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Previous Article | Next Article 
Applied and Environmental Microbiology, October 1998, p. 3854-3859, Vol. 64, No. 10
Laboratory of Microbiology, Department of
Biomolecular Sciences, Wageningen Agricultural University, 6703 CT
Wageningen, The Netherlands
Received 1 April 1998/Accepted 16 July 1998
The diversity of the predominant bacteria in the human
gastrointestinal tract was studied by using 16S rRNA-based approaches. PCR amplicons of the V6 to V8 regions of fecal 16S rRNA and ribosomal DNA (rDNA) were analyzed by temperature gradient gel electrophoresis (TGGE). TGGE of fecal 16S rDNA amplicons from 16 individuals showed different profiles, with some bands in common. Fecal samples from two
individuals were monitored over time and showed remarkably stable
profiles over a period of at least 6 months. TGGE profiles derived from
16S rRNA and rDNA amplicons showed similar banding patterns. However,
the intensities of bands with similar mobilities differed in some
cases, indicating a different contribution to the total active fraction
of the prominent fecal bacteria. Most 16S rRNA amplicons in the TGGE
pattern of one subject were identified by cloning and sequence
analysis. Forty-five of the 78 clones matched 15 bands, and 33 clones
did not match any visible band in the TGGE pattern. Nested PCR of
amplified 16S rDNA indicated preferential amplification of a sequence
corresponding to 12 of the 33 nonmatching clones with similar
mobilities in TGGE. The sequences matching 15 bands in the TGGE pattern
showed 91.5 to 98.7% homology to sequences derived from different
Clostridium clusters. Most of these were related to strains
derived from the human intestine. The results indicate that the
combination of cloning and TGGE analysis of 16S rDNA amplicons is a
reliable approach to monitoring different microbial communities in
feces.
The human gastrointestinal tract
harbors a diverse community of microorganisms which include a large
number of mainly anaerobic bacteria. These have largely been studied by
plate count analysis of fecal samples, which usually contain
1010 to 1011 CFU per g (9, 13, 29).
One of the limitations in using conventional microbiological methods is
that only easily cultivable organisms are counted. Bacteria which have
obligate interactions with the host or other microorganisms, or which
require unknown growth conditions, will not be selected this way.
Estimates of culturability of bacteria in the gastrointestinal tract
vary from 10 to 50% (16, 20, 37). Other limitations of
cultivation include the selectivity of the medium used, the stress
imposed by cultivation procedures, and the necessity of strictly anoxic conditions. As a consequence, insight into the interaction between the
host and the microbial community, and into the influence of environmental factors on microbial composition, is still lacking.
This decade has shown an explosive development in the application of
molecular techniques based on 16S and 23S rRNA to the study of
microbial diversity in ecosystems (reviewed in references 1 and 32). So far, the rRNA
approach has been used only incidentally to study human intestinal
microbial ecology, and only specific groups of bacteria, such as
Bifidobacterium and Lactobacillus, have been
studied (16, 19). In addition, PCR has been used to quantify
specific groups of bacteria in human feces (35), and random
cloning approaches have been used to analyze the microbial diversity of
feces from one individual (37). Although these studies
report significant information on specific bacteria and specific
individuals, the approaches are time-consuming, expensive, and
unsuitable for characterizing complex microbial communities. Methods
such as denaturing gradient gel electrophoresis (10) or
temperature gradient gel electrophoresis (TGGE) (28) have been developed to analyze microbial communities rapidly, based on
sequence-specific separation of 16S rDNA amplicons (8, 22). The aim of the present study was to use molecular approaches to describe the bacterial diversity in human fecal samples and to investigate to what extent this diversity is affected by the host. We
analyzed PCR-amplified V6 to V8 regions of 16S rRNA (23) by
TGGE to describe the diversity of the predominant bacteria in fecal
samples. Since the ratio of 16S ribosomal DNA (rDNA) and rRNA is
dependent on cellular activity (33), we compared TGGE
patterns derived from 16S rRNA and rDNA amplicons. Finally, to gain
insight into the phylogenetic positions of the most prominent bacteria,
we prepared a 16S rDNA clone library and sequenced clones corresponding
to dominant bands in the TGGE pattern of a single individual.
Experimental approach.
To describe the bacterial diversity
in the human gastrointestinal tract, we used a molecular approach based
on the sequence variability of the 16S rRNA gene (Fig.
1). RNA and DNA were simultaneously isolated from fecal samples and were used as templates for
amplification by reverse transcriptase PCR (RT-PCR) and regular PCR,
respectively, of fragments of the 16S rRNA gene. Amplicons of the V6 to
V8 regions were analyzed by TGGE. Migration distances from different
gels were compared by using a marker which consisted of amplified V6 to
V8 regions from nine clones with different mobilities. Additionally, a
clone library of 16S rDNA amplicons (Escherichia coli
positions 8 to 1510) from a fecal sample of one individual was
prepared. The mobilities of cloned amplicons were screened by TGGE, and those corresponding to specific bands in the RNA-derived profile were
sequenced.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Temperature Gradient Gel Electrophoresis Analysis of 16S rRNA
from Human Fecal Samples Reveals Stable and Host-Specific Communities
of Active Bacteria
ABSTRACT
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
INTRODUCTION
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
MATERIALS AND METHODS
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
View larger version (16K):
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FIG. 1.
Outline of the molecular approaches used to analyze the
fecal bacterial communities. PCR 968-1401 represents the RT-PCR with
primers U968-GC and L1401, which amplify the V6 to V8 regions. PCR
8-1510 represents the PCR with primers 8f and 1510r, which amplify the
complete 16S rDNA.
Recovery, preparation, and storage of fecal samples.
Fresh
fecal samples were collected from 16 unrelated individuals (A to P)
from different geographical locations within The Netherlands and
Finland, differing in dietary preferences, age (25 to 78 years), and
sex (7 men and 9 women). Four fecal samples from individual A (male; 25 years old) were taken within a 6-month period at 2-month intervals, and
two samples from individual B (female; 43 years old) were taken within
a 7-month period. Three grams (wet weight) of fecal samples was
homogenized in 50 ml of ice-cold 0.05 M potassium phosphate buffer (pH
7.0), and aliquots of 1 ml were stored at 
20°C.
Parallel RNA and DNA isolation. Fecal samples (1 ml) were centrifuged at 9,000 × g for 5 min. The pellets were resuspended in 1 ml of a buffer containing 10 mM Tris-HCl (pH 8.0) and 150 mM NaCl (6). After the addition of 150 µl of acid phenol, consisting of phenol buffered in a solution containing 10 mM sodium acetate (pH 5.0) and 140 mM NaCl (6), 0.3 g of zirconium beads (diameter, 0.1 mm) was added. The samples were treated at 5,000 rpm for 3 min in a mini-bead beater (Biospec Products, Bartlesville, Okla.). After the addition of 150 µl of CI solution, consisting of chloroform and isoamyl alcohol in a 24:1 (vol/vol) ratio, the tubes were vortexed briefly and centrifuged for 5 min at 15,000 × g. The aqueous phase was split in two aliquots of 0.5 ml, one for RNA isolation and one for DNA isolation.
For RNA isolation, phenol-chloroform extractions were performed with 150 µl of acid phenol and 150 µl of CI solution. These steps were repeated until a clear interface between the aqueous and phenol-chloroform layers was obtained after centrifugation. Subsequently, an extraction with 300 µl of CI solution was performed. Finally, nucleic acids were precipitated with 2 volumes of ethanol and 1/10 volume of 3 M sodium acetate (pH 5.2) at20°C for 30 min.
After centrifugation at 15,000 × g for 20 min, the
pellet was washed with 500 µl of 70% ethanol, air dried, and
resuspended in 500 µl of a buffer containing 20 mM Tris-HCl (pH 7.5),
10 mM NaCl, 6 mM MgCl2, and 10 mM CaCl2
(6). Five units of RNase-free DNase (Promega, Madison,
Wisc.) was added, followed by incubation at 37°C for 30 min. After
phenol-chloroform extractions, RNA was precipitated as previously
described and resuspended in 100 µl of 10 mM Tris-HCl (pH 8.0). The
RNA solutions were checked for the presence of residual amounts of DNA
by performing PCR as described in the section "RT-PCR and PCR
amplification." When necessary, the DNase treatment was repeated to
eliminate all DNA.
For the parallel DNA isolation, 50 µl of 3 M sodium acetate (pH 5.2)
was added to the residual aliquots. Subsequently, phenol-chloroform extractions were performed with 150 µl of phenol buffered in TE, which consisted of 10 mM Tris-HCl (pH 8.0) and 1 mM EDTA
(18), and 150 µl of CI solution. After an additional
chloroform extraction, DNA was precipitated with 2 volumes of ethanol
at 20°C for 30 min. After centrifugation and washing with 70%
ethanol, the pellet was resuspended in 500 µl of TE. Five units of
DNase-free RNase (Promega) was added, and the sample was incubated at
37°C for 15 min. After phenol-chloroform extractions and an
extraction with chloroform only, DNA was precipitated as before and
resuspended in 100 µl of TE.
The amount and integrity of the nucleic acids was determined visually
after electrophoresis on a 1.2% agarose gel containing ethidium
bromide.
RT-PCR and PCR amplification. Primers U968-GC (5' CGC CCG GGG CGC GCC CCG GGC GGG GCG GGG GCA CGG GGG GAA CGC GAA GAA CCT TAC) and L1401 (5' GCG TGT GTA CAA GAC CC) (24) were used to amplify the V6 to V8 regions of the bacterial 16S rRNA. The GC clamp in primer U968-GC creates RT-PCR products suitable for separation by TGGE (22).
RT-PCR was performed with the Geneamp Thermostable rTth Reverse Transcriptase RNA PCR kit (Perkin-Elmer, Norwalk, Conn.). Reverse transcriptase reaction mixtures of 10 µl contained 10 mM Tris-HCl (pH 8.3), 90 mM KCl, 1 mM MnCl2, 200 mM each deoxynucleoside triphosphate (dNTP), 2.5 U of rTth DNA polymerase, 7.5 pmol of primer L1401, and 1 µl of 10-times-diluted RNA (approximately 5 ng). The mixtures were incubated at 68°C for 15 min. After this incubation, 40 µl of the PCR additive was added. The additive consisted of 5% glycerol, 10 mM Tris-HCl (pH 8.3), 100 mM KCl, 0.05% Tween 20, 0.75 mM EGTA, 3.75 mM MgCl2, 50 mM each dNTP, and 7.5 pmol of primer U968-GC. The samples were amplified in a Geneamp PCR system 2400 (Perkin-Elmer) by using the following program: 94°C for 1 min; 30 cycles of 94°C for 30 s, 56°C for 30 s, and 68°C for 1 min; and finally, 68°C for 7 min. Aliquots of 5 µl were analyzed by electrophoresis on a 1.2% (wt/vol) agarose gel containing ethidium bromide to check the sizes and amounts of the amplicons. PCR was performed with the Taq DNA polymerase kit from Life Technologies (Gaithersburg, Md.). PCR mixtures of 50 µl contained 20 mM Tris-HCl (pH 8.4), 50 mM KCl, 3 mM MgCl2, 50 mM each dNTP, 1.25 U of Taq polymerase, 5 pmol of the primers L1401 and U968-GC, and 1 µl of 10-times-diluted DNA (approximately 1 ng). Amplification and analysis by agarose gel electrophoresis were performed as described above for the RT-PCR, with the exception that the first incubation at 94°C was performed for 3 min instead of 1 min.Cloning of the PCR-amplified products. PCR was performed with primers 8f [5' CAC GGA TCC AGA GTT TGA T(C/T)(A/C) TGG CTC AG] and 1510r [5' GTG AAG CTT ACG G(C/T)T ACC TTG TTA CGA CTT] (15) by using the Taq DNA polymerase kit from Life Technologies to amplify the bacterial 16S rDNA. PCR was performed under the following conditions: 94°C for 3 min; 30 cycles of 94°C for 30 s, 52°C for 30 s, and 68°C for 1.5 min; and finally 68°C for 7 min. The PCR products were purified with the Qiaquick PCR purification kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions. Purified PCR products were quantified by electrophoresis on a 1.2% (wt/vol) agarose gel with a DNA solution of known concentration as the concentration standard and were cloned in E. coli JM109 by using the Promega pGEM-T vector system. Colonies of ampicillin-resistant transformants were transferred with a sterile toothpick to 50 µl of TE and were boiled for 15 min to lyse the cells. Subsequently, PCR was performed with pGEM-T-specific primers T7 (5' AAT ACG ACT CAC TAT AGG) and SP6 (5' ATT TAG GTG ACA CTA TAG) to check the size of the inserts by using the cell lysates as the template. The plasmids containing inserts of approximately 1.6 kb in the cell lysates were used to amplify the V6 to V8 regions. The amplified V6 to V8 regions were compared to the rRNA-derived TGGE profile from the same fecal sample. Plasmids containing an insert of a clone corresponding to a dominant band were purified by the Wizard Plus miniprep DNA purification system (Promega) and were used for sequence analysis.
TGGE analysis of PCR amplicons. The Diagen (Düsseldorf, Germany) TGGE system was used for sequence-specific separation of RT-PCR products. Electrophoresis was performed in a 0.8-mm polyacrylamide gel (6% [wt/vol] acrylamide, 0.1% bisacrylamide, 8 M urea, 20% [vol/vol] formamide, 2% [vol/vol] glycerol) with 40 mM Tris-acetate (pH 8.0) as the electrophoresis buffer at a fixed voltage of 120 V (±9 mA) for 18 h. A gradient from 36 to 45°C was applied parallel to the electrophoresis running direction. After the completion of electrophoresis, the gel was stained with AgNO3 and developed (3).
Sequence analysis. Purified plasmid DNA (1 µl) was used for sequence analysis of the cloned 16S rDNA by using the Sequenase (T7) sequencing kit (Amersham, Slough, United Kingdom) according to the manufacturer's instructions with Infrared Dye 41 (MWG-Biotech, Ebersberg, Germany)-labeled primers 515r (5' ACC GCG GCT GCT GGC AC) (15), 338f (5' ACT CCT ACG GGA GGC AGC), and 968f (5' AAC GCG AAG AAC CTT AC) (24) as sequencing primers. The sequences were automatically analyzed on a LI-COR (Lincoln, Nebr.) DNA sequencer 4000L and corrected manually. The fraction of unidentified bases was 1% or less. The sequences were checked for reading errors with the alignment programs of the ARB package, which are based on secondary structures of rRNA (31). Homology searches of the ARB, EMBL, and GenBank DNA databases for these partial sequences were performed with FASTA (25), and the homologies were checked with the ARB programs. The complete 16S rDNA sequences were checked for chimerical constructs by using the CHECK-CHIMERA program of the Ribosomal Database Project (17) and the ARB software package.
Nucleotide sequence accession numbers. The sequences of the fecal rDNA clones were deposited in the GenBank database. The new sequences from subject A (with their accession numbers in parentheses) are A03 (AF052408), A07 (AF052409), A09 (AF052410), A10 (AF052411), A11 (AF052412), A12 (AF052413), A13 (AF052414), A14 (AF052415), A19 (AF052416), A20 (AF052417), A21 (AF052418), A22 (AF052419), A27 (AF052420), A54 (AF052421), A57 (AF052422), and A71 (AF052423).
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RESULTS |
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Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
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Nucleic acid extraction and reproducibility of TGGE patterns. Nucleic acids were extracted from the fecal samples by a mechanical procedure which has been shown to be effective in disrupting bacterial cells from a variety of ecosystems (6, 11, 26, 37). To optimize the efficiency of the nucleic acid extraction, the effect of increased bead-beating time on the concentration of the nucleic acids, as well as on their integrity and competence to generate a reproducible TGGE pattern, was determined. With 1 to 5 min of bead beating, no effect on the amount of nucleic acids extracted or on their integrity, as analyzed by agarose gel electrophoresis (data not shown), was observed. No nucleic acids were detected in the samples that had not been subjected to the bead-beating procedure or in the supernatant of the potassium phosphate buffer used to homogenize the fecal samples, indicating that lysis was limited. The TGGE patterns of the rRNA-based amplicons of fecal samples tested remained constant after increased bead-beating time (data not shown). However, in the rDNA-derived pattern of subject A, a new amplicon appeared only after 3 min of bead beating, suggesting the presence of a bacterium which was difficult to lyse (Fig. 2). Since further treatment did not affect the TGGE profiles, 3 min of bead beating was used in further experiments.
|
Comparison between RNA- and DNA-derived TGGE profiles. TGGE profiles derived from fecal RNA and DNA amplicons were compared in order to determine the expression levels of the 16S rRNA genes of the most prominent bacteria, which may reflect their contributions to total activity (Fig. 3). The TGGE patterns derived from RNA and DNA from the same fecal sample were highly similar. However, some bands were more prominent in the RNA-derived profile than in the DNA-derived profile in both subjects, indicating that these bacteria could be very active metabolically. In contrast, few bands in the rRNA-derived pattern were faint, while bands at this position in the DNA-derived pattern were more prominent in both subjects. Such bands probably represent predominant bacteria in the feces that became inactive at the end of the large intestine.
|
Host-dependent TGGE patterns. TGGE analysis of PCR products of fecal samples from 14 individuals (Fig. 4) was performed, and their TGGE profiles were compared to those of PCR products from individuals A and B (Fig. 3). Remarkable differences in individual banding patterns were observed. Differences were found in both the positions of specific bands and the number of bands (up to 38 in the profile of subject profile C). While most prominent bands were found at different positions, some distinct bands were observed in all fecal samples (indicated in Fig. 3 and 4). This indicates that each individual harbors a specific bacterial community in the intestine but that a few dominant bacterial species may be present in many individuals.
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Stability of TGGE patterns over time. Since the observed differences in banding patterns could also be influenced by temporal variation, the fecal samples of two healthy individuals, A and B, were monitored over time (Fig. 5). Four samples from individual A were taken within a period of 6 months. The two fecal samples from individual B were taken within a period of 7 months. In both individuals, the RNA-derived banding patterns were highly constant over a period of approximately half a year. Only some slight differences in the intensities of the bands were observed in both individuals. Similar results were found in the DNA-derived patterns (data not shown). This indicates that the dominant microbial composition remains quite constant over time for these healthy individuals.
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Phylogenetic analysis of dominant bands in a TGGE pattern. To gain insight into the phylogenetic positions of the predominant bacteria, 16S rDNA from fecal samples of individual A was amplified and cloned into E. coli JM109 by using pGEM-T. The V6 to V8 regions of the 16S rDNA of the cell lysates of 78 transformants were amplified, and their mobilities after TGGE were compared to the rRNA-derived pattern of individual A (Fig. 1). In this way, 45 clones were each assigned to 1 of the 15 prominent bands in the TGGE pattern, while 33 did not match any of the detectable bands (Fig. 6). Twelve of the 33 clones which did not match any band in the pattern showed similar mobilities during TGGE. The sequence showed the highest homology (98.9%) to an unidentified rumen bacterium (GenBank accession no. AF018503) (36a). The next closest relative was Prevotella veroralis (89.9%). Nested amplification of the V6 to V8 regions of the 16S rDNA amplicons showed the appearance of this band in the pattern (data not shown), indicating a preferential amplification of this sequence in the first PCR amplification.
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DISCUSSION |
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Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
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In this study we have shown that TGGE analysis of the V6 to V8 amplicons of fecal 16S rRNA and rDNA is a powerful tool for analysis of complex microbial communities in fecal samples. TGGE patterns were unique for each individual. Since no major changes in banding patterns were found during amplification or dilution of the template, the differences in the patterns must reflect the differences in fecal composition among individuals. The results indicate that each individual has his or her own personal and unique microbial community, extending previous work based on the composition of Lactobacillus spp. and Bifidobacterium spp. (19) in selective plate counts (9, 13, 19, 29).
RT-PCR products and PCR products from the same fecal sample were very similar. Because eubacterial primers which show very limited efficiency in the amplification of Archaea and Eucarya have been used, the TGGE pattern reflects the predominant bacteria in fecal samples. The differences between intensities of specific bands in the 16S rDNA- and 16S rRNA-derived patterns are most probably due to differences in the activities of different groups of bacteria. The amount of rRNA per cell is dependent on the type of species and the physiological condition of the cell. In addition, differences in the copy number of the rRNA operon per species (2) also play a role in differences in intensity. Some bacteria which have reached high numbers in the intestine could have been inactivated by losing contact with the mucosa or by exposure to oxygen during the collection of the fecal samples.
In comparisons of the TGGE profiles of fecal samples with those of clones, it appeared that 42% of the clones did not match any band in the TGGE profile. Twelve clones with similar mobilities during TGGE did not correspond to any dominant band in the rRNA- and rDNA-derived profiles of individual A. The partial sequence showed the highest homology with an unidentified rumen bacterium and was grouped in the Prevotella cluster. However, this amplicon was found in the DNA-derived pattern after nested amplification of the V6 to V8 regions of amplified 16S rDNA. This result supports the existence of PCR and cloning biases as reported previously (27, 32, 34, 37). Another reason for the difference between the results of cloning and TGGE analysis was described by Felske et al. (7). Analysis of a PCR amplicon by TGGE visualizes only the dominant fraction of the population, while a cloning approach randomly selects 16S rDNA amplicons. As a consequence, hundreds of bacteria which represent a numerically important part of the total community do not form visible bands in the TGGE profiles, although some of them will be selected by cloning.
The 15 clones corresponding to dominant bands in the TGGE patterns of individual A showed the highest homology with sequences derived from different Clostridium clusters (4). Only two partial 16S rDNA sequences showed more than 97% identity to a sequence in the databases. The other complete and partial 16S rDNA sequences did not match any of the sequences found in the ARB, GenBank, and EMBL databases. Furthermore, their similarities were below the 97% threshold for being considered the same species (30), and they could therefore be considered to be derived from new bacterial species. The identity values of clones corresponding to Coprococcus eutactus could be underestimated, since the sequence of this species in the databases contains a large number of unidentified nucleotides.
Two complete sequences corresponding to two bands in the TGGE pattern showed the highest homology with Clostridium celerecrescens. These sequences showed 97.5% identity and differed by at least 9 bases in the V6 to V8 regions. This explains the different locations of these clones in the TGGE profiles. Ruminococcus obeum-like and Fusobacterium prausnitzii-like amplicons were also found several times among the most prominent bacteria. Previously, similar observations have been reported for closely related Bacillus benzoevorans-like sequences in Drentse A grassland soils (8). These observations could be due to 16S rDNA sequence heterogeneity of bacterial strains (24). However, one of the three R. obeum-like sequences derived from a species which was difficult to lyse, indicating the presence of at least two different types of R. obeum-like species.
Sequences derived from R. obeum showed high-intensity bands in both rRNA- and rDNA-derived patterns in individual A, and they could therefore be considered numerically important in composition and in the total activity. The genera Ruminococcus and Coprococcus are anaerobic cocci, and members of this group, especially Ruminococcus and Peptostreptococcus, have been found numerically important in fecal samples (9, 21).
Clones corresponding to two dominant bands showed the highest homology with an F. prausnitzii sequence described previously (36). It was reported that this sequence was not clustering in the Fusobacterium group and that this strain was one of the most common species in human feces, based on PCR quantitation (35, 36). F. prausnitzii, and also Roseburia cecicola and Butyrivibrio fibrisolvens, are known to be gram-negative species but are phylogenetically related to low-G+C gram-positive species in the Clostridium group described by Collins et al. (4).
The other clones traced in the TGGE profiles showed the highest homology to Eubacterium spp. and Ruminococcus productus (also known as Peptostreptococcus productus) (5). Eubacterium plautii was found as an endosymbiont of Entamoeba histolytica (12). The other eubacteria have been found previously in human fecal samples (9, 21).
All individual-specific patterns had some bands in common. Sequences corresponding to these bands were found in the clone library and showed the highest homologies to R. obeum, Eubacterium hallii, and F. prausnitzii. This indicates that these bacteria have an important function at the end of the gastrointestinal tract in all individuals. Eubacteria and ruminococci are known to have a fermentative metabolism, while fusobacteria in general have a weakly fermentative metabolism (14).
Surprisingly, Bacteroides spp. were not found in the TGGE profile of subject A. Since we used bacterial primers, we did not select to the benefit of Bacteroides spp. The TGGE profile represents only 90 to 99% of the total bacterial community. This means that bacteria which reach levels of 109 cells or fewer (this number is not unusual for Bacteroides spp.) per g of feces will not be visualized on TGGE, assuming that 1 g of feces contains 1011 cells.
Overall, it can be concluded that the results support the hypothesis that each healthy person has his or her own unique fecal flora and that the dominant active flora is stable over time. Since the individuals were unrelated, were of different ages, and had different dietary preferences, the reasons for this uniqueness are likely to be found in host factors. The conclusions are based on an approach which could be biased by irregular cell lysis and primer specificity, which are general drawbacks of molecular microbial ecology. Even though the quality and reproducibility of the extraction of nucleic acids and their amplification have been investigated, the possibility that some important, hitherto unknown bacteria were missed cannot be excluded. The approach reported here can be useful in studying the effects of certain diets, food components, probiotics, prebiotics, and antibiotics, as well as the genetic background of the host, on the stability and composition of the dominant microbial community.
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ACKNOWLEDGMENTS |
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This study was partly supported by VTT Biotechnology and Food Research (Helsinki, Finland).
We thank all individuals who provided the fecal samples for this study. In particular, we thank Atte von Wright and Minna Alander from VTT Biotechnology and Food Research for sending us the fecal samples from the Finnish individuals.
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FOOTNOTES |
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* Corresponding author. Mailing address: Laboratory of Microbiology, Wageningen Agricultural University, Hesselink van Suchtelenweg 4, 6703 CT, Wageningen, The Netherlands. Phone: 31 317 483486. Fax: 31 317 483829. E-mail: antoon.akkermans{at}algemeen.micr.wau.nl.
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REFERENCES |
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Abstract
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Materials & Methods
Results
Discussion
References
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