Bacterial isolates and genomic DNA preparation The detection limits and specificities of the assays were evaluated using genomic materials from the bacterial strains and other sources displayed in Additional file 1 Table S1. The pathogen panel included (besides a variety of Eukaryal organisms): 8 B. anthracis strains and 31 near relatives (22 B. cereus, 5 B. thuringiensis and 4 B. mycoides), 21 F. tularensis

strains (16 subspecies holarctica, 4 tularensis and 1 novicida) and 4 of the closest related species F. philomiragia, 23 Y. pestis (including Antiqua, Mediaevalis and Orientalis biovars) and 3 strains from the closest relative Y. pseudotuberculosis and 7 strains from Y. enterocolitica. From most of the B. anthracis, F. tularensis and Y. pestis strains we only had genomic DNA (lysates) available to verify specificity of our assays. this website Several strains

were available as live cultures in our laboratory and these were used as resource for the production of larger quantities of genomic DNA. B. anthracis and Y. pestis strains were acquired from the NCTC (National Culture Type Collection, UK) and the Pasteur Institute (France). https://www.selleckchem.com/products/bmn-673.html The Francisella holarctica strain was a patient isolate. Other genomic materials were lysates from bacterial cultures provided by other researchers as mentioned in the acknowledgements. Cultivation of these strains was carried out in a BSL3 glove-box.

Colonies from B. anthracis, F. tularensis and Y. pestis were grown on Columbian sheep blood agar plates and chocolate agar plates. Single colonies were transferred to liquid BHI (Brain Heart Infusion, 27 g/L) medium. After cultures had grown to visible turbidity, 1.4 ml cell culture was centrifuged and the pellet was resuspended in 250 μl TE pH 8. Cells were incubated for 30 minutes at 100°C. Lysed cultures were filtered through a 0.22 μm sterile Ultrafree-MC spinfilter (Millipore, Selleckchem LCZ696 Amsterdam, the Netherlands) and the filtrate Sunitinib concentration was subsequently transported from the BSL3 facility for handling under normal laboratory conditions. Cultures from non-target bacteria that were used in the specificity panel were obtained from the culture collection at the RIVM. These cultures were cultivated under BSL2 conditions and lysates of these cultures were used for specificity testing. DNA extraction and purification was carried out by using NucliSens Magnetic Extraction Reagents (bioMérieux, Boxtel, the Netherlands) following the manufacturers instructions. This method performed best with regard to efficiency and ease-of-use when compared to other kits. This comparison was carried out as follows. Dilution series of a mixture of genomic DNA from B. anthracis, Y. pestis and F. tularensis, and spores from B.