Evaluation of four protocols for the detection and isolation of thermophilic Campylobacter from different matrices

M. Ugarte-Ruiz, S. Gómez-Barrero, M. C. Porrero, J. Álvarez, M. García, M. C. Comerón, T. M. Wassenaar, L. Domínguez

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

Aims: To identify the optimal method for detection of thermophilic Campylobacter at various stages in the food chain, three culture-dependent (direct plating, Bolton and Preston enrichment) and one molecular method (qPCR) were compared for three matrices: poultry faeces (n=38), neck skin (n=38) and packed fresh meat (n=38). Methods and Results: Direct plating was compared to enrichment with either Bolton broth (ISO 10272:2006-1) or Preston broth, followed by culture on two selective agars: modified charcoal cefoperazone desoxycholate agar (mCCDA) and Campyfood agar (CFA). Direct plating on CFA provided the highest number of positive samples for faeces and neck skin samples. Enrichment of meat samples in Preston followed by plating on mCCDA gave significantly higher number of positives than the recommended ISO method. Real-time qPCR yielded the highest number of positive samples. Conclusion: Direct plating on CFA is optimal for Campylobacter isolation from highly contaminated samples such as faeces or neck skin. When enrichment is required for less-contaminated samples such as poultry meat, Preston broth is the best choice. The maximum of detectable cells predicted by qPCR is a sensitive and powerful evaluation tool. Significance and impact of the study: The recommended ISO protocol had the least sensitivity, and application of this method could result in underreporting. We detected a high prevalence of Campylobacter on packed meat to be distributed, which suggests this is still a significant risk for consumers.

Original languageEnglish (US)
Pages (from-to)200-208
Number of pages9
JournalJournal of Applied Microbiology
Volume113
Issue number1
DOIs
StatePublished - Jul 1 2012

Keywords

  • Campylobacter
  • Detection methods
  • Enrichment
  • Matrices
  • Quantification
  • Real-time PCR

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