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Title:The LexA regulated genes of the Clostridium difficile
Authors:ID Walter, Beata Maria (Author)
ID Rupnik, Maja (Author)
ID Hodnik, Vesna (Author)
ID Anderluh, Gregor (Author)
ID Dupuy, Bruno (Author)
ID Paulič, Nejc (Author)
ID Žgur-Bertok, Darja (Author)
ID Butala, Matej (Author)
Files:.pdf BMC_Microbiology_2014_Walter_et_al._The_LexA_regulated_genes_of_the_Clostridium_difficile.pdf (1,16 MB)
MD5: 3D831395DDD4C95165600CBBEEEA3552
 
URL http://bmcmicrobiol.biomedcentral.com/articles/10.1186/1471-2180-14-88
 
Language:English
Work type:Scientific work
Typology:1.01 - Original Scientific Article
Organization:MF - Faculty of Medicine
Abstract:Background: The SOS response including two main proteins LexA and RecA, maintains the integrity of bacterial genomes after DNA damage due to metabolic or environmental assaults. Additionally, derepression of LexA-regulated genes can result in mutations, genetic exchange and expression of virulence factors. Here we describe the first comprehensive description of the in silico LexA regulon in Clostridium difficile, an important human pathogen. Results: We grouped thirty C. difficile strains from different ribotypes and toxinotypes into three clusters according to lexA gene/protein variability. We applied in silico analysis coupled to surface plasmon resonance spectroscopy (SPR) and determined 16 LexA binding sites in C. difficile. Our data indicate that strains within the cluster, as defined by LexA variability, harbour several specific LexA regulon genes. In addition to core SOS genes: lexA, recA, ruvCA and uvrBA, we identified a LexA binding site on the pathogenicity locus (PaLoc) and in the putative promoter region of several genes involved in housekeeping, sporulation and antibiotic resistance. Conclusions: Results presented here suggest that in C. difficile LexA is not merely a regulator of the DNA damage response genes but also controls the expression of dozen genes involved in various other biological functions. Our in vitro results indicate that in C. difficile inactivation of LexA repressor depends on repressor`s dissociation from the operators. We report that the repressor`s dissociation rates from operators differentiate, thus the determined LexA-DNA dissociation constants imply on the timing of SOS gene expression in C. difficile.
Keywords:Clostridium difficile, antibiotic resistance, toxin regulation, SOS system, surface plasmon resonance, SPR, LexA repressor
Publication status:Published
Publication version:Version of Record
Year of publishing:2014
Number of pages:str. 1-20
Numbering:Letn. 14
PID:20.500.12556/DKUM-66507 New window
ISSN:1471-2180
UDC:577.2
ISSN on article:1471-2180
COBISS.SI-ID:3097423 New window
DOI:10.1186/1471-2180-14-88 New window
NUK URN:URN:SI:UM:DK:WMFMKAWB
Publication date in DKUM:29.06.2017
Views:1550
Downloads:390
Metadata:XML DC-XML DC-RDF
Categories:Misc.
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Record is a part of a journal

Title:BMC Microbiology
Shortened title:BMC Microbiol.
Publisher:BioMed Central
ISSN:1471-2180
COBISS.SI-ID:2441492 New window

Document is financed by a project

Funder:EC - European Commission
Funding programme:FP7
Project number:237942
Name:A Clostridal Biology Network to Facilitate European-wide Medical Countermeasures and Commercial Exploitation
Acronym:CLOSTNET

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:29.06.2017

Secondary language

Language:Slovenian
Keywords:Clostridium difficile, rezistenca na antibiotike, odpornost na antibiotike, regulacija toksinov, sistem SOS, površinska plazmonska resonanca, SPR, represor LexA


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