The TIR domain containing locus of Enterococcus faecalis is predominant among urinary tract infection isolates and downregulates host inflammatory response

dc.contributor.authorKraemer, Thomas Daniel
dc.contributor.authorQuintanar Haro, Orlando Daniel
dc.contributor.authorDomann, Eugen
dc.contributor.authorChakraborty, Trinad
dc.contributor.authorTchatalbachev, Svetlin
dc.date.accessioned2022-11-18T09:50:37Z
dc.date.available2015-02-16T13:53:25Z
dc.date.available2022-11-18T09:50:37Z
dc.date.issued2014
dc.description.abstractBased on Toll/interleukin-1 receptor (TIR) domain structure homology, we detected a previously uncharacterized gene encoding for a TIR domain containing protein (Tcp) in the genome of Enterococcus faecalis. We assigned this gene the name tcpF (as in Tcp of E. faecalis). Screening of E. faecalis samples revealed that tcpF is more common in isolates from urinary tract infections (UTIs) than in human faecal flora. tcpF alleles showed moderate single nucleotide polymorphism (SNP) among UTI isolates. Infection of mouse RAW264.7 macrophages with a tcpF knock-out mutant led to elevated cytokine response compared to the isogenic wild type E. faecalis strain. In silico analysis predicted significant tertiary structure homology to the TIR domain of human TLR1 (TLR1-TIR). When transiently expressed in cultured eukaryotic cells, TcpF caused suppression of TLR2-dependent NF-?B activation suggesting for TcpF a role as a factor in E. faecalis that benefits colonization by modulating the host´s immune responses.en
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:hebis:26-opus-113232
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/9096
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-8484
dc.language.isodede_DE
dc.rightsNamensnennung 3.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/*
dc.subject.ddcddc:610de_DE
dc.titleThe TIR domain containing locus of Enterococcus faecalis is predominant among urinary tract infection isolates and downregulates host inflammatory responseen
dc.typearticlede_DE
local.affiliationFB 11 - Medizinde_DE
local.opus.fachgebietMedizinde_DE
local.opus.id11323
local.opus.instituteInstitute of Medical Microbiologyde_DE
local.source.freetextInternational Journal of Microbiology 2014:Article ID 918143de_DE
local.source.urihttps://doi.org/10.1155/2014/918143

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