A PLASMID-ENCODED RFB(O/54) GENE-CLUSTER IS REQUIRED FOR BIOSYNTHESIS OF THE O/54 ANTIGEN IN SALMONELLA-ENTERICA SEROVAR BORREZE

被引:35
作者
KEENLEYSIDE, WJ
PERRY, M
MACLEAN, L
POPPE, C
WHITFIELD, C
机构
[1] UNIV GUELPH,DEPT MICROBIOL,GUELPH N1G 2W1,ON,CANADA
[2] NATL RES COUNCIL CANADA,DIV BIOL SCI,OTTAWA K1A 0R6,ON,CANADA
[3] AGR CANADA,HLTH ANIM LAB,GUELPH N1G 3W4,ON,CANADA
关键词
D O I
10.1111/j.1365-2958.1994.tb00325.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous studies demonstrated that the presence of a 7-8kb plasmid is correlated with expression of the lipopolysaccharide (LPS) O:54 antigen in several Salmonella enterica serovars. In this study, a 6.7kb 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 0:54 serotype. SDS-PAGE analysis of other O: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)-beta-D-ManpNAc-(1-->3)-beta-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 Delta rfb, pWQ800 directed the synthesis of authentic O:54 polysaccharide. Polymerized O:54 polysaccharide was also produced in S. entericaserovar Typhimurium rfb and rfc mutants. From these data, we conclude that pWQ800 carries the rfb(O:54) gene cluster and synthesis of the O:54 polysaccharides 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.
引用
收藏
页码:437 / 448
页数:12
相关论文
共 68 条
[61]   A SENSITIVE SILVER STAIN FOR DETECTING LIPOPOLYSACCHARIDES IN POLYACRYLAMIDE GELS [J].
TSAI, CM ;
FRASCH, CE .
ANALYTICAL BIOCHEMISTRY, 1982, 119 (01) :115-119
[62]  
USOV AI, 1969, ZH OBSHCH KHIM, V39, P912
[63]   RELATEDNESS OF O-SPECIFIC LIPOPOLYSACCHARIDE SIDE-CHAIN GENES FROM STRAINS OF SHIGELLA-BOYDII TYPE-12 BELONGING TO 2 CLONAL GROUPS AND FROM ESCHERICHIA-COLI O7-K1 [J].
VALVANO, MA ;
MAROLDA, CL .
INFECTION AND IMMUNITY, 1991, 59 (11) :3917-3923
[64]  
WANG L, 1992, GENETICS, V130, P429
[65]   VARIATION OF THE RFB GENE CLUSTERS IN SALMONELLA-ENTERICA [J].
XIANG, SH ;
HAASE, AM ;
REEVES, PR .
JOURNAL OF BACTERIOLOGY, 1993, 175 (15) :4877-4884
[66]   ACETYLATION OF O-SPECIFIC LIPOPOLYSACCHARIDES FROM SHIGELLA-FLEXNERI 3A AND SHIGELLA-FLEXNERI 2A OCCURS IN ESCHERICHIA-COLI K-12 CARRYING CLONED SHIGELLA-FLEXNERI 3A AND SHIGELLA-FLEXNERI 2A RFB GENES [J].
YAO, ZJ ;
LIU, HM ;
VALVANO, MA .
JOURNAL OF BACTERIOLOGY, 1992, 174 (23) :7500-7508
[67]   MOLECULAR-CLONING AND CHARACTERIZATION OF FORM-I ANTIGEN GENES OF SHIGELLA-SONNEI [J].
YOSHIDA, Y ;
OKAMURA, N ;
KATO, J ;
WATANABE, H .
JOURNAL OF GENERAL MICROBIOLOGY, 1991, 137 :867-874
[68]  
[No title captured]