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Appl Environ Microbiol, March 1998, p. 907-913, Vol. 64, No. 3
AgResearch Grasslands, Palmerston North, New
Zealand
Received 7 August 1997/Accepted 4 December 1997
A competitive PCR technique was used to enumerate the proteolytic
bacterium Clostridium proteoclasticum from the rumen. A PCR
primer, which circumscribes this organism and several closely related
strains, was designed for a variable region within their 16S rRNA genes
and was used in conjunction with a universal forward primer. This
primer pair was tested for specificity against 85 ruminal bacterial
strains. An internal control DNA was constructed for use in competitive
PCRs and was shown to amplify under the same reaction conditions and
with the same amplification efficiency as the target DNA. DNA from a
known number of C. proteoclasticum cells was
coamplified with the internal control to construct a standard curve.
Rumen samples were collected from eight dairy cows fed four diets in
rotation: high nitrogen, high nitrogen supplemented with carbohydrate,
low nitrogen, and low nitrogen supplemented with carbohydrate. DNA
extracted from these and spiked with internal control DNA was amplified
with the C. proteoclasticum primer pair. The relative
intensities of the PCR products were used to quantitate the numbers of
C. proteoclasticum cell equivalents from the rumen
samples. The numbers ranged from 2.01 × 106
ml New Zealand ruminants graze a fresh
forage diet which is high in protein and low in soluble carbohydrates
(10). Up to 50% of the protein available from this diet can
be lost due to the rapid microbial breakdown of plant protein
(16). Bacteria are thought to be responsible for the
majority of this protein degradation in the rumen (8). The
proteolytic bacteria in forage-fed New Zealand cattle are dominated by
species of the genera Streptococcus, Eubacterium,
and Butyrivibrio (2), while a novel, highly
proteolytic strain, Clostridium proteoclasticum, has also
been isolated. To determine the significance of these particular
proteolytic bacteria within the New Zealand ruminant, we have set out
to develop a sensitive and specific method of quantitation of microbial
populations directly from rumen samples.
rRNA probes have been successfully used for the detection and
enumeration of bacteria within the rumen (7, 11, 17-20, 27). This technique expresses the abundance of a particular rRNA
sequence in relation to total RNA extracted from a sample. However, it
is relatively insensitive, only detecting down to 106
bacteria per ml of rumen fluid (27). PCR has been used to
detect bacteria in many environments (5, 6), and its
sensitivity has allowed the detection of a single bacterium
(28). Conventional PCR amplifies target DNA exponentially,
making it difficult to use the technique in a quantitative manner.
Competitive PCR (cPCR), however, has been used to determine bacterial
numbers in a range of environments (12, 14, 15). The
addition of an internal DNA standard controls for the variation among
reactions, allowing reliable PCR quantitation. The internal DNA
standard contains the same primer binding sites as the target, and the
two DNAs compete for reaction reagents to produce PCR products of
different sizes, which can be separated in an agarose gel. The log
ratio of intensities of amplified target DNA to internal control DNA is
determined by the equation log
(Nn1/Nn2) = log
(N01/N02) + n
log (eff1/eff2) (29). If the
efficiencies of amplification (eff1 and eff2)
are equal, the ratio of amplified products
(Nn1/Nn2) is dependent on
the log ratio of starting products
(N01/N02)
(29). Even if the efficiencies of the two reactions are not
equal, the values still hold assuming that
eff1/eff2 is constant and amplification is in
the exponential phase. With this technique, amounts of target DNA can
be determined by amplification with known amounts of internal control
DNA. The resulting log ratio of intensities of PCR products is compared to standard curves derived from serial dilutions of known target DNA
amplified with known amounts of internal control DNA.
C. proteoclasticum is a gram-positive, straight
to slightly curved rod which was first isolated from a
pasture-grazed cow in New Zealand (4). Its most
distinguishing feature is its extremely high proteinase activity, and
because of this feature we were interested in quantifying this organism
to estimate its contribution to rumen proteolysis. Since its
description as a new species, it has become apparent that the 16S rRNA
gene (rDNA) sequence of C. proteoclasticum is very
similar to those of Butyrivibrio fibrisolvens NCDO 2435, 2434, 2222, and 2398. However, the description of C. proteoclasticum as a new species is justified since
C. proteoclasticum and these Butyrivibrio
fibrisolvens strains are phylogenetically closely related to
each another (96.9 to 99.5% 16S rRNA sequence similarity) but are
distantly related to the Butyrivibrio fibrisolvens type
strain NCDO 2221T (93.1 to 94.1% similarity). We have
developed a cPCR technique which detects C. proteoclasticum and these closely related B. fibrisolvens strains directly from rumen samples. PCR primers were
designed against a common region of the C. proteoclasticum and B. fibrisolvens 16S rRNA genes.
These primers have been tested for specificity against DNA from 85 rumen bacterial strains, and the sensitivity of detection in a mixed
rumen bacterial background has been investigated. We have used this
cPCR approach to enumerate C. proteoclasticum cell
equivalents in rumen samples from dairy cows fed four different diets:
high nitrogen, high nitrogen supplemented with carbohydrate, low
nitrogen, and low nitrogen supplemented with carbohydrate.
Bacterial strains and growth.
The bacterial strains used are
listed in Table 1. Bacteria were grown on
CC medium (13), except that the rumen fluid was not
preincubated to remove soluble carbohydrates and carbon sources were
replaced by either 1.0% (wt/vol) glucose or cellobiose.
Clostridium aminophilum, C. sticklandii, and
Peptostreptococcus anaerobius were grown in CC medium in
which no carbon source was added and tryptone (1.5% [wt/vol]; Difco,
Detroit, Mich.) replaced trypticase.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Detection of Clostridium proteoclasticum
and Closely Related Strains in the Rumen by Competitive PCR
ABSTRACT
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
1 to 3.12 × 107 ml1.
There was no significant effect on the numbers of C. proteoclasticum detected in rumen samples among cows fed the four
diets. The utility of the competitive PCR approach for quantifying
ruminal bacterial populations in vivo and the occurrence of
C. proteoclasticum in forage-fed dairy cows are
discussed.
INTRODUCTION
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
MATERIALS AND METHODS
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
TABLE 1.
Bacterial strains used in this study
Rumen samples.
Eight fistulated, lactating, Friesian dairy
cows were fed four different diets in rotation: high nitrogen, high
nitrogen with carbohydrate, low nitrogen, and low nitrogen with
carbohydrate. Ryegrass pasture, containing less than 5% clover, was
top dressed with 20 kg of nitrogen (as urea) per ha for low-nitrogen
diets and 90 kg of nitrogen per ha for high-nitrogen diets. Urea was applied 21 to 28 days before cutting, and the nitrogen was 2.11 and
2.82% of dry matter for the low- and high-nitrogen diets, respectively. Carbohydrate was supplied as a 50:50 mixture of dextrose
and corn flour on an energy basis and was drenched at 9:00 a.m., 11:00
a.m., 4:00 p.m., and 6:00 p.m., supplying 10% of the minimum energy
intake. The cows were fed at 9:00 a.m. and 4:00 p.m. and were
maintained on each diet for 12 days before the samples were taken.
Whole rumen samples of approximately 250 ml were collected before the
last 4:00 p.m. feed, frozen immediately in liquid nitrogen, and stored
at 
80°C until DNA extraction. Immediately before DNA extraction,
the samples were thawed in a 37°C water bath and diluted with an
equal weight of mineral salts (MS) buffer (3) before
homogenization in a Sorvall tissue homogenizer (Du Pont Co.,
Wilmington, Del.).
DNA extraction.
General techniques of DNA precipitation and
phenol-chloroform extractions were performed as described by Sambrook
et al. (26). For determination of primer specificity,
bacterial cultures were grown overnight and DNA was extracted by the
enzymatic lysis procedure described by Saito and Miura (25).
To eliminate possible bias introduced by enzymatic cell wall lysis and
to maximize DNA extraction efficiencies, physical disruption was used
to extract DNA from rumen samples and from C. proteoclasticum for sensitivity experiments and standard curve
construction. Unless otherwise stated, DNA was extracted from
triplicate samples. A 1-ml volume of homogenized rumen contents or
1010 C. proteoclasticum cells was added to
1.2 g of sterile zirconia-silica beads (Biospec Products) followed
by centrifugation at 12,000 × g for 10 min at room
temperature. The pellet and beads were rinsed twice in saline-EDTA
solution (0.15 M NaCl, 0.1 M EDTA) before final resuspension in 750 µl of saline-EDTA. Physical disruption was then performed with a
Mini-beadbeater (Biospec Products) at maximum speed for two intervals
of 2 min each, with a 1-min incubation on ice between each treatment.
Phenol-chloroform-isoamyl alcohol (25:24:1) was added and mixed, and
the mixture was centrifuged at 12,000 × g for 5 min at
room temperature. The aqueous phase was removed, and the interface
was reextracted with TE buffer (10 mM Tris-HCl, 1 mM EDTA [pH
8.0]). The combined aqueous phases were repeatedly extracted with the
phenol-chloroform-isoamyl alcohol until no protein remained at the
interface. A final chloroform-isoamyl alcohol extraction was performed
before the nucleic acids were precipitated with ethanol and centrifuged
at 10,000 × g for 20 min at 4°C. The air-dried
pellet was resuspended in TE buffer, RNase A (1 mg ml1
[final concentration]) was added, and the mixture was incubated at
37°C for 60 min. RNase A was removed by phenol-chloroform-isoamyl alcohol extraction followed by ethanol precipitation and
centrifugation. The air-dried DNA pellet was resuspended in TE buffer
and was stored at 20°C, until required. DNAzol reagent (Gibco BRL,
Life Technologies, Auckland, New Zealand) was used for chemical
extraction of DNA. Cells were suspended in 1 ml of DNAzol reagent
before being subjected to bead beater treatment as described above. The DNA was then precipitated as specified by the manufacturer. The concentration and purity of the DNA were determined
spectrophotometrically by measuring the absorbances at 260 and 280 nm
(A260/280) with a Spectramax microplate
spectrophotometer (Molecular Dynamics).
PCR primers and amplification. The primers used for the amplification of the 16S rRNA genes were as follows: universal forward primer (S-*-Univ-0008-a-S-19; 5' GAG TTT GAT CCT GGC TCA G 3'), universal reverse primer (S-*-Univ-1528-a-A-17; 5' AAG GAG GTG ATC CAG CC 3'), and the C. proteoclasticum primer (S-S-Cprot-0832-a-A-21; 5' CTG AAT GCC TAT GGC ACC CAA 3'). The S-S-Cprot-0832-a-A-21 primer was screened for specificity with the PROBE CHECK program of the Ribosomal Database Project (21) and the BLAST (Basic Local Alignment Search Tool) facility at the National Center for Biotechnology. PCR amplification of C. proteoclasticum DNA produces an 830-bp product when amplified with the universal forward primer and S-S-Cprot-0832-a-A-21. Because the S-S-Cprot-0832-a-A-21 primer also detects some closely related B. fibrisolvens strains in rumen samples, in these instances cell numbers are expressed as C. proteoclasticum cell equivalents.
The PCR mixtures contained 20 mM Tris-HCl (pH 8.4), 50 mM KCl, 2.5 mM MgCl2, 0.2 mM each dATP, dCTP, dGTP and dTTP, 1 µM each primer, and 0.5 U of Taq DNA polymerase (Gibco BRL). The PCRs were performed in a final volume of 20 µl sealed in a capillary tip, and thermocycling was carried out in a model FTS-1 capillary thermal sequencer (Corbett Research, Sydney, Australia). The PCR amplification conditions for S-S-Cprot-0832-a-A-21 and the universal forward primers were as follows: denaturation at 95°C for 3 min followed by 6 cycles of 95°C for 30 s, 62°C for 15 s, and 72°C for 30 s and 25 cycles of 95°C for 15 s, 62°C for 5 s, and 72°C for 30 s, with a final cycle of 72°C for 3 min. Amplification with the universal forward and reverse primers differed only in the annealing temperature, which was 55°C. PCR products were separated by electrophoresis in agarose gels, stained with ethidium bromide, and visualized by UV transillumination.Construction of the internal control.
The 830-bp PCR product
from C. proteoclasticum DNA amplified
with the universal forward and S-S-Cprot-0832-a-A-21 primers contains
two AluI sites (Fig. 1). To
produce an AluI deletion, the 830-bp fragment was digested
with AluI as specified by the manufacturer (Boehringer,
Mannheim, Germany) and the restriction endonuclease was removed with
phenol treatment followed by ethanol precipitation. The AluI
fragments were ligated with T4 DNA ligase (Gibco BRL), 2 µl of the
ligation reaction was used in a PCR with the universal forward and
S-S-Cprot-0832-a-A-21 primers, and the products were separated by
agarose gel electrophoresis. One of the PCR products was a 480-bp
fragment expected from the deletion of the 350-bp internal
AluI fragment. The 480-bp fragment was purified from the gel
and used as an internal control for the cPCRs. The concentration of the
internal control was estimated from photographs of the gel to be
approximately 100 ng ml1. However, the DNA concentration
was too low to obtain an accurate A260/280
reading, and so the internal control was expressed as a dilution of the
concentrated mixture.
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Preparation of C. proteoclasticum cells for sensitivity testing.
C. proteoclasticum was grown in 100-ml
overnight cultures, and a sample was counted by phase-contrast
microscopy with a WSI counting chamber (Weber Scientific International
Ltd., Middlesex, England). The cells were pelleted by centrifugation
and resuspended to a final concentration of 1010 cells
ml1. DNA extractions were performed on 1010
cells; 10-fold serial dilutions of this DNA were amplified to determine
the detection limit.
Quantitation of PCR products. PCR products were quantitated by photographing agarose gels with Polaroid 665 film (Polaroid, St. Albans, England), which produces a negative image of the photograph. The negative was scanned with a GS-670 imaging densitometer (Bio-Rad, Hercules, Calif.) and analyzed with Molecular Analyst software version 1.4 (Bio-Rad). To correct for differences in the fluorescence of ethidium bromide-stained PCR fragments of different sizes (23), the intensity of the internal control was multiplied by the ratio 830/480.
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RESULTS |
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Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
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Primer specificity and sensitivity. Alignment of the C. proteoclasticum 16S rDNA sequence with other sequences from the Ribosomal Database Project and closely related B. fibrisolvens sequences retrieved from BLAST searches identified a region at bp 832 to 851 (E. coli numbering) that was common to C. proteoclasticum and B. fibrisolvens NCDO 2435, 2222, 2398, and 2434. A primer, S-S-Cprot-0832-a-A-21, complementary to the sense strand of this region facing the 5' end of the 16S rRNA gene was designed. This enabled it to be used with the universal forward primer in PCRs to generate an 830-bp product. The primer pair was tested for specificity against DNA from 85 bacterial strains, mostly of rumen origin (Table 1). Only C. proteoclasticum genomic DNA amplified with these two primers at an annealing temperature of 62°C (Table 1); closely related strains (B. fibrisolvens-like C21b and C122b) failed to amplify under these conditions. At an annealing temperature of 60°C, some amplification occurred from unrelated Enterococcus faecalis NCTC 775 and Streptococcus bovis RF-2. This nonspecific amplification was eliminated once the annealing temperature was raised to 62°C. The DNA from each of the rumen strains was also tested with the universal forward and reverse primers at an annealing temperature of 55°C. All the strains produced a PCR fragment of approximately 1,500 bp, corresponding to the approximate size of the 16S rRNA gene, demonstrating that the DNA from each strain was amplifiable.
The sensitivity of the S-S-Cprot-0832-a-A-21 primer in PCRs was investigated by amplification of a serial dilution of DNA from known numbers of C. proteoclasticum cells. The results show that 50 fg of DNA (the equivalent of DNA from 25 C. proteoclasticum cells) was the lower limit of detection when coamplified with a 2 × 106 dilution of the internal control DNA (Fig. 2).
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DNA extraction. To determine the most efficient method of recovering DNA from bacterial samples, 1010 C. proteoclasticum cells were subjected to three methods of DNA extraction: enzymatic cell lysis, chemical extraction, and physical disruption. A260/280 readings demonstrated that physical disruption was the most efficient method of extraction, recovering 67 µg of DNA from 1010 cells. Enzymatic lysis and chemical extraction recovered 43 and 1.01 µg of DNA per 1010 cells, respectively.
Internal-control amplification efficiency.
The relative
amplification efficiencies of target and internal-control DNAs can be
determined from a plot of the ratio of log target intensity to internal
control intensity against the log concentration of internal control
DNA. Coamplification of DNA from 103 C. proteoclasticum cells with dilutions of the
internal control (Fig. 3) results in a
line with a slope of 0.94 and a regression of 0.999. This indicates
equivalent amplification efficiencies of the target and control DNAs.
The line intersects the x axis at 5.9, indicating that the
optimal dilution of internal control for detection of 103
C. proteoclasticum cells is 1.26 × 106.
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Standard curve.
Since cPCR is most accurate when the target
and internal control are coamplified in equimolar proportions, it was
necessary to determine the optimal internal-control concentrations to
use with DNA extracted from rumen samples. Dilutions of internal
control were coamplified with DNA from selected samples, and the
optimal dilution of the internal control was found to be
106. This concentration of internal control was used to
construct a standard curve by coamplification with C. proteoclasticum DNA extracted from a known number
of cells (Fig. 4). The results show that
DNA from 1 × 104 to 5 × 101 cells
gave a linear response and could be used for quantitation of samples
within this range.
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Detection of C. proteoclasticum
added to rumen fluid.
To test whether C. proteoclasticum could be detected by cPCR within a
background of nonspecific DNA from rumen fluid, samples of rumen
contents were spiked with known numbers of C. proteoclasticum cells. DNA from each of the
samples was coamplified under optimal cPCR conditions, and the results
show a linear relationship between the number of cells added and the
number of cells detected. The assay slightly overestimated the number
of C. proteoclasticum cells added
compared to the ideal (y = x), and this was
particularly evident at the higher concentrations of cells (Fig.
5). A population of 6.25 × 106 C. proteoclasticum cell
equivalents ml1 was detected in the unspiked rumen
samples.
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Detection of C. proteoclasticum
and closely related strains in vivo.
To examine the application of
the cPCR approach to determining bacterial numbers directly from
animals, rumen samples were collected from eight lactating dairy cows
fed four different diets in rotation. The number of C. proteoclasticum cell equivalents detected ranged
from 2.01 × 106 to 3.12 × 107
ml1 of rumen contents (Fig.
6). Within individual animals there were significant responses to diet, but overall there was no significant difference between the diets.
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DISCUSSION |
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Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
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C. proteoclasticum is a proteolytic bacterium that was isolated from the rumen contents of a forage-fed cow (2). It has a predominately serine-type proteinase activity (3) but also some cysteine- and metallo-type proteinase activity. It seems most likely to be involved with primary hydrolysis of feed protein, but the significance of C. proteoclasticum to rumen microbial ecology has not yet been determined. Since no suitable selective media are available for enumeration of C. proteoclasticum, we set out to develop a method to quantify this organism directly from rumen samples.
PCR is an extremely sensitive and specific method for the amplification of DNA, and when it is used in conjunction with an internal DNA control, the products of the amplification reactions can be quantified. This technique, cPCR, was originally developed for quantitation of human immunodeficiency virus type 1 3B long terminal repeat DNA (29). Its use has since been extended to bacterial quantitation in the environment (12, 14, 15). In the present study, a cPCR method was developed to quantify C. proteoclasticum and closely related strains from rumen samples. PCR primers, based on both conserved and hypervariable regions of the 16S rRNA gene, were used to amplify DNA in the presence of an internal control which allowed quantitation of the PCR products. The primer pair used circumscribes C. proteoclasticum and four closely related B. fibrisolvens strains and did not amplify DNA from any other bacterium tested. The specificity of the assay stems from the selection of 16S rDNA as the target for amplification and the primer design. The semiconserved nature of rRNA genes allows the use of regions of hypervariable sequence as targets for group-, genus-, species-, and strain-specific amplification (22). The primer was designed to match, as closely as possible, the length, G+C content, and Tm of the universal forward primer so that the forward primer "anchored" the PCR at the 5' end of the 16S rRNA gene. This approach limits the range of suitable specific primers which can be designed within a particular region but avoids the need to design two specific primers for a given organism. Using the 16S rRNA gene as the amplification target also allows primers to be checked against the existing entries in DNA sequence databases, thereby reducing the effort needed to test primer specificity.
A critical factor in ensuring the accuracy of cPCR is to demonstrate
that coamplifications of the target and internal control are equivalent
(24). This can be done by plotting the log ratio of target
to internal-control DNA intensities against the log dilution of
internal-control DNA. Coamplification of C. proteoclasticum DNA with dilutions of internal
control gave a straight line with a slope of 0.94, indicating that
the amplification efficiencies of the two DNAs are essentially equal.
The small deviation from equivalence may be due to a slightly more
efficient amplification of the smaller internal control (480 bp) than
of the target (830 bp). This effect was taken into account by using
standard curves to relate the log ratio of target to internal control
to the log of cell numbers. These standard curves also account for the
rRNA gene copy number, which can vary anywhere from 2 to 10 copies per
genome (1, 9). Each standard curve, generated by
coamplification of a single dilution of internal control with DNA from
different numbers of C. proteoclasticum
cells, gives a substantial working range of cell numbers of
approximately 103- to 104-fold. Indeed, in the
application of the assay to rumen samples, only a single standard curve
was required to encompass the entire range of C. proteoclasticum numbers encountered in differently fed dairy cows.
In a similar manner, dilutions of internal control can be used to
determine the absolute sensitivity of the assay. Theoretically, the
detection of one copy of the target sequence is possible
(28). However, in cPCR, the target and internal control
compete for amplification reagents, reducing the sensitivity of
detection. In our assay, DNA from the equivalent of 25 C. proteoclasticum cells could be detected when
coamplified with a 2 × 106 dilution of the internal
control. However, it was found that a 100-fold dilution was necessary
to overcome an inhibitory effect in DNA extracted from rumen samples.
Thus, in practice, the sensitivity of the assay is limited to 2.5 × 103 cells. The exact nature of the inhibitory factor is
not known, but high A260/280 readings from these
DNA samples indicate that it is not proteinaceous and that it may be a
water-soluble polysaccharide or polyphenolic compound similar in nature
to the humic acids described by Leser (14) as interfering
with the PCRs. The level of detection compares favorably with that in
similar studies of bacterial populations from other environments. Leser
(14) detected DNA from 40 Pseudomonas cells in
cPCR assays of samples from a marine environment. Radiolabelled
oligonucleotides used to probe rRNA from rumen bacteria (7, 11,
17-20, 27) are less sensitive, being able to detect 0.01% of
the total rumen population, or approximately 106 cells
ml1 (27). It should be noted that the cPCR
technique does not discriminate between living and dead cells and
therefore is likely to overestimate viable populations. This is in
contrast with oligonucleotide probing, where microbial abundance is
expressed in terms of a proportion of total rRNA. Since the rRNA
content in cells changes according to the growth phase, this technique
provides an approximation of relative cell numbers (20),
which reflects their contribution to total metabolic activity
(27). However, the estimation of total rRNA abundance
depends on universal probes, and recent evidence suggests that
domain-specific variations in dissociation temperatures of universal
probes could lead to significant biases in quantifying microbial
populations from environmental samples (30). Estimates of
both absolute cell numbers and the percent contribution to total rRNA
may be the best approach to gain an accurate assessment of the
importance of microbial populations in environmental samples.
After the development of the cPCR assay in vitro, it was necessary to test its ability to detect C. proteoclasticum cells in the complex mixture of plant and microbial DNA present in rumen fluid. Mechanical disruption was chosen for DNA extraction from rumen contents since the efficiency of extraction was greatest with bead beating followed by phenol-chloroform extractions. Also, this method allowed entire rumen contents to be sampled, thereby enabling the quantitation of populations adherent to plant tissue. Previous methods have sampled only filtered rumen contents (7, 17, 27). The addition of C. proteoclasticum cells to rumen fluid followed by cPCR quantitation demonstrated the usefulness of the technique in vivo. There was good correlation between the number of cells added and those detected by the assay. A slight overestimation of absolute numbers of cells compared to the ideal (y = x) is probably due to the resident population of C. proteoclasticum and closely related B. fibrisolvens strains in the rumen fluid used.
When the assay was applied to rumen samples collected from animals fed diets differing in nitrogen and carbohydrate content, the C. proteoclasticum cell equivalents detected ranged from 2.01 × 106 cells per ml in the carbohydrate-supplemented, high-nitrogen diet to 3.12 × 107 cells per ml in the high-nitrogen diet. These numbers represent the population of C. proteoclasticum and closely related B. fibrisolvens strains present in the samples and are consistent with the original isolation of C. proteoclasticum from a 108 dilution of rumen contents (4). These results indicate that this group of organisms is common among forage-fed ruminants in New Zealand. Within individual animals, the diet had some effects on C. proteoclasticum cell equivalents, but overall, between the animals there were no significant differences (Fig. 6). The relatively small range of cell numbers detected indicates that the population is stable and unresponsive to changes in dietary content. This is a little surprising since one might expect the proteolytic population of C. proteoclasticum to be influenced by nitrogen supply. However, the population density of C. proteoclasticum does not necessarily reflect its overall contribution to proteolytic activity, which may well vary significantly under the conditions tested. Previously, it was shown that C. proteoclasticum has a high chymotrypsin-like proteinase activity (3), and, based on its specific activity for the artificial chymotrypsin substrate N-succinyl alanine-alanine-proline-phenylalanine-p-nitroanilide and the populations detected in this study, it may be responsible for up to 20% of this type of activity in forage-fed dairy cows. More detailed investigations of specific C. proteoclasticum proteinase activities are required before the contribution of this organism to ruminal protein breakdown can be estimated more precisely.
We have found cPCR to be an easy, accurate, and reliable method of bacterial quantitation. Collection of rumen samples, DNA extraction, preliminary PCR amplification with internal control dilutions, and cPCR followed by scanning densitometry can be accomplished within 10 h. Testing primers for specificity and constructing internal DNA controls are the most time-consuming steps in developing the method, but once these have been carried out, they need not be repeated. The precision of the technique is good, with the coefficient of variation between replicate PCRs of the same sample averaging 2.5% and that between samples from the same animal averaging 7.5%. The technique combines the specificity of 16S rDNA-targeted oligonucleotides with the sensitivity of PCR in a format which allows quantitation of bacterial populations from a complex microbial ecosystem. The technique is currently being extended to other protein-degrading genera and will eventually allow us to examine how proteolytic bacterial populations are influenced by changes in the rumen ecosystem.
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ACKNOWLEDGMENTS |
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This work was funded by Public Good Science Funding from the Foundation for Research in Science and Technology and a Lottery Science Research Grant from the New Zealand Lotteries Grant Board.
We thank Vicky Carruthers of the Dairying Research Corporation for the rumen samples and Raymond Bennett and Doug Hopcroft of HortResearch for the development of photographs. Constructive criticisms of the manuscript by Barry Scott and K. N. Joblin are also gratefully acknowledged.
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FOOTNOTES |
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* Corresponding author. Mailing address: AgResearch, Ruminant Digestion and Metabolism, Grasslands Research Centre, Tennent Drive, Private Bag 11008, Palmerston North, New Zealand. Phone: 64 6 356 8019. Fax: 64 6 351 8003. E-mail: attwoodg{at}agresearch.cri.nz.
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Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
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