One hundred and forty soil samples, collected from 30-cm soil depth in Nampong District, Khon Kaen Province, Thailand, were used for phage isolation using the basic enrichment method selleck inhibitor (Kutter & Sulakvelidze, 2005). Five grams of soil were inoculated into 20 mL of brain–heart infusion broth (Oxoid, Basingstoke, UK), mixed and incubated at 37 °C for 16–18 h.

Five milliliters of the culture were centrifuged at 4000 g, 4 °C for 30 min and the supernatant filtered through 0.22-μm filters and used as phage lysate or stored at 4 °C until use. The spot test method was used to screen for the presence of lytic phage activity (Chopin et al., 1976). Approximately 1 mL of mid-log phase B. pseudomallei P37 (1 × 109 CFU mL−1) was flooded onto a plate containing nutrient agar with 3.6 mM CaCl2, the excess removed and allowed to dry open in a laminar flow biosafety cabinet. Twenty microliters of phage lysate from each soil sample were then dropped

onto the plate and incubated at 37 °C overnight and the clear zone formation was observed. Each clear and isolated plaque was cored out by a sterile Pasteur pipette into nutrient broth, shaken for 1 h and centrifuged at 2500 g, at 4 °C for 20 min. Supernatants were filtered through 0.22-μm filter membranes and purified by the BGJ398 soft agar method (Sambrook & Russell, 2001). The purification steps for each phage were repeated three times to ensure the homogeneity of the phage stock and finally phage titers were calculated as PFU mL−1. A ADAM7 mid-log phase culture of B. pseudomallei P37 (1 × 109 CFU mL−1) in 100 mL nutrient broth (Oxoid) containing 3.6 mM CaCl2 was mixed with the purified phage suspension at a multiplicity of infection (MOI) of 0.1 and incubated at 37 °C for 3–5 h. After bacterial lysis was observed, the solution was centrifuged and the supernatant containing phage particles was filtered through

0.22-μm filter membranes and used as the phage suspension. One hundred microliters of each B. pseudomallei isolate’s overnight culture were spread on the surface of nutrient agar plates and 20 μL of each phage suspension (∼108–109 PFU mL−1) was spotted and incubated at 37 °C for 18–24 h. The results were recorded as negative if there were no plaques and positive if clear plaques were observed. The host range of selected phages was further evaluated with species closely related to Burkholderia (Table 1) by the agar overlay method (Sambrook & Russell, 2001). The negative staining method was performed to visualize phage morphology using transmission electron microscopy (Jamalludeen et al., 2007). Ten microliters of phage suspension (>108 particles mL−1) were used for staining with 10 μL of 2% uranyl acetate for 10 min. Photographs were taken under a transmission electron microscope (JEM-2100, JEOL LAB6, Japan). Size was determined from the average of three independent measurements.