Your browser doesn't support javascript.
loading
A rapid and accurate method for screening T-2 toxin in food and feed using competitive AlphaLISA.
Zhang, Liwen; Lv, Qingyu; Zheng, Yuling; Chen, Xuan; Kong, Decong; Huang, Wenhua; Liu, Peng; Jiang, Hua; Jiang, Yongqiang.
Affiliation
  • Zhang L; Anhui Medical University, Hefei, Anhui 230032, China.
  • Lv Q; State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.
  • Zheng Y; State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.
  • Chen X; State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.
  • Kong D; State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.
  • Huang W; State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.
  • Liu P; State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.
  • Jiang H; State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.
  • Jiang Y; State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, Beijing 100071, China.
FEMS Microbiol Lett ; 368(6)2021 04 22.
Article de En | MEDLINE | ID: mdl-33755724
ABSTRACT
T-2 is a common mycotoxin contaminating cereal crops. Chronic consumption of food contaminated with T-2 toxin can lead to death, so simple and accurate detection methods in food and feed are necessary. In this paper, we establish a highly sensitive and accurate method for detecting T-2 toxin using AlphaLISA. The system consists of acceptor beads labeled with T-2-bovine serum albumin (BSA), streptavidin-labeled donor beads and biotinylated T-2 antibodies. T-2 in the sample matrix competes with T-2-BSA for antibodies. Adding biotinylated antibodies to the test well followed by T-2 and T-2-BSA acceptor beads yielded a detection range of 0.03-500 ng/mL. The half-maximal inhibitory concentration was 2.28 ng/mL and the coefficient of variation was <10%. In addition, this method had no cross-reaction with other related mycotoxins. This optimized method for extracting T-2 from food and feed samples achieved a recovery rate of approximately 90% in T-2 concentrations as low as 1 ng/mL, better than the performance of a commercial ELISA kit. This competitive AlphaLISA method offers high sensitivity, good specificity, good repeatability and simple operation for detecting T-2 toxin in food and feed.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Contamination des aliments / Analyse d&apos;aliment / Aliment pour animaux Type d'étude: Diagnostic_studies / Screening_studies Langue: En Journal: FEMS Microbiol Lett Année: 2021 Type de document: Article Pays d'affiliation: Chine

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Contamination des aliments / Analyse d&apos;aliment / Aliment pour animaux Type d'étude: Diagnostic_studies / Screening_studies Langue: En Journal: FEMS Microbiol Lett Année: 2021 Type de document: Article Pays d'affiliation: Chine