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Applied and Environmental Microbiology, December 1999, p. 5293-5302, Vol. 65, No. 12
Laboratorium voor Microbiologie, Universiteit Gent, Gent,
Belgium2; Microbiology Section, Swiss
Federal Veterinary Office, Liebefeld-Bern,1
and Istituto Cantonale Batteriosierologico,
Lugano,3 Switzerland; and International
Centre for Diarrhoeal Disease Research, Bangladesh (ICDDRB),
Dhaka-2, Bangladesh4
Received 20 May 1999/Accepted 22 September 1999
We found 73.1 to 96.9% similarity by aligning the cytolytic
enterotoxin gene of Aeromonas hydrophila SSU (AHCYTOEN;
GenBank accession no. M84709) against aerolysin genes of
Aeromonas spp., suggesting the possibility of selecting
common primers. Identities of 90 to 100% were found among the eight
selected primers from those genes. Amplicons obtained from
Aeromonas sp. reference strains by using specific primers
for each gene or a cocktail of primers were 232 bp long. Of
hybridization group 4/5A/5B (HG4/5A/5B), HG9, and HG12 or
non-Aeromonas reference strains, none were positive. PCR-restriction fragment length polymorphism (PCR-RFLP) with
HpaII yielded three types of patterns. PCR-RFLP 1 contained
two fragments (66 and 166 bp) found in HG6, HG7, HG8, HG10, and HG11.
PCR-RFLP 2 contained three fragments (18, 66, and 148 bp) found in HG1, HG2, HG3, and HG11. PCR-RFLP 3, with four fragments (7, 20, 66, and 139 bp), was observed only in HG13. PCR-amplicon sequence analysis
(PCR-ASA) revealed three main types. PCR-ASA 1 had 76 to 78% homology
with AHCYTOEN and included strains in HG6, HG7, HG8, HG10, and HG11.
PCR-ASA 2, with 82% homology, was found only in HG13. PCR-ASA 3, with
91 to 99% homology, contained the strains in HG1, HG2, HG3, and HG11.
This method indicated that 37 (61%) of the 61 reference strains were
positive with the primer cocktail master mixture, and 34 (58%) of 59 environmental isolates, 93 (66%) of 141 food isolates, and 100 (67%)
of 150 clinical isolates from around the world carried a virulence
factor when primers AHCF1 and AHCR1 were used. In conclusion, this
PCR-based method is rapid, sensitive, and specific for the detection of
virulence factors of Aeromonas spp. It overcomes the
handicap of time-consuming biochemical and other DNA-based methods.
Aeromonas spp. comprise
mesophilic motile and psychrophilic nonmotile gram-negative ubiquitous
bacteria. Worldwide studies have demonstrated that Aeromonas
spp. are universally distributed and widely isolated from clinical
(38), environmental (29, 38, 44), and food
samples (2, 5), where they may grow even at low temperatures
(46). They are an example of emerging bacterial pathogens.
Even though they have been recognized as primary fish pathogens for a
long time, their status as primary human pathogens was not clear until
recently (18, 42). It is estimated that aeromonads may cause
up to 13% of the reported gastroenteritis cases in the United States
(10). Aeromonas spp. are opportunistic pathogens
that are at the same time infectious (4, 33) and
enterotoxigenic (12, 16).
Routine detection of pathogenic Aeromonas spp. was not
efficient until now due to the diversity of the hybridization groups (HGs), and also, 17% of isolates could not be grouped into any of the
known HGs with biochemical tests (19).
By definition, the detection of a pathogen requires rapid and specific
methods for isolation, identification, and enumeration. Such procedures
may assist in the control of potentially pathogenic microorganisms from
environmental and food samples, which are mostly regarded as the main
transport vectors to human populations.
According to the International Commission on Microbiological
Specifications for Food (30), many classical microbial
procedures for the detection of Aeromonas spp. are laborious
and time consuming or do not allow quantitative assessment of these
organisms. A complete review of methodologies for the isolation,
identification, and enumeration of Aeromonas spp. from
clinical, environmental, and food samples has been done by Joseph and
coworkers (34). Since then, other isolation methods have
been evaluated and compared for the ability to isolate or detect
Aeromonas spp. in food and environmental items (20, 48,
51) and this indicates the need for a reliable, universal, and
standard method for the detection of these pathogens in clinical,
environmental, and food samples.
The identification of mesophilic Aeromonas spp. remains
difficult in routine surveys due to the complex classification of Aeromonas bacteria into phenotypically defined phenospecies
and into genomospecies delineated on the basis of DNA-DNA hybridization studies. At least 15 genospecies or HGs related to 14 phenospecies have
been validated or proposed (13). Biochemical allocation of
unknown aeromonads into HGs usually involves a large series of tests,
ranging from 9 (1) to 136 (35) in number.
Well-equipped laboratories can perform cellular fatty acid methyl ester
(FAME) composition analysis (27), DNA fingerprinting by
amplified fragment length polymorphism analysis (28),
multilocus enzyme electrophoresis (MEE), or ribotyping (50)
to identify Aeromonas spp. to the genomospecies level.
Nevertheless, the above-mentioned methods cannot reveal the pathogenic
or nonpathogenic character of unknown Aeromonas sp. isolates
(39).
An interesting approach for the direct detection of potentially
pathogenic Aeromonas sp. isolates is the use of virulence determinants as genetic markers. A significant number of
Aeromonas sp. virulence genes have been described, including
the aerolysin genes (15, 24, 25, 26); hemolysin genes from
A. hydrophila and A. sobria (22),
A. salmonicida (23), and A. caviae
(52); an extracellular lipase gene from A. hydrophila (7); a cytolytic enterotoxin gene of
A. hydrophila (16); and a hemolytic toxin gene of
A. trota (36). The first study using the PCR
technique for specific detection of an A. hydrophila
virulence gene, the hole-forming toxin gene (25), was
accomplished in Canada by Pollard and coworkers (47). Using
a pair of primers designed on the basis of this known gene sequence,
the authors were able to detect beta-hemolysin-positive A. hydrophila strains from patients with diarrhea, whereas control
strains of hemolytic A. sobria, nonhemolytic
Aeromonas spp., and A. caviae strains, even those producing cytotoxin or enterotoxin, were negative with these primers. A
Swedish study (8) using the same primers confirmed the
Canadian findings (47) when screening for the presence of
the aerolysin gene in water, fish, and foods isolates. Another PCR
technique for the detection of two hemolysin genes of A. sobria was conducted in Japan (49), where none of the
virulence factors found with other Aeromonas spp. were detected.
The present report describes the development of a new PCR method that
detects cytolytic enterotoxin and aerolysin genes in Aeromonas spp. by using one pair of primers for a specific
gene or a cocktail of primers for the most known virulence genes of Aeromonas spp. In combination with PCR-restriction fragment
length polymorphism (PCR-RFLP) and/or PCR-amplicon sequence analysis (PCR-ASA), the described PCR assay also allows partial determination of
the HG of a potentially virulent isolate from a clinical,
environmental, or food sample.
Bacterial strains and cultural media. (i) Bacterial strains.
For the reference strains and the clinical, environmental, and food
isolates used in this investigation, see Tables 2 and 3. All strains
were identified by either FAME, MEE, or ribotyping as described
previously (6, 27, 39, 50) or by serotyping with a
unpublished serology test developed at the National Veterinary Laboratory, Aarhus, Denmark.
(ii) Isolate preservation.
All strains were purified on
Columbia sheep blood agar (bio-Merieux, Geneva, Switzerland) upon
receipt in our laboratory. Subsequently, a typical colony was grown in
Tryptone soya broth (Oxoid CM 129; Fakola AG, Basel, Switzerland) at
28°C for 16 h. For preservation purposes, stock cultures were
prepared in 30% sterilized glycerol (Glycerol G-5150; Sigma, Buchs,
Switzerland) and maintained at Bacterial DNA extraction for PCR.
Approximately 100 µl of
a Tryptone soya broth (Oxoid) culture grown for 16 h at 28°C was
used for DNA extraction using the InstaGene matrix (Bio-Rad
Laboratories AG, Glattbrugg, Switzerland) in accordance with the
manufacturer's instructions. Subsequently, 5 µl of the DNA solution
was used as a template for PCR amplification.
Strategies for primer design.
An A. hydrophila
cytolytic enterotoxin gene (AHCYTOEN) was described (16) as
a multivirulence gene including lethality in mice, hemolysis,
cytotoxicity, and enterotoxigenicity. Some of those activities are part
of the virulence factors of other Aeromonas spp. For this
reason, the AHCYTOEN gene was chosen as the reference gene in this investigation.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
PCR Detection, Characterization, and Distribution
of Virulence Genes in Aeromonas spp.
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
70°C.
Master mixture preparation and PCR condition optimization. As previewed by the Primer Designer 3 software, the eight selected primers (AHCF1, -2, and -3 and AHCR1, -2, -3, -4, and -5 [see Table 1]) constitute five combinations of primers or a cocktail of all of the primers that produce an amplicon of 232 bp under identical amplification conditions. The annealing temperature indicated by the software was increased by 10°C in order to increase the stringency of primer annealing and to avoid nonspecific binding. Of the five possible primer combinations, only the combination of AHCF1 and AHCR1 was used for clinical, environmental, and food isolates because they displayed 100% homology with the counterpart AHCYTOEN gene and an extracellular hemolysin gene (EMBL accession no. X65045) (21), which represented the two main groups of virulence factors in the genus Aeromonas, i.e., enterotoxins and hemolysins. The cocktail master mixture containing all eight primers was used only for the reference strains, which were found to be negative for the AHCF1-AHCR1 primer combination master mixture. All primers were purchased from MWG-Biotech GmbH (Ebersberg, Germany).
Optimization of the PCR protocol was performed by using 50 µl of a PCR mixture containing 5 µl of template DNA, 8 µl of a mixture containing each deoxynucleoside triphosphate at 0.2 mM (Roche Diagnostics AG, Rotkreuz, Switzerland), 5 µl of GeneAmp 10× PCR buffer II (Perkin-Elmer, Rotkreuz, Switzerland), 5 µl of a 25 mM MgCl2 solution (3.0 mM final concentration; Perkin-Elmer), 0.25 µl of a 200 µM solution of each primer (1 µM final concentration), 0.10 µl of Tween 20 (2% final concentration) (Sigma), 0.25 µl of AmpliTaq Gold at 5 U/µl (1.25-U final concentration) (Perkin-Elmer), and 26.15 µl of sterile double-distilled water, to make the final volume 50 µl. The PCR mixture was made in a sterile, laminar-airflow environment in a large volume to produce approximately 100 tubes of 45 µl each, combining all of the ingredients except the template DNA, and stored at20°C.
PCR amplification was performed with a GeneAmp 9600 PCR system
(Perkin-Elmer) by using the following temperature program: 1 cycle of
denaturation for 10 min at 95°C; 25 cycles of melting at 95°C for
15 s, annealing at 66°C for 30 s, and elongation at 72°C
for 30 s; and a final extension round at 72°C for 10 min. The
PCR amplicons were separated electrophoretically by loading a total
amplicon volume of 20 µl including 6 µl of stop solution buffer
onto a 2.5% agarose gel (pulsed-field-certified agarose; Bio-Rad
Laboratories AG). Electrophoresis was performed in 0.5×
Tris-borate-EDTA buffer-double-distilled water (Roche Diagnostics AG)
for 1 h at 100 V. Amplicons were visualized with UV light after
the agarose gel had been soaked for 15 min in an ethidium bromide
solution (0.5 g/ml; Bio-Rad Laboratories AG).
Characterization of amplicons. The PCR products were purified by using the QIAquick PCR Purification Kit (QIAGEN AG, Basel, Switzerland) and quantified by using the GeneQuant instrument (Pharmacia-Biotech Europe GmbH, Dübendorf, Switzerland) in accordance with the instructions provided by the manufacturers. PCR-RFLP analysis using the endonuclease HpaII as indicated by the Clone Manager software (Scientific & Educational Software) and PCR-ASA were used to characterize the 135 amplicons available for this purpose.
The following procedure was used for PCR-RFLP analysis. A 10-µg sample of the purified PCR product was digested for 16 h at 37°C with endonuclease HpaII (Roche Diagnostics AG) in accordance with the manufacturer's instructions. The fragments were separated by electrophoresis of 20 µl of the digested product in 3.5% agarose gel (pulsed-field-certified agarose; Bio-Rad) and subsequently visualized with ethidium bromide fluorescence. For PCR-ASA, the cycle sequencing reaction mixture was prepared with the Big Dye Terminator Cycle Sequencing Ready Reaction Kit (PE Applied Biosystems, Rotkreuz, Switzerland). Excess terminators were removed by the Centri-Sep Spin Column Purification System (PE Applied Biosystems) before preparation and loading of the samples onto the ABI PRISM 310 Genetic Analyzer System (PE Applied Biosystems) as specified by the manufacturer's protocol. The obtained sequences were aligned with the amplicon of the AHCYTOEN gene predicted by the Primer Designer 3 software by using the Bestfit program of the GCG software.| |
RESULTS |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
|
|---|
Sequence alignment and primer design strategies.
Results of
sequence alignment and the primer design strategies are detailed in
Table 1. Alignment of the AHCYTOEN gene
with the aerolysin genes of Aeromonas spp. revealed high
sequence similarities ranging from 73.1 to 96.9% (Table 1). The most
commonly shared region of the AHCYTOEN gene was ORF2, with its 1,515-bp
length. The search for primers within this ORF provided two 22-bp
primers unique to the AHCYTOEN gene, i.e., AHCF1 (5'-GAG AAG GTG ACC
ACC AAG AAC A-3') and AHCR1 (5'-AAC TGA CAT CGG CCT TGA ACT C-3'). Comparison of these primers to sequences in the GenBank database generated six more primers, including forward primers AHCF2 and AHCF3
and reverse primers AHCR2, AHCR3, AHCR4, and AHCR5 (Table 1), from the
other aerolysin genes with high sequence identities to AHCF1 and AHCR1
ranging from 90 to 100%. More base mismatches in the generated primers
were found with AHCR1 than with AHCF1.
|
PCR amplification. Results of PCR amplification using well-characterized reference strains and wild-type isolates are reported in Tables 2 and 3. For the reference strains, PCR amplification using a specific combination of primers for a specific gene or using the cocktail master mixture produced an amplicon of 232 bp, as predicted by the Primer Designer 3 software. Of the 61 Aeromonas reference strains tested, the 30 (49.2%) that were positive for the primer combination AHCF1-AHCR1 master mixture were found in HG1 (A. hydrophila), HG2 (A. bestiarum), HG3 (A. hydrophila and A. salmonicida), HG6 (A. eucrenophila), HG7 (A. sobria), and HG8 (A. veronii biogroup sobria). When the cocktail master mixture was used, 37 (61%) of the 61 reference strains were positive. Some of the reference strains negative with the AHCF1-AHCR1 mixture, e.g., in HG6 (A. eucrenophila), HG10 (A. veronii biogroup veronii), HG11 (A. encheleia), and HG13 (A. trota), turned out to be positive with the primer cocktail master mixture. No representatives of HG4/5A/5B (A. caviae-A. media complex), HG9 (A. jandaei), or HG12 (A. schubertii) were found to be positive for the targeted genes. Two positive representative reference strains of each HG were tested with all five combinations, including the cocktail master mixture. Some of them produced more than one amplicon as evidence that they possess more than one virulence factor, e.g., strain ATCC 43979T (HG7) (results not shown). The application of this PCR procedure to isolates from clinical, environmental, and food isolates when using the primer combination AHCF1-AHCR1 showed that 227 (65%) of 351 strains were positive for the targeted virulence markers. Use of the primer combination AHCF1-AHCR1 for the clinical, environmental, and food isolates was justified by the fact that almost all of the isolates received in our laboratory for this investigation were in HG1, HG2, HG3, HG4, HG5A, HG5B, or HG8. The reference strains in these HGs always reacted positively or negatively with both primers AHCF1 and AHCR1 and the cocktail master mixture. Of the 55 isolates which were not characterized to the genotype (HG) level because they could not grow on the culture medium required for identification by the FAME method or which were only serotyped (fish isolates), 31 (56%) were positive for one of the virulence factors.
Specificity of primers.
The specificity of the primer
combination AHCF1-AHCR1 and the cocktail master mixture for the
amplification of the 232-bp amplicon in Aeromonas spp. was
demonstrated by the negative PCR results
obtained with all of the non-Aeromonas reference strains (Table 2).
|
PCR-RFLP characterization. Results of the characterization of the reference strains and isolates by PCR-RFLP are presented in Tables 2 and 3, respectively. The characterization of the 232-bp PCR product from reference strains by restriction enzyme digestion (PCR-RFLP) using endonuclease HpaII revealed three types of amplicons, as predicted by the Clone Manager software (Fig. 1 and 2). PCR-RFLP type 1 (PCR-RFLP 1), exhibiting two restriction fragments of 66 and 166 bp, was found in HG6, HG7, HG8, HG10, and HG11 (e.g., strain A926; Table 2). PCR-RFLP 2, displaying three restriction fragments of 18, 66, and 148 bp, was found in HG1, HG2, HG3, and HG11 (e.g., strain A1653; Table 2). PCR-RFLP 3, with four fragments of 7, 20, 66, and 139 bp, was found only in HG13. PCR-RFLP characterization of amplicons of Aeromonas isolates from clinical, environmental, and food samples by either FAME, MEE, or ribotyping generally produced the same values as the reference strains. All 18 amplicons of the A. veronii complex isolates tested were found to be of PCR-RFLP 1. Of the 57 amplicons of HG1, HG2, HG3, and the HG4/5A/5B complex tested, only 2 (1 of HG1, isolated from water in Belgium, and 1 from a clinical isolate of HG4 from Bangladesh) were of PCR-RFLP 1 instead of PCR-RFLP 2. Divergent results were found when the HGs of the isolates were not identified or when they were serotyped by the Danish National Veterinary Laboratory serotyping system, except for A. salmonicida, for which all six of the amplicons tested were of PCR-RFLP 2.
|
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PCR-ASA characterization.
The results of PCR-ASA for the
reference strains demonstrated the existence of three PCR-ASA groups in
Aeromonas (Table 2). Similarly to PCR-RFLP 1, PCR-ASA group
1 (PCR-ASA 1) includes strains of the A. veronii complex in
HG6, HG7, HG8, HG10, and HG11. All six of the positive strains of this
complex tested for this analysis showed sequence similarities ranging
from 76 to 78% compared to the reference amplicon of the AHCYTOEN
gene. PCR-ASA 2, with 82% sequence similarity, was found exclusively
in HG13. PCR-ASA 3 contained HG1, HG2, HG3, and HG11, with sequence
similarities to the reference amplicon of the AHCYTOEN gene varying
from 91 to 99%. The results of PCR-ASA of amplicons from clinical,
environmental, and food isolates characterized by either FAME, MEE, or
ribotyping as for PCR-RFLP characterization were similar to those
obtained with the reference strains. Again, as for the PCR-RFLP test,
the isolates which were not characterized with respect to HG and
serotype gave divergent results (Table
3), except for isolates identified as A. salmonicida by serotyping. All six of
these isolates of A. salmonicida had the PCR-ASA 3 profile.
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DISCUSSION |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
|
|---|
The results of alignment analysis have shown that high sequence homologies exists between the AHCYTOEN gene and other aerolysin genes, ranging from 73.1 to 96.7%, thus confirming clearly the high level of DNA relatedness of Aeromonas sp. virulence factors. This enabled us to retrieve specific primers from their common regions (Table 1). We found that the ORF2 region within the AHCYTOEN gene was the most common region of the aligned genes. The systematic search for specific primers from ORF2 within the AHCYTOEN gene led to the selection of primers AHCF1 (forward) and AHCR1 (reverse). These primers were selected for their uniqueness to this gene, but when these primers were compared to sequences in the GenBank database, high sequence similarities to eight other described virulence genes of the Aeromonas complex were revealed by gene alignment analysis (Table 1). From the primer comparison results, six more primers were generated, including AHCF2, AHCF3, AHCR2, AHCR3, AHCR4, and AHCR5, each with the ability to amplify the same amplicon from its specific gene. The master mixture using all eight primers (cocktail master mixture) also produced the 232 bp in reference strains.
Among the described virulence factors of Aeromonas spp., two major groups are frequently associated with its pathogenicity, namely, the aerolysins and the enterotoxins (11). The specific and rapid detection of the virulence genes (Table 1) by means of molecular techniques has been the subject of many studies during the last decade (8, 14, 35, 41, 47). However, many of these investigations were limited to the detection of one specific virulence gene. Theoretically, primers AHCF1 and AHCR1 used in this investigation were designed to target both the AHCYTOEN gene and the extracellular hemolysin gene with EMBL database accession no. X65045 (22) of A. hydrophila on the basis of 100% sequence homology. In practice, however, these primers produced amplicons in almost all of the HGs of the reference strains except HG9, HG10, HG11, HG12, and HG13. Also, we observed that these particular HGs were practically absent in the wild-type strains we received from different laboratories for this investigation. This observation demonstrates the multigene detection characteristics of the two-primer set AHCF1-AHCR1 used in this work for wild-type isolates and its greater usefulness than previously described primers (14, 46, 49).
The results of PCR-RFLP analysis of Aeromonas reference strains with endonuclease HpaII have revealed that three main types or clusters of virulence genes coexist in the 15 HGs of Aeromonas spp. (Fig. 1 and 2).
As for the PCR-RFLP, the PCR-ASA of the 232-bp amplicons showed that representatives of all known Aeromonas HGs can also be divided into three types (Tables 2 and 3). In Aeromonas sp. taxa, amplicons from A. hydrophila HG1 and A. encheleia HG11 (e.g., strain A1653; this strain was recently moved from HG6 [A. eucrenophila] to HG11 [A. encheleia]) reference strains were most closely related to the AHCYTOEN gene sequence, with homologies between 97 and 99%. The strains of A. bestiarum HG2 were more versatile in their homology to the AHCYTOEN gene, with 91 to 95% sequence homology, whereas all of the reference strains of HG3, including A. hydrophila and A. salmonicida, exhibited 91% of homology to the AHCYTOEN gene. These data clearly illustrated the stability of this gene in these HGs (Table 2).
The reference strains of A. caviae (HG4/5A/5B) could not be classified in any of the defined PCR-RFLP or PCR-ASA types because all representatives were negative for the 232-bp amplicon with the primer set AHCF1-AHCR1 and the cocktail master mixtures. The lack of these genes in A. caviae (HG4/5A/5B) is in agreement with previous reports (3, 21, 31, 32, 53) which suggested that this group of aeromonads are less virulent and less cytotoxigenic than other Aeromonas taxa. Nevertheless, recent studies have demonstrated the production of cytotoxin by A. caviae strains under specific culture conditions and its implications for the generation of diarrhea in very young children and old people (40, 45). Negative 232-bp amplicon detection results were also obtained with the A. jandaei (HG9) and A. schubertii (HG12) reference strains. Since only a limited number of strains were included, it is not possible to report on the distribution of hemolytic or enterotoxin genes in these Aeromonas HGs.
The PCR-RFLP and PCR-ASA assays performed on Aeromonas reference strains have proven to be helpful tools for the detection and characterization of potential enterotoxigenic and hemolytic aeromonads. This characterization can be performed in any molecular laboratory, depending on the availability of equipment, principally a thermocycler and the restriction endonuclease HpaII. The application of these procedures to clinical, environmental, and food isolates will permit not only the detection of the virulence genes but also their characterization and the distribution of these genes in wild isolates from different sources or in their HGs.
Of the total of 350 clinical, environmental, and food isolates of Aeromonas spp. included in this study, 65% harbored virulence genes. Fifty percent of the human clinical isolates originating from Bangladesh, Ivory Coast, and Switzerland were positive by PCR for virulence factors and belonged mainly to the A. caviae complex (HG4/5A/5B), A. hydrophila (HG1), and A. veronii (HG8/10) (Table 3). Although it is very likely that clinical isolates possess at least one virulence gene, it should be kept in mind that Aeromonas spp. are well recognized as opportunistic organisms that may be present in diarrheal stool as commensals rather than as primary pathogens (3). In addition, the primers used for PCR identification in this study may not be specific for other virulence genes of Aeromonas spp. (Table 1). Interestingly, all of the Swiss human and environmental isolates of A. caviae were found to be negative for the targeted genes whereas 25% of the A. caviae isolates originating from Bangladesh harbored virulence genes. This may confirm the previously published observations that geographical variation in virulence factors for this Aeromonas species may exist (3).
A total of 22 amplicons from human clinical isolates belonging to A. bestiarum (n = 1), A. caviae (n = 4), A. hydrophila (n = 5), and A. veronii (n = 12) were included for PCR-RFLP and PCR-ASA assays. All positive A. caviae isolates from Bangladesh were classified as members of HG4 and belonged to PCR-RFLP 2 and PCR-ASA 3 with amplicon sequence homologies ranging from 93 to 100%. Clearly, these amplicons show high relatedness to the reference sequence of the multivirulence AHCYTOEN gene found mostly in A. hydrophila HG1. In this study, amplicons of reference strains and clinical and environmental isolates of HG1 exhibited 97 to 100% homology with the AHCYTOEN gene (Table 3). In addition, it was found that the PCR-RFLP and PCR-ASA profiles of HG1 isolates were similar to those of HG1 reference strains, suggesting that these isolates possess a multiple-virulence gene comparable to the AHCYTOEN gene. Previous clinical studies (37, 43) have suggested that the expression of multiple biological activities, as in the case of the AHCYTOEN gene, is necessary for the expression of microbial pathogenicity.
All of the 23 clinical isolates of A. veronii included in this investigation contained the 232-bp amplicon. Of the 12 amplicons characterized by PCR-RFLP and PCR-ASA assays, all were of PCR-ASA 1 and PCR-RFLP 1, regardless their origin. From the literature, it is known that A. veronii represents one of the more virulent species in the genus Aeromonas, as was proven by its pronounced invasiveness and lower 50% lethal doses (17). Similar to A. hydrophila HG1, A. veronii isolates originated mainly from clinical and environmental samples, suggesting that the aquatic environment acts as a reservoir of potentially virulent Aeromonas spp.
Fresh water is known to be a source and reservoir of Aeromonas spp. Among the 60 water isolates, 58% were found to be potentially pathogenic. Virulence genes were found in a high proportion in all species but in none of 15 A. caviae (HG4/5A/5B) isolates. All A. bestiarum and A. hydrophila isolates were found to be of PCR-ASA 3 and PCR-RFLP 2. A strain of A. hydrophila of HG1 and one of A. caviae of HG4 were found to be of PCR-ASA 1 and PCR-RFLP 1; these were the only cases of FAME-characterized isolates to be found so among all of the reference strains and wild isolates.
The Aeromonas sp. fish isolates under study were dominated by A. salmonicida (n = 52), followed by A. hydrophila (n = 12) and A. veronii (n = 8), as determined by serotyping. In contrast to the reference strains, the distribution of virulence genes determined by the PCR-RFLP and PCR-ASA tests among the PCR-RFLP 1 or 2 and PCR-ASA 1 or 2 amplicons in isolates classified as A. veronii or A. hydrophila demonstrated the lack of specificity of the serotyping technique in the classification of Aeromonas spp. Furthermore, it was interesting to note such a proportion (85%) of PCR-positive A. salmonicida isolates, among which almost all of the amplicons belonged to PCR-RFLP 2 and PCR-ASA 3. The fact that all of the fish isolates were isolated from moribund fish may confirm the high pathogenicity of A. salmonicida for fish.
A total of 67% of the food isolates originating from beef, minced meat, pork, poultry, seafoods, perch, salmon, and vegetables possessed one of the targeted virulence genes. The majority of these food isolates were identified as A. bestiarum HG2 and A. hydrophila HG3. The virulence genes of these isolates, as shown by molecular analysis, belonged to PCR-RFLP 2 and PCR-ASA 2. Representatives of the A. caviae complex were rarely isolated from foods of animal origin, and none of them was positive for the virulence genes. These strains mostly originated from vegetables sampled in Belgium, and 29% were found to be positive for the targeted virulence genes. Also, A. veronii HG8/10 was not frequently found among the food isolates; the few positive amplicons all belonged to PCR-RFLP 1 and PCR-ASA 1.
In conclusion, we found that the alignment and comparison analysis of the described aerolysins, hemolysins, and AHCYTOEN genes of Aeromonas spp. confirm the high homologies reported in the literature. The primers designed from the 10 Aeromonas sp. virulence factor genes permit the detection of any of the above virulence markers according to a specific need. The results of the application of the PCR-RFLP and PCR-ASA assays to Aeromonas reference strains and clinical, environmental, and food isolates demonstrated that the detection and identification of potentially pathogenic Aeromonas spp. have become more specific, faster, and easier to perform than conventional phenotyping methods. The PCR procedure did not detect the targeted virulence genes in reference strains of A. caviae; however, there were 10 (15%) of 68 well FAME-characterized positive A. caviae isolates, including 4 clinical isolates of HG4 from Bangladesh and 6 vegetable isolates from Belgium, of which 4 were identified as belonging to the A. caviae complex. In this context, the geographic variation in virulence and/or the failure of actual characterization systems for A. caviae isolates should be considered. Virulence genes were detected and characterized in well-typed reference strains. They were also found and characterized in 65% of wild isolates of Aeromonas spp. from around the world which originated from different samples, proving the universality of the procedures described here. The characterization of the PCR products by PCR-RFLP using endonuclease HpaII and PCR-ASA revealed three major types or clusters of amplicons. It may suggest the classification of pathogenic Aeromonas sp. virulence genes into three main groups (aerolysins-hemolysins, cytolytic enterotoxins, and cytotonic enterotoxins) with PCR-RFLP 1, 2, and 3 and PCR-ASA 1, 2, and 3. The PCR, PCR-RFLP, and PCR-ASA systems may prove to be important tools for the detection, identification, differentiation, and distribution of virulence markers in HGs. These tools will give microbiologists an alternative way to understand pathogenicity in Aeromonas spp. and their distribution in isolates from different sources and HGs.
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ACKNOWLEDGMENTS |
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We thank M. Altwegg and J. Lüthy-Hottenstein, University of Zürich, Zürich, Switzerland; T. Wahli and J. Graf, University of Bern, Bern, Switzerland; M. Jermini of the Cantonal Health Laboratory of Ticino, Lugano, Switzerland; M. Uyttendaele and K. Neyts of the University of Ghent for providing us with Aeromonas sp. isolates; A. Caminada of the Cantonal Institute of Bacteriology, Lugano, Switzerland; P. Meyer of Perkin-Elmer Switzerland; and E. Lüthi and D. Howald of the Swiss Federal Veterinary Office for their exceptional technical support.
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FOOTNOTES |
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* Corresponding author. Mailing address: Microbiology Section, Swiss Federal Veterinary Office, Schwarzenburgstrasse 161, CH-3003 Liebefeld-Bern, Switzerland. Phone: 41 31 322 22 63. Fax: 41 31 323 85 70. E-mail: cesar.kingombe{at}bvet.admin.ch.
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REFERENCES |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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