This family of ABC transporters represents domain II of the carbohydrate find more uptake proteins that transport only monosaccharides. In E. coli, mutations in any of these genes (rbsa, rbsb, rbsc) eliminates

transport of ribose, indicating that these components form a transport system that is responsible for high-affinity ribose transport [64]. The gene galU, which encodes for glucose-1-phosphate uridylyltransferase, Adavosertib cost was also highly upregulated and is responsible for catalyzing the reversible production of UDP-glucose. The gene galU plays a pivotal role in the synthesis of the carbohydrate moieties of glycolipids, glycoproteins, and proteoglycans. galU is also essential for capsular polysaccharide biosynthesis in Streptococcus pneumoniae [65]. In H. influenzae, galU is an essential housekeeping gene that is important in generating sugar precursors needed for polysaccharide formation and LOS outer core synthesis [66]. The H. somni GalU in this locus is 70% similar to that of H. influenzae at the amino GDC-0068 nmr acid level. Of interest was that in 129Pt only 5 of the genes in these two loci were significantly upregulated when the bacteria were grown under conditions favorable to biofilm formation, which is much thinner and less substantial

than that of 2336 [29], and much less EPS can be isolated from the biofilm of 129Pt (data not shown). Therefore, these experiments support the premise that these genes encode for proteins responsible for EPS biosynthesis. It will be important to determine if all or most strains of H. somni produce an antigenically identical or similar EPS, and if antibodies to the EPS can be used to differentiate infected animals from healthy, colonized animals. Preliminary ELISA experiments with antibodies to the EPS indicated that most strains do produce this EPS. Serological studies with infected and healthy animals are in progress. Conclusions We describe the isolation and structure of an H. somni EPS. The EPS was upregulated under

stress-like conditions, and appeared to be a major component of the matrix of the H. somni biofilm. An attractive hypothesis is that formation of EPS and a biofilm is, in part, responsible for the capability of H. somni to ID-8 persist in tissues and cause chronic infections. Since biofilm formation in the bovine host occurs during disease [49], it will be important to determine if compounds that inhibit EPS production will reduce biofilm formation in the host and hasten recovery. The putative genes responsible for EPS synthesis were also identified, which will lead to the development of mutants unable to synthesize EPS and determine the role of the EPS and biofilm in virulence. Furthermore, if EPS is produced primarily during the disease process, this antigen may prove useful in serological assays for diagnosis of H. somni infection.