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Why? - Successful Pseudomonas aeruginosa clones with a focus on clone C

期刊

FEMS MICROBIOLOGY REVIEWS
卷 44, 期 6, 页码 740-762

出版社

OXFORD UNIV PRESS
DOI: 10.1093/femsre/fuaa029

关键词

disaggregase; FtsH; genomic island; protein homeostasis; pulsed field gel electrophoresis; whole genome sequencing

资金

  1. Bundesministerium fur Bildung und Forschung [0315827A]
  2. Deutsche Forschungsgemeinschaft [SFB 900]
  3. Swedish Research Council [K2012-56X-22034-01-3]

向作者/读者索取更多资源

The environmental species Pseudomonas aeruginosa thrives in a variety of habitats. Within the epidemic population structure of P. aeruginosa, occassionally highly successful clones that are equally capable to succeed in the environment and the human host arise. Framed by a highly conserved core genome, individual members of successful clones are characterized by a high variability in their accessory genome. The abundance of successful clones might be funded in specific features of the core genome or, although not mutually exclusive, in the variability of the accessory genome. In clone C, one of the most predominant clones, the plasmid pKLC102 and the PACGI-1 genomic island are two ubiquitous accessory genetic elements. The conserved transmissible locus of protein quality control (TLPQC) at the border of PACGI-1 is a unique horizontally transferred compository element, which codes predominantly for stress-related cargo gene products such as involved in protein homeostasis. As a hallmark, most TLPQC xenologues possess a core genome equivalent. With elevated temperature tolerance as a characteristic of clone C strains, the unique P. aeruginosa and clone C specific disaggregase ClpG is a major contributor to tolerance. As other successful clones, such as PA14, do not encode the TLPQC locus, ubiquitous denominators of success, if existing, need to be identified.

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