Abstract
In this study, we developed a microplate sandwich analysis of Escherichia coli and Staphylococcus aureus bacterial pathogens based on the interaction of their cell wall carbohydrates with natural receptors called lectins. An immobilized lectin-cell-biotinylated lectin complex was formed in this assay. Here, we studied the binding specificity of several plant lectins to E. coli and S. aureus cells, and pairs characterized by high-affinity interactions were selected for the assay. Wheat germ agglutinin and Ricinus communis agglutinin were used to develop enzyme-linked lectinosorbent assays for E. coli and S. aureus cells with the detection limits of 4 × 106 and 5 × 105 cells/mL, respectively. Comparison of the enzyme-linked immonosorbent assay and the enzyme-linked lectinosorbent assay demonstrated no significant differences in detection limit values for E. coli. Due to the accessibility and universality of lectin reagents, the proposed approach is a promising tool for the control of a wide range of bacterial pathogens.
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Original Russian Text © O.D. Hendrickson, N.I. Smirnova, A.V. Zherdev, V.K. Gasparyan, B.B. Dzantiev, 2017, published in Prikladnaya Biokhimiya i Mikrobiologiya, 2017, Vol. 53, No. 1, pp. 96–103.
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Hendrickson, O.D., Smirnova, N.I., Zherdev, A.V. et al. Enzyme-linked lectinosorbent assay of Escherichia coli and Staphylococcus aureus . Appl Biochem Microbiol 53, 107–113 (2017). https://doi.org/10.1134/S0003683817010082
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DOI: https://doi.org/10.1134/S0003683817010082