To our knowledge, the expression of genes involved in the gliding motility of F. columnare has not been described previously. Mucus from the skin and gills of catfish has been demonstrated to promote the chemotaxis of

F. columnare (Klesius et al., 2008; LaFrentz & Klesius, 2009). The mechanisms involved in the chemotactic response of F. columnare to mucus are largely unknown. In this study, the effects of sodium metaperiodate and different carbohydrate treatments on F. columnare chemotactic activities to catfish skin mucus were examined. Furthermore, the effect of catfish skin mucus treatment on the transcriptional levels of three gliding motility genes (gldB, gldC and gldH) in F. columnare was evaluated. The F. Epacadostat clinical trial columnare ALG-00-530 strain was used in this study. This strain was isolated from channel catfish with columnaris disease in Alabama. The ALG-00-530 is a genomovar II strain that is highly virulent to channel catfish (Arias et al., 2004; Shoemaker et

al., 2007). This strain was demonstrated to be chemotactic to mucus from the skin of channel catfish (Klesius et al., 2008). The bacteria were cultured in modified Shieh broth (0.5% tryptone, Y-27632 clinical trial 0.2% yeast extract, 45.6 μM CaCl2·2H2O, 1.1 mM KH2PO4, 1.2 mM MgSO4·7H2O, 3.6 μM FeSO4·7H2O, pH 7.2) for 24 h at 28 °C on an orbital shaker set at 90 rotations min−1 (Klesius et al., 2008; LaFrentz & Klesius, 2009). The bacteria were harvested by centrifugation at 2800 g for 15 min, washed twice with sterile phosphate-buffered saline (PBS), pH 7.2 and resuspended in Hanks’ balanced salt solution (HBSS, pH 7.2, Sigma, St. Louis, MO) to an OD540 nm of 1.0 (1 × 109 CFU mL−1 (LaFrentz & Klesius, 2009). Healthy channel catfish NWAC-103 strain (50–100 g) were cultured in 57-L glass aquaria with aeration and flowthrough water. Fish were anesthetized with 100 mg−1 tricane methanesulfonate (Argent Chemicals, Redmond, CA). The anesthetized fish were held vertically and mucus was collected from the skin by gently stroking with a soft rubber spatula into Petri dishes. Special care was taken to prevent damage to the skin and

avoid contamination with blood or other extraneous products. Farnesyltransferase The mucus from individual fish were pooled together and centrifuged at 6000 g for 15 min and the pellet (epithelium cells and cellular debris) was discarded. The mucus protein concentration was determined using the Micro BCA™ Protein assay (Pierce, Rockford, IL) and adjusted to 0.1–0.2 μg μL−1 with HBSS. Pooled mucus samples (10 μL) were streaked for bacterial isolation onto tryptic soy agar and modified Shieh agar plates and incubated at 28 °C for 72 h to check for contamination. The pooled mucus samples were stored at −80 °C before use. Chemotaxis assays with F. columnare were performed using blind-well chambers (Corning Costar, Cambridge, MA) as described previously (LaFrentz & Klesius, 2009).