Probe labeling and hybridization were performed using the ECL Direct Nucleic Acid Labeling and Detection system (Amersham Bioscience) according to the manufacturer’s instructions. The membrane was exposed to Hyper Film™ ECL for visualization. The tester-specific clones were sequenced using M13F and/or M13R primers. Cycle sequencing was performed using the BigDye Terminator v3.1 Cycle Sequencing kit, and the sequencing reactions were analyzed on an automated DNA sequencer (model 3730; Applied

selleck chemicals Biosystems, Foster City, CA). The sequences generated from the automatic sequencer were edited by removing the vector and adaptor sequences. Sequence assembly and further editing were performed with the clustal_x 1.81 program (Thompson et al., 1994), and blastn, blastx, and tblastx analyses against the database of the National Center for Biotechnology Information (NCBI) were performed for each sequence to determine homology with other microorganisms and to annotate their functions.

The nucleotide sequences obtained in this study were deposited in the dbGSS (database of Genome Survey Sequences) of NCBI GenBank under accession numbers JM426692–JM426710 for SSH libraries of L. garvieae (Table 2). PCR primers were designed for the clones CAUF58 (garF58F, 5′-CGGAGTAGCCGATAATTCCA-3′ and garF58R, Apitolisib research buy 5′-GCAGGTACCCTGAAAAAGGA-3′) and CAUF64 (garF64F, 5′-GTGCTGAACGTCACCTTGAA-3′ and garF64R, 5′-CGTTTGCCATGATTTTTCCT-3′) using primer3 software (Rozen & Skaletsky, 2000). PCRs were performed with 100 ng genomic DNA template in 20-μL reaction mixtures containing 1 μM each primer, 2 μL 10× reaction buffer, 0.2 mM dNTPs, 1.5 mM MgCl2, and 2.5 U Taq polymerase. Amplification was carried out in a GeneAmp PCR system 9700 (Applied Biosystems) under the following conditions: initial denaturation at 94 °C for 5 min, followed by 30 cycles at 94 °C for 30 s, 58 °C for 30 s, and 72 °C for 40 s, with a final extension at 72 °C for 10 min. The primer specificities were evaluated using 12 L. garvieae, six other Lactococcus, 12 Streptococcus, and two Enterococcus strains and were compared with the specificities of previously reported Oxalosuccinic acid primers targeting

the 16S rRNA gene [pLG-1 and pLG-2 (Zlotkin et al., 1998), SA1B10-1-F and SA1B10-1-R (Aoki et al., 2000), and LcG-F and Lc-R (Odamaki et al., 2011)] using the published PCR conditions. After PCR amplification, 5 μL of each PCR product was resolved on a 1.2% Seakem LE agarose gel (FMC Bioproducts, Rockland, ME) and was visualized on the GelDoc xR image-analysis system (BioRad) after ethidium bromide staining. DNA signatures are nucleotide sequences that can be used to detect the presence of an organism and to distinguish that organism from all other species (Phillippy et al., 2007). In this study, the DNA signatures specific for L. garvieae were investigated through the identification of sequences present in L. garvieae but absent in a closely related species.