A sequence type (ST), based on the allelic profile of the seven amplicons, was assigned to each strain. The sequences of all new alleles and the composition of the new STs identified are available from http://pubmlst.org/sagalactiae/. Strains were grouped into clonal complexes (CCs) with eBURST software [35]. An eBURST clonal complex (CC) was defined as all allelic profiles sharing six identical alleles with at least one other member of the group. The term “”singleton ST”" refers to a ST that did not cluster into a CC. Identification of VNTR loci Tandem repeats were
identified in the sequenced genomes of the three reference strains, NEM316, A909 and 2603 V/R, with the Microbial Tandem Repeats Database http://minisatellites.u-psud.fr[36] and the Tandem https://www.selleckchem.com/products/ca-4948.html Repeats Finder program [37]. AZD1390 datasheet We determined the size of the repeat sequence and the number of repeat units for the three reference strains. BLAST analysis was carried out to determine
whether the repeats were located within or between genes and to identify a hypothetical function for the open reading frame involved. The TR locus name was defined according to the following nomenclature: common name_size of the repeat sequence_size of the amplicon for the reference strain_corresponding number of repeats (Table 1). The primers used for amplification targeted the 5′ and 3′ flanking
regions of selected loci and matched the sequences present at these positions in the Protein kinase N1 genomes of strains NEM316, A909 and 2603 V/R. We initially selected and evaluated 34 tandem repeats with repeat units of more than 9 bp in length. Some TRs were not present in all the strains, some were present in all strains and displayed no polymorphism, and others were too large for amplification in standard conditions. Six TRs were retained for this study, selected on the basis of their greater FHPI price stability and discriminatory power for four of the six (Table 1). Table 1 Characteristics of the 6 VNTR loci selected for MLVA scheme to genotype the 186 strains of S. agalactiae VNTR1 Repeat size bp2 Putative function3 Expected number of repeats4 PCR product bp5 Number of alleles min-max size of amplicons (bp) HGDI 6 2603 V/R A909 NEM316 SAG2_32pb_244pb_3U 32 Non-cds7 3 3 3 244 3 212 – 276 0.474 [0.427 - 0.522] SAG3_24pb_126pb_2U 24 Protein DnaJ 3 2 3 126 2 126 – 150 0.481 [0.452 - 0.511] SAG4_60pb_114pb_1U (SATR1)* 60 Hypothetical protein 3 1 1 114 6 114 – 414 0.713 [0.691 - 0.735] SAG7_18pb_285pb_8U (SATR2)* 18 Hypothetical protein 6 8 – 285 9 231-573 0.745 [0.701 - 0.789] SAG21_48pb_783pb_14U (SATR5)* 48 FbsA – 14 18 783 26 117 – ≈2000 0.893 [0.867 - 0.919] SAG22_159pb_928pb_5U 159 Hypothetical protein 2 5 2 928 7 292 – 1246 0.713 [0.666 – 0.