Fungal diversity associated with diverse tomato organs (18S). Searching for Salmonella Using a cutoff of 97% similarity across 97% of sequence, a few hits to Salmonella from the 16S amplicon

libraries were identified. Closer phylogenetic inspection (Figures 5 and 6) using tree-based methods with maximum likelihood suggests that the putative Salmonella hits were more likely closely related taxa and not in fact, Salmonella. Clustering of putative Salmonella individuals using the program STRUCTURE corroborated these phylogenetic results and suggested that a representative set of Salmonella reference sequences form Genbank belonged to a single cluster and our putative Salmonella sequences from the tomato anatomy samples composed a second cluster (Additional file 2: Table S2). Using the IMG pipeline described in the methods section, no Salmonella was detected RGFP966 order in any of the shotgun-sequenced metagenomic samples. Figure 5 Tree based examination of Salmonella 16S sequences. Phylogenetic placement of putative Salmonella 16S rRNA gene sequences from different anatomical regions of tomato plants. Blue sequences are Salmonella reference samples (Additional file 2: Table S2) and red sequences are from the tomato anatomy data. A single tip label is used in instances where a clade consists

of predominantly one taxa. Phylogenetic placement of putative Salmonella 16S rRNA gene sequences from different anatomical regions of tomato plants. Blue sequences are Salmonella reference samples (Additional file 2: Table S2) and red sequences are from the tomato anatomy dataset. Figure 6 The clustering of individuals using the program

selleck chemical STRUCTURE corroborate the phylogenetic results in that Salmonella reference samples are primarily distinct from the isolates identified as being putative Salmonella based on BLAST results (Figure 5 ). At K = 2, the reference sequences belong to one cluster and the anatomy samples comprise the second cluster. Evolving habitat The Cobimetinib mw tomato (Solanum lycopersicum syn. Lycopersicon esculentum) has been heavily cultivated since the point when it shared a common ancestor with other Solanum species such as potato (Solanum tuberosum), pepper (Capsicum sp., and eggplant (Solanum melongena) some 23 million years ago [23]. Breeding has largely without our noticing, impacted the dynamic interplay of the tomato and its microbial environment for the last 500 years. Quality trait loci (QTL) focused breeding, relying on genomic methods, has drastically sped up the rate of phenotypic change in commercial tomato plants. Thousands of markers across tomato’s 12 chromosomes are correlated to phenotypic characteristics such as thickened pericarps for improved transport durability, joint-less pedicels for ease of processing, ethylene insensitivity for manipulation of ripening dynamics, viral, fungal, nematode and bacterial resistance traits, and many more.