To further investigate if the capsular polysaccharide accumulated in the cell, as would be anticipated if the exportation of capsule were interrupted, immunoblots and stains-all/silver stain with different cell fractions were performed (Figure 6). There was no difference in K-antigen present outside or inside the cells between the Δwzabc mutant and the wild type. Therefore, our results suggested that the wza, wzb and wzc exportation system was not required by either K6-antigen or O3-antigen production in V. parahaemolyticus O3:K6. Figure

6 Immuno blot and stains-all/silver-stain of cell fractions. Outer membrane (OM) and cytoplasmic (CP) fractions were separated on polyacrylamide gel, then were either transferred to PVDF membrane and probed with K6 specific antiserum (A), or stained with stains-all/silver CFTRinh-172 supplier stain (B). Lane1, wild type CP; lane 2, ∆wzabc CP; lane 3, ∆EPS CP; lane 4, wild type OM; lane 5, ∆wzabc OM; lane 6, ∆EPS OM. However, a K-antigen processing system similar to the O-antigen/capsule

polysaccharide genes in V. cholerae O139 [13, 20, 21] is present in V. parahaemolyticus. VP0219-0221 are homologous to wbfE, wbfF and wzz genes in V. cholerae O139, sharing 49%, 69% and 54% amino acid identities. Therefore a similar capsule processing mechanism may exist for both taxa. We generated an in frame deletion of VP0220, the wbfF homolog. Mutant ∆0220 displayed an intermediate level of translucence. Immunoblots indicated that deletion of VP0220 did not affect O3 antigen synthesis (Figure 4). However, the midpoint of the K-antigen band shifted NVP-BSK805 in this mutant, suggesting a role of VP0220 in the later PTK6 stage of the K-antigen processing. Complementation of ∆0220 with over expressed wild type VP0220 gene restored mostly the pattern of the wild type K antigen (Figure 4). However, there was more reactive material away from the midpoint of the K-antigen band in the complemented mutant than the wild type (Figure 4), possibly due to the over expression of VP0220 or other reasons that remain unclear. Other K-antigen region features

A complete set of genes of the rhamnose pathway rmlBADC are present in the K-antigen genes of V. parahaemolyticus. However, four open reading frames, VP0225-0228, are inserted between the rmlD and rmlC genes. Analysis of the GC percentage SB202190 mw revealed that the average GC percentage in VP0225-0228 is lower than the rest of the genes in this operon (Figure 2). The unusual arrangement of the rhamnose gene order and the mosaic GC percentage pattern indicated that there was a recent recombination event in the K antigen genes. Between gmhD and the K-antigen operon like genes, there are four genes (VP0215-0218) transcribed to the opposite direction (Figure 2). In frame deletion of these four genes led to the over expression of K-antigen polysaccharides (Figure 4), suggesting these genes may have a regulatory role in capsule expression.