jejuni and C. coli. Resistance observed in these strains has the potential to complicate the effectiveness of treatment for poultry-acquired Campylobacter infections in humans should they remain on the processed product. Molecular subtyping using fla typing and PFGE provided additional information on antimicrobial-resistant Campylobacter from processed turkey. Fla-PFGE types were relatively diverse and associated with a specific plant and species. Some ciprofloxacin and/or erythromycin resistant isolates with the same fla-PFGE types were recovered from processing

both before and after chilling. Factors contributing to the occurrence of antimicrobial-resistant Campylobacter in processed turkey warrant further investigation. Methods Campylobacter isolates Campylobacter #Anlotinib randurls[1|1|,|CHEM1|]# isolates in A-1210477 purchase this study (n = 801, Table 2) were obtained from two unrelated Midwestern processing plants (A and

B) prior to the FDA ban of enrofloxacin use in poultry [8]. Plant A received turkeys from independent producers belonging to a farmers’ cooperative, while plant B received turkeys from producers under contract with a large turkey processing company. Isolates were recovered and identified by Logue et al. as previously described [8]. Briefly, isolates were recovered from whole carcass swabs collected from randomly selected carcasses at two points on the processing line: pre chill and post chill, from plants visited monthly over a period of 12 months

[8]. Samples of the chill water were also collected. Birds sampled on a single day were usually from one supplier or farm. Throughout all parts of the study, isolates were removed from -80°C storage in Brucella broth (Becton Dickinson, Cockeysville, Md.) with 20% glycerol Non-specific serine/threonine protein kinase and cultured onto sheep blood agar (BBL Prepared Media Trypticase Soy Agar II, 5% Sheep Blood; Becton Dickinson, Sparks, Md.). All cultures were incubated in a microaerobic environment of approximately 14% CO2 and 6% O2 generated by Pack-Micro Aero (Mitsubishi Gas Chemical, New York, N.Y.). Antimicrobial susceptibility testing Antimicrobial susceptibility testing on all isolates (n = 801) was conducted using the agar dilution method [52, 53] with testing ranges of 0.008-4 μg/ml for ciprofloxacin (Serologicals Proteins, Kankakee, Ill.) and 0.06-32 μg/ml for erythromycin (Sigma Chemical, St. Louis, Mo.). C. jejuni ATCC #33560 was used as a quality control strain [11, 53]. Resistance breakpoints were ≥ 4 μg/ml for ciprofloxacin and ≥ 32 μg/ml for erythromycin [54]. Isolates (n = 241) with an MIC of > 4 μg/ml for ciprofloxacin and/or an MIC of > 32 μg/ml for erythromycin were re-tested with extended antimicrobial concentrations of 0.5-32 μg/ml for ciprofloxacin and 2.0-128 μg/ml for erythromycin. One hundred isolates (n = 51, plant A and n = 49, plant B) were selected for further characterization.