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Development of a Synthetic Peptide ELISA Assay for the Detection of Foot-and-Mouth Disease Virus Nonstructural Protein Antibodies 被引量:1

Development of a Synthetic Peptide ELISA Assay for the Detection of Foot-and-Mouth Disease Virus Nonstructural Protein Antibodies
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摘要 In order to develop an ELISA assay with synthetic peptides for the detection of antibody to the nonstructural proteins of foot-and-mouth disease virus, specific peptides were synthesized by a solid-phase method according to FMDV NSPs B-cell epitopes, and were conjugated to carrier protein BSA. An ELISA system was developed to detect FMDV NSPs antibody with the conjugated proteins as the coating antigen. The optimal coating concentration of the antigen was determined as 2.5 μg mL-1. The comparative study of this assay with UBI NSP ELISA kit and national commercial 3ABC ELISA kit in the detection of 199 serum samples showed that they were very coincident, and the identity rates were 96.48 and 97.48%, respectively. The development of ELISA using the synthetic peptides as coating antigen is specific, reproducible, stable, and easy, and can be used to differentiate FMDV infected pigs from immunized pigs. In order to develop an ELISA assay with synthetic peptides for the detection of antibody to the nonstructural proteins of foot-and-mouth disease virus, specific peptides were synthesized by a solid-phase method according to FMDV NSPs B-cell epitopes, and were conjugated to carrier protein BSA. An ELISA system was developed to detect FMDV NSPs antibody with the conjugated proteins as the coating antigen. The optimal coating concentration of the antigen was determined as 2.5 μg mL-1. The comparative study of this assay with UBI NSP ELISA kit and national commercial 3ABC ELISA kit in the detection of 199 serum samples showed that they were very coincident, and the identity rates were 96.48 and 97.48%, respectively. The development of ELISA using the synthetic peptides as coating antigen is specific, reproducible, stable, and easy, and can be used to differentiate FMDV infected pigs from immunized pigs.
出处 《Agricultural Sciences in China》 CAS CSCD 2010年第11期1677-1683,共7页 中国农业科学(英文版)
基金 supported by the National Natural Science Foundation of China (30730068) the National High-Tech R&D Program of China (863 Program,2007AA100606)
关键词 foot and mouth disease virus (FMDV) ELISA synthetic peptide foot and mouth disease virus (FMDV), ELISA, synthetic peptide
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  • 1Alonso A,Martins M A,Gomes Mda P,Allende R,S(o)ndahl M S.1992.Foot-and-mouth disease virus typing by complement fixation and enzyme-linked immunosorbent assay using monovalent and polyvalent antisera.Journal of Veterinary Diagnose Investigation,4,249-253.
  • 2Bergmann I E,Malirat V,Neitzert E,Beck E,Panizzutti N,Sanchez C,Falczuk A.2000.Improvement of a serodiagnostic strategy for foot and mouth disease virus surveillance in cattle under systematic vaccination:a combined system of an indirect ELISA-3ABC with an enzyme-linked immunoelectrotransfer blot assay.Archives of Virology,145,473-489.
  • 3Bronsvoort B M,Toft N,Bergmann I E,Sorensen K J,Anderson J,Malirat V,Tanya V N,Morgan K L.2006.Evaluation of three 3ABC ELISAs for foot-and-mouth disease nonstructural antibodies using latent class analysis.BMC Veterinary Research,2,30.
  • 4Chung W B,Sorensen K J,Liao P C,Yang P C,Jong M H.2002.Differentiation of foot-and-mouth disease virus-infected from vaccinated pigs by enzyme-linked immanosorbent assay using nonstructural protein 3AB as the antigen and application to an eradication program.Journal of Clinical Microbiology,40,2843-2848.
  • 5De Jong A S,de Mattia F,Van Dommelen M M,Lanke K,Melchers W J,Willems P H,van Kuppeveld F J.2008.Functional analysis of picornavirus 2B proteins:effects on calcium homeostasis and intracellular protein trafficking.Journal of Virology,82,3782-3790.
  • 6Fukai K,Morioka K,Ohashi S,Yamazoe R,Yoshida K,Sakamoto K.2008.Differentiation of foot-and-mouth disease virusinfected pigs from vaccinated pigs using a western blotting assay based on baculovirus-expressed nonstructural proteins2C and 3D.Journal of Veterinary Medical Science,70,1353-1357.
  • 7Inoue T,Parida S,Paton D J,Linchongsubongkoch W,Mackay D,Oh Y,Aunpomma D,Gubbins S,Saeki T.2006.Development and evaluation of an indirect enzyme-linked immunosorbent assay for detection of foot-and-mouth disease virus nonstructural protein antibody using a chemically synthesized 2B peptide as antigen.Journal of Veterinary Diagnose Investigation,18,545-552.
  • 8Kitching R P.1999.Foot-and-mouth disease:current world situation.Vaccine,17,1772-1774.
  • 9Lubroth J,Brown F.1995.Identification of native foot-and-mouth disease virus non-structural protein 2C as a serological indicator to differentiate infected from vaccinated animals.Research in Veterinary Science,59,70-78.
  • 10Lu Z J,Cao Y M,Guo J H,Qi S Y,Li D,Zhang Q,Ma J W,Chang H Y,Liu Z X,Liu X T,et al.2007.Development and validation of a 3ABC indirect ELISA for differentiation of foot-and-mouth disease virus infected from vaccinated animals.Veterinary Microbiology,125,157-169.

同被引文献24

  • 1ApSimon J W. Structure, synthesis, and biosynthesis of fumonisin B and related compounds [ J ]. Environmental Health Perspectives ,2001,109 (2) : 245 -249.
  • 2Dupuy J, Bars P L, Boudra H, et al. Thermostability of fumonisin B1 , a mycotoxin from Fusarium moniliforme, in corn [ J]. Applied and Environmental Microbiology, 1993,59 ( 9 ) :2864-2867.
  • 3Reverberi M, Rieelli A, Zjalic S, et al. Natural functions of mycotoxins and control of their biosynthesis in fungi [ J]. Appl Microbiol Biotechnol, 2010,87:899-911.
  • 4Stepieh L, Koczyk G, Wakiewicz A. FUM cluster divergence in fumonisins-producing Fusarium species [ J ]. Fungal Biology,2011,115 : 112 - 123.
  • 5de Oliveira Rocha L, Reis G M, da Silva V N, et al. Molecular characterization and fumonisin production by Fusarium verticillioides isolated from corn grains of different geographic origins in Brazil [ J ] International Journal of Food Microbiology,2011,145:9-21.
  • 6Pereira P, Nesci A, Castillo C, et al. Impact of bacterial biological control agents on fumonisin B1 content and Fusarium verticillioides infection of field-grown maize[ Jl. Biological Control,2010,53:258-266.
  • 7Bernabucci U, C olaveeehia L, Danieli P P, et al. Aflatoxin B1 and fumonisin Bl affect the oxidative status of bovine peripheral blood mononuelear cells [ J ]. Toxicology in Vitro,2011,25:684-691.
  • 8Malovrh T,Jakovac-Strajn B. Feed contaminated with fusarium toxins alter lymphocyte proliferation and apoptosis in primiparous sows during the perinatal period[J]. Food and Chemical Toxicology,2010,48:2907-2912.
  • 9Minervini F, Lacalandra G M, Filannino A, et al. Toxic effects induced by myeotoxin fumonisin B1 on equine spermatozoa: assessment of viability, sperm ehromatin structure stability, ROS production and motility [ J ]. Toxicology in Vitro, 2010,24 : 2072-2078.
  • 10Ren Y, Zhang Y, Han S, et al. Simultaneous determination of fumonisins B1 , B2 and B3 contaminants in maize by ultra high-performance liquid chromatography tandem mass spectrometry [ J ]. Anal Chim Acta, 2011,692 : 138 - 145.

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