RELATION BETWEEN STRUCTURE AND IMMUNOLOGICAL PROPERTIES OF THE VI CAPSULAR POLYSACCHARIDE

被引:94
作者
SZU, SC [1 ]
LI, XR [1 ]
STONE, AL [1 ]
ROBBINS, JB [1 ]
机构
[1] NIMH, INTRAMURAL RES PROGRAM, BETHESDA, MD 20892 USA
关键词
D O I
10.1128/IAI.59.12.4555-4561.1991
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Vi capsular polysaccharide of Salmonella typhi is a linear homopolymer of poly-alpha(1 --> 4)GalNAcp variably O acetylated at the C-3 position. Serum antibodies elicited by this antigen confer protective immunity against typhoid fever. The relation between the immunologic properties and structure of Vi was investigated by carboxyl reduction, O deacetylation, and acid hydrolysis. The immunogenicity of Vi was closely related to its degree of O acetylation. Partial O deacetylation slightly increased immunogenicity; complete O deacetylation eliminated the immunogenicity of Vi. O-deacetylated Vi, however, still reacted with antisera prepared by injection of whole bacteria. Carboxyl reduction, in contrast, had a comparatively slight effect upon both the immunogenicity and antigenicity of Vi. Retention levels of antigenicity after acid treatment were greater for both the native and carboxyl-reduced Vi than for the O-deacetylated product. The Courtauld-Koltun space-filling model of a pentamer of Vi demonstrated that the bulky nonpolar O-acetyls, which protrude in rows on both sides, make up most of the surface. The carboxyls are less exposed and are partially shielded by the O-acetyls. The molecular model thus provides an explanation for the dominant role of the O-acetyls, as well as the lesser effect of carboxyl reduction, upon the immunologic properties of Vi.
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页码:4555 / 4561
页数:7
相关论文
共 33 条
[1]   PREVENTION OF TYPHOID-FEVER IN NEPAL WITH THE VI CAPSULAR POLYSACCHARIDE OF SALMONELLA-TYPHI - A PRELIMINARY-REPORT [J].
ACHARYA, IL ;
LOWE, CU ;
THAPA, R ;
GURUBACHARYA, VL ;
SHRESTHA, MB ;
CADOZ, M ;
SCHULZ, D ;
ARMAND, J ;
BRYLA, DA ;
TROLLFORS, B ;
CRAMTON, T ;
SCHNEERSON, R ;
ROBBINS, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (18) :1101-1104
[2]   IDENTIFICATION OF A SUBGROUP ANTIGEN ON NEISSERIA-MENINGITIDIS GROUP-C CAPSULAR POLYSACCHARIDE [J].
APICELLA, MA .
JOURNAL OF INFECTIOUS DISEASES, 1974, 129 (02) :147-153
[3]   POLYURONIDES - THEIR MOLECULAR ARCHITECTURE [J].
ATKINS, EDT ;
ISAAC, DH ;
NIEDUSZY.IA ;
PHELPS, CF ;
SHEEHAN, JK .
POLYMER, 1974, 15 (05) :263-271
[4]   Chemoimmunological studies on the soluble specific substance of Pneumococcus I. The isolation and properties of the acetyl polysaccharide of Pneumococcus Type I [J].
Avery, OT ;
Goebel, WF .
JOURNAL OF EXPERIMENTAL MEDICINE, 1933, 58 (06) :731-755
[5]   STRUCTURAL STUDIES OF THE ESCHERICHIA-COLI K93 AND K53 CAPSULAR POLYSACCHARIDES [J].
BAX, A ;
SUMMERS, MF ;
EGAN, W ;
GUIRGIS, N ;
SCHNEERSON, R ;
ROBBINS, JB ;
ORSKOV, F ;
ORSKOV, I ;
VANN, WF .
CARBOHYDRATE RESEARCH, 1988, 173 (01) :53-64
[6]  
BHATTACHARJEE AK, 1975, J BIOL CHEM, V250, P1926
[7]  
Felix A, 1934, LANCET, V2, P186
[8]   ESCHERICHIA-COLI K51 AND K93 CAPSULAR POLYSACCHARIDES ARE CROSSREACTIVE WITH THE GROUP-A CAPSULAR POLYSACCHARIDE OF NEISSERIA-MENINGITIDIS - IMMUNOCHEMICAL, BIOLOGICAL, AND EPIDEMIOLOGICAL-STUDIES [J].
GUIRGUIS, N ;
SCHNEERSON, R ;
BAX, A ;
EGAN, W ;
ROBBINS, JB ;
SHILOACH, J ;
ORSKOV, I ;
ORSKOV, F ;
KHOLY, AE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (06) :1837-1851
[9]  
HESTRIN S, 1949, J BIOL CHEM, V180, P249
[10]  
HEYNS K., 1967, CARBOHYD RES, V3, P340, DOI 10.1016/S0008-6215(00)82210-7