is a clinically dominant form among the other virulent species of complex (Bcc). In the present study, we sequenced and analyzed the genomes of seven nosocomial Bcc isolates, five of which were isolated from the bloodstream infections and two isolates were recovered from the hospital setting during the surveillance. Genome-based species identification of the Bcc isolates using a type strain explicitly identified the species as Moreover, single nucleotide polymorphism analysis revealed that the six isolates were clonal and phylogenetically distinct from the other . Comparative genomics distinctly revealed the larger genome size of six clonal isolates as well as the presence of a novel 107 kb genomic island named as BcenGI15, which encodes putative pathogenicity-associated genes. We have shown that the BcenGI15 has an ability to actively excise from the genome and forming an extrachromosomal circular form suggesting its mobile nature. Surprisingly, a homolog of BcenGI15 was also present in the genome of a clinical isolate named strain EY1. This novel genetic element is present only in the variants of and isolates suggesting its interspecies existence in the main pathogenic species of the genus . In conclusion, the whole genome analysis of the genomically distinct clinical isolates has advanced our understanding of the epidemiology and evolution of this important nosocomial pathogen as well as its relatives.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382208PMC
http://dx.doi.org/10.3389/fmicb.2017.00590DOI Listing

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