Colicin Z, a structurally and functionally novel colicin type that selectively kills enteroinvasive Escherichia coli and Shigella strains.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
31 07 2019
Historique:
received: 08 04 2019
accepted: 16 07 2019
entrez: 2 8 2019
pubmed: 2 8 2019
medline: 29 10 2020
Statut: epublish

Résumé

Colicin production in Escherichia coli (E. coli) strains represents an important trait with regard to microbial survival and competition in the complex intestinal environment. A novel colicin type, colicin Z (26.3 kDa), was described as a product of an original producer, extraintestinal E. coli B1356 strain, isolated from the anorectal abscess of a 17 years-old man. The 4,007 bp plasmid (pColZ) was completely sequenced and colicin Z activity (cza) and colicin Z immunity (czi) genes were identified. The cza and czi genes are transcribed in opposite directions and encode for 237 and 151 amino acid-long proteins, respectively. Colicin Z shows a narrow inhibitory spectrum, being active only against enteroinvasive E. coli (EIEC) and Shigella strains via CjrC receptor recognition and CjrB- and ExbB-, ExbD-mediated colicin translocation. All tested EIEC and Shigella strains isolated between the years 1958-2010 were sensitive to colicin Z. The lethal effect of colicin Z was found to be directed against cell wall peptidoglycan (PG) resulting in PG degradation, as revealed by experiments with Remazol Brilliant Blue-stained purified peptidoglycans and with MALDI-TOF MS analyses of treated PG. Colicin Z represents a new class of colicins that is structurally and functionally distinct from previously studied colicin types.

Identifiants

pubmed: 31366939
doi: 10.1038/s41598-019-47488-8
pii: 10.1038/s41598-019-47488-8
pmc: PMC6668396
doi:

Substances chimiques

Colicins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

11127

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Auteurs

Lenka Micenková (L)

Research Centre for Toxic Compounds in the Environment, Faculty of Science, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic.

Juraj Bosák (J)

Department of Biology, Faculty of Medicine, Masaryk University, Kamenice 5, Building A6, 625 00, Brno, Czech Republic.

Jiri Kucera (J)

Department of Biochemistry, Faculty of Science, Masaryk University, Kamenice 5, Building A5, 625 00, Brno, Czech Republic.

Matěj Hrala (M)

Department of Biology, Faculty of Medicine, Masaryk University, Kamenice 5, Building A6, 625 00, Brno, Czech Republic.

Tereza Dolejšová (T)

Department of Genetics and Microbiology, Faculty of Science, Charles University, Viničná 5, 128 44, Prague 2, Czech Republic.

Ondrej Šedo (O)

Central European Institute of Technology, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic.

Dirk Linke (D)

Department of Biosciences, University of Oslo, P.O. Box 1066, Blindern, 0316, Oslo, Norway.

Radovan Fišer (R)

Department of Genetics and Microbiology, Faculty of Science, Charles University, Viničná 5, 128 44, Prague 2, Czech Republic.

David Šmajs (D)

Department of Biology, Faculty of Medicine, Masaryk University, Kamenice 5, Building A6, 625 00, Brno, Czech Republic. dsmajs@med.muni.cz.

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Classifications MeSH