Cultures were incubated at 37 °C. Butyrivibrio proteoclasticus and E. faecalis conjugations,

procedures and culture conditions for the purification of transconjugants were performed as described previously (Hespell & Whitehead, 1991; Hussein et al., 2008; Villas-Bôas et al., 2008). Briefly, donor and recipient bacterial cultures (10 mL, 24 h at 37 °C) were pelleted by centrifugation, washed twice with carbohydrate-free RGM medium (buffer) and resuspended in 2 mL of RGM buffer. Donor and recipient cells were mixed (1 : 1 and 1 : 2 ratios), resuspended to approximately BIBW2992 nmr 100 μL in the same buffer and dispensed onto a sterile filter (type GS, 0.22 μm pore size; Millipore Corp.) placed on a DM or a TYAR agar plate (no antibiotics). After incubation (3.5 h at 37 °C), the filter was washed in phosphate-buffered saline (pH 7.3). Dilutions were plated out onto DM or TYAR agar plates supplemented with tetracycline (10 μg mL−1) and ciprofloxacin JQ1 cell line (25 μg mL−1) and incubated for 2–5 days. Presumptive transconjugants were purified by picking well-spaced colonies and subculturing at least twice onto the corresponding antibiotic-containing medium (Hussein et al., 2008). B316T cells were enumerated for determining

the conjugation efficiency by plating dilutions of the recipient mix onto RGM agar. Total genomic DNA was recovered from transconjugants with standard cell lysis methods using lysozyme, proteinase K and sodium dodecyl sulphate, followed by phenol chloroform extraction. Genomic DNA was precipitated by the addition of isopropanol, washed once with 70% ethanol, resuspended in 100 μL distilled water and stored at −20 °C until required. Approximately 500 ng of total genomic DNA from transconjugants was digested overnight at 37 °C with HindIII. Cut DNA was then electrophoresed

on a 0.8% (w/v) agarose gel, depurinated, denatured and neutralized, and transferred to a nitrocellulose membrane (Hybond N+, GE Healthcare) according to the manufacturer’s instructions. The number of Tn916 insertions per transconjugant was determined by probing blots with a HindIII–KpnI fragment from Tn916 corresponding to the tet(M) gene labelled using an AlkPhos kit (GE Healthcare) method. Hybridization proceeded overnight at 62.5 °C, with posthybridization washes at 62.5 °C and subsequent Dolutegravir cell line chemiluminescence detection of the hybridized probe using CDP-Star (GE Healthcare). Approximately 100 ng of HindIII digested B316T total genomic DNA from transconjugants having only a single Tn916 insertion was ligated overnight at 16 °C (Ready-to-Go T4 DNA ligase, GE Healthcare). The ligase was denatured by incubating at 65 °C for 15 min. Circularized HindIII DNA fragments were purified using sodium acetate and ethanol precipitation and resuspended in 20 μL distilled water. Inverse PCR was performed using the primers Tn916L (5′-CGTGAAGTATCTTCCTACAGT-3′) and TetM5′ (5′-CCTAATTCTGTAATCGCTCCACTG-3′) using circularized HindIII DNA as a template (Villas-Bôas et al., 2008).