) is the most predominant fumonisin found in food/feed commodities. Recombinant antibody can be deployed to analyze the fumonisin toxicological mechanism and develop a simple and cost-effective method for the detection of fumonisins, which is vitally important for monitoring and preventing fumonisins from entering food/feed chains. In this study, FB1 conjugated to keyhole limpet hemocyanin was used to immunize mice, from which RNA was isolated to construct a recombinant antibody library. Successive panning of the library by phage display was used to select monoclonal phage clones reactive to FB1 conjugated to bovine serum albumin. Subsequent phage ELISA and sequencing analyses revealed four different reactive scFv antibodies specific to FB1. Soluble expression and ELISA analysis showed that one scFv antibody, FBMA1, had the highest reactivity and could be purified from bacterial cells in large quantities. Surface plasmon resonance measurements further revealed that the FBMA1 scFv antibody had a binding kinetics of K D = 1.89 × 10–7 M. Molecular modeling and docking analyses suggested that the FBMA1 antibody shaped a proper cavity to embed the whole FB1 molecule and that a steady-state complex was formed relying on intermolecular forces, including hydrogen bonding, electrostatic force and hydrophobic interactions. Thus, the scFv antibody can be applied for mechanistic studies of intermolecular interactions and fumonisin toxicity, and for the development of an immunoassay for fumonisin-contaminated food/feed samples.
Similar content being viewed by others
References
Munkvold, G. P. and A. E. Desjardins (1997) Fumonisin in maize: Can we reduce their occurrence? Plant Dis. 81: 556–565.
Yazar, S. and G. Z. Omurtag (2008) Fumonisins, trichothecenes and zearalenone in cereals. Int. J. Mol. Sci. 9: 2062–2090.
Soriano, J. M. and S. Dragacci (2004) Occurrence of fumonisins in foods. Food Res. Int. 37: 985–1000.
Rheeder, J. P., W. F. Marasas, and H. F.Vismer (2002) Production of fumonisin analogs by Fusarium species. Appl. Environ. Microbiol. 68: 2101–2105.
Scott, P. M. (2012) Recent research on fumonisins: A review. Food Addit. Contam. Part A Chem. Anal. Control Expo. Risk Assess. 29: 242–248.
Wang, J. H., J. B. Zhang,; H. P. Li, A. D. Gong, S. Xue, R. S. Agboola, and Y. C. Liao (2014) Molecular identification, mycotoxin production and comparative pathogenicity of Fusarium temperatum isolated from maize in China. J. Phytopathol. 162: 147–157.
Soriano, J. M., L. Gonzalez, and A. I. Catala (2005) Mechanism of action of sphingolipids and their metabolites in the toxicity of fumonisin B1. Prog. Lipid Res. 44: 345–356.
Stockmann-Juvala, H. and K. Savolainen (2008) A review of the toxic effects and mechanisms of action of fumonisin B1. Hum. Exp. Toxicol. 27: 799–809.
Rheeder, J. P., W. F. Marasas, P. G. Thiel, E. W. Sydenham, G. S. Shephard, and D. J. van Schalkwyk (1992) Fusarium moniliforme and fumonisins in corn in relation to human esophageal cancer in Transkei. Phytopathol. 82: 353–357.
Myburg, R. B., M. F. Dutton, and A. A. Chuturgoon (2002) Cytotoxicity of fumonisin B1, diethylnitrosamine, and catechol on the SNO esophageal cancer cell line. Environ. Health Perspect. 110: 813–815.
Sun, G., S. Wang, X. Hu, J. Su, T. Huang, J. Yu, L. Tang, W. Gao, and J. S. Wang (2007) Fumonisin B1 contamination of homegrown corn in high-risk areas for esophageal and liver cancer in China. Food Addit. Contam. 24: 181–185.
Ueno, Y., K. Iijima, S. D. Wang, Y. Sugiura, M. Sekijima, T. Tanaka, C. Chen, and S. Z. Yu (1997) Fumonisins as a possible contributory risk factor for primary liver cancer: A 3-year study of corn harvested in Haimen, China, by HPLC and ELISA. Food Chem. Toxicol. 35: 1143–1150.
Castegnaro, M. and C. P. Wild (1995) IARC activities in mycotoxin research. Nat. Toxins 3: 327–331.
Azcona-Olivera, J. I., M. M. Abouzied, R. D. Plattner, W. P. Norred, and J. J. Pestka (1992) Generation of antibodies reactive with fumonisins B1, B2, and B3 by using cholera toxin as the carrier-adjuvant. Appl. Environ. Microbiol. 58: 169–173.
Quan, Y., Y. Zhang, S. Wang, N. Lee, and I. R. Kennedy (2006) A rapid and sensitive chemiluminescence enzyme-linked immunosorbent assay for the determination of fumonisin B1 in food samples. Anal. Chim. Acta 580: 1–8.
Azcona-Olivera, J. I., M. M. Abouzied, R. D. Plattner, and J. J. Pestka (1992) Production of monoclonal antibodies to the mycotoxins fumonisins B1, B2 and B3. J. Agric. Food Chem. 40: 531–534.
Barna-Vetró, I., E. Szabó, B. Fazekas, and L. Solti (2000) Development of a sensitive ELISA for the determination of fumonisin B1 in cereals. J. Agric. Food Chem. 48: 2821–2825.
Min, W. K., Y. J. Cho, J. B. Park, Y. H. Bae, E. J. Kim, K. Park, and J. H. Seo (2010) Production and characterization of monoclonal antibody and its recombinant single chain variable fragment specific for a food-born mycotoxin, fumonisin B1. Bioproc. Biosyst. Eng. 33: 109–115.
Zhou, H. R., J. J. Pestka, and L. P. Hart (1996) Molecular cloning and expression of recombinant phage antibody against fumonisin B1. J. Food Prot. 59: 1208–1212.
Zou, L., Y. Xu, Y. Li, Q. He, B. Chen, and D. Wang (2014) Development of a single-chain variable fragment antibody-based enzyme-linked immunosorbent assay for determination of fumonisin B1 in corn samples. J. Sci. Food Agric. 94: 1865–1871.
Lauer, B., I. Ottleben, H. J. Jacobsen, and T. Reinard (2005) Production of a single-chain variable fragment antibody against fumonisin B1. J. Agric. Food Chem. 53: 899–904.
Li, X., P. Li, Q. Zhang, Y. Li, W. Zhang, and X. Ding (2012) Molecular characterization of monoclonal antibodies against aflatoxins: A possible explanation for the highest sensitivity. Anal. Chem. 84: 5229–5235.
Rosok, M. J., M. Eghtedarzadeh-Kondri, K. Young, J. Bajorath, S. Glaser, and D. Yelton (1998) Analysis of BR96 binding sites for antigen and anti-idiotype by codon-based scanning mutagenesis. J. Immunol. 160: 2353–2359.
Shrivastava, D., V. Nain, S. Sahi, A. Verma, P. Sharma, P. C. Sharma, and P. A. Kumar (2011) Insights from molecular modeling and dynamics simulation of pathogen resistance (R) protein from brinjal. Bioinformation 5: 326–330.
Sala, E., L. Guasch, J. Iwaszkiewicz, M. Mulero, M. J. Salvadó, M. Pinent, V. Zoete, A. Grosdidier, S. Garcia-Vallvé, O. Michielin, and G. Pujadas (2011) Identification of human IKK-2 inhibitors of natural origin (part I): Modeling of the IKK-2 kinase domain, virtual screening and activity assays. PLoS One 6: e16903.
Hu, Z. Q., J. L. Liu, H. P. Li, S. Xing, S. Xue, J. B. Zhang, J. H. Wang, G. Nölke, and Y. C. Liao (2012) Generation of a highly reactive chicken-derived single-chain variable fragment against Fusarium verticillioides by phage display. Int. J. Mol. Sci. 13: 7038–7056.
Peschen, D., H. P. Li, R. Fischer, F. Kreuzaler, and Y. C. Liao (2004) Fusion proteins comprising a Fusarium-specific antibody linked to antifungal peptides protect plants against a fungal pathogen. Nat. Biotechnol. 22: 732–738.
Hu, Z. Q., H. P. Li, J. B. Zhang, T. Huang, J. L. Liu, S. Xue, A. B. Wu, and Y. C. Liao (2013) A phage-displayed chicken singlechain antibody fused to alkaline phosphatase detects Fusarium pathogens and their presence in cereal grains. Anal. Chim. Acta 764: 84–92.
Liu, J. L., Z. Q. Hu, S. Xing, S. Xue, H. P. Li, J. B. Zhang, and Y. C. Liao (2012) Attainment of 15-fold higher affinity of a Fusarium-specific single-chain antibody by directed molecular evolution coupled to phage display. Mol. Biotechnol. 52: 111–122.
Rosenfeld, R. J., D. S. Goodsell, R. A. Musah, G. M. Morris, D. B. Goodin, and A. J. Olson (2003) Automated docking of ligands to an artificial active site: Augmenting crystallographic analysis with computer modeling. J. Comput. Aided Mol. Des. 17: 525–536.
Cecchini, M., A. Houdusse, and M. Karplus (2008) Allosteric communication in myosin V: From small conformational changes to large directed movements. PLoS Comput. Biol. 4: e1000129.
Schoonbroodt, S., M. Steukers, M. Viswanathan, N. Frans, M. Timmermans, A. Wehnert, M. Nguyen, R. C. Ladner, and R. M. Hoet (2008) Engineering antibody heavy chain CDR3 to create a phage display Fab library rich in antibodies that bind charged carbohydrates. J. Immunol. 181: 6213–6221.
Nishi, M., N. Jian, K. Yamamoto, H. Seto, Y. Nishida, Y. Tonoyama, N. Shimizu, and Y. Nishi. (2014) Ligation-based assembly for constructing mouse synthetic scFv libraries by chain shuffling with in vivo-amplified VH and VL fragments. J. Immunol. Methods 412: 53–69.
Fukuda, I., K. Kojoh, N. Tabata, N. Doi, H. Takashima, E. Miyamoto-Sato, and H. Yanagawa (2006) In vitro evolution of single-chain antibodies using mRNA display. Nucleic Acids Res. 34: e127.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Hu, ZQ., Li, HP., Liu, JL. et al. Production of a phage-displayed mouse ScFv antibody against fumonisin B1 and molecular docking analysis of their interactions. Biotechnol Bioproc E 21, 134–143 (2016). https://doi.org/10.1007/s12257-015-0495-0
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12257-015-0495-0


