- Methodology article
- Open Access
Molecular beacon-based real-time PCR detection of primary isolates of Salmonella Typhimurium and Salmonella Enteritidis in environmental and clinical samples
BMC Microbiology volume 9, Article number: 97 (2009)
A fast and simple two-step multiplex real-time PCR assay has been developed to replace the traditional, laborious Salmonella serotyping procedure. Molecular beacons were incorporated into the assay as probes for target DNA. Target sequences were regions of the invA, prot6E and fliC genes specific for Salmonella spp. Salmonella Enteritidis and Salmonella Typhimurium, respectively, the two most clinically relevant serotypes. An internal amplification positive control was included in the experiment to ensure the optimal functioning of the PCR and detect possible PCR inhibition. Three sets of primers were used for the amplification of the target sequences. The results were compared to those of the Kauffmann-White antigenic classification scheme.
The assay was 100% sensitive and specific, correctly identifying all 44 Salmonella strains, all 21 samples of S. Enteritidis and all 17 samples of S. Typhimurium tested in this work. Therefore, the entire experiment had specificity and sensitivity of 100%. The detection limit was down to 10 copies of DNA target per 25 μl reaction.
The assay can amplify and analyse a large number of samples in approximately 8 hours, compared to the 4 to 5 days conventional identification takes, and is thus considered a very promising method for detecting the two major serotypes of Salmonella quickly and accurately from clinical and environmental samples.
Salmonella is a gram-negative, facultative anaerobic, flagellated bacterium. It is the pathogenic agent of salmonellosis, a major cause of enteric illness and typhoid fever, leading to many hospitalisations and a few rare deaths if no antibiotics are administered. Salmonella outbreaks are linked to unhygienic food preparation, cooking, reheating and storage practices. The bacterium can be isolated from raw meat and poultry products as well as from milk and milk-based products . The detection of Salmonella therefore remains a highly important issue in microbiological analysis for food safety and standards.
Because the nomenclature for the Salmonella genus is at times confusing, this publication will follow the current literature [2, 3]. The CDC  distinguishes two Salmonella species (or subgenera): S. enterica and S. bongori. S. enterica is further divided into six subspecies, of which S. enterica subsp. enterica is the most clinically significant, causing 99% of Salmonella infections. In the present study we are concerned with its two main serovars: Salmonella enterica serovar Typhimurium (group D) denoted S. Typhimurium, and Salmonella enterica serovar Enteritidis (group B) denoted S. Enteritidis, which are the most commonly isolated Salmonellae from food-borne outbreaks.
Identification of the disease-causing Salmonella serovars is currently a lengthy process, and its initial isolation from food samples can be difficult as the bacteria can be present in small numbers and many closely related bacteria may be found within the same sample . For this reason, pre-enrichment steps are required for all samples [5, 6]. The current accepted method for isolation of Salmonella from foodstuffs is a well established procedure – ISO 6579, laborious and time-consuming, taking up to 5 days to complete [7, 8]. The most widely-used method used to characterise Salmonella into its subspecies is the Kauffman-White serotyping system , based on the variability of the O, H and Vi antigens [9–11]. Apart from being arduous, this method can not identify a small number of S. enterica samples that lack either the O antigen alone or both the O and the H antigens . Therefore there is a need for fast, sensitive and specific "in the field" detection, using nucleic acid-based technologies such as molecular beacon-based real-time PCR, to reduce the time needed to complete the assay, but also improve the level of accuracy and reliability.
In this study, molecular beacons [13–15] and real-time PCR technology are combined to develop a fast, sensitive, clear-cut method of detection of Salmonella spp. and its two most clinically significant serotypes from clinical, food and environmental specimens, which reduces the time taken to identify the Salmonella strain from an environmental sample, and is precise enough to distinguish between serovars. PCR-based methods targeting various genes are usually more rapid and sensitive than culture-based methods, and the high specificity and high sensitivity of molecular beacons means they can be successfully combined with real-time PCR assays, and so provide a quick, accurate method for detection and analysis, making them ideal for routine diagnosis. Recent studies show that real-time PCR is gradually replacing gel electrophoresis [16–24] as it is suitable for large numbers of samples and involves automatic and fast analysis, as well as being able to execute multiplex protocols. Also, like in all probe-based assays, molecular beacons offer additional specificity. Recent studies have employed molecular beacons in PCR for the detection of Salmonella [25–27].
Here the detection of Salmonella and the discrimination between S. Typhimurium and S. Enteritidis serotypes is done by targeting 133–136 nt regions of three genes, while an artificial internal amplification control (IAC) is also incorporated. The target for Salmonella spp is invA, as it is highly conserved in almost all Salmonella serotypes [28, 29], and its specificity is apparent from its continuous use in previous studies [18, 24, 28, 30–43]. The target for the specific detection of S. Enteritidis is prot6E, whose absence from S. Enteritidis strains appears to be very rare , and the fliC gene has been chosen as a single target for the presence of S. Typhimurium. The method described here for the detection of Salmonella spp. from environmental and food specimens, not only reduces the time taken to identify the Salmonella strain, but is also precise enough to distinguish between its clinically significant serovars.
The primary Salmonella samples used in this study (Table 1) were obtained from various animal, food and environmental sources at the Cyprus Veterinary Services (Ministry of Agriculture, Natural Resources and Environment, Nicosia, Cyprus), which is the National Reference Laboratory of Salmonella for Cyprus. The commercially available bacterial strains listed in Table 2 were obtained from the American Type Culture Collection (ATCC, Manasas, USA), the National Collection of Type Cultures (NCTC, Health Protection Agency, London, UK) and MERCK KGaA (Darmstadt, Germany). The reference S. enterica serovars listed in Table 3 were obtained from the Community Reference Laboratory for Salmonella at the National Institute for Public Health and the Environment (RIVM, Bilthoven, the Netherlands). Thirty-eight S. Typhimurium and S. Enteritidis samples as well as six different Salmonella serovars have been incorporated to ensure that the assay could correctly identify and differentiate between serotypes of S. enterica. Eighteen non-Salmonella bacterial samples were also included to ensure accurate experimental design and specificity to the Salmonella genus.
Bacterial cultures and serotyping
The detection of Salmonella spp. was performed based on the ISO 6579:2002 method. In brief, 25 g of clinical specimen (10 g in the case of minced meat in accordance with the EC regulation 2073/2005 – Microbiological Criteria for Foodstuffs) were added to 225 ml of buffered peptone water in a Stomacher® bag, sealed and placed in a Stomacher® blender for 3 min. The blended sample was incubated for 18 h at 37°C and a 0.1 ml aliquot of sample was inoculated into 10 ml Rappaport-Vassiliadis medium with Soya (RVS) and into 10 ml Muller-Kauffmann tetrathionate/novobiocin (MKTTn) broth; these cultures were incubated for 24 h at 41.5°C and 37°C, respectively. Each culture was inoculated into xylose lysine deoxycholate agar (XLD) and brilliant green agar (BGA) and incubated at 37°C for 24 h. One colony was selected from each XLD and BGA plate and spread onto nutrient agar for incubation at 37°C for 24 h. The resulting colonies were subject to biochemical analysis and serotyping. Salmonella spp. was characterised into different serovars on the basis of their surface (LPS, O-antigens) and flagellar antigens (H-antigens) as defined by the Kauffman-White Scheme [10, 44] and based on the Global Salm-Surv laboratory protocol of the World Health Organisation (Global Salm-Surv, Serotyping of Salmonella enterica O and H antigen, Level 3 Training Course, WHO, 6th edition, Jan. 2004).
To extract DNA for use in the molecular detection assay, bacteria were cultured on the XLD agar and one colony was selected and grown on nutrient agar. A colony was then selected and incubated in 5 ml nutrient broth, 1 ml of which was transferred into a 1.5 ml tube for centrifugation for 10 min at 18,000 rcf. The supernatant was discarded and the cell pellet was kept at -80°C until DNA extraction.
Bacterial genomic DNA preparation
Bacterial genomic DNA was extracted from the cell pellets using QIAGEN DNeasy Blood and Tissue Kit (Hilden, Germany) according to the manufacturer's instructions. The purified DNA was eluted in 100 μl of AE buffer and the concentration was determined by measuring the optical density at 260 nm using a NanoDrop UV spectrophotometer (NanoDrop Technologies, USA). The extracted DNA was kept at -30°C until further use.
Internal amplification control
An artificial 129 nt oligonucleotide fragment was designed as an IAC to be amplified by the same primers as the invA target. The IAC is a completely synthetic and unique oligonucleotide, designed to avoid sequence homology with any entries in the GenBank database, tested using the BLAST (Basic Local Alignment Search Tool) software .
Primer and beacon design
All primers and molecular beacons described here were designed de novo for this study (See additional file 1: Oligonucleotide primers and molecular beacons in the real-time PCR assay). Small regions (133–136 nt) of the invA, prot6E and fliC genes were used as target sequences for the detection of Salmonella spp. S. Enteritidis and S. Typhimurium, respectively. The primers and the molecular beacons were designed based on sequences of the above genes found in the GenBank database http://www.ncbi.nlm.nih.gov/Genbank/index.html using BLAST . The molecular beacons, target oligonucleotides and primers were synthesised by MWG-Biotech AG Ltd (Ebersberg, Germany) and the Midland Certified Reagent Company, Incorporated (Texas, USA). For the stem formation, the ends of each beacon were designed to have a high GC content and to be complementary to each other. All beacons were labelled with DABCYL, i.e., 4'-(4'-dimethylaminophenylazo) benzoic acid at the 3' end and with one of four fluorophores at the 5' end. Molecular beacon MBinvA, was labelled with the fluorophore FAM (Fluorescein); MBprot6E with TET (Tetrachloro-6'-carbofluorescein); MBfliC with HEX (hexachlorofluorescein); and MBIAC, with ROX (6'-carboxy-X-rhodamine). Within the loop element, each beacon contains a 22–25 nucleotide-long probe sequence complementary to the target. In addition to the probe sequence, each beacon has 4–5 of the 12 bases of its two arms also complementary to the target. In this non-traditional way, once the beacon is in the open structure, it binds more forcefully to the target and the hybrid formed is more stable, and the maximum distance possible between fluorophore and quencher is created.
Thermal denaturation characteristics of the molecular beacons
To assess the thermodynamic characteristics, the quality and the purity of the molecular beacons used in this study, a melting curve analysis was performed on each using the 7900 HT Fast Real-Time PCR System (Applied Biosystems, Foster City, CA, USA). Briefly, the reaction consisted of a 25 μl solution containing 12.5 μl Platinum® PCR Supermix (Invitrogen), 1 μl of the beacon probe at the appropriate concentration with or without 1 μl (100 pmol) of a single-stranded oligonucleotide perfectly complementary to the probe. The cycling parameters were as follows: 1 cycle for 2 min at 95°C followed by 50 cycles, each consisting of the data collection step for 30 s and a second step for 10 s, each starting at 80°C and employing auto-incrementation of -1°C per half-minute cycle until 31°C. Changes in fluorescence were measured at 490 nm and the data was collected at each temperature interval.
PCR target standards synthesis, amplification and quantification
PCR target standards of the fliC, invA, prot6E and IAC target sequences were synthesised by PCR amplification using long overlapping primers. Each PCR reaction was performed in a 50-μl reaction volume containing 45 μl of Platinum® PCR Supermix (Invitrogen, Inc., Carlsbad, CA, USA) and 25 pmoles each of the following primer pairs: for the fliC target, TFfliC and TRfliC; for the invA target, TFinvA and TRinvA; for the prot6E target, TFprot6E and TRprot6E; and for the IAC, TFIAC and TRIAC (See additional file 1: Oligonucleotide primers and molecular beacons in the real-time PCR assay). Amplification was performed with an activation step of 94°C for 30 s, followed by 20 cycles, each consisting of 94°C for 20 s, 68°C for 30 s and 72°C for 20 s, followed by a final extension step of 72°C for 5 min in an Eppendorf Mastercycler (Eppendorf AG, Hamburg, Germany). Three μl of the product from the first PCR was used in a secondary PCR in a 50-μl reaction volume containing 1 × of Platinum® PCR Supermix (Invitrogen, Inc., Carlsbad, CA) and 20 pmoles each of the following PCR primer pairs: for the fliC target, 585 and 717; for the invA target, 302 and 437; for the prot6E target, 438 and 572; and for the IAC, 302 and 437 (See additional file 1: Oligonucleotide primers and molecular beacons in the real-time PCR assay). Amplification was performed with an activation step of 94°C for 30 s, followed by 40 cycles, each consisting of 94°C for 20 s, the annealing temperature for 30 s and 72°C for 20 s, followed by a final extension step of 72°C for 5 min in an Eppendorf Mastercycler (Eppendorf AG, Hamburg, Germany). The annealing temperature for the fliC primers was 59°C, for the invA primers 58°C, for the prot6E primers 56°C and for the IAC primers 58°C. The resulting product was then cleaned using the QIAquick PCR Purification Kit (QIAGEN GmbH, Hilden, Germany) and eluted in 50 μl of EB buffer. The PCR products were run on a 2% agarose gel with a 50 bp DNA ladder (Invitrogen) and the DNA concentration of each was measured on the NanoDrop ND-1000 UV Spectrophotometer (Wilmington, DE). The number of molecules per unit volume was calculated from the measured concentration and the molecular weight of each oligonucleotide. The amplified targets were then diluted to concentrations of 106, 105, 104, 103, 102 and 10 copies per 5 μl to be used as target standards of known concentration.
Uniplex real-time PCR reactions were performed on 10-fold serial dilutions of the PCR targets, synthesised and prepared as described above. Reactions of 25 μl volume were set up, containing 12.5 μl Platinum® qPCR Supermix-UDG (Invitrogen, Carlsbad, CA), 1 μl of forward primer and 1 μl of reverse primer (20 pmol/μl), 1 μl of the corresponding molecular beacon at the concentration determined appropriate from the melting curve analysis (4.9 pmol/μl MBinvA, 10 pmol/μl MBfliC, 4.4 pmol/μl MBprot6E and 50 pmol/μl MBIAC) 4.5 μl H2O and 5 μl of the PCR target standard. The reactions were performed on the 7900 HT Real-Time PCR System (Applied Biosystems, Foster City, CA, USA) and the cycling parameters were as follows: activation step at 95°C for 10 min, followed by 50 cycles, each consisting of 95°C for 15 s, 50°C for 30 s (data collection step) and 72°C for 30 s.
Uniplex real-time PCR
The real-time PCR analysis was made with by the 7900 HT Fast Real-Time PCR System (Applied Biosystems) using the Platinum® Quantitative PCR SuperMix-UDG (Invitrogen) on all of the samples described above. Each 25 μl uniplex PCR reaction contained 5 μl of the extracted DNA, and was carried out as described above. The fluorescence given out on hybridisation between each beacon and its target DNA was measured directly and the resulting amplification curves were processed immediately with the 7900 HT Sequence Detection Systems software v2.2.2 (Applied Biosystems, Foster City, CA). To verify that the fluorescence signals were due to PCR amplification of the template DNA and not any other contaminant, negative or non-template controls were also run, where sterile water replaced the DNA template in the reaction mixture.
Double duplex real-time PCR
Having tested all sets of beacons and primers in uniplex reactions, the samples were run again in a two-step duplex assay. In step 1, 25 μl reactions were set up, containing 12.5 μl of Platinum Quantitative Supermix-UDG (Invitrogen), 1 μl of each of primers 302 and 437 (20 pmol/μl), 1 μl of MBIAC (50 pmol/μl), 1 μl of MBinvA (4.9 pmol/μl), 0.5 μl of the synthetic IAC (2 × 105 copies/μl). To this, 2 μl of 100-fold dilution of sample DNA were added and the volume was made up with sterile water or, in the case of non-template controls, the sample DNA was replaced with sterile water. In step 2, each reaction had a total volume of 25 μl consisting of 12.5 μl of Platinum Quantitative Supermix-UDG (Invitrogen), 1 μl of each of 572, 585 and 717 (20 pmol/μl), 1 μl of MBprot6E (4.4 pmol/μl) and 2 μl of MBfliC (10 pmol/μl). The final volume was reached by the addition of 2 μl of sample DNA and 3.5 μl of sterile water or, in the case of non-template negative control reactions, 5.5 μl of sterile water only. For both steps, PCR cycling conditions were as described for the standard curve analysis and uniplex reactions. The fluorescence given out on hybridisation between beacon and its target was measured at each cycle.
Thermal denaturation characteristics of molecular beacons
Normalised fluorescence signals for both the beacon and the beacon-target hybrid were plotted against temperature to give a thermal denaturation profile for each beacon (Fig. 1). These profiles were created using an ABI 7900 HT Fast Real-Time PCR System (Applied Biosystems, Foster City, CA) to determine the optimal hybridisation temperature between the beacon and its target sequence. Perfectly complementary beacon-target hybrids exist at lower temperatures giving out a bright fluorescence signal. A progressive increase in temperature causes the hybrids to dissociate, followed by a marked decrease in fluorescence. Conversely, the beacons alone unravelled at high temperatures and exhibited a melting temperature above 60°C in all cases. In the temperature interval from 31 to 55°C, the probe-target hybrids elicited significantly stronger fluorescence than the probe alone, thus allowing the detection of target sequence at these temperatures. A temperature of 50°C was chosen as an optimal annealing temperature for subsequent real-time PCR studies. At this temperature the difference in fluorescence signal between beacon alone and beacon-target hybrids is large; in the absence of target any fluorescence detected is background level and the temperature is high enough to prevent less energetically favourable hybrids from forming, e.g., primer dimers or beacon-primer dimers. In the process of carrying out the melting curve analysis for all beacons, different concentrations were tested, to find the appropriate concentration at which the fluorescence signal was neither too low nor saturated. The concentrations at which the particular beacons exhibited the desired amount of fluorescence signal in these reactions were: MBIAC, 50 pmol/μl; MBinvA, 4.9 pmol/μl; MBprot6E, 4.4 pmol/μl; and MBfliC, 10 pmol/μl. Finally, these thermal denaturation profiles illustrate the good quality of the molecular beacons and their efficiency in hybridising with the appropriate target sequence.
Standard curves and limit of detection
Standard curves were initially plotted to ensure the ability of each molecular beacon to detect its specific Salmonella target and the detection limit of the assay. The copy numbers of target standards used ranged from 101 to 106 copies per reaction. These plots represent how the amplification of DNA progresses with each log increase of target copy number. The small standard errors calculated from multiple values of the threshold cycle at which significant DNA amplification was observed (threshold cycle, CT) for each reaction and indicated on the graphs with horizontal lines above and below each plotted point, suggest that the PCR amplification is highly reproducible. The CT values for the target sequences depended on the initial DNA amount in each reaction as shown by the linear relationship of standard curves along a 6-log range which yields an R2 correlation value higher than 0.994 in all three cases (Fig. 2). The correlation was 0.995 with 76% efficiency for invA, 0.997 and 84% efficiency for prot6E and 0.999 and 100% efficiency for fliC. As the reactions worked well for all target standard concentrations tested, the lower limit of detection for the assay was set to be 10 copies of the required target fragment per reaction. Based on the standard curves and the limit of detection of this assay, negative results were defined as those exhibiting CT values higher than 45.
Detection of S. enterica alleles in bacterial samples by molecular beacon-based uniplex real-time PCR
The molecular beacon-based real-time PCR assay designed in this study was tested on environmental and food samples of S. Enteritidis and S. Typhimurium (Table 1), as well as several commercially available bacterial strains (Table 2) and various Salmonella serovars obtained from a reference laboratory for Salmonella (Table 3). All samples were investigated first by uniplex assays to detect invA, prot6E and fliC (Table 4). In the reaction for detection of invA, all 44 Salmonella samples were positive and all 18 non-Salmonella samples were undetectable. Positive results (≤ 10 copies of DNA per reaction) had CT values ranging from 15 to 25. In the prot6E reaction, all 21 S. Enteritidis samples gave positive PCR results and all 41 non-Enteritidis samples were negative. Positive samples for the prot6E gene had CT values ranging between 15 and 18 with one exception, the commercially available specimen of S. Enteritidis (Table 3) for which fluorescence detection significantly increased around cycle 30. Finally, in the fliC reaction, all 17 S. Typhimurium samples gave positive PCR results and all 45 non-Typhimurium samples were negative. Positive results had CT values ranging from 15 to 18 cycles. These results showed that the primers and beacons for each reaction work well individually and that they amplify and detect their target sequence with very high specificity and sensitivity. The CT values exhibited by the samples in these experiments, compared to the plot of the standards of known concentration, indicated that the extracted DNA from the bacterial samples was higher than the range of concentrations tested by the standards (>107 copies per reaction). Therefore 100-fold dilutions of all extracted DNA samples were prepared for use in the two-step duplex assay, so that the resulting CT values would fall within the range seen on the standard curves.
Detection of S. enterica alleles in bacterial samples by molecular beacon-based two-step duplex real-time PCR
All samples were subsequently tested employing a double duplex strategy, where the first step of the assay involved a real-time PCR reaction containing the primers and beacons for the amplification and detection of both the invA gene and the IAC, a quantity of which was inserted into each reaction. This step of the assay determined the presence or absence of the invA gene to verify whether the sample was Salmonella or not. Simultaneous amplification and detection of the IAC in all samples ensured accurate PCR performance, therefore excluding the possibility of false-negative results. Amplification and detection of both invA and the IAC were clear in all Salmonella samples, whereas only the IAC amplification was detected in non-Salmonella samples. Representative amplification plots from Salmonella and other bacteria for the first step reaction are seen in Fig. 3. The results demonstrate that this reaction correctly recognises samples in which Salmonella exist from samples in which it does not.
All samples found positive for invA in the first step were then tested in the second step of the assay, another duplex real-time PCR reaction containing the components for amplification and detection of both prot6E and fliC targets. In all S. Typhimurium samples fliC was the only target detected, in all S. Enteritidis samples prot6E was the only target detected and in all other Salmonella samples, both targets were undetected. The results show that this reaction clearly and accurately distinguishes between S. Typhimurium strains, S. Enteritidis strains and other Salmonella serotypes. Representative amplification plots from S. Typhimurium, S. Enteritidis and other Salmonellae for the second step reaction are seen in Fig. 4, clearly showing that the prot6E and fliC components designed in this study work well together in a multiplex real-time PCR reaction.
In both the uniplex and double duplex assays, non-template controls were included to verify the absence of false-positive results. In all cases they exhibited undetectable amplification of the targets (CT >45).
Selectivity of the real-time assay
The selectivity and accuracy of the test is measured by calculating the values for specificity and sensitivity. Specificity is the probability that the PCR will be negative among specimens that should not possess the gene and is calculated using the formula: true negative/(true negative + false positive). Sensitivity shows the strength of the test in recognising what we are looking for, i.e., in correctly identifying the specific serotype. The formula used for estimation of sensitivity is: true positive/(true positive + false negative). For the reaction targeting the invA gene, all 44 Salmonella samples investigated were positive indicating a sensitivity of 100%. The specificity was also 100% since all non-Salmonella samples gave negative results, with undetectable fluorescence signals after 50 cycles. In the prot6E reaction all S. Enteritidis samples analysed were identified correctly with positive PCR results and all non-Enteritidis samples were negative for this target. Thus, this reaction also had sensitivity and specificity of 100%. Similarly, in the assay for fliC detection, all S. Typhimurium samples tested were positive for the target. The assay's sensitivity was 100%, matched by an equal specificity value as all non-Typhimurium samples tested gave negative PCR results.
Traditional serotyping of S. enterica is based on the detection of certain antigens using microbiological techniques and culturing, which are time-consuming and laborious. This study exploits real-time PCR, molecular beacons and genetic variation between different serotypes to devise a quick, accurate and simple assay to reliably identify a bacterial sample as Salmonella enterica and further distinguish it as serotypes S. Typhimurium or S. Enteritidis, the two serovars most commonly associated with food-borne gastroenteritis. The assay described in this study can analyse a large number of samples very quickly, and can also identify as few as 10 copies of target DNA per reaction, potentially even in the presence of thousands of copies of other serotypes. The short completion time of this assay and the ability of PCR to detect even dead bacterial cells, even though these are no longer infectious, highlight the drawbacks of the culturing method and the need to start using modern molecular techniques as opposed to conventional microbiology methods where applicable. PCR sensitivity is superior to that of the bacteriological culturing methods, as it can detect Salmonellas with atypical biochemical features, reducing false-negative results, and it will not mistakenly detect non-Salmonella bacteria, reducing the chances of false-positive data . However, further research is necessary to ensure that molecular assays alone can efficiently detect Salmonella spp. and its serotypes.
A variety of bacterial samples were used to test the specificity of the assay in the detection of the genus Salmonella. At the same time a number of Salmonella strains were included to ensure that the detection tests for serovars S. Typhimurium and S. Enteritidis were specific. The study includes strains from clinical and environmental samples as well as commercially available strains, and a significant number of S. Typhimurium and S. Enteritidis samples as well as other Salmonella serotypes and non-Salmonella bacteria. This broad range of samples was included to test the efficacy of the assay. Three genes were specifically targeted: the invA gene specific to the genus Salmonella; the prot6E gene specific to S. Enteritidis; and the fliC gene specific to S. Typhimurium. Due to its specificity, the invA gene is an excellent potential target for the detection of S. enterica strains alone [18, 24, 28, 30–43]. The fact that it is unique for S. enterica and rarely absent from it , ensures high specificity and sensitivity in detection assays. The prot6E gene is located on a highly conserved, low copy number, 60-kb virulence plasmid specific to S. Enteritidis and its absence appears to be very rare . Finally, the fliC gene codes for the H1 antigen of Salmonella. Targeting the fliC-i allele greatly increases the specificity for S. Typhimurium identification. In order to detect S. Typhimurium with the highest specificity, three genes could ideally be targeted, coding for antigens O:4, H1:i and H2:1,2, as it is the only serovar with this antigen combination . However, this would not only raise the costs of the assay but would compromise the simplicity of design and the potential for including further molecular beacons in the multiplex reaction for identification of other target serotypes. Thus, in this study, as in some other studies [48, 49], the fliC gene has been chosen as a single target for the presence of S. Typhimurium. By designing the fliC beacon using a S. Typhimurium sequence from the GenBank database as a template, the assay exhibits high sensitivity. However, although it performed with 100% specificity with this particular set of samples, in a different set of samples, e.g., with other S. enterica serotypes like Kentucky that also possess the H1:i antigen, it might yield different results. Many different genes have been targeted in previous studies [16, 22, 25, 26, 30, 47, 48, 50–54]. However, the above targets did not prove to be specific enough for unique detection and identification.
The IAC used is a synthetic and unique oligonucleotide designed de novo for this study. The fact that this IAC is co-amplified with the invA fragment using the same primer set but detected by a distinct beacon, does not appear to alter the precision and accuracy of the real-time PCR, and quantification of original target DNA is still possible even in the presence of the control. However, the standard curve protocol for invA in the presence of the IAC should be performed for a correct quantitative approach if the assay is to be used for quantification. The invA gene has been used as an internal amplification control in other studies , but its application is limited to Salmonella assays alone. Furthermore, it has been found that in some rare cases, this gene may be absent and is therefore unreliable as an amplification control even for studies incorporating Salmonella specimens alone. This IAC sequence matches no organism in the NCBI libraries and could potentially be used in any such detection assays.
The assays for the invA, fliC and prot6E genes all had a sensitivity and specificity score of 100%. All 45 Salmonella samples were positive, with 100% sensitivity. Positive results (>10 copies of DNA per reaction) had CT values ranging from 15 to 25. One exception, the commercially available specimen of S. Enteritidis (Table 3), had a CT value of approximately 30. Since the prot6E gene is located on a virulence plasmid, its absence would not be surprising. Plasmid profiling should be performed to explain the unusually high CT value observed for this specific specimen. This raises the question of whether selecting a target on a plasmid is a wise choice, but this absence of this plasmid has been found to be rare from S. Enteritidis and the low copy numbers (1–2) of the plasmid in the cells make possible the conversion of the assay to a quantitative one which would be correct to a factor of 2. Therefore, using this target for quantification would depend on the accuracy required.
Our study is the first to incorporate four molecular beacons with real-time PCR in a double duplex PCR protocol to detect Salmonella spp., Salmonella Enteritidis and Salmonella Typhimurium in a single assay. Strong fluorescence signals were observed in all positive PCR results in both the uniplex and the duplex assays, indicating the efficiency of the design in the primers and beacons. The sensitivity and specificity of the design and procedure described here give the assay the potential to be converted into a quantitative method, directly applied to samples without the requirement of pre-enrichment stages, making use of the standard curves.
This molecular beacon-based real-time PCR assay is extremely useful for any laboratory in possession of a real-time PCR. It is a fast, reproducible, simple, specific and sensitive way to detect nucleic acids, which could be used in clinical diagnostic tests in the future. The design of the assay gives it potential to be used for quantification, for detection of multiple other serotypes of Salmonella or to be modified for the detection of other bacterial samples. Also, more significantly, the sensitivity of the test and its confirmed low limit of detection, are promising factors for the important switch to direct detection from real clinical and environmental samples which have not been previously cultured and have low numbers of bacteria.
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The authors would like to thank the staff at the Department of Veterinary Services, Nicosia for assisting in sample collection; S. Gilliland and J. Hezka for technical assistance.
This work was supported by research funds from the University of Cyprus (awarded to L. G. Kostrikis) and the Birch Biomedical Research LLC.
AVH participated in the assay design, sample preparation, real-time PCR experimental procedures, the analysis and interpretation of the results and drafted the manuscript. VLD carried out sample preparation, real-time experimental procedures, analysis and interpretation of results and drafted the manuscript. MAE carried out the bacterial culturing and serotyping techniques, sample selection, bacterial pellets isolation and helped with the manuscript preparation. CKK participated in sample selection and donated samples for this study. LGK conceived and designed the assay, coordinated the study and participated in sample selection and analysis and interpretation of results. All authors read and approved the final manuscript.
Andreas V Hadjinicolaou, Victoria L Demetriou contributed equally to this work.
Electronic supplementary material
Additional File 1: Oligonucleotide primers and molecular beacons in the real-time PCR assay. Table of primer and molecular beacon sequences used in this study. (DOC 63 KB)
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Hadjinicolaou, A.V., Demetriou, V.L., Emmanuel, M.A. et al. Molecular beacon-based real-time PCR detection of primary isolates of Salmonella Typhimurium and Salmonella Enteritidis in environmental and clinical samples. BMC Microbiol 9, 97 (2009). https://doi.org/10.1186/1471-2180-9-97
- Molecular Beacon
- invA Gene
- Internal Amplification Control
- Bacterial Sample
- fliC Gene