Temporal stability analysis of the microbiota in human feces by denaturing gradient gel electrophoresis using universal and group-specific 16S rRNA gene primers

被引:204
作者
Vanhoutte, T
Huys, G
De Brandt, E
Swings, J
机构
[1] Ghent Univ, Microbiol Lab, B-9000 Ghent, Belgium
[2] BCCM, LMG Bacteria Collect, B-9000 Ghent, Belgium
关键词
temporal stability; human fecal microbiota; DGGE;
D O I
10.1016/j.femsec.2004.03.001
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
According to the current insights, the predominant bacterial community in human feces is considered to be stable and unique for each individual over a prolonged period of time. In this study, the temporal stability of both the predominant population and a number of specific subpopulations of the fecal microbiota Of four healthy volunteers was monitored for 6-12 weeks. For this purpose, a combination of different universal (V-3 and V-6-V-8) and genus- or group-specific (targeting the Bacteroides fragilis subgroup, the genera Bifidobacterium and Enterococcus and the Lactobacillus group, which also comprises the genera Leuconostoc, Pediococcus and Weisella) 16S rRNA gene primers was used. Denaturing gradient gel electrophoresis (DGGE) was used to analyze the 16S rRNA gene amplicons generating population fingerprints which were compared visually and by numerical analysis. DGGE profiles generated by universal primers were relatively stable over a three-month period and these profiles were grouped by numerical analysis in subject-specific clusters. In contrast, the genus- and group-specific primers yielded profiles with varying degrees of temporal stability. The Bacteroides fragilis subgroup and Bifidobacterium populations remained relatively stable which was also reflected by subject-specific profile Clustering. The Lactobacillus group showed considerable variation even within a two-week period and resulted in complete loss of subject-grouping. The Enterococcus population was detectable by DGGE analysis in only half of the samples. In conclusion, numerical analysis of 16S rRNA gene-DGGE profiles clearly indicates that the predominant fecal microbiota is host-specific and relatively stable over a prolonged time period. However, some subpopulations tended to show temporal variations (e.g., the Lactobacillus group) whereas other autochthonous groups (e.g., the bifidobacteria and the Bacteroides fragilis subgroup) did not undergo major population shifts in time. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:437 / 446
页数:10
相关论文
共 33 条
[1]
Design and evaluation of a 16S rRNA-targeted oligonucleotide probe for specific detection and quantitation of human faecal Bacteroides populations [J].
Dore, J ;
Sghir, A ;
Hannequart-Gramet, G ;
Corthier, G ;
Pochart, P .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 1998, 21 (01) :65-71
[2]
DRASAR BS, 1985, ASPECTS MICROBIOLOGY, V10, P28
[3]
Duncan SH, 2002, INT J SYST EVOL MICR, V52, P2141, DOI [10.1099/ijs.0.02241-0, 10.1099/00207713-52-6-2141]
[4]
Duncan SH, 2002, INT J SYST EVOL MICR, V52, P1615, DOI 10.1099/00207713-52-5-1615
[5]
Molecular monitoring of succession of bacterial communities in human neonates [J].
Favier, CF ;
Vaughan, EE ;
De Vos, WM ;
Akkermans, ADL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (01) :219-226
[6]
Finegold S.M., 1983, HUMAN INTESTINAL MIC, P3
[7]
Molecular diversity of Lactobacillus spp. and other lactic acid bacteria in the human intestine as determined by specific amplification of 16S ribosomal DNA [J].
Heilig, HGHJ ;
Zoetendal, EG ;
Vaughan, EE ;
Marteau, P ;
Akkermans, ADL ;
de Vos, WM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (01) :114-123
[8]
Overview of gut flora and probiotics [J].
Holzapfel, WH ;
Haberer, P ;
Snel, J ;
Schillinger, U ;
Huis in't Veld, JHJ .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1998, 41 (02) :85-101
[9]
Analysis of fecal populations of bifidobacteria and lactobacilli and investigation of the immunological responses of their human hosts to the predominant strains [J].
Kimura, K ;
McCartney, AL ;
McConnell, MA ;
Tannock, GW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (09) :3394-3398
[10]
QUANTITATIVE FLUORESCENCE IN-SITU HYBRIDIZATION OF BIFIDOBACTERIUM SPP WITH GENUS-SPECIFIC 16S RIBOSOMAL-RNA-TARGETED PROBES AND ITS APPLICATION IN FECAL SAMPLES [J].
LANGENDIJK, PS ;
SCHUT, F ;
JANSEN, GJ ;
RAANGS, GC ;
KAMPHUIS, GR ;
WILKINSON, MHF ;
WELLING, GW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (08) :3069-3075