Lipopolysaccharide with an altered O‐antigen produced in Escherichia coli K‐12 harbouring mutated, cloned Shigella flexneri rfb genes

Cloning of the rfb genes of Shigella flexneri 2a into Escherichia coli K‐12 strain DH1 results in the synthesis of lipopolysaccharides (LPS) with an O‐antigen chain having type antigen IV and group antigens 3,4. During genetic studies of these rfb genes in E. coli K‐12, we observed that strains harbouring plasmids with certain mutations (inversion and transposon insertions) which should have blocked O‐antigen synthesis nevertheless still produced LPS with O‐antigen chains. These LPS migrated differently on silver‐stained SDS—polyacrylamide gels, compared with the LPS produced by wild‐type rfb genes, and the group 3,4 antigens were barely detectable, suggesting that the O‐antigen was altered. Investigation of the genetic determinants for production of the altered O‐antigen/LPS indicated that: (i) these LPS are produced as a result of mutations which are either polar on rfbF or inactivate rfbF ; (ii) the rfbX gene product (or a similar protein in the E. coli K‐12 rfb region) is needed for production of the altered O‐antigen in the form of LPS; (iii) the rfbG gene product is required for the production of both the parental and altered LPS; (iv) the dTDP‐rhamnose biosynthesis genes are required. Additionally, an E. coli K‐12 gene product(s) encoded outside the rfb region also contributes to production of the O‐antigen of the altered LPS. An antiserum raised to the altered LPS from strain DH1(pPM2217 ( rfbX ::Tn 1725 )) was found to cross‐react with nearly all S. flexneri serotypes, and with the altered LPS produced by other DH1 strains harbouring plasmids with different rfb mutations, as described above. The reactivity of the altered LPS with a panel of monoclonal antibodies specific for various S. flexneri O‐antigen type and group antigens demonstrated that their O‐antigen components were closely related to that of S. flexneri serotype 4. The RfbF and RfbG proteins were shown to have similarity to rhamnose transferases, and we identified a motif common to the N‐termini of 6‐deoxy‐hexose nucleotide sugar transferases. We propose that the E. coli K‐12 strains harbouring the mutated S. flexneri rfb genes produce LPS with a hybrid O‐antigen as a consequence of inactivation of RfbF and complementation by an E. coli K‐12 gene product. Analysis of the genetic and immunochemical data suggested a possible structure for the O‐antigen component of the altered LPS.