columnare not exposed to catfish mucus. qPCR results revealed that the transcriptional level of gldH was significantly (P<0.001) upregulated at 5 min postexposure to the catfish mucus (Fig. 3). However, the transcriptional levels of gldB and gldC in mucus-treated F. columnare were not significantly different from that in F. columnare not treated by mucus. As a negative control, the expression of the gene encoding Hsp90 of F. columnare was not affected by the mucus treatment (Fig.
3). The relative transcriptional levels of three gliding motility genes (gldB, gldC and gldH) of d-mannose-treated Selleckchem AZD1208 F. columnare following exposure to catfish mucus were compared with that of treated F. columnare not exposed to catfish mucus. qPCR results revealed that the transcriptional level of gldB, gldC and gldH in mucus-treated F. columnare was similar to that in the PBS-treated F. columnare (Fig. 4). Similarly, the transcriptional level
of the negative control Hsp90 was not affected by the mucus treatment in the d-mannose-pretreated F. columnare (Fig. 4). When F. columnare cells were pretreated by sodium metaperiodate, their chemotactic response to catfish skin mucus was significantly inhibited. Sodium metaperiodate treatment also resulted in a partial loss of its capsule. A previous study demonstrated that sodium metaperiodate treatment of a F. columnare isolate resulted in significant inhibition of adherence to gill tissue and a 90% loss Lapatinib price of capsule (Decostere et Adenosine al., 1999). Decostere et al. (1999) hypothesized that sodium metaperiodate treatment removed or inactivated the lectin chemotactic receptor associated with the capsule by cleaving the C–C bond between vicinal hydroxyl groups of sugar, thus removing or loosening the capsule of F. columnare. We hypothesize that the sodium metaperiodate treatment removed or inactivated the sugar-binding receptor associated with capsule, thus inhibiting the F. columnare chemotactic response to mucus. The treatments of d-mannose, d-glucose and N-acetyl-d-galactosamine resulted in significant inhibition of the chemotactic responses of F. columanare to catfish skin mucus, suggesting that
at least three carbohydrate-binding receptors of the capsule are involved in chemotactic responses. These receptors may recognize and bind to the d-mannose, d-glucose and N-acetyl-d- galactosamine structure of the chemoattractants associated with the fish mucus. d-Glucose and N-acetyl-d-galactosamine treatment of F. columnare was previously shown to significantly inhibit adherence to gill tissue (Decostere et al., 1999). Several genes are required for F. johnsoniae gliding motility (Agarwal et al., 1997; Hunnicutt & McBride, 2000, 2001; Hunnicutt et al., 2002). The GldH protein is a lipoprotein and has been demonstrated to be required for F. johnsoniae gliding motility (McBride et al., 2003). We examined the expression of gldB, gldC and gldH following the exposure of F.
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