The list of the 40 primer combinations for each IS629 site and PCR conditions can be found in Additional file 5, Table S4. IS629 presence/I-BET151 ic50 absence parsimony tree analysis IS629 PCR

fragments sizes indicating IS629 presence/absence and IS629 target site presence/absence identified by PCR using primers specific for each IS629 observed in 4 E. coli O157:H7 genomes were entered as binary characters (+ or -) into BioNumerics version 6.0 (Applied Maths, Saint-Martens-Latem, Belgium). IS629 presence/absence and IS629 target site presence/absence were used to create a phylogenetic parsimony tree rooted to A5 CC strains for A5/A6 CC strains analysis (Figure 1B) and statistical support of ZD1839 in vivo the nodes was assessed by 1000 bootstrap re-sampling. IS629 target site presence/absence were used to create a phylogenetic parsimony tree rooted to A1/A2 CC strains for strains of the entire model (A1 – A6) (Figure 1C) and statistical support of the nodes was assessed by 1000 bootstrap re-sampling. IS629 phylogenetic analysis Minimum evolution tree for IS629 sequences present in 4 E. coli O157:H7 genomes, two IS629 in O55:H7 genome, IS629 sequences from Shigella, two other IS629 isoforms (IS1203 and IS3411), and ISPsy21 (a member of the IS3 family buy MK0683 and sharing only 68% homology

with IS629) as out-group (Pseudomonas syringae pv. savastanoi TK2009-5) was constructed using Mega version 4.0 [29]. The evolutionary distances were computed using the Kimura 2-parameter method [30] and are in the units of the number of base substitutions per site. All

positions containing gaps and missing data were eliminated from the dataset (Complete deletion option). There were a total of 299 positions in the final dataset. The statistical support of the nodes in the ME tree was assessed by 1000 bootstrap re-sampling. Acknowledgements and Funding The authors thank Eric W. Brown for his helpful comments. This project was supported by an appointment to LVR through the Research Fellowship Program for the Center for Food Safety and Applied Nutrition administered by the Oak Ridge Associated Universities through a contract Myosin with the FDA. Electronic supplementary material Additional file 1: “”Figure S1″”. Schematic representation of the strategy used for primer design. Primer pairs: A: presence/absence of IS629 at specific loci, B: IS629 internal primer. A) Amplification product for locations where the IS629 element is present; B) Amplification product for locations where the IS629 element is absent, although the up-and downstream flanking region is present in the genome but not carrying an insertion. (DOC ) Additional file 2: “”Table S1″”. Genomes and plasmids investigated by “”in silico”" analysis. (DOCX 25 KB) Additional file 3: “”Table S2″”.