Methods Bacterial C188-9 strains and growth conditions For Suppression Subtractive Hybridization (SSH) we used APEC strain IMT5155 (O2:K1:H5) [10] and human UPEC strain CFT073 (O6:K2:H5) [41]. IMT5155 was isolated in 2000 from the internal organs of a laying hen in Germany with clinical symptoms of septicemia. It has been included in large-scale phylogenetic analysis and was grouped into one of the most dominant

lineages, namely phylogenetic group B2 and multi locus sequence type (ST) 140 of ST complex 95 complex [10, 37, 42]. Chicken infection studies using a systemic infection model [43] showed that APEC strain IMT5155 as well as UPEC strain CFT073 cause severe symptoms of systemic infection in 5-week-old SPF chickens and can selleck products be isolated from all internal organs in comparable numbers (C. Ewers, unpublished data). Non-pathogenic E. coli K-12 strain was

used as control strain in SSH KU55933 supplier analysis. To determine the distribution of the putative adhesin gene aatA among ExPEC and commensal E. coli strains, a strain collection (n = 779) available at the Institute of Microbiology and Epizootics, Freie Universität Berlin (n = 691), and at the College of Veterinary Medicine, Nanjing Agricultural University (n = 88) was screened. The strain set included 336 APEC, 149 UPEC, 25 newborn meningitis-causing E. coli (NMEC), and 44 pathogenic strains from diverse extraintestinal locations, referred to as “”other ExPEC”". The majority of ExPEC strains originated from birds (n = 336), companion animals (n = 90), and humans (n = 89). In addition, a total of 225 commensal strains from humans (n = 89), birds (n = 103), and from non-avian animal pheromone sources (n = 33) were included. E. coli DH5α was used for cloning procedures, BL21(DE3)pLysS was included in protein expression analysis [44] and the fim negative E. coli strain AAEC189 [20] was used for adhesion assay experiments. All E. coli strains were grown at 37°C in LB medium, supplemented with ampicillin (100 μg/ml LB), where necessary. Suppression

Subtractive Hybridization (SSH) SSH was carried out between APEC strain IMT5155 and UPEC strain CFT073 using Clontech PCR-Select™ Bacterial Genome Subtraction Kit (Clontech, Heidelberg, Germany) according to the manufacturer’s manual. Briefly, genomic DNA (1.5-2.0 μg/subtraction) of IMT5155 and CFT073 served as tester and driver DNA, respectively. The extracted genomic DNA of tester and driver was digested with restriction enzyme RsaI. Tester DNA was subdivided into two portions, which were then ligated with Adaptor 1 and Adaptor 2R, respectively, provided with the kit. After that, two hybridizations were performed. First, an excess of driver DNA was added to each adaptor-ligated tester sample. The samples were then heat-denatured and allowed to anneal. During the second hybridization, the two primary hybridization samples were mixed together without denaturing.