Literature DB >> 25791007

Effect of exposure to stress conditions on propidium monoazide (PMA)-qPCR based Campylobacter enumeration in broiler carcass rinses.

A Duarte1, N Botteldoorn2, W Coucke3, S Denayer2, K Dierick2, M Uyttendaele4.   

Abstract

Campylobacter quantification by qPCR is unable to distinguish viable vs. dead cells in contrast to the culture-based ISO 10272-2 reference method. Propidium monoazide (PMA) has been used to overcome this disadvantage. A Campylobacter PMA-qPCR enumeration method was evaluated for its consistency and compared to the culture-based enumeration for both artificially and natural contaminated broiler carcass rinses. The PMA effect was further evaluated on stressed cells. Five conditions, commonly encountered during the slaughter process and storage (acid, heat, cold, oxidation and freezing), were inflicted to the broiler carcass rinses artificially contaminated with Campylobacter jejuni or Campylobacter coli. A better correlation between the reference method and the qPCR enumeration was obtained when PMA was used. The two cultured-based methods used showed a significant CFU reduction for heat, cold and acid stresses although the PMA-qPCR enumeration showed that viable bacteria were underestimated. Freezing showed the highest reduction effect, while the reduction extend was also overestimated by the microbiological enumeration procedure. Exposure to a mild oxidative stress was the only stress condition applied at temperatures permitting adaptation of Campylobacter and did not lead to either reduction in CFU nor in the PMA-qPCR signal.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Alternative method; Campylobacter; Injured membrane / stressed cells; Propidium monoazide; qPCR

Mesh:

Substances:

Year:  2015        PMID: 25791007     DOI: 10.1016/j.fm.2014.12.011

Source DB:  PubMed          Journal:  Food Microbiol        ISSN: 0740-0020            Impact factor:   5.516


  4 in total

1.  Viability Quantitative PCR Utilizing Propidium Monoazide, Spheroplast Formation, and Campylobacter coli as a Bacterial Model.

Authors:  Thomai P Lazou; Eleni G Iossifidou; Athanasios I Gelasakis; Serafeim C Chaintoutis; Chrysostomos I Dovas
Journal:  Appl Environ Microbiol       Date:  2019-10-01       Impact factor: 4.792

2.  Method-Dependent Implications in Foodborne Pathogen Quantification: The Case of Campylobacter coli Survival on Meat as Comparatively Assessed by Colony Count and Viability PCR.

Authors:  Thomai P Lazou; Athanasios I Gelasakis; Serafeim C Chaintoutis; Eleni G Iossifidou; Chrysostomos I Dovas
Journal:  Front Microbiol       Date:  2021-03-01       Impact factor: 5.640

3.  Two-Round Treatment With Propidium Monoazide Completely Inhibits the Detection of Dead Campylobacter spp. Cells by Quantitative PCR.

Authors:  Ayaka Okada; Mizuki Tsuchida; Md Matiur Rahman; Yasuo Inoshima
Journal:  Front Microbiol       Date:  2022-04-25       Impact factor: 5.640

4.  Chicken Skin Decontamination of Thermotolerant Campylobacter spp. and Hygiene Indicator Escherichia coli Assessed by Viability Real-Time PCR.

Authors:  Imke F Wulsten; Maja Thieck; André Göhler; Elisabeth Schuh; Kerstin Stingl
Journal:  Pathogens       Date:  2022-06-18
  4 in total

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