The fluorescence labelled PCR products of vc0147 (FAM), vc0437 (VIC), vc1457 (PET), vc1650 (NED) in one sample and vca0171 (PET) and PLX-4720 chemical structure vca0283 (NED) in a second sample were pooled for capillary electrophoresis on an Automated GeneScan Analyser ABI3730 (Applied Biosystems) at the sequencing facility of the School of Biotechnology and Biomolecular Sciences, the

University of New FDA approved Drug Library order South Wales. The fragment size was determined using the LIZ600 size standard (Applied Biosystems) and analysed using GeneMapper v 3.7 software (Applied Biosystems). Sequencing was performed to confirm the number of repeats for representative alleles. Phylogenetic analysis A Minimum spanning tree (MST) using pairwise difference was generated using Arlequin v. 3.1, available from BMS345541 solubility dmso http://​cmpg.​unibe.​ch/​software/​arlequin3,

in which if alternative connections of equal distance were present, the connection between isolates with closest geographical or temporal proximity was selected. The Simpson’s Index of Diversity (D value) [30] was calculated using an in-house program, MLEECOMP package [31]. Acknowledgements The authors thank Gordon Stevenson for technical assistance. This research was supported by a Goldstar award from the University of New South Wales. The authors also thank strain donors, including M.J. Albert, A. Dodin, P. Eccheveria, J. Kaper, T. Popovic, R.B.

Sack, C. Salles, W.C. Yam. Electronic supplementary material Additional file 1: Figure S1.Minimum Spanning trees of 66 V. cholerae isolates using MLVA of A) 6 VNTR loci and B) 4 VNTR loci from chromosome I. Each circle represents a MLVA profile, with the isolate Erythromycin number/s belonging to the MLVA type within the circles. The colour of each circle denotes the group to which each isolate belongs according to SNP typing [12] (see Figure 2). If isolates from different SNP groups shared a MLVA profile, the circle was divided to reflect the proportion of isolates in each SNP group. Thick solid connecting lines represent differences of one repeat unit, thin solid lines and dashed lines represent 1 and 2 loci differences respectively, and longer dashed lines represent more than 2 loci differences. The size of each circle reflects the number of isolates within the circle. (PDF 183 KB) References 1. Chatterjee SN, Chaudhuri K: Lipopolysaccharides ofVibrio cholerae. I. Physical and chemical characterization. Biochim Biophys Acta 2003, 1639:65–79.PubMedCrossRef 2. Reeves PR, Lan R: Cholera in the 1990s. Br Med Bull 1998, 54:611–623.PubMedCrossRef 3. Barua D, Greenough WB: Cholera. In Current Topics In Infectious Disease. Plenum, New York; 1992. 4. WHO: Cholera. Wkly Epidemiol Rec 2010, 85:16. 5.