ABSTRACT
A multiplex PCR assay for detection of genes for staphylococcal enterotoxins A to E (entA, entB,entC, entD, and entE), toxic shock syndrome toxin 1 (tst), exfoliative toxins A and B (etaA and etaB), and intrinsic methicillin resistance (mecA) was developed. Detection offemA was used as an internal positive control. The multiplex PCR assay combined the primers for sea tosee and femA in one set and those foreta, etb, tst, mecA, and femA in the other set. Validation of the assay was performed using 176 human isolates of Staphylococcus aureus. This assay offers a very specific, quick, reliable, and inexpensive alternative to conventional PCR assays used in clinical laboratories to identify various staphylococcal toxin genes.
It is well documented that strains of Staphylococcus aureus produce a variety of extracellular protein toxins, including enterotoxins, toxic shock syndrome toxin 1 (TSST-1), exfoliative toxin (ET), hemolysins, and coagulase (15). S. aureus is one of the most commonly found pathogenic bacteria and is hard to eliminate from the human environment. It is responsible for many nosocomial infections, besides being the main causative agent of food intoxication by virtue of its variety of enterotoxins (15).
According to serological classification, to date six staphylococcal enterotoxin (SE) groups have been recognized: SEA, SEB, SEC, SED, and SEE (15) and the recently described SEH (22, 27). These enterotoxins are small peptides (26 to 29 kDa) and have a great deal of similarity at the amino acid level (21). They are the main source of food poisoning and cause intensive intestinal peristalsis. The toxic shock syndrome of humans and animals is caused by the presence of S. aureus isolates producing TSST-1. The enterotoxins, as well as TSST-1, belong to a family of superantigens (25). The two ETs ETA and ETB, in conjunction or independently, are implicated in the cause of staphylococcal scalded-skin syndrome (15).
Over the last few decades, there has been an enormous increase and emergence of S. aureus strains resistant to the antibiotic methicillin (MRSA strains), particularly in nosocomial settings (13). The intrinsic resistance to these antibiotics is attributed to the presence of mecA, whose product is a 78-kDa protein called penicillin binding protein 2a (14, 28). Identification of mecA in such MRSA strains has led to some knowledge regarding the use of the antibiotic vancomycin (9). The femA gene encodes a factor which is essential for methicillin resistance and is universally present in allS. aureus isolates. The femA gene product, a 48-kDa protein, has been implicated in cell wall metabolism and is found in large amounts in actively growing cultures (17, 29).
For epidemiological surveillance, the methods most frequently used for the detection of staphylococcal toxins are immunodiffusion, agglutination, radioimmunoassay, and enzyme-linked immunosorbent assay (15, 18). Among the techniques used to identify toxin genotypes, DNA-DNA hybridization and PCR have been reported to be very successful and reliable, and our laboratory previously designed specific primers for the successful and reliable detection of SEs, TSST-1, and ETs by PCR (18).
There are several reports in the literature describing the use of multiplex PCR for detection of MRSA strains, but most of these techniques are designed to detect only two or three gene fragments (1, 8, 12, 24, 26, 29, 30). In this report, we describe two multiplex PCR primer sets which can detect the presence of 10 staphylococcal genes simultaneously, in just two reactions. As an internal positive control for each reaction, we incorporated primers specifically designated to amplify femA, which has been reported to be specific to S. aureus (29). Validation of the multiplex PCR primers was performed and interpreted using 176 isolates of S. aureus which were first characterized for their toxin gene profiles by using individual primers (18). We conclude that the multiplex primer sets described here are reliable and specific in detecting the toxin genes of S. aureus.
MATERIALS AND METHODS
Bacterial strains and culture media.A total of 176 S. aureus strains were used in this study. Of these, 107 strains were isolated from nasal swabs of a control (healthy) population, 47 strains were from The Netherlands, and 19 MRSA strains were from a national surveillance study in Canada. The remaining three strains were isolated from clinical specimens. All strains were stored on suitable maintenance media in the culture collection in the National Laboratory for Bacteriology, Laboratory Center for Disease Control. The control strains had been previously defined in terms of toxigenicity with respect to enterotoxins, ETs, and TSST-1. The following strains were used as positive controls in this study: ATCC 13565 (SEA), ATCC 14458 (SEB), ATCC 19095 (SEC), 90-S-1025 (SED), ATCC 27664 (SEE), 88-S-8902 (ETA), 88-S-8620 (ETB), 92-S-1344 (TSST-1), and 95-S-739 (mecA). The non-ATCC strains mentioned above were obtained from the culture collection of the Laboratory Center for Disease Control and were characterized for their toxin production by using semiquantitative reversed passive latex agglutination toxin detection kits (SET-RPLA and TST-RPLA; Oxoid Ltd., Basingstoke, Hampshire, England). The two ET-producing strains were originally identified by immunodiffusion tests (18). Disk diffusion tests for MRSA isolates were performed as described previously (21a). Bacterial cultures were grown in brain heart infusion broth prior to extraction of total DNA.
DNA isolation.Total DNA was isolated from 0.5 ml of brain heart infusion broth culture grown overnight for all the bacterial strains used in the study. The procedure used for DNA isolation has been described previously (18). DNA samples were dissolved in Tris-EDTA buffer (10 mM Tris chloride, 1 mM EDTA [pH 8.0]), and the concentration was determined as micrograms per milliliter according to A260 values. Template DNA in amounts ranging from 10 to 1,000 ng was used in the study.
Primers.Oligonucleotides ranging from 18- to 24-mers were selected from the published DNA sequences of the S. aureusgenes (Table 1) using Oligo software (version 3.4). Synthesis of oligonucleotides was carried out at the DNA Core Facility at the Laboratory Center for Disease Control. For multiplex PCRs, two primers sets were prepared: set A was designed to amplify sea, seb, sec, sed,see, and femA, whereas set B was designed to amplify mecA, eta, etb, andtst as well as femA. The primer sequences used in the multiplex PCRs are described in Table 1.
Nucleotide sequences, gene locations, and anticipated sizes of PCR products for the S. aureus gene-specific oligonucleotide primers used in this study
Multiplex PCR conditions.Two sets of primer mixes were prepared according to the master mixes of components from the GeneAmp kit (Perkin-Elmer, Norwalk, Conn.), with slight modifications to the given instructions. Multiplex primer set A contained 200 μM deoxynucleoside triphosphates; 5 μl of 10× reaction buffer (100 mM Tris-HCl [pH 8.3], 500 mM KCl); 1.5 mM MgCl2; 20 pmol (each) of sea, seb, sec,see, and femA primers; 40 pmol of sedprimer; 2.5 U of Taq DNA polymerase (AmpliTaq DNA polymerase; Perkin-Elmer), and 10 to 1,000 ng of template DNA. The volume of this mix was adjusted to 50 μl with sterile water. Multiplex primer set B included the same constituents as in set A except for the MgCl2 concentration (2.0 mM) and the primers, which were used at 50 pmol for eta and 20 pmol each for etb, tst, mecA, andfemA. Evaporation of the reaction mixture was prevented by addition of 100 μl of sterile mineral oil. DNA amplification was carried out in a Perkin-Elmer thermocycler with the following thermal cycling profile: an initial denaturation at 94°C for 5 min was followed by 35 cycles of amplification (denaturation at 94°C for 2 min, annealing at 57°C for 2 min, and extension at 72°C for 1 min), ending with a final extension at 72°C for 7 min.
RESULTS
Multiplex PCR for detection of selected staphylococcal genes.The reaction conditions for the multiplex PCR assay were optimized to ensure that all of the target gene sequences were satisfactorily amplified. The primers were designed to target the coding regions of the genes; care was taken to avoid areas of homology within the structural genes for the enterotoxins. The primers used in each set had almost equal annealing temperatures, which reduced the possibility of occurrence of unwanted bands originating from nonspecific amplification. Figure 1 shows the presence of the amplified products after agarose gel electrophoresis, when DNA extracted from a representative toxigenic S. aureusstrain (positive control) was used as the template in the PCR using the multiplex primer sets. Reliable amplification of six bands in set A (for sea, seb, sec, sed,see, and femA) was obtained when a mixture of DNAs from the same strains was tested (Fig. 1). Similarly, five bands were obtained when a mixture of DNAs from the corresponding strains in set B (for eta, etb, tst,mecA, and femA) was tested (Fig. 1). The sizes of the amplicons obtained from the various control strains corresponded to the predicted sizes (Table 1). As a negative control, both sets were tested with sterile water, and no amplicons were observed (Fig. 1). Genomic DNA in amounts ranging from 10 to 1,000 ng/reaction was used, with no apparent change in sensitivity and ability to detect all of the genes in the sample (data not shown).
Agarose gel electrophoresis patterns showing multiplex PCR amplification products for the S. aureus genes. Lanes M, DNA molecular size marker (100-bp ladder; Bethesda Research Laboratories Inc., Gaithersburg, Md.); lanes 1 to 7, PCR amplicons from primer set A; lanes 8 to 13, PCR amplicons from set B. Lanes: 1,sea plus femA; 2, seb plusfemA; 3, sec plus femA; 4,sed plus femA; 5, see plusfemA; 6, sea, seb, sec,sed, see, and femA simultaneously; 7, negative control; 8, eta plus femA; 9,etb plus femA; 10, tst plusfemA; 11, mecA plus femA; 12,eta, etb, tst, mecA, andfemA; 13, negative control.
To further test the specificity of the assay, DNA templates from oneCampylobacter jejuni strain and two Escherichia coli strains were used with the multiplex PCR primer sets (A and B), and no amplified products were obtained (data not shown).
To substantiate the multiplex PCR technique, 176 strains of S. aureus that were tested by multiplex PCR were also screened for the presence of individual toxin genes by using the method described previously (18). Full agreement of the two methods was observed. In order to test for 10 toxin genes individually, a total of 1,760 PCRs were required, whereas when multiplex primer sets were used, only 352 PCRs were needed. The multiplex primers sets were seen to be very reliable, since no discrepancy was observed in the results obtained using the two methods. An internal control of femAwas present in all of the samples, confirming the presence of S. aureus and also validating the PCR conditions. Other workers have used primers for 16S rRNA as the internal control when designing multiplex primers to detect mecA (24, 26).
Primary validation of the amplicons.The sizes of the amplicons obtained by the multiplex primer sets were identical to those predicted from the design of the primers (Tables 1 and2). The amplicons from the control strains were subjected to further confirmation and characterization by digestion with restriction endonucleases with cleavage sites within the amplicon. The restriction enzymes used and the predicted product sizes are given in Table 2. Enzyme fragments with the anticipated sizes were obtained in each case (data not shown).
Predicted sizes of restriction fragments and enzymes used for restriction fragment length polymorphism analysis to validate the amplified products of multiplex PCR
Analysis of the results.Among the 176 strains tested, 107 strains were collected from nasal swabs of healthy humans. Of these 107 strains, 21 (19.6%) were positive for sea, 26 (24.3%) were positive for the TSST-1 gene (tst), 6 (5.6%) were found to be seb positive, 8 (7.5%) were positive for sec, and 2 (1.9%) contained the gene for sed. None were positive for see, eta, etb, or mecA. Of the 47 strains obtained from The Netherlands, 6 were positive forsea, 1 was positive for seb, 3 were positive forsec, 4 were positive for eta, and 11 were positive for tst. Among the three clinical isolates tested, all were positive for eta as well as etb.
Among the 19 strains obtained from the national MRSA surveillance study, 18 were mecA positive, indicating thatmecA is responsible for methicillin resistance in those strains. The single remaining oxacillin-resistant isolate (which wasmecA negative) must be methicillin resistant by virtue of some other mechanism (9). Of these MRSA isolates, three were positive for sea, two were positive for seb, three were positive for sec, two were positive forsed, three were positive for see, and one contained the gene for TSST-1. All of the 176 samples tested contained the femA gene.
DISCUSSION
We have described a multiplex PCR-based diagnostic protocol to detect the genes for enterotoxins A to E, ETA, ETB, and TSST-1 and themecA gene in DNA extracted from human isolates of S. aureus. This procedure is an improvement over our previously described PCR protocols, where individual primers were used to identify the staphylococcal toxin genes (18). The multiplex PCR primer sets were shown to be very specific, reliable, and, most importantly, very efficient in detection of all 10 genes. As an internal control, femA was found to be present in all of the strains studied. The gene product of femA has been suggested to have a role in cell wall metabolism and is reported to be present in all S. aureus species during the active growth phase (17, 29).
Six pairs of primers were used in multiplex primer set A to target the structural genes for enterotoxins A to E (sea,seb, sec, sed, and see), along with femA. In the multiplex primer set B, five pairs of primers were mixed together to target the structural genes formecA, eta, etb, and tst, along with femA. All of the primers were gene specific, as demonstrated by restriction fragment lengths obtained after specific restriction endonuclease digestion of the amplicons. The multiplex primers were shown to be specific for S. aureus, since no amplification product was obtained when either C. jejuni orE. coli DNA was used as the template.
In this study, the toxin genotypes of S. aureus strains isolated from healthy human carriers are also demonstrated. Of 107 such isolates tested, 24.3% possessed the gene for TSST-1 and 19.6% were positive for SEA. These results are in accordance with previous findings that many healthy individuals are carriers of toxin-producing strains of S. aureus (10).
The use of multiplex PCR to characterize staphylococcal strains and their resistance to methicillin has been well documented (1, 8, 12, 29, 30). Those reports focus on detection of the gene responsible for methicillin resistance (mecA) along with either the femA, 16S rRNA, nuc, or IS431 gene as a positive control(s) (1, 8, 12, 29). A recent study describes the use of two multiplex PCR assays for detection of S. aureus exotoxin genes: one is designed to detect the enterotoxin genes, and the other is designed to detect the tst, eta, and etb genes (3). Becker et al. have used DNA enzyme immunoassays to validate the specificity of the PCR products, using oligonucleotide probes derived from the sequences of the S. aureus toxin genes (3).
The study described in this paper provides detailed information aboutS. aureus toxin genes as well as mecA. The inclusion of an internal positive control (femA) in the reaction provides assurance against false-negative results. Use of this multiplex PCR assay will help provide the information required for appropriate therapy and infection control during outbreaks of S. aureus. It is important to recognize that this technique only will identify strains harboring the toxin genes and is independent of the expression and secretion of the toxin. To verify toxin production by any given isolate, time- and labor-intensive immunological methods may be used to detect the excreted toxins.
Considering the low cost and much shorter time required to detect the 10 genes of S. aureus by multiplex PCR, we believe this to be a powerful tool for studying the genotypes of staphylococcal isolates. This procedure was specially developed to fit into the daily work pattern of a routine clinical laboratory, since genotypic detection of drug resistance and the presence of toxin genes is becoming an important component of the diagnostic inventory of such laboratories.
ACKNOWLEDGMENTS
We are grateful to J. W. Cohen Tervaert for the strains from The Netherlands and to M. Mamelak for the strains from healthy controls. We also thank Russell Easy and Hugh Cai for technical assistance and M. R. Mulvey for critical review and reading of the manuscript.
M.M. was funded by a postdoctoral fellowship from a grant to W.M.J. by the Canadian Bacterial Disease Network.
FOOTNOTES
- Received 30 August 1999.
- Returned for modification 27 October 1999.
- Accepted 5 December 1999.
- Copyright © 2000 American Society for Microbiology
