Thermophilic Campylobacter were cultured at 41.5°C in microaerobic conditions.

For direct streaking and selective enrichment, the Campylobacter suspect colonies on Karmali or Butzler plates were confirmed by microscopy (cell morphology) and conventional PCR [24]). The number of CFU/g of faeces or feed as well as the number of CFU/m2 for the environmental samples were thus calculated. Finally, material from Campylobacter suspect colonies was suspended in TE buffer and subdued to DNA extraction and the species-specific PCR described by Denis et al. (1999) www.selleckchem.com/products/Dasatinib.html [24] for differentiation between C. coli and C. jejuni. Real-time PCR primers and probes To detect C. jejuni and C. coli, we have used sequences described by Lagier et al. (2004) [33], which are based (i) on the single-copy hipO gene (benzoylglycine Selleck VX-809 amidohydrolase) responsible

for the hippurate activity exclusively found within the C. jejuni genome, and (ii) on the single-copy glyA gene (serine hydroxymethyltransferase) in an unique nucleotide region within the C. coli glyA open reading frame identified as specific for C. coli [58] (Table 5). Table 5 PCR primers and probes used in the species-specific real-time PCR assays Primer or Probea Nucleotide sequence 5′-3′ Location within Selleck Verteporfin target Origin Target Gene detectedb glyA-F forward F: AAACCAAAGCTTATCGTGTGC 297-320 This study   glyA-R reverse R: AGTGCAGCAATGTGTGCAATG 422-359 Lagier et al. (2004) Campylobacter coli glyA gene (125 bp) glyA-P MGB Probe P: FAM-CAACTTCATCCGCAAT 346-330 This study   hipO-F forward F: CTTGCGGTCATGCTGGACATAC 340-360 This study   hipO-R reverse R: AGCACCACCCAAACCCTCTTCA 464-444 This study Campylobacter jejuni hipO gene (124 bp) hipO-P MGB Probe P: VIC-ATTGCTTGCTGCAAAGT 424-409 This study   bp, length in base pairs of the species specific PCR products aPrimers and probes Fossariinae were designed by using the program Primer Express version 2.0 (Applied Biosystems, Foster city, CA, USA). The TaqMan® MGB probes were dual-labelled with either fluorescent

reporter dyes FAM (6-carboxyfluorescein, C. coli specific probe) or VIC (C. jejuni specific probe) on the 5′end, and quenched by a non fluorescent quencher associated with a minor groove binder at the 3′end (Applied Biosystems). bThe nucleotide sequences were retrieved from the GenBank™ sequence database http://​www.​ncbi.​nlm.​nih.​gov/​Genbank/​index.​html under accession numbers: [GenBank: Z36940] for C. jejuni hipO gene and [GenBank: AF136494] for C. coli glyA gene. To optimize the real-time PCR reaction and to improve the specificity and the mismatch discrimination, shorter Minor Groove Binder (MgB) probes have been designed [59–62]. At the 5′end, the C. coli probe was linked to the fluorophore FAM and the C. jejuni probe to the fluorophore VIC. The C. jejuni and C.