Promoter orientation of the immunomodulatory Bacteroides fragilis capsular polysaccharide A (PSA) is off in individuals with inflammatory bowel disease (IBD)

被引:43
作者
Blandford, Lucy E. [1 ]
Johnston, Emma L. [2 ,3 ]
Sanderson, Jeremy D. [2 ,3 ]
Wade, William G. [1 ]
Lax, Alistair J. [1 ]
机构
[1] Kings Coll London, Guys Hosp, Dent Inst, London, England
[2] Guys & St Thomas NHS Fdn Trust, Dept Gastroenterol, London, England
[3] Kings Coll London, London, England
关键词
Bacteroides fragilis; inflammatory bowel disease; capsular polysaccharide; phase variation; interleukin-10; invertible promoter; mucosal colonisation; ANTIGENIC VARIATION; BIOSYNTHESIS LOCUS; HUMAN COMMENSAL; GUT; COLONIZATION; SYMBIOSIS; MOLECULE; STRAIN; CELLS;
D O I
10.1080/19490976.2018.1560755
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Bacteroides fragilis is a member of the normal microbiota of the lower gastrointestinal tract, but some strains produce the putative tumourigenic B. fragilis toxin (BFT). In addition, B. fragilis can produce multiple capsular polysaccharides that comprise a microcapsule layer, including an immunomodulatory, zwitterionic, polysaccharide A (PSA) capable of stimulating anti-inflammatory interleukin-10 (IL-10) production. It is known that the PSA promoter can undergo inversion, thereby regulating the expression of PSA. A PCR digestion technique was used to investigate B. fragilis capsular PSA promoter orientation using human samples for the first time. It was found that approximately half of the B. fragilis population in a healthy patient population had PSA orientated in the 'ON' position. However, individuals with inflammatory bowel disease (IBD) had a significantly lower percentage of the B. fragilis population with PSA orientated 'ON' in comparison with the other patient cohorts studied. Similarly, the putative tumourigenic bft-positive B. fragilis populations were significantly associated with a lower proportion of the PSA promoter orientated 'ON'. These results suggest that the proportion of the B. fragilis population with the PSA promoter 'ON' may be an indicator of gastrointestinal health.
引用
收藏
页码:569 / 577
页数:9
相关论文
共 31 条
[1]   STRUCTURAL ELUCIDATION OF 2 CAPSULAR POLYSACCHARIDES FROM ONE STRAIN OF BACTEROIDES-FRAGILIS USING HIGH-RESOLUTION NMR-SPECTROSCOPY [J].
BAUMANN, H ;
TZIANABOS, AO ;
BRISSON, JR ;
KASPER, DL ;
JENNINGS, HJ .
BIOCHEMISTRY, 1992, 31 (16) :4081-4089
[2]   Loss of resistance to ingestion and phagocytic killing by O- and K- mutants of a uropathogenic Escherichia coli O75:K5 strain [J].
Burns, SM ;
Hull, SI .
INFECTION AND IMMUNITY, 1999, 67 (08) :3757-3762
[3]   Trans locus inhibitors limit concomitant polysaccharide synthesis in the human gut symbiont Bacteroides fragilis [J].
Chatzidaki-Livanis, Maria ;
Weinacht, Katja G. ;
Comstock, Laurie E. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (26) :11976-11980
[4]   A Family of Transcriptional Antitermination Factors Necessary for Synthesis of the Capsular Polysaccharides of Bacteroides fragilis [J].
Chatzidaki-Livanis, Maria ;
Coyne, Michael J. ;
Comstock, Laurie E. .
JOURNAL OF BACTERIOLOGY, 2009, 191 (23) :7288-7295
[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]   Role of glycan synthesis in colonization of the mammalian gut by the bacterial symbiont Bacteroides fragilis [J].
Coyne, Michael J. ;
Chatzidaki-Livanis, Maria ;
Paoletti, Lawrence C. ;
Comstock, Laurie E. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (35) :13099-13104
[7]   Mpi recombinase globally modulates the surface architecture of a human commensal bacterium [J].
Coyne, MJ ;
Weinacht, KG ;
Krinos, CM ;
Comstock, LE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (18) :10446-10451
[8]   Plasmacytoid Dendritic Cells Mediate Anti-inflammatory Responses to a Gut Commensal Molecule via Both Innate and Adaptive Mechanisms [J].
Dasgupta, Suryasarathi ;
Erturk-Hasdemir, Deniz ;
Ochoa-Reparaz, Javier ;
Reinecker, Hans-Christian ;
Kasper, Dennis L. .
CELL HOST & MICROBE, 2014, 15 (04) :413-423
[9]   Patients with familial adenomatous polyposis harbor colonic biofilms containing tumorigenic bacteria [J].
Dejea, Christine M. ;
Fathi, Payam ;
Craig, John M. ;
Boleij, Annemarie ;
Taddese, Rahwa ;
Geis, Abby L. ;
Wu, Xinqun ;
Shields, Christina E. DeStefano ;
Hechenbleikner, Elizabeth M. ;
Huso, David L. ;
Anders, Robert A. ;
Giardiello, Francis M. ;
Wick, Elizabeth C. ;
Wang, Hao ;
Wu, Shaoguang ;
Pardoll, Drew M. ;
Housseau, Franck ;
Sears, Cynthia L. .
SCIENCE, 2018, 359 (6375) :592-+
[10]   Gut microbiota utilize immunoglobulin A for mucosal colonization [J].
Donaldson, G. P. ;
Ladinsky, M. S. ;
Yu, K. B. ;
Sanders, J. G. ;
Yoo, B. B. ;
Chou, W. -C. ;
Conner, M. E. ;
Earl, A. M. ;
Knight, R. ;
Bjorkman, P. J. ;
Mazmanian, S. K. .
SCIENCE, 2018, 360 (6390) :795-+