- Research article
- Open Access
Recovery of a Burkholderia thailandensis-like isolate from an Australian water source
© Gee et al; licensee BioMed Central Ltd. 2008
Received: 08 August 2007
Accepted: 02 April 2008
Published: 02 April 2008
Burkholderia thailandensis, a close relative of Burkholderia pseudomallei, has previously been reported only from Southeast Asia and North America. It is biochemically differentiated from B. pseudomallei by the ability to utilize arabinose. During the course of environmental sampling for B. pseudomallei in the Northern Territory of Australia, an isolate, MSMB 43, was recovered that is arabinose positive.
Genetic analysis using 16S rDNA sequencing and DNA/DNA hybridization indicates that MSMB 43 is most similar to B. thailandensis although multi-locus sequence typing indicates that this isolate is divergent from both B. pseudomallei and other described B. thailandensis.
We report the isolation and initial characterization of strain MSMB 43, which is a B. thailandensis-like isolate recovered in Australia.
Burkholderia thailandensis is a less virulent close relative of Burkholderia pseudomallei, the causative agent of melioidosis . B. thailandensis can be differentiated biochemically from B. pseudomallei by its ability to assimilate arabinose [1, 2]. During the course of environmental surveys for B. pseudomallei in the rural region outside Darwin, Northern Territory, Australia, an arabinose assimilating isolate, designated strain MSMB 43, was recovered from a bore water source that also yielded B. pseudomallei from the same and subsequent samples.
We report the initial characterization of a B. thailandensis-like isolate, the first of its kind, in Australia. In this study we characterize strain MSMB 43 using phenotypic tests, 16S rDNA gene sequencing, multi-locus sequence typing (MLST), and DNA-DNA hybridization.
Results and Discussion
Standard biochemical testing, including arabinose assimilation, identified strain MSMB 43 as B. thailandensis. However, MSMB 43 did not grow at 42°C and produced little to no gas from nitrate [1, 3]. A B. pseudomallei-specific real-time PCR method targeting a gene in the type III secretion system (TTS) was performed as previously described. Strain MSMB 43 was negative by TTS real-time PCR suggesting that it was not a B. pseudomallei .
The accession numbers for the 16S rDNA sequences determined for strains MSMB 43 and Burkholderia thailandensis ATCC 700388T are [GenBank: EF114404] and [GenBank: EF535235] respectively. The 16S rDNA sequence of strain MSMB 43 has 99.7% similarity and 98.9% identity to the 16S rDNA sequence of the B. thailandensis type strain. The discrepancy between the % similarity and % identity is due to multiple heterogeneous base calls in the sequence for MSMB 43, probably resulting from differences in alleles of the 16S rDNA, which has been previously noted for B. pseudomallei, but not in B. thailandensis [1, 5].
DNA-DNA hybridization using labeled DNA from MSMB 43 and from the Burkholderia thailandensis type strain.
Source of unlabeled DNA
Results with labeled DNA from B. thailandensis ATCC 700388T
Results with labeled DNA from strain MSMB 43
B. thailandensis ATCC 700388T
Burkholderia pseudomallei is a major cause of community acquired septicemia in Thailand and in tropical northern Australia, especially the Darwin region of the Northern Territory [10, 11]. As an environmental saprophyte, it has a wide distribution in endemic areas and poses a hazard for those who are exposed to it. In northern Australia, the ability to distinguish the pathogen B. pseudomallei from less or non-pathogenic species is important since public health action may result [4, 5, 9, 10]. For instance, the misidentification in the U.S. of B. thailandensis as B. pseudomallei could potentially trigger an unnecessary bioterrorism investigation.
Strain MSMB 43 appears distinct from B. thailandensis, B. pseudomallei, and B. oklahomensis by analysis of MLST sequences, but unexpectedly the percent DNA-DNA hybridization is above the 70% threshold that fulfills part of the current gold standard for species definition .
B. thailandensis is a close relative of B. pseudomallei, but is much less virulent in animal models such as hamsters [1, 2]. Since access to B. pseudomallei is restricted due to its classification as a category B select agent, B. thailandensis and other less virulent related strains may serve as acceptable substitutes for training and research [13, 14]. B. thailandensis has also been the subject of increased investigation recently, especially in genome sequence comparison studies, to reveal virulence factors in B. pseudomallei [14–16].
We report the isolation and characterization of strain MSMB 43 from bore water in the rural Darwin region of tropical northern Australia. This is the first report of a B. thailandensis-like isolate in Australia. Further genomic characterization of MSMB 43 may yield insights into the phylogenetic relatedness of B. thailandensis strains and may allow identification of yet undescribed virulence factors in B. pseudomallei. The relationship of this isolate to B. thailandensis strains from southeast Asia and to endemic Australian Burkholderia species requires further elucidation. The genome of MSMB 43 is currently being fully sequenced along with a collection of B. pseudomallei, B. mallei and B. thailandensis strains from various locations . The sequencing project should help unravel the phylogeny of these Burkholderia and ascertain if MSMB 43 represents environmental Burkholderia species in Australia which are ancestral to both Southeast Asian B. thailandensis and B. pseudomallei. Recent data show that Australian B. pseudomallei strains are probably ancestral to those from southeast Asia [18, 19]. The origins of B. pseudomallei may therefore be linked to environmental Burkholderia species in Australia such as MSMB 43. In addition, comparison of B. pseudomallei and closely related Burkholderia strains collected concurrently from environmental sources may provide further insights into horizontal gene transfer among these species .
Standard biochemical testing was performed as outlined in Weyant et al . Arabinose assimilation was tested using a minimal salts solution with 10% L-arabinose.
Whole cell suspensions of bacteria were used for this study as previously described . Bacteria were grown by plating one loop (1 μl) of stock cell suspension in defibrinated rabbit blood (stored at -70°C until use) on trypticase soy agar with 5% defibrinated sheep blood (SBA) (BBL Microbiology systems, Cockeysville, MD) and incubated aerobically 1–2 days at 37°C. A single colony was suspended in 200 μl of 10 mM Tris, pH 8.0 in a 1.5 ml Millipore 0.22 μm filter unit (Millipore, Bedford, MA), heated at 95°C for 30 min, and centrifuged at 6000 × g for 5 min.
16S rDNA sequencing
Sequencing and analysis of 1488 bp of the 16S rDNA was performed as previously described . In brief, we used the Expand Hi Fidelity PCR system (Roche, Indianopolis, IN). The amplification mix consisted of 1× buffer #2, 200 μM dNTP mix, 0.4 μM primers F229 and R1908, 5 units Expand Polymerase, and 2 μl of cell extract in a total volume of 50 ul. Reactions were first incubated for 5 min at 95°C. Then, 35 cycles were performed as follows: 15 sec at 94°C, 15 sec at 60°C, and 1 min and 30 sec at 72°C. Reactions were then incubated at 72°C for an additional 5 min. PCR products were purified with Qiaquick PCR purification kit (Qiagen, Valencia, CA).
Sequencing primers were chosen from a panel of previously described oligonucleotides . Sequencing was performed using an Applied Biosystems (ABI) BigDye terminator cycle sequencing ver 3.1 kit as per the manufacturer's instructions, except 0.25 μl of BigDye 3.1 were used for each reaction instead of 8 μl (Applied BioSystems, Foster City, CA). Sequencing products were purified by using Centri-Sep spin columns (Princeton Separations, Adelphia, NJ) and were resolved using an Applied Biosystems model 3130xl automated DNA sequencing system (Applied BioSystems, Foster City, CA). BestFit in the Wisconsin package (Accelrys, San Diego) was used to assess the percent identity between sequences.
Multi-locus sequence typing
We used the panel of primers described on the MLST Web site and in Godoy et al. for both amplification and sequencing [6, 7]. For amplification, we used the Expand Hi Fidelity PCR system. Amplification mix consisted of 1× buffer #2, 200 μM dNTP mix, 0.4 μM forward and reverse primers, 0.9 units Expand Polymerase, and 1 μl of cell extract in a total volume of 25 ul. Conditions consisted of an initial 5 min hold at 95°C, followed by 35 cycles at 95°C for 30 sec, 60°C for 30 sec, and 72°C for 1 min with a final hold at 72°C for 10 min. PCR products were purified and sequenced as described above for the 16S rDNA sequencing except using the MLST primer set.
To determine relatedness to other Burkholderia strains, the sequences of the seven alleles were concatenated and analyzed using the Neighbor-joining, Kimura 2-parameter method with 1000 step bootstrap in MEGA 3.1 [6, 20]. BestFit was used to assess the percent identity between concatenated sequences.
DNA-DNA hybridization was performed using MSMB 43 and the type strain of B. thailandensis, strain ATCC 700388T. Cells were harvested and lysed, and the chromosomal DNA was isolated and purified as previously described . DNA from strain MSMB 43 and strain ATCC 700388T were labeled with [32P]dCTP using a commercial nick translation kit (Invitrogen Life Technologies, Carlsbad, CA) and tested for reassociation to unlabeled DNA from the same strain (homologous reaction), as well as to each other (heterologous reactions). Relative binding ratios and percent divergence were calculated as described previously .
We thank Heidi Smith-Vaughan and Yvonne Wood for assistance with bacterial isolation and identification. This publication made use of the Multi Locus Sequence Typing (MLST) website at Imperial College London developed by David Aanensen and Man-Suen Chan and funded by the Wellcome Trust .
The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the Centers for Disease Control and Prevention.
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