Genome evolution and pathoadaptation of Shigella

The genus comprises a polyphyletic group of facultative intracellular pathogens that evolved from genomes have accumulated mobile elements, which may have been caused by decreased effective population size and concomitant reduction of purifying selection that allowed their proliferation. Here, we investigated the interplay of the accumulation of genomic repeats with genomic rearrangements and their impact on adaptation in bacterial evolution. We studied 414 genomes of and strains to assess the contribution of genomic rearrangements to pathoadaptation. We show that accumulated a variety of insertion sequences (ISs), experienced exceptionally high rates of intragenomic rearrangements and had a decreased rate of homologous recombination. IS families differ in the expansion rates in lineages, as expected given their independent origin. In contrast, the number of IS elements and, consequently, the rate of genome rearrangements in the enteroinvasive strain (EIEC) strain are comparable to those in other . We found two chromosomal E3 ubiquitin-protein ligases (putative IpaH family proteins) that are functional in all strains, while only one pseudogenised copy is found in the EIEC strain and none in other . Taken together, our data indicate that ISs played an important role in the adaptation of strains to a intracellular lifestyle and that the composition of functional types of ubiquitin-protein ligases may explain the differences in the infectious dose and disease severity between and EIEC pathotypes.