P5 Mechanism of impairment of testicular function by immune evasive mechanism of uropathogenic Escherichia coli (UPEC)
We aim to investigate if UPEC can silence NFκB regulated pro-inflammatory gene transcription by NFAT activated histone deacetylases (HDAC1) chromatin remodeling. Moreover, an influence of UPEC on peroxisome proliferator activated receptor (PPAR)y to repress NFκB-mediated inflammatory response will be investigated. An established rat in vivo orchitis infection model will be used to link our in vitro studies and the human biopsy investigations. Extra- and intracellular persistence of UPEC and mutants will be monitored to provide information up to what time post-infection UPEC may be detectable in biopsy specimens to help guiding diagnosis. Initial results show the presence of bacterial DNA in testis biopsies with inflammatory infiltrates, but could not reveal the species. New automated sample extraction combined with DHPLCbased profiling and subsequent sequencing of microbial marker genes allows discrimination of uropathogens and opportunistic bacteria. In vivo UPEC immunosuppressive properties seen in vitro shall be validated e.g. by examining the hypothesized shift from a Th1 to a Th2 immune response. The role of reproductive tract specific antimicrobial peptides (isoforms of SPAG11 & beta-defensins) will be examined by substitution in the in vivo infection model.