Intestinal TM7 bacterial phylogenies in active inflammatory bowel disease

被引:144
作者
Kuehbacher, Tanja [1 ]
Rehman, Ateequr [2 ]
Lepage, Patricia [2 ]
Hellmig, Stephan [1 ]
Foelsch, Ulrich R. [1 ]
Schreiber, Stefan [1 ,2 ]
Ott, Stephan J. [1 ,2 ]
机构
[1] Univ Hosp Schleswig Holstein, Dept Med 1, Clin Gen Internal Med, D-24105 Kiel, Germany
[2] Univ Kiel, Inst Clin Mol Biol IKMB, D-24105 Kiel, Germany
关键词
D O I
10.1099/jmm.0.47719-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
TM7 is a recently described subgroup of Gram-positive uncultivable bacteria originally found in natural environmental habitats. An association of the TM7 bacterial division with the inflammatory pathogenesis of periodontitis has been previously shown. This study investigated TM7 phylogenies in patients with inflammatory bowel diseases (IBDs). The mucosal microbiota of patients with active Crohn's disease (CD; n=42) and ulcerative colitis (UC; n=31) was compared with that of controls (n=33). TM7 consortia were examined using molecular techniques based on 16S rRNA genes, including clone libraries, sequencing and in situ hybridization. TM7 molecular signatures could be cloned from mucosal samples of both IBD patients and controls, but the composition of the clone libraries differed significantly. Taxonomic analysis of the sequences revealed a higher diversity of TM7 phylotypes in CID (23 different phylotypes) than in UC (10) and non-IBD controls (112). All clone libraries showed a high number of novel sequences (21 for controls, 34 for CID and 29 for UC). A highly atypical base substitution for bacterial 16S rRNA genes associated with antibiotic resistance was detected in almost all sequences from CID (97.3%) and UC (100%) patients compared to only 65.1% in the controls. TM7 bacteria might play an important role in IBD similar to that previously described in oral inflammation. The alterations of TM7 bacteria and the genetically determined antibiotic resistance of TM7 species in IBD could be a relevant part of a more general alteration of bacterial microbiota in IBD as recently found, e.g. as a promoter of inflammation at early stages of disease.
引用
收藏
页码:1569 / 1576
页数:8
相关论文
共 37 条
[1]   How bacteria talk to each other: regulation of gene expression by quorum sensing [J].
Bassler, BL .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (06) :582-587
[2]   Prevalence of bacteria of division TM7 in human subgingival plaque and their association with disease [J].
Brinig, MM ;
Lepp, PW ;
Ouverney, CC ;
Armitage, GC ;
Relman, DA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (03) :1687-1694
[3]   CONTROLLED TRIAL OF INTRAVENOUS METRONIDAZOLE AS AN ADJUNCT TO CORTICOSTEROIDS IN SEVERE ULCERATIVE-COLITIS [J].
CHAPMAN, RW ;
SELBY, WS ;
JEWELL, DP .
GUT, 1986, 27 (10) :1210-1212
[4]   The Ribosomal Database Project (RDP-II): previewing a new autoaligner that allows regular updates and the new prokaryotic taxonomy [J].
Cole, JR ;
Chai, B ;
Marsh, TL ;
Farris, RJ ;
Wang, Q ;
Kulam, SA ;
Chandra, S ;
McGarrell, DM ;
Schmidt, TM ;
Garrity, GM ;
Tiedje, JM .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :442-443
[5]   The role of microbes in Crohn's disease [J].
Eckburg, Paul B. ;
Relman, David A. .
CLINICAL INFECTIOUS DISEASES, 2007, 44 (02) :256-262
[6]   RAPID DETECTION OF HERPES-SIMPLEX VIRUS-DNA IN HUMAN-BRAIN TISSUE BY INSITU HYBRIDIZATION [J].
FORGHANI, B ;
DUPUIS, KW ;
SCHMIDT, NJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1985, 22 (04) :656-658
[7]   A reproducible grading scale for histological assessment of inflammation in ulcerative colitis [J].
Geboes, K ;
Riddell, R ;
Öst, A ;
Jensfelt, B ;
Persson, T ;
Löfberg, R .
GUT, 2000, 47 (03) :404-409
[8]  
Geboes K, 2002, GUT, V50, P37
[9]   THE POPULATION FREQUENCIES OF SPECIES AND THE ESTIMATION OF POPULATION PARAMETERS [J].
GOOD, IJ .
BIOMETRIKA, 1953, 40 (3-4) :237-264
[10]  
Hooper LV, 1998, BIOESSAYS, V20, P336, DOI 10.1002/(SICI)1521-1878(199804)20:4&lt