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Applied and Environmental Microbiology, April 2004, p. 2296-2306, Vol. 70, No. 4
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.4.2296-2306.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Direct Quantification of Campylobacter jejuni and Campylobacter lanienae in Feces of Cattle by Real-Time Quantitative PCR{dagger}

G. Douglas Inglis* and Lisa D. Kalischuk

Agriculture and Agri-Food Canada Research Centre, Lethbridge, Alberta T1J 4B1, Canada

Received 15 July 2003/ Accepted 17 November 2003

Campylobacter species are fastidious to culture, and the ability to directly quantify biomass in microbiologically complex substrates using real-time quantitative (RTQ) PCR may enhance our understanding of their biology and facilitate the development of efficacious mitigation strategies. This study reports the use of nested RTQ-PCR to directly quantify Campylobacter jejuni and Campylobacter lanienae in cattle feces. For C. jejuni, the single-copy mapA gene was selected. For C. lanienae, the three-copy 16S rRNA gene was targeted. RTQ-PCR primers were tested alone or they were nested with species-specific primers, and amplification products were detected using the intercalating dye SYBR Green. Nesting did not increase the specificity or sensitivity of C. jejuni quantification, and the limit of quantification was 19 to 25 genome copies ({approx}3 x 103 CFU/g of feces). In contrast, nested RTQ-PCR was necessary to confer specificity on C. lanienae by targeting the 16S rRNA gene. The limit of quantification was 1.8 genome copies ({approx}250 CFU/g of feces), and there was no discernible difference between the two C. lanienae secondary primer sets evaluated. Detection and quantification of C. jejuni in naturally infested cattle feces by RTQ-PCR were comparable to the results of culture-based methods. In contrast, culturing did not detect C. lanienae in 6 of 10 fecal samples positive for the bacterium and substantially underestimated cell densities relative to nested RTQ-PCR. The results of this study illustrate that RTQ-PCR can be used to directly quantify campylobacters, including very fastidious species, in a microbiologically and chemically complex substrate. Furthermore, targeting of a multicopy universal gene provided highly sensitive quantification of C. lanienae, but nested RTQ-PCR was necessary to confer specificity. This method will facilitate subsequent studies to elucidate the impact of this group of bacteria within the gastrointestinal tracts of livestock and studies of the factors that influence colonization success and shedding.

* Corresponding author. Mailing address: Agriculture and Agri-Food Canada Research Centre, 5403 1st Ave. S, Lethbridge, AB T1J 4B1, Canada. Phone: (403) 317-3355. Fax: (403) 382-3156. E-mail: inglisd{at}agr.gc.ca.

{dagger} Contribution 03036 from the Agriculture and Agri-Food Canada Research Centre, Lethbridge, Alberta, Canada.

Applied and Environmental Microbiology, April 2004, p. 2296-2306, Vol. 70, No. 4
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.4.2296-2306.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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