(A) The phylogenetic tree was inferred with ML method based on the conserved
genomic sequences. The S. Typhimurium strains are rooted
to S. Typhi Ty2. The upper-left subtree shows the phylogenetic
relationship of the five strains in a smaller scale. The relationship was
supported by the bootstrapping values shown on the subtree. The distance (marked
in red) based on the number of SNPs was also presented on the phylogenetic
tree. The right panel shows the complete genome alignment of the five strains
generated in MAUVE [93].
The regions conserved among all genomes are colored in purple and the regions
conserved among subsets of the genomes are colored differently. If the areas
contain sequence elements not aligned, those are marked in white. Regions
that are not colored indicate no detectable homology among the five genomes
in MAUVE. The distinguished phages and phage remnants are marked on the alignment
(black: detected among all of the five strains, red: detected in a subset
of strains). (B) Comparison of the lengths of genomes, phages, and genomes
excluding phage regions among the five S. Typhimurium strains.
Length of phages is displayed on the second Y-axis due to the relatively small
value of phages in contrast to the whole genome size. (C) Alignment of the
UK-1 Gifsy-1 sequence segment harboring the two UK-1 unique genes with sequences
from the other four S. Typhimurium strains. The sequence
alignments were generated in MAUVE. The color scheme used for the alignment
is described in Fig. 2A.
The predicted genes in these regions are shown with red solid arrays. Each
gene name is indicated with the strain name (UK indicates UK-1, STM indicates
LT2, 14- indicates 14028s, MW indicates D23580, and SL indicates SL1344) followed
by its locus number obtained from each of the annotation files. The two UK-1
unique genes are marked in red in the UK-1 genome.