These sensors were purchased from Vernier (Beaverton, Tideglusib manufacturer OR). A double bagging system was used to avoid air leaks during the ABT-263 cell line measurements taken with the O2 sensors during incubation. Changes in O2 concentration were measured in all subsamples. The O2 Gas Sensor was calibrated to the environment within the plastic bag which produces condensation (100% humidity), and therefore
was started at 20.1 O2 in percentage by volume. The DO sensor was positioned in the enrichment bag with the collection tip of the sensor placed at the bottom of the enrichment broth with the subsample. The O2 sensor was placed in the head space of the bag above the liquid. The excess air was expelled from the bag before sealing and incubation for 48 h. The DO sensor was calibrated by pre-warming the probe for 10 min in the broth before starting the readings. Throughout incubation, the sensors were connected to a laptop computer with the Logger Lite™ data collection program (version 1.4) that recorded readings every 1 min. The data were analyzed using
Microsoft Excel (Microsoft Corporation, Redmond, WA). Statistical analyses An unpaired sample design was used where the number of Campylobacter positive subsamples enriched under microaerobic conditions (reference method) was compared to the number of Campylobacter positive subsamples enriched under aerobic conditions TGF-beta inhibitor (alternative method). Statistical comparisons were made using the formula mcnemar. test (x, y, correct = TRUE) of R [41], which is the McNemar’s chi-squared (γ2) test for count data, and it is based on McNemar’s Test for correlated proportions [42]. The accuracy, sensitivity, specificity,
and Kappa values for the test were calculated using 2-by-2 tables according to Hanrahan and Madupu [43]. A receiver operating characteristic (ROC) curve was determined with a web-based calculator with an ordinal rating scale of 1 through 4, where 1 represents samples that were negative FER for Campylobacter spp. in both subsamples, and 4 represents samples that were positive for both subsamples [44]. Acknowledgements We thank Leslie Speegle for her assistance in collecting the sensor data and Kennedy Wekesa for allowing us access to the phase contrast microscope. JK work was supported by grant 0754966 from the Research Experiences for Undergraduates Program of the Biology Directorate of the National Science Foundation. The work of S.B. is supported by Science Foundation Ireland (UCD 09/IN.1/B2609). References 1. Anon: European Food Safety Authority. Trends and sources of zoonoses, zoonotic agents and antimicrobial resistance in the European Union in 2004 2006, 96–16. 2. Anon: Isolation, identification, and enumeration of Campylobacter jejuni / coli / lari from poultry rinse and sponge samples. [http://www.fsis.usda.gov/PDF/MLG_41_01.pdf] Laboratory Guidebook, MLG 41.