VNTRs might possibly contribute to the genomic polymorphism
and/or evolution. Comparative genomics of pathogenic Mycobacterium tuberculosis showed that a variation in size and number of repeats, located in coding regions, can result in a variable expression of surface-exposed proteins that play a role in pathogenicity [54]. These changes could possibly help the pathogen to avoid the host immune click here response. Expansion or reduction of the number of tandem repeats can influence the expression, structure and activity of cellular proteins. Tandem repeats located within regulatory regions can result in a modification of gene expression at the transcriptional level [55]. All tested Clav-VNTR loci were found in putative coding regions
(Table 2). At least two of them were found within genes linked to processes taking place in a cell envelope (Clav-VNTR-13: putative NAD (FAD)-dependent dehydrogenase and Clav-VNTR 16: putative glycine/betaine ABC transporter). We Smoothened antagonist could speculate that variability observed within these regions might possibly help bacteria to alternate the proteins of a cell envelope. However, more research has to be performed on the role of tandem repeat copy, and virulence in Cmm. The genetic structure of the studied strains was assessed by the sequence analysis of two housekeeping genes, gyrB and dnaA, which were previously reported to be good molecular markers for studying populations of the genus Clavibacter[32, 38]. The phylogenetic position of Cmm strains was supported by high bootstrap values in a Maximum Likelihood tree. High similarity of Belgian strains from recent outbreaks was detected both, in a gene sequence analysis and by an MLVA typing method, supporting the hypothesis about their monomorphic nature. The percentages of polymorphic sites observed for the concatenated set of gyrB and dnaA genes (Table 4) was higher than the value obtained from five concatenated genes described in Phosphoribosylglycinamide formyltransferase a recently published MLSA scheme of Clavibacter
michiganensis subsp. michiganensis, (12 versus 8.8) [33]. Based on these parameters the genes selected in this work can be applied in MLST studies to investigate highly similar Cmm populations. Table 4 Discrimination indices for Clavibacter typing methods Typing technique Hunter-Gaston diversity index Number of haplotypesb Number of polymorphic sitesb Number of sites % of polymorphic sites gyrB 0.586b 10 47 440 10.7 dnaA 0.662b 12 87 675 12.9 Concatenated gyrB-dnaA 0.758b 17 134 1115 12.0 MLVA 0.800a 25 na na na aCalculated in discriminatory Power Calculator (http://insilico.ehu.es/mini_tools/discriminatory_power/) based on 56 Cmm strains. bCalculated in DnaSP v.5 [44] based on 56 Cmm strains. na- not applicable. In this study, MLVA was successfully applied to investigate a genetic relationship of Cmm strains from recent Belgian outbreaks.