Issue 19, 2013

Phage receptor binding protein-based magnetic enrichment method as an aid for real time PCR detection of foodborne bacteria

Abstract

We present a novel phage receptor binding protein-based magnetic separation and pre-enrichment method as an alternative to the immunomagnetic separation methods by replacing antibodies with bacteriophage receptor binding proteins (RBPs). We couple the proposed RBP-based magnetic separation with real time PCR for rapid, sensitive and specific detection of Campylobacter jejuni cells in artificially contaminated skim milk, milk with 2% fat and chicken broth. Recovery rates, assessed by real time PCR, were greater than 80% for the samples spiked with as low as 100 cfu mL−1 of C. jejuni cells. The specificity of capture was confirmed using Salmonella Typhimurium as a negative control where no bacteria were captured on the RBP-derivatized magnetic beads. The combination of RBP-based magnetic separation and real time PCR improved PCR sensitivity and allowed the detection of C. jejuni cells in milk and chicken broth samples without a time consuming pre-enrichment step through culturing. The total sample preparation and analysis time in the proposed RBP-based enrichment method coupled with real time PCR was less than 3 h.

Graphical abstract: Phage receptor binding protein-based magnetic enrichment method as an aid for real time PCR detection of foodborne bacteria

Article information

Article type
Paper
Submitted
03 Jun 2013
Accepted
19 Jul 2013
First published
22 Jul 2013

Analyst, 2013,138, 5619-5626

Phage receptor binding protein-based magnetic enrichment method as an aid for real time PCR detection of foodborne bacteria

S. Poshtiban, M. A. Javed, D. Arutyunov, A. Singh, G. Banting, C. M. Szymanski and S. Evoy, Analyst, 2013, 138, 5619 DOI: 10.1039/C3AN01100C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements