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“The Gram-negative, non spore forming bacillus Burkholderia pseudomallei is the cause of melioidosis and classified by CDC as a Category B select agent. Burkholderia pseudomallei is present in the environment in northern Australia and across much of southeast Asia, where human infection is acquired by bacterial

inoculation, inhalation or ingestion. 1 and 2 In the absence of a vaccine, strategies for the prevention of melioidosis are based on reduction of exposure. These could potentially include efforts to reduce the bioburden of B. pseudomallei in specific environments, including clean-up operations in geographic areas that have become contaminated for the first time through accident or bioterrorist activity. This is likely to be hampered, however, by the extreme hardiness of this organism. In 1995,

www.selleckchem.com/products/ABT-263.html we reported that B. pseudomallei strain E32 had survived in distilled water (DW) for three years. 3 Here, we extend these observations and report on the survival and preliminary characterisation of a strain of B. pseudomallei maintained in DW at 25 °C for 16 years. Burkholderia pseudomallei strain 207a was isolated in 1986 from blood taken from a rice farmer presenting to Sappasithiprasong Hospital in northeast Thailand, and stored in trypticase soya broth (TSB) with 15% glycerol at –80 °C. In 1994, the organism was sub-cultured Obeticholic Acid onto Columbia agar and inoculated into 9 ml DW to obtain 3.0 x 1010 cfu/ml contained in a plain plastic tube with a screw cap that was tightened and then loosened by a half turn. This

was maintained in a cupboard at 25 °C. In December 2008, the volume was noted to be around 2.5 ml and DW was added once to a total volume of 15 ml. In January 2010, an aliquot Progesterone of 5 ml was removed for the work described below. Gram stain and light microscopy of bacilli from the original freezer vial demonstrated typical Gram-negative rods, while bacilli from DW were pale pink cocci or coccobacilli. The proportion of live versus dead bacteria in DW was defined using the LIVE/DEAD® BacLightTM viability stain according to the manufacturer’s recommendations (Invitrogen, Carlsbad, California, USA). The estimated number of live and dead B. pseudomallei was 3.8 x 107 cells/ml and 1.4 x 105 cells/ml, respectively. Live bacteria were non-motile. A colony count was performed of the bacilli from DW on Ashdown agar (ASH) after serial dilution, spread plating, and incubation in air at 37 °C for four days. The count of 1.0 x 106 cfu/ml was less than the estimated number of live bacteria using the viability kit, suggesting that a proportion of cells may be in a viable but non-culturable state. The entire original freezer vial (a volume of 80 μl) was subcultured onto ASH and incubated in air at 37 °C for four days. This resulted in a total of just 236 colonies, suggestive of cell death during freezing.