Bacteroides fragilis NCTC9343 produces at least three distinct capsular polysaccharides:: Cloning, characterization, and reassignment of polysaccharide B and C biosynthesis loci

被引:39
作者
Coyne, MJ
Kalka-Moll, W
Tzianabos, AO
Kasper, DL
Comstock, LE
机构
[1] Brigham & Womens Hosp, Channing Lab, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02115 USA
关键词
D O I
10.1128/IAI.68.11.6176-6181.2000
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bacteroides fragilis produces a capsular polysaccharide complex (CPC) that is directly involved in its ability to induce abscesses. Two distinct capsular polysaccharides, polysaccharide A (PS A) and PS B, have been shown to be synthesized by the prototype strain for the study of abscesses, NCTC9343. Both of these polysaccharides in purified form induce abscesses in animal models. In this study, we demonstrate that the CPC of NCTC9343 is composed of at least three distinct capsular polysaccharides: PS A PS B, and PS C, A previously described locus contains genes whose products are involved in the biosynthesis of PS C rather than PS B as was originally suggested. The actual PS B biosynthesis locus was cloned, sequenced, and found to contain 22 genes in an operon-type structure. A mutant with a large chromosomal deletion of the PS B biosynthesis locus was created so that the contribution of PS B to the formation of abscesses could be assessed in a rodent model. Although purified PS B can induce abscesses, removal of this polysaccharide does not attenuate the organism's ability to induce abscesses.
引用
收藏
页码:6176 / 6181
页数:6
相关论文
共 19 条
[1]   Identification of the fucose synthetase gene in the colanic acid gene cluster of Escherichia coli K-12 [J].
Andrianopoulos, K ;
Wang, L ;
Reeves, PR .
JOURNAL OF BACTERIOLOGY, 1998, 180 (04) :998-1001
[2]  
Bethesda Research Laboratories, 1986, FOCUS, V8, P9
[3]   Interstrain variation of the polysaccharide B biosynthesis locus of Bacteroides fragilis:: Characterization of the region from strain 638R [J].
Comstock, LE ;
Coyne, MJ ;
Tzianabos, AO ;
Kasper, DL .
JOURNAL OF BACTERIOLOGY, 1999, 181 (19) :6192-6196
[4]   Genetic diversity of the capsular polysaccharide C biosynthesis region of Bacteroides fragilis [J].
Comstock, LE ;
Pantosti, A ;
Kasper, DL .
INFECTION AND IMMUNITY, 2000, 68 (11) :6182-6188
[5]   Analysis of a capsular polysaccharide biosynthesis locus of Bacteroides fragilis [J].
Comstock, LE ;
Coyne, MJ ;
Tzianabos, AO ;
Pantosti, A ;
Onderdonk, AB ;
Kasper, DL .
INFECTION AND IMMUNITY, 1999, 67 (07) :3525-3532
[6]   PLASMID TRANSFER FROM ESCHERICHIA-COLI TO BACTEROIDES-FRAGILIS - DIFFERENTIAL EXPRESSION OF ANTIBIOTIC-RESISTANCE PHENOTYPES [J].
GUINEY, DG ;
HASEGAWA, P ;
DAVIS, CE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (22) :7203-7206
[7]   A SMALL COSMID FOR EFFICIENT CLONING OF LARGE DNA FRAGMENTS [J].
HOHN, B ;
COLLINS, J .
GENE, 1980, 11 (3-4) :291-298
[8]   TAXONOMY OF BACTEROIDES .1. DEOXYRIBONUCLEIC-ACID HOMOLOGIES AMONG BACTEROIDES-FRAGILIS AND OTHER SACCHAROLYTIC BACTEROIDES-SPECIES [J].
JOHNSON, JL .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1978, 28 (02) :245-256
[9]   FLOW CYTOMETRIC ANALYSIS OF WITHIN-STRAIN VARIATION IN POLYSACCHARIDE EXPRESSION BY BACTEROIDES-FRAGILIS BY USE OF MURINE MONOCLONAL-ANTIBODIES [J].
LUTTON, DA ;
PATRICK, S ;
CROCKARD, AD ;
STEWART, LD ;
LARKIN, MJ ;
DERMOTT, E ;
MCNEILL, TA .
JOURNAL OF MEDICAL MICROBIOLOGY, 1991, 35 (04) :229-237
[10]   CAPSULAR POLYSACCHARIDE OF BACTEROIDES-FRAGILIS AS A VIRULENCE FACTOR - COMPARISON OF PATHOGENIC POTENTIAL OF ENCAPSULATED AND UNENCAPSULATED STRAINS [J].
ONDERDONK, AB ;
KASPER, DL ;
CISNEROS, RL ;
BARTLETT, JG .
JOURNAL OF INFECTIOUS DISEASES, 1977, 136 (01) :82-89