For the NB-Seas subset, STs that occurred multiple times were eit

For the NB-Seas subset, STs that occurred multiple times were either recovered from North Sea isolates (ST758, ST760 and ST764) or Baltic Sea isolates (ST481) but not from both (Figure 2E). Two STs were found in the retail samples too: ST394 was found in a sample taken from Sri Lankan prawn farms

and in a German retail sample find more originating from the Indian Ocean; ST540 isolates were recovered from Ecuadorian Nutlin-3a in vitro prawn farms as well as from a German retail sample originating from Ecuador. Phylogenetic analysis Global dataset The UPGMA analysis based on the concatenated sequences revealed a high genetic diversity among the analyzed strains (Figure 3). However, groups of isolates were identified by clustering of STs. These clusters contain strains with > 99% similarity. The two main clusters (marked by I and II) of the UPGMA showed a different composition in terms of geographic origin of strains. A higher proportion of South American (54%) and European STs (65%) was located in cluster I, whereas a higher proportion of Asian STs (60%) was located in cluster II. Nine of the 20 clusters (marked www.selleckchem.com/products/pci-32765.html by boxes) largely consisted of strains originating from the same continent (Figure 3A). The CCs that were identified by goeBURST clustered together and the DLVs and TLVs were closely related in the UPGMA too (Figure 3A). Figure 3 UPGMA tree constructed from the concatenated nucleotide (A) and peptide (B) sequences

of 130 isolates. Squares next to the tree are colored regarding geographical origin (Asia-red, South America-green, Europe-blue and diverse origin-black). A STs of strains are shown and asterisks (*) mark STs found in more than one isolate originating from the same continent. Boxes mark cluster of isolates with more than 99% similarity. Coloring of boxes indicates the origin of majority of strains, while light grey boxes are indicative of clusters of diverse origins. Smaller dark grey boxes indicate doublets AMP deaminase and CCs. Main clusters are indicated by Roman numerals. B pSTs of strains are shown and asterisks (*) mark pSTs representing more than one ST. Boxes mark clusters

of pSTs with more than 99.95% similarity. All pSTs except pST79 and pST164 belong to a single CC. In contrast, the pSTs were grouped into one major cluster, except for pST79 and pST164 from Ecuador that were DLV and TLV, respectively (Figure 3B). The AA-UPGMA revealed no clustering depending on the geographic origin of strains. The pSTs that were more common and belonged to different STs did not originate from the same continent as indicated by the black squares. Therefore neither geographic dependency of pST affiliation nor clustering depending of origin was present. Comparing the results obtained by UPGMA analysis of MLST and AA-MLST data, clusters on nucleotide level were not always found on peptide level (Figures 3A and B). All STs that form a CC or doublet were characterized by the same pST (CC410 and doublet ST246-ST56 were pST1; doublet ST760-ST412 was pST6).

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