DGGE was used to observe shifts in the Prevotella community as a result of diet change. The analysis was carried out in a Bio-Rad DCode universal mutation detection system (Hercules, CA). The g-Prevo primers used for real-time PCR were used to amplify the

V5–V8 regions of the 16S rRNA gene of Prevotella. An amplicon of around 530 bp for DGGE analysis was obtained by modifying the forward primer by addition of a 40-bp GC clamp (5′-CGCCCGCCGCGCGCGGCGGGCGGGGCGGGGGCACGGGGGG-3′). KPT-330 clinical trial PCR was conducted using a GeneAmp PCR 2400 thermal cycler (Perkin-Elmer, Yokohama, Japan). A reaction mixture containing 20 pmol of each primer, 5 μL of 10 × ExTaq buffer, 10 pmol of each dNTP, 1.25 U polymerase (ExTaq, Takara, Otsu, Japan) and 10 ng of template DNA in a total volume of 50 μL was prepared. The temperature program for cycling consisted of an initial denaturation at 94 °C for 5 min, followed by 35 cycles of 94 °C for 30 s, annealing at 55 °C for 30 s and extension at 72 °C for 30 s with a final extension at 72 °C for 5 min. PCR-amplified 16S rRNA gene fragments were separated using an 8% polyacrylamide gel with 0.5 × TAE buffer (20 mM Tris-acetate, 10 mM sodium acetate, 0.5 mM EDTA, pH 8.0) and a 35–60% linear gradient of denaturant (100% denaturant corresponded to 40% v/v deionized formamide and 7 M urea). The gel was run at 60 °C, 80 V for 16 h, and then placed in fixing solution (10% ethanol and

0.5% acetic acid) for 2 h, stained in 0.1% w/v silver nitrate CYTH4 solution for 20 min and developed in 1.5% sodium PF-562271 hydroxide (w/v), 0.1% sodium borohydride (w/v) and 0.4% formaldehyde (v/v) for 8 min. Thereafter, the gel was rinsed and kept in distilled water till the image was scanned. Gel images were analyzed using bionumerics software version

4.5 (Applied Maths, Kortrijk, Belgium). Normalized banding patterns were used to generate dendrograms by calculating Dice’s similarity coefficient and using an unweighted pair group method with the arithmetic averages clustering algorithm. Two clone libraries were constructed for the respective feeding conditions from composite samples; the samples were obtained from rumen content DNA from three animals under the same dietary conditions. PCR products were generated by g-Prevo primers with the same reaction and amplification conditions as those described for DGGE, with the exception of the forward primer without a GC clamp. PCR products were cloned using a pGEM-T Easy Vector System (Promega, San Luis Obispo, CA) according to the manufacturer’s instructions. Clones containing the correct insert were sequenced at Takara Bio (Yokkaichi, Japan). Clone nomenclature was as follows: for the hay-associated Prevotella library, clone names begin with ‘HAPC’, followed by the clone number. Clone names in the concentrate-associated Prevotella library begin with ‘CAPC’, followed by the clone number.