Comparison of Media for the Detection of Campylobacter jejuni Using a Commercial RT-PCR System

The accurate quantification of in poultry samples is critical for ensuring food safety and compliance with regulatory standards. This study evaluated the performance of three enrichment media-Mueller-Hinton Broth (MHB), Bolton's Blood-Free Broth 2x (BFBB2x), and Buffered Peptone Water (BPW)-in...

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Published inPathogens (Basel) Vol. 14; no. 2; p. 166
Main Authors Olson, Elena G, Bodie, Aaron R, Tarcin, Haley A, Rubinelli, Peter M, Applegate, Savannah F, Stephens, Tyler P, Rothrock, Jr, Michael J, Ricke, Steven C
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 08.02.2025
MDPI
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Summary:The accurate quantification of in poultry samples is critical for ensuring food safety and compliance with regulatory standards. This study evaluated the performance of three enrichment media-Mueller-Hinton Broth (MHB), Bolton's Blood-Free Broth 2x (BFBB2x), and Buffered Peptone Water (BPW)-in supporting detection and quantification using the BAX Q7-RT PCR system and traditional plate count methods. Results demonstrated high reliability across all media types, with BFBB2x and MHB showing the strongest correlations (R = 0.99) for the BAX system. BFBB2x exhibited the lowest RMSE (0.13), while MHB balanced precision (RMSE = 0.4) with sensitivity. For plate counts, MHB and BPW achieved the highest correlations (R = 0.99) and precision (RMSE = 0.26), with MHB demonstrating the lowest detection limit (2.56 log CFU/mL) compared to BFBB2x (2.93 log CFU/mL) and BPW (3.31 log CFU/mL). The findings underscore MHB's robustness as an enrichment medium, offering consistent performance across both molecular and culture-based methods. The current study supports MHB as the more effective medium for the reliable and precise quantification of in poultry-associated matrices, highlighting its utility in minimizing contamination risks and enhancing food safety. Future research should explore its applicability in diverse poultry products and production environments.
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ISSN:2076-0817
2076-0817
DOI:10.3390/pathogens14020166