A plasmid-encoded rfbO:54gene cluster is required for biosynthesis of the O:54 antigen in Salmonella enterica serovar Borreze
- 1 February 1994
- journal article
- Published by Wiley in Molecular Microbiology
- Vol. 11 (3) , 437-448
- https://doi.org/10.1111/j.1365-2958.1994.tb00325.x
Abstract
Previous studies demonstrated that the presence of a 7–8 kb plasmid is correlated with expression of the lipopolysaccharide (LPS) O:54 antigen in several Salmonella enterica serovars. In this study, a 6.7 kb plasmid from a field isolate of S. enterica serovar Borreze was shown to encode enzymes responsible for the synthesis of the O:54 polysaccharide. Curing the plasmid results in simultaneous loss of smooth O-polysaccharide-substituted LPS molecules and O:54 serotype. SDS-PAGE analysis of other 0:54 isolates indicated that the O:54 O-polysaccharide can be co-expressed with an additional O-polysaccharide, likely encoded by chromosomal genes. The structure of the O:54 polysaccharide was determined by a combination of chemical and nuclear magnetic resonance (NMR) methods and was found to be an unusual homopolymer of N-acetylmannosamine (D-ManNAc) residues. The polysaccharide contained a disaccharide repeating unit with the structure: →4)-β-d-MANpNAc-(1→3)-β- d-ManpNAc-(1 → This structure does not resemble other O-polysaccharides in S. enterica. To examine the role played by plasmid functions in synthesis of the O:54 polysaccharide, the 6.7 kb plasmid was cloned to produce a hybrid plasmid (pWQ800) in pGEM-7Zf(+). In Escherichia coli K-12 Δrfb, pWQ800 directed the synthesis of authentic O:54 polysaccharide. Polymerized O:54 polysaccharide was also produced in S. enterica serovar Typhimurium rfb and rfc mutants. From these data, we conclude that pWQB00 carries the rfbO:54 gene cluster and synthesis of the O:54 poiysaccharides does not require host chromosomal rfb functions. However, synthesis of the O:54 polysaccharide requires the function of the rfe and rffE genes which are part of the gene cluster encoding enzymes involved in biosynthesis of enterobacterial common antigen. The rffE gene product synthesizes the O:54 precursor, uridine diphospho-N-acetylmannosamine. This is the first description of a plasmid-encoded rfb gene cluster in Salmonella.Keywords
This publication has 47 references indexed in Scilit:
- Function of the rfb gene cluster and the rfe gene in the synthesis of O antigen by Shigella dysenteriae 1Molecular Microbiology, 1993
- Cloning and structure of group C1 O antigen (rfb gene cluster) from Salmonella enterica serovar montevideoJournal of General Microbiology, 1992
- Cloning of the rfb gene cluster of a group C2 Salmonella strain: comparison with the rfb regions of groups B and DMolecular Microbiology, 1991
- Genetic analysis of the rfb region of Shigella flexneri encoding the Y serotype O‐antigen specificityMolecular Microbiology, 1991
- Molecular cloning and characterization of form I antigen genes of Shigella sonneiJournal of General Microbiology, 1991
- Correlation of proton and nitrogen-15 chemical shifts by multiple quantum NMRJournal of Magnetic Resonance (1969), 1983
- Correlation of proton chemical shifts by two-dimensional Fourier transform NMRJournal of Magnetic Resonance (1969), 1981
- Biosynthesis of uridine diphosphate N-acetyl-D-mannosaminuronic acid from uridine diphosphate N-acetyl-D-glucosamine in Escherichia coli: Separation of enzymes responsible for epimerization and dehydrogenationBiochemical and Biophysical Research Communications, 1975
- Enzymatic formation of uridine diphosphate N‐acetyl‐D‐mannosaminuronic acidFEBS Letters, 1974
- Calcium-dependent bacteriophage DNA infectionJournal of Molecular Biology, 1970