MNGCs were defined as cells containing 3 or more nuclei The erro

MNGCs were defined as cells containing 3 or more nuclei. The error bars represent the standard error of the mean derived from at least 10 fields of view. ND = not detected. (B-C) Representative confocal micrographs of cells at 8 hrs post infection with B. thailandensis strain E264 (B) and B. oklahomensis strain C6786 (C). In both panels, bacteria appear red due to expression of RFP from the modified broad-host-range vector pBHR4-groS-RFP. Filamentous actin click here was stained green with FITC-phalloidin conjugate and nuclei were stained with DAPI. Scale bars represent 20 μm. B. thailandensis but not B. oklahomensis exhibits actin-based motility in J774A.1 macrophages Actin-based motility on infection of eukaryotic cells has previously

been demonstrated for B. pseudomallei [20, 21] and B. thailandensis strain E30 [22]. To determine whether other B. thailandensis strains and B. oklahomensis are also able to migrate using actin-based motility, J774A.1 macrophages were infected with strains that expressed red fluorescent protein from plasmid pBHR4-groS-RFP. In preliminary studies, we showed that the presence of the plasmid did not affect the growth of the bacteria in LB broth or inside macrophages, and the plasmid was stably maintained for the course of the intracellular replication assay. At different time points post infection, macrophages were stained with Phalloidin conjugated to FITC and analysed by confocal microscopy. Both B. thailandensis

and B. oklahomensis were visualised in the cells. Actin tails were visible and associated with B. thailandensis (Figure 3B) but were not visible Pim inhibitor Adenosine triphosphate in B. oklahomensis infected cells (Figure 3C). Infection of Galleria mellonella larvae with Burkholderia Galleria mellonella (wax moth) larvae were challenged with approximately 100 cfu of B. pseudomallei, B. thailandensis or B. oklahomensis and survival was recorded at 24 hrs post-challenge. B. pseudomallei strains 576 or K96243 caused 100% mortality, but no deaths were observed after challenge with

B. pseudomallei 708a (Figure 4A). Challenge with B. oklahomensis strains C6786 or E0147 also did not result in death of the larvae at 24 hrs post infection. The B. thailandensis strains showed different degrees of virulence in this model. 100% mortality was recorded after challenge with B. thailandensis CDC272 or CDC301. Challenge with B. thailandensis Phuket or E264 resulted in mortality of approximately 80% and 50% of larvae, respectively (Figure 4A). At 20 hrs post challenge, just prior to the onset of paralysis and death, larvae were sacrificed and the number of bacteria in the haemocoel was enumerated. For all of the strains tested, the bacterial numbers at 20 hrs post infection were higher than the input number (Figure 4B). Similar to the cell culture model, B. pseudomallei strains 576 and K96243 and B. thailandensis strains CDC272, CDC301 and Phuket showed increased bacterial numbers relative to B. pseudomallei 708a, B.

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