4.7 Article

Poly-L ysine-functionalized magnetic beads combined with polymerase chain reaction for the detection of Staphylococcus aureus and Escherichia coli O157:H7 in milk

期刊

JOURNAL OF DAIRY SCIENCE
卷 104, 期 12, 页码 12342-12352

出版社

ELSEVIER SCIENCE INC
DOI: 10.3168/jds.2021-20612

关键词

Staphylococcus aureus; Escherichia coli O157:H7; poly-L-lysine; magnetic bead; foodborne pathogen detection

资金

  1. National Key R&D Program of China [2018YFC1602500]
  2. Research Foundation from Academic and Technical Lead-ers of Major Disciplines in Jiangxi Province, China [20194BCJ22004]
  3. State Key Laboratory of Food Science and Technol-ogy, Nanchang University, Nanchang, China [SKLF-ZZA-201912]

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The study established a poly-L-lysine-functionalized magnetic beads (PLL-MB) strategy combined with a PCR assay for the detection of Staphylococcus aureus, achieving high capture efficiency in milk samples. The method showed a lower limit of detection, simplicity of operation, and cost-effectiveness, demonstrating its potential applications in foodborne pathogen detection.
Rapid and credible detection of pathogens is essential to prevent and control outbreaks of foodborne diseases. In this study, a poly-L-lysine-functionalized magnetic beads (PLL-MB) strategy combined with a PCR assay was established to detect Staphylococcus aureus. We also detected Escherichia coli O157:H7 to further verify the strategy for gram-negative bacteria detection. Poly-r,-lysine has strong positive charges because of its amino groups, which can conjugate with the carboxyl of carboxyl magnetic beads. Furthermore, it can be used to combine with bacteria through electrostatic adsorption. Under optimum conditions, the developed PLL-MB complexes showed 90% capture efficiency in phosphate-buffered saline and 85% capture efficiency in milk for S. aureus detection. The limit of detection of the PLL-MB-PCR assay was 10(2) cfu/mL (1.8 x 10(2) cfu/mL for S. aurrus and 7 x 10(2) cfu/mL for E. coli O157:H7) in phosphate-buffered saline and milk samples. The whole assay can be performed within 4 h. The proposed strategy showed a lower limit of detection when compared with the conventional PCR assay without enrichment. In addition, this method exhibited the advantages of a high-efficient, cost-efficient, and simple operation, indicating its potential applications in foodborne pathogen detection.

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