In this study, GSK1210151A we were able to assess the usefulness of VNTRs for the study of Xam populations. Remarkably, only 5 VNTR loci offered a very similar panorama of the pathogen populations to that obtained by 57 AFLP loci.
This finding is relevant for further studies on the population dynamics of Xam, because VNTR markers provide a faster and less expensive characterization of bacterial isolates, as has been reported for several pathogenic microorganisms [22, 24, 25, 49]. The fact that amplification of VNTRs requires neither a complex DNA extraction procedure, nor compounds different from those used in a regular PCR, makes VNTRs ideal when a large PND-1186 solubility dmso number of isolates are considered and when funding is limiting. Moreover, sharing information between laboratories would be considerably more straightforward with VNTRs than with AFLPs, because results from VNTRs can be more easily coded [17]. For future Xam survey studies we recommend the use of VNTRs. The rising number of sequenced
genomes available nowadays, provides an additional advantage to identify new VNTR loci, hence improving the characterization of several pathogens [19, 21, 50, 51]. Recently, 65 partial genomes of Xam strains have been released [52], providing a valuable opportunity to detect VNTRs with high discriminatory power. Currently, we are focusing on the prediction and evaluation of new VNTR loci into a core of the representative Xam strains using the information obtained from the 65 draft genome sequences. Our goal is to obtain a small sets of VNTRs with a high discriminatory Ribonucleotide reductase Tanespimycin concentration power, aiming to implement them in studies that involve a large number of isolates to provide a more accurate description of evolving processes taking place in Xam populations. Conclusions This study represents the first attempt to type populations of Xam using VNTRs as molecular markers. Here we demonstrated that a small number
of VNTR loci could offer a similar panorama of the status of the pathogen to that offered by AFLPs markers. Because VNTRs represent a fast and simple tool to type Xam populations, their implementation will allow a constant and adequate surveillance of the pathogen, which could provide information to improve the efficiency of strategies for disease control, such as the deployment of resistant varieties. Availability of supporting data The data sets supporting the results of this article are available in the Dryad Digital Repository: http://doi.org/10.5061/dryad.t173v. DNA sequences are available in Genbank database: (Accession numbers XaG1_02: KJ736838 – KJ736944; XaG1_29: KJ736945 – KJ737053; XaG2_52: KJ737163 – KJ737268; XaG1_67: KJ737269 – KJ737369; XaG1_73: KJ737054 – KJ737162). Ethics statement This study did not involve any human material, or human data.