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Journal of Clinical Microbiology, May 2006, p. 1821-1827, Vol. 44, No. 5
0095-1137/06/$08.00+0 doi:10.1128/JCM.44.5.1821-1827.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Division of Bacteriology, Osaka Prefectural Institute of Public Health, 3-69, Nakamichi 1-chome, Higashinari-ku, Osaka 537-0025, Japan
Received 19 September 2005/ Returned for modification 6 November 2005/ Accepted 20 February 2006
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ABSTRACT |
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INTRODUCTION |
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Cases of V. parahaemolyticus diarrhea in humans are commonly diagnosed by isolating this pathogen from a stool specimen by a bacterial culture test. The test procedure includes the plating of stool or its enrichment culture onto selective agar medium and the subsequent identification of suspected colonies on the agar medium. The identification includes biochemical tests, serotyping of O and K antigens, and examination for the presence of the tdh and trh genes (12, 20). Since the bacterial culture test requires at least 3 days and a complicated and time-consuming procedure, a simple and rapid method for the diagnosis of V. parahaemolyticus diarrhea has been desired.
Virulence factors are regarded as useful markers for the detection of pathogenic bacteria because they are almost completely specific for a particular pathogenic bacterium. For example, in the case of V. parahaemolyticus diarrhea, when a stool specimen containing tdh-positive V. parahaemolyticus is cultured in enrichment broth medium, the pathogen is expected to release TDH into the fecal enrichment culture, because TDH is a bacterial exotoxin. TDH is highly specific to tdh-positive V. parahaemolyticus, although some Vibrio cholerae non-O1 and Vibrio mimicus strains and all strains of Vibrio hollisae have been reported to produce hemolysins similar to TDH (22, 23, 25). Therefore, the occurrence of TDH in fecal enrichment culture is regarded as a useful marker for the detection of tdh-positive V. parahaemolyticus isolates in stool specimens. Since most cases of V. parahaemolyticus diarrhea are caused by tdh-positive strains (1, 2, 16, 17, 18), the detection of TDH in fecal enrichment cultures appears to be useful as an adjunct to the diagnosis of V. parahaemolyticus diarrhea. For this purpose, a rapid, simple, and sensitive method to detect TDH is necessary. Several methods, including the latex agglutination assay (KAP-RPLA; Denka Seiken Co., Ltd., Tokyo, Japan) and enzyme-linked immunosorbent assays (ELISAs) (6, 9, 10), have already been used for the detection of TDH. Each method has advantages and disadvantages. KAP-RPLA is commercially available and simple to perform, but it lacks sensitivity and requires a long incubation time before the test results are available. On the other hand, although ELISAs have excellent sensitivity, they require a complicated and time-consuming procedure. Considering the limitations mentioned above, the conventional TDH detection methods appear to be unsuitable for rapid, simple, and sensitive detection of TDH in fecal enrichment cultures.
The purpose of the present study was to develop a rapid, simple, and sensitive method to detect TDH and to evaluate the utility of the new method for the diagnosis of V. parahaemolyticus diarrhea. Using the combination of an immunochromatographic technique with monoclonal antibodies (MAbs) to TDH, a method that can detect levels of TDH in picograms per milliliter within 10 min was successfully developed. Here, we report in detail the development and the evaluation of an immunochromatographic assay to detect TDH (TDH-ICA).
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MATERIALS AND METHODS |
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Production of MAbs to TDH. TDH was purified from Kanagawa hemolysin (Sigma Chemical Co., St. Louis, MO) using a modification of a protocol described previously by Huntley et al. (11). Briefly, Kanagawa hemolysin was subjected to ion-exchange chromatography with a monoQ column (Amersham Biosciences, Piscataway, NJ) and was fractionated with an NaCl gradient of 0 to 1 M. The peak fractions (detected by measurement of the A280) were assayed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, pooled, concentrated, and loaded onto a Superose12 gel filtration column (Amersham). The purified TDH was recognized on the basis of its molecular weight by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and was used as an immunogen for the production of MAbs and as an antigen in ELISAs. Three female BALB/c mice (8 weeks old) were immunized intraperitoneally with 20 µg of the purified TDH emulsified in Freund's complete adjuvant (Wako Pure Chemical Industries, Osaka, Japan). After 2, 4, and 6 weeks, the mice were boosted intraperitoneally with the same antigen emulsified in Freund's incomplete adjuvant (Wako). At 10 weeks, a final immunization was carried out intraperitoneally with the same antigen alone. Three days after the final immunization, splenocytes of the mice and P3-X63-Ag8.U1 myeloma cells were mixed at a ratio of 5:1 and fused with 40% polyethylene glycol by a modification of a protocol described previously by Galfre and Milstein (3). The resulting hybridoma cells were selected in a hypoxanthine-aminopterin-thymidine medium, and the culture supernatants of actively growing hybridoma cells were then screened for the production of antibody by an ELISA using the purified TDH as the coating antigen. The positive hybridoma cells identified by ELISA were cloned twice by limiting dilution and then amplified in the ascites of pristine (2,6,10,14-tetramethylpentadecane)-primed mice. MAbs were purified from the ascites supernatant by affinity chromatography on a protein A-agarose gel (Affi-Gel Protein A MAPS II kit; Bio-Rad Laboratories, Hercules, CA) after salting out with 50% saturated ammonium sulfate (pH 7.4). Isotyping of MAbs was performed with a mouse monoclonal antibody isotyping kit (IsoStrip; Roche Diagnostics, Indianapolis, IN).
Determination of the best combination of MAbs for TDH-ICA by sandwich ELISA. All of the obtained MAbs were biotinylated with EZ-Link NHS-LC-LC-Biotin (PIERCE, Rockford, IL) for use as the labeling antibody of the sandwich ELISA. Each well of a 96-well ELISA plate (Sumitomo Bakelite Co., Tokyo, Japan) was coated with 100 µl of an unlabeled MAb solution (100 µg/ml in 50 mM sodium bicarbonate buffer, pH 9.6) overnight at 4°C, and the unbound active sites in each well were then blocked with phosphate-buffered saline (PBS) containing 20% horse serum for 1 h at room temperature. After three washes of each well with PBS containing 0.05% Tween 20 (PBS-T), 100 µl of a purified TDH solution (10 ng/ml in PBS-T) and 50 µl of a biotinylated MAb solution (10 µg/ml in PBS-T) were added to each well and incubated for 1 h at room temperature. After four washes with PBS-T, 100 µl of a peroxidase-avidin complex solution prepared according to the manufacturer's instruction manual (VECTASTAIN Elite ABC kit; Vector, Burlingame, CA) was added and incubated for 1 h at room temperature. After five washes with PBS-T, the peroxidase activity in each well was detected by the addition of 3,3',5,5'-tetramethylbenzidine solution (1 mg of 3,3',5,5'-tetramethylbenzidine and 1.5 µl of 30% H2O2 in 10 ml of 50 mM citrate buffer, pH 5.5) as a substrate, followed by incubation for 10 min at room temperature. After the reaction was stopped by the addition of 1 M H2SO4 solution, the absorbance of each well at 450 nm was measured using an EIA microplate reader (model 550; Bio-Rad). Finally, the absorbance values of wells were compared with each other, and the combination of MAbs used in the well that yielded the highest absorbance value was used for TDH-ICA.
TDH-ICA. All solutions and buffers used to prepare the test strip and the colloidal gold conjugate were filtered with 0.22-µm-pore-size membrane filters before use.
The test strips were prepared by using a HiFlowPlus Development Kit-15 (Millipore, Bedford, MA). Briefly, an absorbent pad was attached to a laminated membrane card (HiFlow Plus 135) so that the pad slightly overlapped the membrane, and the assembly was then cut into strips consisting of the membrane (5 by 25 mm) with the absorbent pad (5 by 17 mm). A 1.0-µl aliquot of MAb solution (2 mg/ml in 5 mM borate buffer, pH 8.5) was deposited on the membrane as a 1-mm-wide line at about the midpoint of the length of the membrane as the detection zone of TDH by using a 10-µl syringe. As the control zone, 1.0 µl of goat anti-mouse immunoglobulin G solution (2 mg/ml in 5 mM borate buffer, pH 8.5) (Sigma) was deposited on the membrane as a 1-mm-wide line 5 mm downstream from the detection zone. After drying for 1 h at 37°C and then drying overnight at 4°C, the test strips were stored at 4°C until use.
To prepare the colloidal gold conjugate, 0.3 ml of a MAb solution (0.1 mg/ml in 2 mM borax buffer, pH 9.0) was added to 10 ml of a colloidal gold suspension (40 nm; BBI International, Cardiff, United Kingdom) adjusted to pH 9.0 by the addition of 100 mM K2CO3 solution. After stirring for 30 min at room temperature, 1.0 ml of a 10% bovine serum albumin (BSA) solution (in 2 mM borax buffer, pH 9.0) was added to the mixture. After stirring for 30 min at room temperature, the mixture was centrifuged at 4,500 x g at 5°C for 10 min. The resulting pellet was suspended in 2 mM borax buffer (pH 9.0) containing 1% BSA, and the suspension was then centrifuged at 4,500 x g at 5°C for 10 min. The final pellet (the MAb-gold conjugate) was resuspended in 50 mM Tris-HCl-150 mM NaCl buffer (pH 8.2) containing 1% BSA and 20% glycerol and then stored at –25°C until use.
TDH-ICA testing of samples was performed according to the following procedure. Twenty-five microliters of a sample and 25 µl of the MAb-gold conjugate (diluted 1:10 in 100 mM Tris-HCl buffer, pH 8.0, containing 0.5% BSA and 2% Triton X-100) were added to a well of a 96-well general assay plate (flat-bottom type) (Corning, Acton, MA). After immediate mixing by repeated aspiration and ejection with a micropipette, the test strip was inserted into the mixture in the well. After migration of the mixture through the membrane for 10 min at room temperature, the appearance of red lines at both the detection zone and the control zone was interpreted as positive detection of TDH (Fig. 1).
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TDH-ICA testing of enrichment cultures of V. parahaemolyticus-spiked fecal homogenates. A V. parahaemolyticus strain (serotype O1:K69), which possesses both the tdh and trh genes and yielded a KP-negative result on Wagatsuma agar (13), was used for the preparation of spiked fecal homogenates. This strain was estimated to produce TDH at a very low level because it is tdh positive but KP negative (14). The tdh-positive but KP-negative strain was incubated in 2 ml of APW at 37°C for 16 h. The resulting culture was estimated to contain approximately 2 x 108 CFU/ml by colony counting on marine agar plates (Becton Dickinson). Serial 10-fold dilutions of the culture were made in PBS and were spiked into 10% fecal homogenate (in PBS) to yield concentrations of 2 x 101 to 105 CFU per 1 ml of the fecal homogenate (equivalent to 0.1 g of stool). A loopful of each of the spiked fecal homogenates and the fecal homogenate as 0 CFU/ml was inoculated into 20 ml of APW, which was incubated at 37°C for 16 h without shaking. After centrifugation at 10,000 x g at 5°C for 5 min, the resulting supernatants were tested with TDH-ICA. In parallel, a loopful of each of the spiked fecal homogenates, the fecal homogenate, and their 16-h APW cultures was streaked onto thiosulfate-citrate-bile salts-sucrose (TCBS) agar medium (Eiken Kizai). After incubation at 37°C for 16 h, the resulting sucrose-nonfermenting colonies (green colonies) were identified as V. parahaemolyticus.
TDH-ICA testing of enrichment cultures of stool specimens from patients with diarrhea. A total of 217 stool specimens were obtained from 217 patients with diarrhea derived from 24 different food poisoning incidents that occurred in Osaka prefecture, Japan, between July and October 2004. The specimens, all of which were diarrheal stool samples, were transported to our laboratory from 13 local public health centers in Osaka prefecture and were subjected to bacteriological examination for enteropathogens, including V. parahaemolyticus, within 2 h from the time they arrived in our laboratory. For TDH-ICA testing of fecal enrichment cultures, a loopful of each of the stool specimens was inoculated into 20 ml of APW, which was incubated at 37°C for 16 h without shaking. After centrifugation at 10,000 x g at 5°C for 5 min, the resulting supernatants were tested using TDH-ICA. In parallel, for the isolation of V. parahaemolyticus, a loopful of each of the stool specimens was streaked onto TCBS agar, which was then incubated at 37°C for 16 h. If the 16-h TCBS agar culture was negative for sucrose-nonfermenting colonies (green colonies), a loopful of the 16-h APW culture of the stool specimen was streaked onto TCBS agar. The sucrose-nonfermenting colonies on TCBS agar were screened for V. parahaemolyticus by a battery of biochemical tests, with positive results in the tests for fermentation without gas production of glucose, for lysine decarboxylase, for the production of indole from tryptophan, and for growth in 3, 6, and 8% NaCl and with negative results for fermentation of sucrose and lactose and for growth in 0 and 10% NaCl. The presumptively identified strains were subjected to the serotyping of O and K antigens using a commercially available rabbit antiserum (Denka Seiken) to determine whether they were V. parahaemolyticus strains. All of the isolated V. parahaemolyticus strains were examined for the presence of the tdh and trh genes by the PCR method (19).
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RESULTS |
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) subclass. To select a combination of MAbs for use in a sensitive immunochromatographic test to detect TDH, we screened coating and labeling antibody combinations of the five MAbs for detection sensitivity for TDH in the sandwich ELISA. The results revealed that the sandwich ELISA using MAb 3D2 as the coating antibody and MAb 4E5 as the labeling antibody yielded the highest absorbance value when 1 ng of purified TDH was assayed. Since the range of absorbance values in the sandwich ELISA reflects the detection sensitivity for TDH, the sandwich ELISA that yielded the highest absorbance value has the highest sensitivity for the detection of TDH. The above-described results, therefore, mean that the sandwich ELISA using the combination of MAbs 3D2 and 4E5 had the highest sensitivity for the detection of TDH. MAbs 3D2 and 4E5 were therefore considered to be the best combination for a sensitive immunochromatographic test to detect TDH. Establishment of TDH-ICA. By using MAb 3D2 as the antibody immobilized on test strips and MAb 4E5 as the antibody conjugated with colloidal gold particles, a sandwich-type immunochromatographic assay to detect TDH (TDH-ICA) was established. To determine the minimum detectable concentration of TDH, each TDH solution at various concentrations (0.1, 0.2, 0.5, 1, 100, and 10,000 ng of TDH/ml) and PBS as the zero concentration were tested with TDH-ICA. The red line produced by capturing the MAb-gold conjugate was observed at the control zone of all test strips within 10 min, suggesting that the MAb-gold conjugate migrated by capillary action through the membrane beyond the detection zone without aggregation. Another red line appeared at the detection zone of the test strip within 10 min due to the production of the sandwich immunocomplex of TDH and two MAbs when the concentration of TDH was 0.2 ng/ml or higher. In addition, the detectable concentration range of TDH-ICA extended to 10,000 ng/ml without false-negative results due to the prozone phenomenon. These results indicate that TDH-ICA has a minimum detectable concentration of 0.2 ng of TDH/ml and a wide dynamic range. The test strips of TDH-ICA could be used for at least 4 months when stored at 4°C.
TDH-ICA testing of broth cultures of V. parahaemolyticus and other bacterial strains. Although the tdh gene of V. parahaemolyticus has some variants, their nucleotide sequences are well conserved (>97% identity), and their protein products are immunologically indistinguishable (14). However, we considered it necessary to examine whether TDH-ICA could detect TDH produced by various tdh-positive strains of V. parahaemolyticus before using TDH-ICA as a TDH detection method. For this purpose, broth cultures of 113 tdh-positive strains of V. parahaemolyticus were tested with TDH-ICA. Broth cultures of 10 tdh-negative, trh-negative strains of V. parahaemolyticus were tested as negative controls. The results are summarized in Table 1. The 113 tdh-positive strains included 39 different serotypes of O and K antigens and were derived from 55 different food poisoning incidents. The amount of TDH production by tdh-positive V. parahaemolyticus strains differs from strain to strain, and tdh-positive but KP-negative strains produce TDH at very low levels (14). The 113 tdh-positive strains, therefore, included 19 tdh-positive but KP-negative strains for the purpose of evaluating the ability of TDH-ICA to detect the small amount of TDH produced by tdh-positive but KP-negative strains. When broth cultures of the 113 tdh-positive strains were tested with KAP-RPLA, TDH was detected in broth cultures of the 94 tdh-positive, KP-positive strains but not in broth cultures of the 19 tdh-positive but KP-negative strains. This result revealed that the amounts of TDH produced by the 19 tdh-positive but KP-negative strains were very small. TDH-ICA, however, was able to detect TDH in all broth cultures of the 113 tdh-positive strains regardless of their KP reaction. TDH-ICA yielded negative results for all broth cultures of the tdh-negative, trh-negative strains tested as negative controls.
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In addition to tdh-positive V. parahaemolyticus strains, some V. cholerae non-O1 and V. mimicus strains and all strains of V. hollisae have been reported to possess the tdh gene (14) and to produce hemolysin similar to TDH (NAG-rTDH, Vm-rTDH, and Vh-rTDH are used throughout the text to denote hemolysin similar to TDH produced by V. cholerae non-O1 strains, V. mimicus strains, and V. hollisae strains, respectively) (22, 23, 25). Of these bacterial strains, broth cultures of 11 tdh-positive strains of V. hollisae and 2 tdh-positive strains of V. mimicus were tested with TDH-ICA and KAP-RPLA. The results are summarized in Table 1. The tdh-positive strains of V. mimicus produced Vm-rTDH detectable by TDH-ICA and KAP-RPLA in the broth cultures. This result indicates that TDH-ICA has cross-reactivity with Vm-rTDH from V. mimicus. In contrast, the tdh-positive strains of V. hollisae did not grow well and did not produce Vh-rTDH that was detectable by TDH-ICA and KAP-RPLA in the broth cultures when they were cultured with APW. In the preliminary study, 154 clinical V. cholerae non-O1 strains that were isolated at the Kansai Airport Quarantine Station, Osaka, Japan, from 154 patients with traveler's diarrhea were examined with the PCR method (19), which can also detect also the tdh gene of V. cholerae non-O1 strains. The results, however, indicated that all of the strains were negative for the presence of the tdh gene (data not shown). Since tdh-positive V. cholerae non-O1 strains could not be found, their broth cultures were not tested with TDH-ICA. As shown in Table 1, when broth cultures of the tdh-negative V. cholerae non-O1 and V. mimicus strains were tested with TDH-ICA, they all yielded negative results.
TDH-ICA testing of enrichment cultures of V. parahaemolyticus-spiked fecal homogenates. To evaluate the ability of TDH-ICA to detect TDH in enrichment cultures of stool specimens containing tdh-positive V. parahaemolyticus strains, enrichment cultures of the fecal homogenates spiked with various numbers of tdh-positive V. parahaemolyticus organisms were tested with TDH-ICA. The TDH-ICA results were compared with the culture results of the spiked fecal homogenates and their enrichment cultures on TCBS agar. As shown in Table 2, the results of detection of TDH in the enrichment cultures by TDH-ICA were in accord with the results of recovery of the spiked V. parahaemolyticus organisms from the enrichment cultures by plating onto TCBS agar. TDH-ICA was able to detect TDH in enrichment cultures of the spiked fecal homogenate even when the homogenate did not yield V. parahaemolyticus by direct plating onto TCBS agar. These results suggest that TDH-ICA testing of fecal enrichment cultures is sensitive enough to detect stool specimens containing tdh-positive V. parahaemolyticus strains, compared to a conventional bacterial culture.
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DISCUSSION |
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Before the application of TDH-ICA for the diagnosis of human diarrhea, it is very important to examine the cross-reactivity of TDH-ICA with other related hemolysins. In addition to tdh-positive V. parahaemolyticus strains, some non-V. cholerae O1 and V. mimicus strains and all strains of V. hollisae have been reported to possess the tdh gene (14) and to produce NAG-rTDH, Vm-rTDH, and Vh-rTDH, respectively, which are hemolysins similar to TDH (22, 23, 25). Of these hemolysins, TDH-ICA has cross-reactivity with Vm-rTDH from V. mimicus (Table 1). In the preliminary study, although 154 clinical V. cholerae non-O1 strains were examined by the PCR method (19), tdh-positive strains could not be found (data not shown). The incidence of the tdh gene among clinical V. cholerae non-O1 strains is very low (7, 15). Therefore, we could not test broth cultures of tdh-positive V. cholerae non-O1 strains with TDH-ICA. Since the amino acid compositions of TDH and NAG-rTDH from V. cholerae non-O1 strains are very similar (24), TDH-ICA is also expected to have cross-reactivity with NAG-rTDH. This cross-reactivity of TDH-ICA with NAG-rTDH or Vm-rTDH suggests that TDH-ICA would also yield positive results for enrichment cultures of stool specimens containing tdh-positive V. cholerae non-O1 or tdh-positive V. mimicus strains in addition to tdh-positive V. parahaemolyticus strains. V. cholerae non-O1 and V. mimicus strains, however, can be distinguished from V. parahaemolyticus strains based on the characteristics of their colonies on a chromogenic agar medium (4). Therefore, if TDH-ICA testing of a fecal enrichment culture yields a positive result, whether the causative bacterium is V. parahaemolyticus can be determined easily based on the culture results of the same stool sample on a chromogenic agar medium. While most clinical strains of V. parahaemolyticus possess the tdh gene (1, 2, 16, 17, 18), the incidence of the tdh gene among clinical V. cholerae non-O1 and V. mimicus strains is very low (7, 15). Positive results with TDH-ICA testing of fecal enrichment cultures are therefore expected to almost always be due to tdh-positive V. parahaemolyticus. On the other hand, since the tdh-positive V. hollisae strains did not produce Vh-rTDH that was detectable by TDH-ICA in the broth cultures when they were cultured with APW (Table 1), TDH-ICA appears not to yield positive results for enrichment cultures with APW of stool specimens containing this pathogen.
As shown in Table 1, TDH-ICA could not detect TRH in broth cultures of the strains of V. parahaemolyticus that possessed only the trh gene when the strains were cultured with APW. The lack of reactivity of TDH-ICA with TRH or the lack of TRH production by the strains should be considered as a possible reason for this result. However, regardless of the reason, the result suggests that TDH-ICA would yield negative results for enrichment cultures with APW of stool specimens containing strains of V. parahaemolyticus that possessed only the trh gene. Therefore, TDH-ICA testing of a fecal enrichment culture is unsuitable as a replacement for a conventional bacterial culture to diagnose cases of human diarrhea caused by strains of V. parahaemolyticus that possess only the trh gene. However, since most cases of V. parahaemolyticus diarrhea are caused by tdh-positive strains (1, 2, 16, 17, 18), TDH-ICA testing of a fecal enrichment culture appears to be useful as an adjunct to the diagnosis of V. parahaemolyticus diarrhea.
Among the tdh-positive strains of V. parahaemolyticus, the quantity of TDH produced differs greatly from strain to strain, and tdh-positive but KP-negative strains of V. parahaemolyticus produce TDH at very low levels (14). Therefore, when a stool specimen that contains tdh-positive but KP-negative V. parahaemolyticus is cultured in enrichment broth medium, the amount of TDH that is produced by the pathogen in the fecal enrichment culture is expected to be very small. For the diagnosis of V. parahaemolyticus diarrhea using the presence of TDH in a fecal enrichment culture as a marker, TDH-ICA is needed to detect the very small amount of TDH produced by tdh-positive but KP-negative V. parahaemolyticus organisms in the fecal enrichment culture. We therefore evaluated TDH-ICA testing using enrichment cultures of fecal homogenates spiked with various numbers of tdh-positive but KP-negative V. parahaemolyticus organisms (Table 2). The results suggested that TDH-ICA testing of a fecal enrichment culture is sensitive enough to detect stool specimens containing tdh-positive but KP-negative V. parahaemolyticus strains, compared to a conventional bacterial culture. Therefore, TDH-ICA testing of a fecal enrichment culture also appears to be suitable for diagnosing cases of human diarrhea caused by tdh-positive but KP-negative V. parahaemolyticus strains.
The direct detection of TDH in stool specimens would be a more rapid and simple means for the diagnosis of V. parahaemolyticus diarrhea than the detection of TDH in fecal enrichment cultures. The direct detection of TDH in stool specimens using the ELISA system was evaluated for its utility in the diagnosis of V. parahaemolyticus diarrhea in a previous study (6). The results, however, revealed that the results of direct detection of TDH in stool specimens were not completely compatible with the results of isolation of tdh-positive V. parahaemolyticus from the stool specimens. In the present study, when 217 stool specimens from patients with diarrhea were examined with a bacterial culture test, tdh-positive V. parahaemolyticus was isolated from 50 stool specimens (Table 3). Although we also tested all of the 50 stool specimens directly by TDH-ICA, only 16 stool specimens yielded positive results (data not shown). These results reveal that the direct detection of TDH in stool specimens is an unreliable means for the diagnosis of V. parahaemolyticus diarrhea. Clarification of the reason for discrepancies between the results of the direct detection of TDH in stool specimens and those of bacterial culture will require additional experiments. In contrast, when enrichment cultures of the 217 stool specimens were tested with TDH-ICA, the test results showed 100% sensitivity (50 of 50 samples) and 100% specificity (167 of 167 samples) compared with the results of isolation of V. parahaemolyticus from the stool specimens by a conventional bacterial culture test (Table 3). This result indicates that TDH-ICA testing of a fecal enrichment culture is a more reliable means for the diagnosis of V. parahaemolyticus diarrhea than direct TDH-ICA testing of a stool specimen. Although TDH-ICA testing of a fecal enrichment culture is less rapid and simple than direct TDH-ICA testing of a stool specimen, the total time (approximately 16 h) for the assay is considerably shorter than that (at least 3 days) required for a conventional bacterial culture test. In addition, TDH-ICA testing of a fecal enrichment culture is a simpler procedure than a conventional bacterial culture test.
In conclusion, the presence of TDH in fecal enrichment cultures is regarded as a useful marker for the detection of stool specimens containing tdh-positive V. parahaemolyticus strains. TDH-ICA is a rapid, simple, and sensitive TDH detection method and is suitable for the detection of this marker. TDH-ICA testing of a fecal enrichment culture is useful as an adjunct to facilitate the early diagnosis of V. parahaemolyticus diarrhea.
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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