One of the PCR-positive isolates did not grow on subculture. These five strains were excluded from the study, resulting www.selleckchem.com/products/Pazopanib-Hydrochloride.html in a total of 87 eligible isolates. Of the 87 isolates included in the study there were 17 isolates of Shigella sonnei, two isolates of Shigella flexneri, 18 isolates of Salmonella Typhimurium, 12 isolates of S. Stanley, seven isolates of S. Concord, five isolates of S. Enteritidis and 16 isolates of other non-Typhoid Salmonella. Fecal samples To mimic fecal

samples, we followed the same procedure as has been applied in the Norwegian external quality control program, organized by the NIPH. A fecal suspension from a healthy person was prepared, after controlling for the click here absence of Salmonella and Shigella. The donor fecal material was diluted (approximately 1:5) with isotonic NaCl solution (0.9%). A part of the suspension was heated (80°C, 1 hour) to prevent bacterial overgrowth selleck chemical from intestinal flora on the ESBL screening agars. For each of the 87 samples, 0.9 ml of the heat-treated fecal suspension and 0.1 ml of the non-heated suspension were mixed with 1 ml of Cary-Blair-medium. Table 1 presents the procedure applied to standardize the quantity of ESBL-producing bacteria inoculated on the screening agars. Pure culture of each of the ESBL-producing bacteria was suspended in 0.9% NaCl-solution. The optical density (OD) was then adjusted to 0.40, measured with a spectrophotometer

(Helios Epsilon from Thermo Scientific). 30 μl of each pure-culture suspension containing ESBL-producing isolates was added to the fecal suspensions. In addition, to mimic normal growth, non-ESBL E. coli (50–200 μl with an OD of 0.40) isolated from the donor feces was added to the suspensions from a pure culture. One droplet (50 μl, equivalent to ~8×104 CFU of ESBL-positive culture) of each of the 87 spiked fecal suspensions were spread onto each of the four ESBL screening agars, and on lactose-agar

Flavopiridol (Alvocidib) and XLD-agar as controls. In addition, pure culture from the ESBL-carrying isolates was inoculated onto the four screening agars to ensure that all the ESBL-carrying bacteria did grow on all four media and to facilitate the reading of the corresponding agars inoculated with the fecal specimens. All screening agars were incubated in ambient air at 37°C. After 24 hours incubation, the degree of growth was graded from 0; no growth, to 3; excellent growth. Table 1 Content of the fecal suspension Fecal suspension 1 900 μL Heat treated feces (non-ESBL) 100 μL Non-heated feces (non-ESBL) 1000 μL Cary Blair-medium 30 μL Pure culture (ESBL) OD: 0.4 (1,2×108/mL) 50-200 μL Non-ESBL E. coli OD: 0.4 (1.2×108/mL) ~2100 μL   150 μL from this suspension was inoculated on each screening agar. The preparation, inoculation and interpretation of the culture media were manually performed. ESBL screening media tested Four commercially available selective media designed to detect ESBL-producing bacteria directly from clinical specimens were compared.