Reverse transcriptase real-time PCR for detection and quantification of viable Campylobacter jejuni directly from poultry faecal samples

Thanh Xuan Bui, Anders Wolff, Mogens Madsen, Dang Duong Bang

    Research output: Contribution to journalJournal articleResearchpeer-review

    Abstract

    Campylobacter spp. is the most common cause of bacterial diarrhoea in humans worldwide. Therefore, rapid and reliable methods fordetection and quantification of this pathogen are required. In this study, we have developed a reverse transcription quantitative real-time PCR(RT-qPCR) for detection and quantification of viable Campylobacter jejuni directly from chicken faecal samples. The results of this method anda DNA-based quantitative real-time PCR (qPCR) method were compared with those of a bacterial culture method. Using bacterial culture andRT-qPCR methods, viable C. jejuni cells could be detected for up to 5 days in both the C. jejuni spiked and the naturally contaminated faecalsamples. We found that no RT-qPCR signals were obtained when viable C. jejuni cells could not be counted by the culture method. In contrast,using a DNA-based qPCR method, dead or non-viable Campylobacter cells were detected, and all tested samples were positive, even after 20days of storage. The developed method for detection and quantification of viable C. jejuni cells directly from chicken faecal samples can be usedfor further research on the survival of Campylobacter in the environment.
    Original languageEnglish
    JournalResearch in Microbiology
    Volume163
    Issue number1
    Pages (from-to)64-72
    ISSN0923-2508
    DOIs
    Publication statusPublished - 2012

    Keywords

    • RT-qPCR
    • Campylobacter jejuni
    • Chicken faeces
    • Campylobacter survival
    • mRNA

    Fingerprint Dive into the research topics of 'Reverse transcriptase real-time PCR for detection and quantification of viable Campylobacter jejuni directly from poultry faecal samples'. Together they form a unique fingerprint.

    Cite this