Usefulness of real time PCR for the differentiation and quantification of 652 and JP2 Actinobacillus actinomycetemcomitans genotypes in dental plaque and saliva
The aim of our study is to describe a fast molecular method, able to distinguish and quantize the two different genotypes (652 and JP2) of an important periodontal pathogen: Actinobacillus actinomycetemcomitans. The two genotypes show differences in the expression of an important pathogenic factor: the leukotoxin (ltx). In order to evidence this, we performed a real time PCR procedure on the ltx operon, able to recognize Aa clinical isolates with different leukotoxic potentials.
Methods
The specificity of the method was confirmed in subgingival plaque and saliva specimens collected from eighty-one Italian (Sardinian) subjects with a mean age of 43.9, fifty five (68 %) of whom had various clinical forms of periodontal disease.
Results
This procedure showed a good sensitivity and a high linear dynamic range of quantization (107-102 cells/ml) for all genotypes and a good correlation factor (R2 = 0.97–0.98). Compared with traditional cultural methods, this real time PCR procedure is more sensitive; in fact in two subgingival plaque and two positive saliva specimens Aa was only detected with the molecular method.
Conclusion
A low number of Sardinian patients was found positive for Aa infections in the oral cavity, (just 10 positive periodontal cases out of 81 and two of these were also saliva positive). The highly leukotoxic JP2 strain was the most representative (60 % of the positive specimens); the samples from periodontal pockets and from saliva showed some ltx genotype for the same patient. Our experience suggests that this approach is suitable for a rapid and complete laboratory diagnosis for Aa infection.
Background
Actinobacillus actinomycetemcomitans (Aa) is a gram-negative, facultative anaerobe, implicated in numerous human diseases such as periodontitis, endocarditis, meningitis and osteomyelitis. [1–4]. The primary ecological niches of this bacteria, which causes localized aggressive periodontitis, are dental plaque and periodontal pockets and its presence mainly occurs in chronic adult periodontitis [5–7].Aa has been studied because it produces a powerful leukotoxin (ltx) able to kill human leukocytes [8–13]. Most of the Aa strains isolated from non-diseased periodontal sites produce low levels of leukotoxin, while aggressive forms of Aa -associated periodontitis show highly leukotoxic microrganism clones [8, 46]. The leukotoxin is expressed by an operon consisting of four genes (ltx C, ltx A, ltx B, ltx D); ltx A is the functional toxin while the three remaining genes are required for activating and transporting the leukotoxin [12, 14]. Different transcription levels of ltx can depend on a specific 530-bp sequence in the ltx promoter region, which leads to both lower expression and toxicity (strain 652). When this region is deleted (this occurs in strain JP2) there is a faster ltx production which leads to a better protein transcription than in strain 652: this seems to be responsible for the periodontal destruction [15–18].
Standard culture methods used for Aa detection in clinical samples have some disadvantages such as the need for a required nutritionally complex media for growth and several days of incubation [19, 20]. Molecular assays for Aa detection are based on DNA-probes, PCR and real time PCR methods; they are faster and more sensitive than cultural systems, although they do not allow a simultaneous detection and quantization of the different genotypes [21–34]. To overcome these outbreaks we used a real time PCR method for the differentiation and quantization of Aa 652/JP2 strains, based on the different length of PCR products in the two genotypes; this method is based on the principle that, by using SYBR Green I, the melting temperature (Tm) of the PCR product gives information about the sequence length and also allows different genotype amplicons to be identified and quantified.
Methods
Clinical specimens
Subgingival plaque and saliva samples were collected from 81 male and female subjects, aged from 7 to 81, recruited from the Department of Dental Disease Prevention (University of Cagliari), who had given informed consent to take part in the microbiological analysis. The patient's conditions were: non-diseased (n = 26.32%), with gingivitis (n = 31, 38.3%), with chronic periodontitis (n = 17.21%) and with aggressive periodontitis (n = 7, 8.7%) [35]. Each patient's health status and background were recorded: age, sex, probing pocket depth, clinical attachment level, bleeding on probing (measured in six sites on all teeth present in the mouth). None of the patients who took part in the experiments was under antibiotic therapy during the previous 6 months. At first, 400 μl of saliva was collected from each patient and placed into a sterile tube, afterwards the subgingival plaque samples were obtained (one site per patient) from the deepest periodontal sites in all subjects. The sample area was isolated using sterile cotton rolls and air-dried to avoid saliva contamination; supragingival plaque was removed by using a sterile curette. A sterile paper point ISO 45 (Roeko Dental, Langenau, Germany) was inserted into the pocket and held in place for 30 seconds [36]. The paper point was then removed and placed into a vial containing 800 μl of sterile saline solution, NaCl 0.9%, with 15 glass beads (about 100 mg Bio-Spec Products, Bartesville, USA). After vigorous vortexing, 200 μl of the suspension was immediately used for culture analysis, while the remaining suspension (600 ul) was stored at -20°C and 400 ul of this were used for DNA extraction.
Positive control strains
a) Aa strains
The Aa strains used were: (i) CCUG 37005 (Culture Collection, University of Göteborg, Sweden, genotype 652) and (ii) clinical isolate, strain GO1 (genotype JP2). The two strains were maintained at -80°C in vials containing Schaedler Broth with 15% glycerol and cultured in Columbia agar blood (Microbiol, UTA, Cagliari, Italy) at 37°C with 5% CO2 in jar (Biomérieux Marcy l'Etoile, France). After 1 week of incubation, colonies of each genotype were suspended in a sterile saline solution (NaCl 0.9%) to obtain a concentration of 1 McFarland scale 3*108 cells/ml (counted with the McFarland method) these suspensions were used as follows:
1. to assess specificity: we prepared different suspensions in 400 μl of sterile saliva (obtained by filtration with a 0.5 μm filter, Millipore Molseim, France), (i) containing 106 CELLS/ml of each genotype and (ii) tubes with different proportional mixtures of the two genotypes, 1/2, 1/4, 1/8, 1/10 652/JP2 or vice versa)
2. to assess sensitivity: we prepared 10 fold serial dilutions of each genotype in sterile saliva, ranging from 107 -101 cells/ml.
The exact bacterial concentration of these standards was obtained by colony forming unit (CFU) plate counted in Columbia agar blood (Microbiol, Uta, Cagliari, Italy. These suspensions served as a standard for measuring the method sensitivity and for the quantification curve after DNA extraction.
b) Other periodontal bacteria used as positive control
To assess the role of other periodontal pathogens in these samples, a traditional PCR was used with subsequent positive controls: Porphyromonas gingivalis CCUG 25893, Prevotella intermedia CCUG 24041, (Culture Collection, University of Göteborg, Sweden), Tannerella forsythensis cip 105220 (Institut Pasteur, Paris, France) Treponema denticola DSMZ 14222-Deutsche Sammlung von Mikroorganismen, Braunschweig, Germany. These strains (except T.denticola) were cultured on Shaedler Anaerobe Agar plates (Microbiol, Uta, Cagliari, Italy), incubated in an anaerobic jar for 7 days at 37°C. 1 ml of these bacterial suspensions was used for DNA extraction.
DNA extraction
Genomic DNA from positive controls and clinical samples was obtained by the CTAB modified method. 400 μl of sample were added to 70 μl of 10% sodium dodecyl sulphate (SDS) and 5 μl of proteinase K at 10 mg/ml concentration (SIGMA – Aldrich, ST. Louis, Missouri, USA); after vigorous vortexing, this mixture was incubated for 10 minutes at 65°C. Next, 100 μl of NaCl [5 M] and 100 μl of CTAB/NaCl (0.274 M CTAB, Hexadecyl trimetylammonium bromide and 0.877 M NaCl, Sigma-Aldrich) were added to the tube, which was vortexed briefly and incubated at 65°C for 10 minutes. 750 μl of SEVAG (Chloroform: Isoamyl Alcohol 24:1, Sigma-Aldrich) were added and the mixture was vortexed for 10 sec. After centrifuging for 5 min (at 12000 rpm) 0.6 volumes of isopropanol (Sigma-Aldrich) were added to the supernatant. After 30 min at -20°C and after being centrifuged for 30 min at 12.000 rpm, the pellet was dried at room temperature for 20 min and suspended in 20 μl of molecular biology grade distilled water (Gibco, Invitrogen Paisley, Scotland, UK). 2 μl of this were used as DNA suspension for conventional PCR and real time PCR reaction.
Primers design
Primers for real time PCR were designed using the promoter region on the Leukotoxin operon sequences extracted from the NCBI database GenBank with S68133 and M27399 accession numbers. Figure 1 shows primer sequence and position and the real time PCR mechanism with the two different (652/JP2) Aa genotypes. Possible oligonucleotide dimer formation, self-complementarity and the annealing temperatures of the real time PCR were calculated using the Oligo program vers. 4 (MedProbe, Oslo, Norway). The real time PCR primers (OG155 and OG156) amplified a region of 696 bp in the 652 genotype and 195 bp in the JP2 genotype (Figure 1). The theoretic melting temperatures of the different PCR amplicons (Tms) were calculated using module 1 of the DNA hybridization prediction algorithm program "HYTHER" [37, 50] with the following sets of parameters: (i) monovalent cation concentration at 0.05 mol/L, (ii) Mg2+ at 0.004 mol/L, (iii) a concentration of PCR products (Top/Bottom strands) at 10-7 mol/L and (iv) hybridisation temperature at 37°C. The same procedures have been used to design all the oligonucleotides used in traditional PCR (Table 1).
Figure 1
Structure of Real time PCR design forActinobacillus actinomycetemcomitans652, JP2 genotype detection. Primers were designed to circumscribe a fragment of 530 bp present in 652 but deleted in the JP2 strain. The two different PCR products showed 6 °C difference in Tms after PCR real time melting curve analysis.
Table 1
Primers used and strains detected by conventional PCR.
Name
Target
Strain
Sequence 5'--------------3'
GenBank Accession No
PCR product (bp)
OG 43
16S rRNA
Actinobacillus actimycetemcomitans
CCAAGTGTGATTAGGTAGTT
M75036
226
OG 44
16S rRNA
Actinobacillus actimycetemcomitans
ACCAACCTTCCTCAATAC
M75036
OG53
16S rRNA
Prevotella intermedia
CGTATCCAACCTTCCCTCC
X73965
389
OG54
16S rRNA
Prevotella intermedia
ATTAGCCGGTCCTTATTCGAAG
X73965
OG94
prtC
Porphyromonas gingivalis
GAATCAAATACTTCAGCCGTCT
AB006973
143
OG95
prtC
Porpyromonas gingivalis
TTGCAGTTCGTATCGGATCT
AB006973
OG45
16S rRNA
Tannerella forsythensis
GTCGGACTAATACCTCATAAAACA
L16495
222
OG46
16S rRNA
Tannerella forsythensis
TCGCCCATTGACCAATATT
L16495
OG348
16S rRNA
Treponema denticola
AGAGAAAGGGTAATTTGAAG
AF179264
399
OG349
16S rRNA
Treponema denticola
TATTATTGTCCCTTCTTTCTT
AF179264
Real time PCR
Real time PCR was performed with a LightCycler instrument and a LightCycler DNA Master SYBR Green I kit (Roche Diagnostics Mannheim, Germany), according to the manufacturer's instructions. The 20 μl final volume contained 4 mM MgCl2, 1 μM of each primer (OG155-OG156) and 2 μl of DNA extract. The PCR program was: (i) denaturation at 95°C for 30 sec, (ii) 40 cycles of: 1 sec at 95°C, 10 sec at 49°C, 40 sec at 72°C and 3 sec at 74.3°C. (iii) The melting curve was performed for 0 seconds at 95°C, 45°C, 95°C. Transition rates were: 5°C/s in 72°C segment, 0.1°C/s in 45 °C segment and 20 °C/s for other steps. Fluorescence was detected at the end of the 74.3°C segment in the PCR step (single mode), and at 45°C segment in the melting step (continuous mode) in the F1 channel. During the initial optimization of the real time reaction, products were analyzed using agarose gel to ensure a correct sample product size. After real time PCR, samples were recovered from capillaries by reverse centrifugation into microcentrifuge tubes (Eppendorf 0.2 μl), and mixed with blue loading buffer and finally 10 μl of each sample were utilized in 1% agarose electrophoresis gel (Invitrogen, Palsley, Scotland, UK) and stained with ethidium bromide.
Differentiation between JP2 and 652 genotypes
By using two primers (OG155 and OG156) flanking an ltx promoter region, we obtained two different length PCR products: 696 bp for 652 and 195 bp for the JP2 genotype. These amplicons showed two different Tms melting peaks after the PCR real time reaction with SYBR green I dye. To evaluate product specificity, ltx PCR amplicons were also sequenced by a conventional automated sequencer as described in literature by Ianelli et al.,1998, [38]. The results were edited and analyzed with nucleotide-nucleotide BLAST (blastn) [51] and compared with sequences deposited in the DNA data bank.
Expression of the Aa concentration in dental plaque and saliva
Real time PCR standard curves were performed on different DNA extracts, obtained by different Aa genotype suspensions with a concentration range of 107-101 cells/ml. The number of bacteria was calculated by the interpolation of the clinical sample threshold cycle [39] with a standard curve obtained for each genotype (Figure 4). Bacterial concentration in specimens was expressed in: i) Aa cells/ml paper point suspension for subgingival plaque and ii) Aa cells/ml saliva in saliva samples. We used the following equation to calculate Aa concentration for the paper point specimens.
a) [cells/ml paper point suspension].= ([Aa Rt cells]*2,5.
[Aa Rt cells]= Bacterial cells, calculated by PCR real time standard curve interpolation.
Cultural method
For a sensitivity study, molecular methods were compared with traditional culture analysis for all the clinical samples: 200 μl of saliva and paper point suspensions were diluted 10 and 100 fold in Schaedler Broth (Microbiol, Uta, Cagliari, Italy). 100 μl of each dilution were plated in Columbia agar blood (Microbiol, Uta, Cagliari, Italy) and incubated in a 15% CO2 atmosphere at 37°C in a jar using the Genbox system (Biomérieux Marcy l'Etoile, France). After 6 days of incubation the typical Aa colonies were identified by a biochemical test using API 20A (Biomérieux Marcy l'Etoile, France) according to the manufacturer's instructions.
Conventional PCR
For the 81 analyzed samples we used traditional PCR able to detect: (i) A. actinomycetemcomitans by different DNA target (16S rRNA) and (ii) P. gingivalis, P. intermedia, T. forsythensis, T. denticola. For all bacteria, the reaction was performed in 25 μl reaction volumes using MegaMix 2MM-5 (Microzone Limited, West Sussex, UK) according to the manufacturer's instructions. The primer and target sequences used are shown in Table 1. The mixture contained 7 pmol of each primer, 3.8 mM MgCl2 and 2 μl of DNA suspension. The thermocycler profile was as follows: an initial denaturation at 95° C for 5 min; 35 cycles consisting of 50°C for 1 min, 68° C for 3 min and 40 sec and 95° C for 1 min. PCR products were analysed by electrophoresis on a 1.2 % agarose gel containing ethidium bromide (0.5 mg/ml). With reconstruction experiments this method showed a detection limit range of 10-50 cells/PCR.
Results
Reconstruction experiments: specificity and sensitivity of the method
A reconstruction experiment confirmed the PCR real time selectivity in the DNA extracts of three different suspensions: (i) Aa 652, (ii) Aa JP2 and (iii) a mixture of the two genotypes. Figures 2, 3 shows melting curves and the 1% agarose gel electrophoresis results of PCR real time products. In our study, with reconstruction and with clinical samples, we demonstrated melting temperatures of 76 ± 2 °C in the JP2 positive samples, and 82 ± 2 °C in the 652 positive samples; a double melting peak was obtained with both genotype mixtures tested (Figure 3). The 6 °C difference in Tms allows an easier differentiation of two genotype profiles; no cross-reaction in Tms peaks was detected with strains 652 and JP2, indicating the good selectivity of the method. Only one size band for each genotype was verified and confirmed in agarose gel electrophoresis, respectively 696 bp for 652 and 192 bp for the JP2 strain (Figure 2); this suggests a total absence of non-specific products. Real-time PCR, as evaluated here, has been shown to have a detection limit of 40 Aa 652 or JP2 cells/PCR (100 cells/ml). The wide linear range (107-102cells obtained for two genotypes) as illustrated in Figure .4, indicates the efficiency of this real time PCR. Standard curves showed a similar slope and a good correlation regression coefficient R2 of 0.98–0.97 [40], (Figure 4). In these experiments negative control contained DNA saliva extracts recovered from a non-diseased patient with PCR/negative culture for Aa, the total DNA amount of these samples was about 50 μg/μl. C lanes/curves do not contain aspecific products from previous interaction with human or non-specific bacterial genomic DNA as shown in Figures 2, 3. The DNA sequencing results of the PCR amplicons were a perfect match, with Blast program analysis [51], for the 652 genotype (Gen Bank accession n. S68133) or the JP2 genotype (Gen Bank accession n. X16829).
Figure 2
Real time PCR melting curve and agarose gel electrophoresis results obtained from saliva reconstruction samples containing differentActinobacillus actinomycetemcomitansgenotypes. Curves 1–2: using a suspension containing the 652 or JP2 Aa genotype, the difference in Tms melting peaks was 6°C between the two clones. The presence of a single 696 bp band for 652 and 192 bp for the JP2 strain in 1% agarose electrophoresis gel (Metaphor, BMA, Rockland ME USA) suggests a total absence of non-specific products, gel bands 1–2. Melting peak at 73°C in negative control and the small band in the control samples "C" are primer dimer products.
Figure 3
Real time PCR melting curve and agarose gel electrophoresis results obtained using a suspension containing a mixture of two genotypes: a single curve is obtained with two distinct Tms' peaks which confirm good system selectivity. Melting peak at 73°C in negative control and the small band in the control samples "C" are primer dimer products.
Figure 4
Quantitative standard curves. Linear regressions obtained by real time PCR using a LightCycler instrument with SYBR Green I protocol of serially diluted suspensions for JP2 or 652 Actinobacillus actinomycetemcomitans genotypes (107-102 cells/ml). Threshold cycle (CT) value is directly related to the amount of PCR product and therefore related to the initial amount of target DNA present in the PCR reaction. CT (threshold cycle) represent the fractional PCR cycle number at which the fluorescence signal exceeds background fluorescence [40].
Results with clinical samples
We analyzed plaque and saliva samples collected from 81 patients following the protocols just described. In comparison with the cultural procedure, real time resulted as being a little more sensitive (1 saliva and 2 paper point samples were positive only with molecular methods), while real time and conventional PCR were in accordance. All negative samples with the real time PCR procedure also resulted negative with cultural and conventional PCR methods too. Only one subject in the non-diseased group (26 in total) resulted 652 Aa genotype-positive for the periodontal pocket specimen, with 103 cells/ml bacteria in the paper point suspension and negative in the saliva sample. Table 2 shows that 9 out of 55 diseased patients (16.3%) were infected with Aa and the disease severity was associated with a high bacteria title and/or leukotoxic genotype presence. In accordance with scientific data, we only identified the leukotoxic clone (JP2) in patients with severe forms of periodontitis [41]. However, whenever a similar degree of clinical infection was present, and only the leukotoxic 652 genotype was identified, high bacteria titles were present (about ≥ 104 cells/ml in the paper point suspension). Two patients, with aggressive periodontitis, showed bacteria in saliva samples too; one was found positive for the 652 strain and the other for JP2, the same genotypes were detected respectively in periodontal pockets.
Table 2
Real Time PCR results (title and genotype) in comparison with cultural and conventional PCR methods using saliva and subgingival plaque from 10 Sardinian subjects out of 81, positive for A. actinomycetemcomitans.
Patient
Disease type
Subgingival plaque
Saliva
Aa Real time PCR [cells/ml paper point]
Culture for Aa
Conventional PCR (for 4 periodontal pathogens)
Real time PCR Aa cells/ml
Aa Culture CFU/ml vs Conventional PCR (Aa 16S rRNA only)
C1
aggressive periodontitis
1,9*104 (652)
posit
Aa
3,0*102 (652)
1,5*101/pos
C2
aggressive periodontitis
4,0*103 (JP2)
posit
Aa, Pg
1,3*102 (JP2)
neg/pos
C4
gingivitis
3,6*103 (652)
posit
Aa,
Nd
neg/neg
C5
chronic periodontitis
6,4*103 (JP2)
posit
Aa,Tf
Nd
neg/neg
C6
chronic periodontitis
1,9*103 (JP2)
neg
Aa,Tf
Nd
neg/neg
C7
aggressive periodontitis
2,8*104 (JP2)
posit
Aa,Pi,Tf
Nd
neg/neg
C8
aggressive periodontitis
4,4*104 (JP2)
posit
Aa,
Nd
neg/neg
C25
aggressive periodontitis
2,0*103 (JP2)
posit
Aa,
Nd
neg/neg
C75
aggressive periodontitis
3,0 *104 (652)
posit
Aa, Pg, Pi,Tf
Nd
neg/neg
C80
no disease
1,0*103 (652)
neg
Aa, Pg, Pi,Tf
Nd
neg/neg
Legend:
Aa = A. actinomycetemcomitans, Pg = P. gingivalis, Pi = P. intermedia, Tf = T. forsythensis.
Nd = non-detectable (<102 cells/ml)
Subgingival distribution of different periodontal bacteria
Five periodontopathic bacteria: A. actinomycemcomitans P. gingivalis, P. intermedia, T. forsytensis and T. denticola were detected by a conventional PCR method from the subgingival plaque of all 81 patients. No periodontopathogenic bacterial DNA was observed in 39 of the samples (51%). The percentage of PCR positive samples was: Aa 12.2%, Pg 14.8%, Pi 22%, Tf (the most representative bacteria in these samples) 40.8% and Td 8.7 %. Six specimens resulting positive for Aa, (C2, C5, C6, C7, C75, C80) were associated with at least another periodontal bacteria. The principal pathogen was T. forsythensis present in 50% of the Aa positive samples. Sample C80, isolated in a non-diseased patient (2 mm subgingival pocket), contained all 4 tested pathogens (Table 2). In the PCR results four samples showed Aa DNA only (samples C1, C4, C8, C25) and these results were in accordance with the PCR real time and cultural result s(Table 2).
Discussion
Periodontitis is an inflammatory disease caused by different species of anaerobic bacteria and is the most prevalent human disease; in addition a growing number of studies indicate that severe chronic forms of this disease are not only localized infections, but may also increase of the risk of various systemic conditions such as cardiovascular disease [4, 42].
The multi-factoriality of this infection is due to a complex bacteria population with high dynamicity and adaptability; consequently, treating periodontitis is difficult since the elimination of this pathogenic bacteria, once established in periodontal pockets, may not be possible, even with repetitive treatments. Moreover costs related to maintaining and replacing restoration work like fillings and crowns and those of periodontal treatment are high and similar problems occur with dental implants.
For these reasons in periodontal disease prevention, diagnostic methods able to evaluate the virulence factors of periodontal bacteria are important, particularly in subjects without clinical symptoms but infected with these pathogens; for example patient C80 in our study.
81 patients (diseased and non diseased) showed a sub-gingival distribution of periodontal bacteria in accordance with published data [43]. In fact, at least 1 member of the red complex bacteria (Pg, Tf, Td) 47.2% or orange complex (Pi) 25.9% was found in the majority of diseased patients; ten subjects (0.12%) contained A. actinomicetemcomitans in the periodontal pocket and two of these also in saliva [44].
Different studies have considered Aa as an important etiological microorganism involved in aggressive periodontitis [16, 35, 41, 45, 46] and it has been shown that a high-leukotoxin-producing strain of Aa is mainly found among individuals with severe forms of periodontitis [14–16, 41]. Different authors have recently described PCR real time methods for Aa quantization [26, 27, 34, 47, 48], but with current molecular methods it is not possible to obtain simultaneous bacterial quantization and genotypization.
We have described a fast molecular procedure (2 hours) with good sensitivity and specificity, able to quantify and differentiate strains 652 and JP2 of Aa simultaneously. We analyzed subgingival plaque and saliva samples collected from subjects with different periodontal status and the results showed that in comparison with recent bibliographic data obtained in other geographical regions, the same differences in Aa distribution were also evaluated in Sardinian people [16, 49]. In fact, within the non-diseased patients (n= 26, 3.8%), only one individual resulted Aa positive with all the three methods used; 24 chronic and 8 subjects with aggressive periodontitis (33%) showed the bacteria in oral clinical samples. Genotype JP2 was the most represented in all periodontal patients whose age was >29 mean = 47. None of the adolescent subjects examined in this study (n= 5, age 10 to 15 years) showed periodontal disease.
In comparison with the other periodontal pathogens tested, 4 samples were positive only for Aa; this could mean that in these samples disease severity may depend on the number and genotype of this microorganism. However when other periodontal pathogens were present, high numbers or high leukotoxic Aa genotype were mostly correlated with severe forms of periodontitis. (chronic or aggressive). The presence of this strain in saliva too, (two cases in these patients), has been described by other authors [44]; Our results shows that the same genotype is present in saliva and in periodontal pockets, indicating a possible and continuous bacteria replacement in saliva from an important reservoir which is the periodontal district. Moreover, real time PCR quantification of saliva could explain its role as a means of bacterial transmission in patients with a high infectious dose of Aa.
Conclusion
Experimental results suggest the importance of obtaining both bacterial titre and genotype identification to give the correct microbiological diagnosis in periodontal infections. Further investigations and sample enlargements could give us more answers about the correlation between bacterial status in the oral cavity and disease severity and progression. The presented method/approach is suitable for a rapid and complete laboratory diagnosis of Aa infection.
Abbreviations
CTAB:
Hexadecyl trimetylammonium bromide
Declarations
Authors’ Affiliations
(1)
O.B.L. (Oral Biotechnology Laboratory), Dipartimento di Chirurgia e Odontostomatologia Università degli Studi di Cagliari
(2)
Universita' degli Studi Milano Bicocca, Dipartimento di Neuroscienze, Dottorato di Ricerca in Parodontologia Sperimentale
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