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Applied and Environmental Microbiology, July 1999, p. 3042-3047, Vol. 65, No. 7
Department of Biology, University of New
Brunswick, Fredericton, New Brunswick, Canada E3B 6E1
Received 19 November 1998/Accepted 22 April 1999
A nested reverse transcriptase (RT) PCR assay detected mRNA of the
salmonid pathogen Renibacterium salmoninarum in samples of
RNA extracts of between 1 and 10 cells. Total RNA was extracted from
cultured bacteria, Atlantic salmon (Salmo salar L.) kidney tissue and ovarian fluid seeded with the pathogen, and kidney tissue
from both experimentally challenged and commercially raised fish.
Following DNase treatment, extracted RNA was amplified by both RT PCR
and PCR by using primers specific for the gene encoding the major
protein antigen of R. salmoninarum. A 349-bp amplicon was
detected by polyacrylamide gel electrophoresis and silver stain.
Inactivation of cultured bacteria by rifampin or erythromycin produced
a loss of nested RT PCR mRNA detection corresponding to a loss of
bacterial cell viability determined from plate counts but no loss of
DNA detection by PCR. In subclinically diseased fish, nested RT PCR
identified similar levels of infected fish as determined by viable
pathogen culture. Higher percentages of fish testing positive were
generated by PCR, particularly in samples from fish previously
subjected to antibiotic chemotherapy where 93% were PCR positive, but
only 7% were nested RT PCR and culture positive. PCR can generate
false-positive data from amplification of target DNA from nonviable
pathogen cells. Therefore, nested RT PCR may prove useful for
monitoring cultured Atlantic salmon for the presence of viable R. salmoninarum within a useful time frame, particularly samples
from broodstock where antibiotic chemotherapy is used prior to spawning
to reduce vertical pathogen transmission.
Bacterial kidney disease (BKD)
caused by Renibacterium salmoninarum is a persistent disease
affecting cultivated salmonids in Europe, Japan, and North and South
America (reviewed in reference 10). The frequent
occurrence of subclinically infected carrier fish and the currently
available, less than completely effective, antibiotic chemotherapies
undoubtedly contribute to this persistence. BKD transmission can occur
horizontally from fish to fish or vertically from subclinically
infected female fish to progeny via infected eggs (10).
Control of BKD is attempted through monitoring and culling of
subclinically infected broodstock to prevent vertical transmission. Immunodiagnostic methods developed for this screening (8, 16, 29) lack the necessary sensitivity to identify many subclinical carrier fish (1, 12, 15). Culture of this fastidious
bacterium on selective media is impractical due to the lengthy (many
weeks [6]) incubation required before identification
can be achieved.
More recently, sensitive PCR methods to detect DNA (7, 21, 26,
27) and reverse transcriptase (RT) PCR methods to detect rRNA
(24) from R. salmoninarum in fish kidney tissue, ovarian fluid, and egg samples have been reported. However, it is
becoming increasingly apparent that these methods can produce false-positive results through the amplification of target DNA (18, 25) or rRNA sequences (31) from nonviable
bacteria. In Atlantic salmon intraperitoneally injected with
formalin-treated Aeromonas salmonicida cells, PCR detected
DNA from the dead bacteria in tissues of the live sampled fish for at
least 16 weeks postinjection (17). With R. salmoninarum, this problem may be inflated by the use of
antibiotic chemotherapy not only to treat fish during overt BKD
outbreaks but also to routinely treat broodstock fish prior to spawning
to reduce vertical transmission from subclinical fish. In a survey of
such treated broodstock, only 4 to 5% of the PCR-positive ovarian
fluid and kidney tissue samples were ultimately found to contain viable
R. salmoninarum by culture (27). With
PCR-positive samples not uncommonly representing 10 to 50% of the
total broodstock samples assayed (27), it may become useful
to identify those samples containing viable pathogen cells within a
practical time frame.
Bacterial mRNA has a short half-life, usually measured in minutes
(20), and its detection decreases comparatively quickly with
a loss of bacterial cell viability (31). For this reason, the detection of bacterial mRNA has been investigated recently as a
method to more quickly identify the presence of viable bacteria (4, 5, 19, 28, 31). This report describes a nested RT PCR
assay to detect R. salmoninarum mRNA. A comparison between mRNA detection and R. salmoninarum cell viability was made
in vitro in cultured bacteria inactivated by antibiotics and in situ in
Atlantic salmon.
Bacterial strains and cultivation.
The R. salmoninarum K2A2 strain, isolated from
Atlantic salmon at a hatchery on the Margaree River, Nova Scotia, and
kindly provided by Gilles Olivier, Fisheries and Oceans Canada,
Halifax, Nova Scotia, (14) was subcultured on selective
kidney disease medium (SKDM) (2) agar at 15°C for 3 weeks.
Confluent lawns of bacteria were washed off the agar plates in sterile
phosphate-buffered saline (PBS). Cell numbers were estimated by
absorbance (an optical density at 660 nm of 1.0 corresponded to
approximately 109 cells ml
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
A Sensitive Nested Reverse Transcriptase PCR Assay
To Detect Viable Cells of the Fish Pathogen Renibacterium
salmoninarum in Atlantic Salmon (Salmo salar
L.)
ABSTRACT
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
INTRODUCTION
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
MATERIALS AND METHODS
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
1 from
hemocytometer counts as previously reported [27]).
Serial dilutions of the harvested bacteria in PBS were used to
determine sensitivity of the nested RT PCR assay.
Total RNA extraction from bacterial strains.
Harvested
bacteria in PBS were centrifuged at 6,000 × g for 10 min at 4°C. Cell pellets were suspended immediately in 200 µl of 20 mM sodium acetate, pH 5.5, and 1 mM EDTA followed by the addition of 20 µl of 10% (wt/vol) sodium dodecyl sulfate with mixing and 200 µl
of phenol-chloroform equilibrated with water (1:1) with mixing. Yeast
tRNA (10 µg) was added, and the mixture was agitated at 70°C for 10 min and centrifuged at 12,000 × g for 10 min at 4°C
(23). The aqueous phase was collected, combined with 200 µl of TRIzol reagent (Gibco BRL Life Technologies Inc., Grand Island,
N.Y.), mixed, and set at room temperature for 7 min. Chloroform (100 µl) was added, and the mixture was vortexed, set at room temperature
for 7 min, and centrifuged at 12,000 × g for 15 min at
4°C. The aqueous phase was collected, combined with an equal volume
of isopropanol, set at 
20°C for 30 min, and centrifuged at
12,000 × g for 20 min at 4°C. The extracted RNA
pellet was washed with 75% (vol/vol) ethanol and stored at 70°C
until assayed.
Synthetic oligonucleotide primers. Oligonucleotide primers were selected from the published gene sequence of the major protein antigen (9) produced by R. salmoninarum isolates from a wide geographic range (11) with the assistance of the Oligo software program (National Bioscience Inc., Plymouth, Minn.). The nucleotide sequences of the primers for reverse transcription of the specific mRNA species and preamplification of the cDNA were LP3 (5'TTACCCGATCCAGTTCCC-3'), reverse 3'-position 1483, and UPI (5'ATGTCGCAAGGTGAAGGG-3'), forward 5'-position 127. The primers used for the second amplification reaction (FL7 and RL11) were those previously reported (27). The oligonucleotides were synthesized by Interscience Inc. (Markham, Ontario, Canada).
Nested RT PCR assay to detect R. salmoninarum mRNA. Extracted RNA pellets were air dried, suspended in 175 µl of sterile, distilled, deionized H2O, incubated at 57°C for 10 min, vortexed, and centrifuged at 12,000 × g for 10 min at 4°C. Supernatant aliquots (15 µl) were treated with 10 U of RQ1 RNase-free DNase (Promega Corp., Madison, Wis.) in a total reaction volume of 50 µl, containing 40 mM Tris-HCl (pH 8.0), 3 mM MgCl2, 10 U of RNasin (Promega Corp.), and 1 mM dithiothreitol incubated at 37°C for 30 min. One microliter of 500 mM EDTA was added, and the reaction mixture was centrifuged at 12,000 × g for 1 min, placed at 90°C for 5 min to inactivate DNase, and placed on ice.
For RT PCR, the reaction volume of 50 µl contained 15 µl of the DNase-treated RNA extract, 0.1 µM (each) primers LP3 and UP1, 50 mM Tris-HCl, 75 mM KCl, 12 mM MgCl2, 10 mM dithiothreitol, 2 mM (each) nucleotide triphosphate, 10 U of RNasin, 10 U of Taq polymerase (Gibco BRL Life Technologies Inc.), and 200 U of Moloney murine leukemia virus reverse transcriptase (Gibco BRL Life Technologies Inc.). The reaction mixture was allowed to reach 37°C on a PTC-100 programmable thermal controller (MJ Research Inc., Watertown, Mass.) before addition of reverse transcriptase. The incubation conditions were 37°C for 62 min for RT followed by 95°C for 5 min and 20 cycles of 95°C for 1.5 min (denaturing), 55°C for 1.5 min (annealing), 72°C for 2 min (extension), and 72°C for 10 min for PCR. For the second amplification, the reaction volume of 50 µl contained 15 µl of the preamplification product, 0.2 µM (each) primers FL7 and RL11 (27), 5 µl of 10× PCR buffer (Gibco BRL Life Technologies Inc.), 0.1 mM (each) nucleotide triphosphate, 2% (vol/vol) formamide, 0.001% (wt/vol) gelatin, and 2 U of Taq polymerase. The thermal cycling conditions were 94°C for 5 min and 45 cycles of 93°C for 1 min (denaturing), 60°C for 1 min (annealing), 72°C for 30 s (extension), and 72°C for 2 min. RT was omitted from the first reaction for DNase-digested RNA extract controls to ensure DNA digestion. The nested RT PCR products (10-µl volumes) were subjected to 8% (wt/vol) polyacrylamide gel electrophoresis at a constant 200 V for 30 min by using a Mini Protean II electrophoresis apparatus (Bio-Rad Laboratories Ltd., Hercules, Calif.) and visualized by silver staining (Bio-Rad Laboratories Ltd.).PCR assay to detect R. salmoninarum DNA. DNA was extracted from bacterial cells as previously reported (27). PCR amplification was performed by using 50-µl volumes containing 10 µl of DNA extract, 0.1 µM (each) primers FL7 and RL11 (26), 5 µl of 10× PCR buffer, 1 mM MgCl2, 0.1 mM (each) nucleotide triphosphate, 2% (vol/vol) formamide, 0.001% (wt/vol) gelatin, and 1.5 U of Taq polymerase. Thermal cycling conditions were the same as those used for the second PCR amplification reaction above, except that 35 cycles were used. The PCR products were subjected to polyacrylamide gel electrophoresis and visualized by silver staining as described above.
Sensitivity of nested RT PCR assay of seeded Atlantic salmon
kidney tissue and ovarian fluid.
Kidneys were removed from
Atlantic salmon, homogenized (10% [wet wt/vol]), and stored at
20°C as reported previously (15). Ovarian fluid was
collected from gravid female fish and stored at 20°C as reported
previously (12). Aliquots (50 µl) of presumed-negative samples (by culture on SKDM agar and PCR [27]) were
seeded with serial dilutions of cultivated R. salmoninarum
cells. Seeded kidney homogenate samples were washed twice with 1 ml of
PBS by centrifugation at 13,000 × g for 30 s and
suspended in 50 µl of PBS. Total RNA was extracted from the seeded
ovarian fluid and washed kidney homogenate samples and assayed by
nested RT PCR as described above.
Antibiotic inactivation of cultured R. salmoninarum
cells.
R. salmoninarum was subcultured in 250-ml Erlenmeyer
flasks containing 100 ml of Mueller-Hinton broth containing 0.1%
(wt/vol) cysteine hydrochloride (MHB-C) (3) at 15°C and
150 rpm on a Psychrotherm environmental shaker (model G-26; New
Brunswick Scientific Co. Inc., Edison, N.J.) and used to inoculate
MHB-C with and without rifampin (final concentration, 10 µg
ml1) to a final cell concentration of approximately
106 ml1. Samples (0.5 ml) of each incubated
culture were removed at the times indicated for RNA extraction and
nested RT PCR, DNA extraction and PCR (as described above), and culture
of viable cells. For culture, samples were washed with and suspended in
MHB-C broth. Aliquots (20 µl) of serial 10-fold dilutions of the
washed cell samples were drop plated (15) in triplicate onto
SKDM agar and Trypticase soy agar (TSA), and the number of CFU were
determined after 3, 6, and 8 weeks incubation at 15°C. Growth on SKDM
agar in the absence of growth on TSA was used to confirm colonies as R. salmoninarum (15). Similar experiments were
carried out where erythromycin (final concentration, 200 µg
ml1) was used in place of rifampin.
Comparison of nested RT PCR, PCR, and culture to detect R. salmoninarum in kidney tissue from experimentally challenged and commercially raised Atlantic salmon. For experimentally challenged fish, Atlantic salmon (weight, 25 to 50 g each) were acclimated and maintained at 10 to 11°C as previously described (22). Fish were injected intraperitoneally with approximately 107 CFU of R. salmoninarum K2A2 in 0.2 ml of PBS, the fins were clipped for identification, and 50 fish were placed into each of three tanks containing 50 unchallenged fish to initiate a low-level BKD infection in the cohabitant unchallenged fish. Any fish that died were removed daily and checked for internal clinical signs of BKD (10), and 10% were checked for R. salmoninarum by nested RT PCR, PCR, and culture from kidney tissue. Nested RT PCR and PCR were performed on 10% (wet wt/vol) kidney homogenates as described above. For culture, sterile cotton swabs were dipped into the kidney homogenate and swabbed onto the surface of SKDM agar and TSA plates, and the plates were checked for growth of R. salmoninarum after 6 weeks incubation at 15°C. At week 9 postchallenge, surviving fish challenged by intraperitoneal injection (only 7%) were removed from the tanks. At week 14 postchallenge, samples (10 fish from each tank) of the surviving fish challenged by cohabitation (95%) were sacrificed, and kidney tissue was assayed for R. salmoninarum by nested RT PCR, PCR, and culture. For culture, the number of R. salmoninarum CFU per gram wet weight of kidney tissue was determined by drop plating 20-µl aliquots of serial 10-fold dilutions of kidney homogenates in triplicate on SKDM agar and TSA plates and incubating the plates at 15°C for 6 weeks.
Samples of commercially raised Atlantic salmon from a sea cage site on the Bay of Fundy, New Brunswick, were also obtained and assayed for R. salmoninarum by nested RT PCR, PCR, and culture from kidney tissue.| |
RESULTS |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Nested RT PCR assay to detect R. salmoninarum mRNA. Several PCR assays specifically detecting target DNA from R. salmoninarum isolates from diverse geographic locations (7, 26, 27) have been based on the published sequence of the gene coding the 57-kDa protein (major soluble antigen) from the R. salmoninarum ATCC 33209 type strain (9) and suggest this gene is highly conserved. We have recently sequenced this gene from the R. salmoninarum K2A2 strain used here from bp 127 to 1500 and have found only two differences (a base change at bp 464 and an extra codon between bp 768 and 769) from the published sequence of the ATCC 33209 type strain (32). Therefore, nucleotide sequences for primers for reverse transcription of mRNA and PCR preamplification of cDNA were selected from the published sequence of this gene from the type strain, and PCR as previously reported (27) was used to amplify a 349-bp segment of the cDNA.
Nested RT PCR of DNase-treated RNA extracts from R. salmoninarum K2A2 consistently produced the expected 349-bp amplification product (Fig. 1A, lane 2). Control reactions (RT omitted from the first reaction) consistently failed to produce a detectable 349-bp amplification product, showing that any contaminating R. salmoninarum DNA in the RNA extracts was destroyed (Fig. 1A, lane 3). Lower-molecular-mass bands (of lengths less than 349 bp) were variably seen in both test and control samples (Fig. 1A, lane 2, and Fig. 1B, lanes 2 to 4) but did not hinder interpretation of the results and likely represented residual primers and/or dimerization products of the primers (30).
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Sensitivity and specificity of the nested RT PCR assay. To examine the sensitivity of the nested RT PCR assay, total RNA was extracted from presumed-negative (by culture and PCR) Atlantic salmon kidney tissue homogenate (10% [wet wt/vol]) and ovarian fluid seeded with serial dilutions of cultivated R. salmoninarum cells. The intensity of the stained 349-bp amplification product detected on polyacrylamide gels decreased with the concentration of R. salmoninarum cells in the seeded samples but was consistently detected by the assay with aliquots of the DNase-treated RNA extracts of between 1 and 10 R. salmoninarum cells (Fig. 1B). The nested RT PCR assay of total RNA extracts of cultures of a variety of other bacteria tested did not produce a positive result, as no amplification product of the appropriate size was detected (Fig. 2).
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Effect of antibiotic treatment on R. salmoninarum cell
viability and mRNA detection.
To compare mRNA detection by nested
RT PCR and cell viability by culture, R. salmoninarum cells
were inoculated and incubated in MHB-C broth (3) and
rifampin (10 µg ml1 of broth) or erythromycin (200 µg
ml1 of broth). Viability was defined here as visible
colonies produced from washed cell samples of the broth culture plated
on SKDM agar (2) and incubated at 15°C for 8 weeks.
Rifampin, an inhibitor of mRNA synthesis, and erythromycin, an
inhibitor of protein synthesis, were chosen to inactivate the cells
(20), as they would be less likely to directly cause
destruction of existing mRNA in the cells than other inactivation
methods, such as heat (31).
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Comparison of culture, nested RT PCR, and PCR for detection of R. salmoninarum in experimentally challenged Atlantic salmon. A low-level BKD infection was established in previously unchallenged fish by cohabitation for 9 weeks with fish injected intraperitoneally with R. salmoninarum, by which time most (93%) of the intraperitoneally injected fish had died. All mortalities displayed typical symptoms of BKD (e.g., white granulomatous lesions in kidney tissue [10]), and those mortalities checked (14 fish) were positive for R. salmoninarum by cultivation on SKDM agar, nested RT PCR assay, and PCR assay from kidney tissue.
Most of the live sampled fish challenged by cohabitation and assayed from kidney tissue on week 14 postchallenge were culture positive (66%) with low numbers of R. salmoninarum CFU per gram (wet wt) of kidney tissue (Table 3). The detection limit of the culture method used as the indicator for viable pathogen cells was approximately 5 × 102 to 5 × 103 CFU g1 of kidney tissue. If the detection
limits used for nested RT PCR and PCR did not exceed the detection
limit for culture, then culture could be used to evaluate the nested RT
PCR and PCR methods for detection of viable and/or dead pathogen cells.
Therefore, the detection limits of the nested RT PCR and PCR methods,
as used, were between approximately 7 × 103 and
7 × 104 and between 4 × 103 and
4 × 104 seeded bacterial cell equivalents
g1 kidney tissue, respectively.
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1 by culture tested
positive by nested RT PCR (Table 3). Of eight kidney samples containing
5 × 102 to 3 × 104 CFU
g1, four produced positive results by nested RT PCR,
which may indicate the range where the nested RT PCR detection limit
was being exceeded. Most kidney samples (8 of 10) testing negative by
culture also tested negative by nested RT PCR, but two culture-negative
kidney samples tested weakly positive by nested RT PCR. Some of the
differences between nested RT PCR and culture may have been caused by
chance sampling from kidney homogenates containing low numbers of
unequally distributed viable R. salmoninarum cells, such
that not all aliquots from the same sample contained viable pathogen cells.
A selected number of kidney samples from the live, sampled, challenged
fish also were assayed by PCR (Table 3). While the culture-positive
kidney samples tested were positive by PCR, a number of the
culture-negative and nested RT PCR-negative kidney samples also
produced positive results by PCR.
R. salmoninarum detection in commercially raised Atlantic salmon. Subclinical live fish from a commercial sea cage site in the Bay of Fundy with a recent history of BKD were sampled in May 1997. One sample (16 fish) was obtained from a sea cage of untreated fish, and the other (15 fish) was obtained from a separate sea cage of fish previously subjected to antibiotic chemotherapy (oxytetracycline for 21 days in May and November 1996). Kidney tissue from these fish was assayed in the same manner as tissue from the experimentally challenged fish, except that no serial dilutions of the kidney homogenate samples were plated for culture.
Of the untreated fish, 11 were culture positive and 10 were nested RT PCR positive (Table 4). Some of the culture-positive fish (3) containing very low numbers of R. salmoninarum CFU (1 to 6 colonies per plate, less than approximately 3 × 103 CFU g1 of kidney
tissue) were nested RT PCR negative, and some of the culture-negative
fish (2) produced weak-positive nested RT PCR reactions.
Again, this suggested the range where the detection limits of the
assays, as used, may have been exceeded and where chance sampling of
different aliquots from the same kidney sample may or may not have
contained viable pathogen cells. However, all 16 fish tested were PCR
positive. These results were similar to those observed by using the
subclinical challenged fish. With the fish sample previously subjected
to antibiotic chemotherapy, only one fish was culture-positive (one
colony) and one fish was weakly RT PCR positive, but 14 of the 15 fish
were PCR positive, suggesting the PCR was detecting target DNA from
nonviable R. salmoninarum cells.
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DISCUSSION |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Recent investigations have described the potential use of mRNA detection by RT PCR methods to identify low numbers of viable bacterial cells of human pathogens such as Listeria monocytogenes (19) and Vibrio cholerae (5) in complex environments such as food. These and other reports (4, 28, 31) indicate that, due to the short half-lives of bacterial mRNAs, detection of mRNA may be a good indicator of the presence of viable cells or cells that have died shortly before the time of sampling. Here, the nested RT PCR assay to detect mRNA from the gene coding the major protein antigen of the salmonid fish pathogen R. salmoninarum detected target mRNA from between 1 and 10 pathogen cells in aliquots extracted from seeded Atlantic salmon kidney tissue homogenate or ovarian fluid. The assay was specific and could be completed within 72 h.
Incubation of R. salmoninarum cells in MHB-C broth with rifampin indicated a relationship between mRNA detection by the nested RT PCR assay and R. salmoninarum cell viability. The significant decrease in mRNA detection (99 to 99.9%) in the broth samples corresponding to a significant loss of cell viability (90 to 99.9%) as determined from colony formation after 8 weeks incubation of the broth samples on SKDM agar. Similar results were obtained when R. salmoninarum was incubated in MHB-C broth with erythromycin. The failure to observe any loss of target DNA detection by PCR even after 21 days incubation in the broths with antibiotics showed that PCR amplified target DNA from dead bacterial cells. It is known that detection of DNA by PCR or rRNA by RT PCR may not distinguish between living and dead organisms due to the greater stability of these cellular components (18, 25, 31).
To examine these relationships in situ in Atlantic salmon, a low-level
BKD infection was experimentally established in fish, and kidney tissue
from live sampled fish was assayed. The detection limits, as used, for
the nested RT PCR and PCR assays did not exceed the detection limit of
the culture method. Therefore, culture was used to evaluate the nested
RT PCR and PCR methods for detection of viable and/or dead pathogen
cells. The majority of culture-positive samples tested positive by
nested RT PCR, and the majority of culture-negative samples tested
negative by nested RT PCR. In some kidney samples, differences between
culture and nested RT PCR results were observed where culture results
indicated very low numbers of CFU g1 of kidney tissue or
nested RT PCR reactions were weak. The results suggested that these
latter samples contained very low numbers of viable pathogen cells,
perhaps where detection limits of the assays, as used, were being
exceeded and/or where, due to chance sampling, different aliquots from
the same kidney homogenate may or may not have contained viable
pathogen cells. In contrast, while PCR identified all culture-positive
kidney samples tested, it also produced positive results for many
kidney samples which were negative by culture and nested RT PCR,
suggesting that PCR amplified target DNA from nonviable R. salmoninarum cells in the kidney tissue.
Results similar to those obtained with the experimentally infected fish were produced when a live sample of untreated, commercially raised, sea cage Atlantic salmon with a recent history of BKD were subjected to the same assays. However, an examination of a second live sample of fish from a separate sea cage at the same site, which had previously been subjected to antibiotic chemotherapy, produced a much lower number of fish testing positive by culture and nested RT PCR than was observed for the untreated fish sample. In contrast, PCR produced a number of fish testing positive which was as high as that observed from the untreated fish sample. The results of the fish analyses indicated that the nested RT PCR detection of R. salmoninarum mRNA is a better indicator of the presence of viable pathogen cells in kidney samples from Atlantic salmon and that PCR produced significant false-positive data through amplification of target DNA from nonviable pathogen cells particularly evident in fish subjected to antibiotic chemotherapy. The results also indicated a potential use for the nested RT PCR assay as a method to more quickly assess the efficacy of any antibiotic chemotherapy.
The detection limit used for the nested RT PCR assay of kidney tissue
for experimental comparison purposes most likely contributed to its
failure to identify some of the culture-positive kidney samples
containing low numbers of viable R. salmoninarum cells. However, this detection sensitivity can be increased greater than 10-fold (i.e., tested to approximately 5 × 102 to
5 × 103 cell equivalents g1 of kidney
tissue) without affecting the assay. There are components of kidney
tissue which may have an inhibitory effect on the assay (27)
at higher concentrations of kidney tissue extracts which are presently
under investigation. However, the data show that the nested RT PCR
assay has potential use as a sensitive assay to monitor Atlantic salmon
kidney tissue and ovarian fluid for the presence of viable R. salmoninarum within a practical time frame, especially where
broodstock are routinely subjected to antibiotic chemotherapy prior to
spawning to reduce vertical pathogen transmission.
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ACKNOWLEDGMENTS |
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This research was supported in part by a grant from the Natural Sciences and Engineering Research Council of Canada and in part by a grant from the Huntsman Marine Science Centre.
We gratefully acknowledge the capable technical assistance of L. Hutchins and K. Melville (Research and Productivity Council of New Brunswick).
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FOOTNOTES |
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* Corresponding author. Mailing address: Department of Biology, University of New Brunswick, Bag Service #45111, Fredericton, N.B., Canada E3B 6E1. Phone: (506) 453-4733. Fax: (506) 453-3583. E-mail: wlynch{at}unb.ca.
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REFERENCES |
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Applied and Environmental Microbiology, July 1999, p. 3042-3047, Vol. 65, No. 7
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