Detection of Periodontal Markers in Chronic Periodontitis
Åsa Leonhardt1, *, Anette Carlén2, Lisbeth Bengtsson2, Gunnar Dahlén2
Identifiers and Pagination:Year: 2011
First Page: 110
Last Page: 115
Publisher Id: TODENTJ-5-110
Article History:Received Date: 5/1/2011
Revision Received Date: 19/3/2011
Acceptance Date: 8/4/2011
Electronic publication date: 7/7/2011
Collection year: 2011
open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
The aim was to compare the detection frequency of periodontopathogens by using the Pado Test 4.5 and checkerboard DNA-DNA hybridization technique in chronic periodontitis patients.
Thirty patients with chronic periodontitis were tested cross-sectionally with DNA/RNA oligogenomic probe method (IAI Pado Test 4.5) and DNA/DNA whole genomic probe (checkerboard) method. Samples were taken by two paper points at the deepest site in each of the four quadrants and pooled into one sample for each of the two methods. The samples were sent to the two laboratories (IAI, Zuchwil, Switzerland, and Oral Microbiology Laboratory, University of Gothenburg, Sweden) and were analyzed in a routine setting for the presence and amount of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia and Treponema denticola.
While Pado Test 4.5 detected the four periodontal pathogens in 11 (36.7%) of the patients, the checkerboard method showed presence in all patients (100%) using the lower score (Score 1 corresponding to 104 bacterial cells) and 16 (53.3%) using a higher treshold (score 3 corresponding to between >105 and 106 cells).
The results of the present study showed low agreement for a positive microbiological outcome using the two diagnostic methods. It was also concluded that microbiological analysis in practice should include a larger number of bacterial species to better serve as markers for a diseased associated flora in chronic periodontitis cases.
Diagnosis of periodontal disease and evaluation of periodontal therapy are usually based on clinical parameters including attachment loss (AL), probing pocket depth (PPD) and bleeding on probing (BOP). While they are decisive for the diagnosis and the initial treatment they need to be supported in non-responders after the initial therapy for decision for further therapy . A microbiological diagnosis has thus been suggested to complement the clinical diagnosis and to be used for guidance for more aggressive treatment such as surgery and antibiotics [2-6]. There is confusion both scientifically and in practice on the criteria for sampling, when, where and how to sample, what microorganisms should be tested, which methods should be used and how to interpret the results .
Several methods have been used for microbiological testing in periodontitis . Most methods are focused on the presence of Aggregatibacter actinomycetemcomitans and the three “red complex” bacteria Porphyromonas gingivalis, Tannerella forsythus and Treponema denticola. Many techniques have not been fully accepted due to low sensitivity or specificity and they are sometimes slow, laborious and expensive. In recent years molecular biology methods such as whole genomic probes or oligogenomic based probes (Checkerboard DNA-DNA hybridization technology) and quantitative or qualitative PCR based methods have been introduced [9-17]. Despite some of the comparisons made we still do not know which method is the most appropriate in a given case. This could partly be explained by the lack of a gold standard. Culture techniques were used in the past as a gold standard but is less usable dealing with “difficult to culture” or “unculturable” bacteria. Consequently, comparisons between such methods based on different principles needs to be performed in clinical settings that best can answer the question on the presence and proportions of the bacterial species (markers) and serve as a guidance for the treatment strategy.
Several methods for microbiological testing have become commercialized. One such test is the IAI PadoTest 4.5 based on oligonucleotid probes against the 16S rRNA gene of 4 target species claimed to be indicators species for disease activity [18, 19]. Although the PadoTest 4.5 has been used in several investigations [20-22] it has not been evaluated with other methods used in clinical practice, except for one study  where the PadoTest 4.5 (IAI, Zuchvil, Switzerland) was compared with a similar DNA/RNA based method (MERI, Gaba GmbH, Lörrach, Germany). In the present study, the PadoTest 4.5 method was compared with the checkerboard DNA-DNA hybridization method against four bacterial marker species in chronic periodontitis patients.
MATERIALS AND METHODS
30 adults, 21 females and 9 males, with generalized chronic periodontitis (bone loss >2/3 of the root length at several teeth) were recruited for the study. They were referred to a specialist clinic for treatment of chronic periodontitis. The clinic regularly uses microbiological samples in the treatment planning and risk evaluation of cases with advanced periodontitis. The patients were all informed about the sampling and none refused to participate.
Clinical Registration and Radiographs
Full mouth recordings were taken at six sites per tooth except for third molars. Plaque (PlI) and Bleeding on probing (BoP) was scored as being absent or present (0 or 1) and % sites with plaque and BoP were calculated. Probing pocket depths (PPD) were measured and recorded in mm using a periodontal probe (Hu Friedy, Chicago, IL, USA) and were rounded to the nearest upper millimeter. Radiographs were taken to confirm the extent of bone loss.
In each of 4 quadrants, one site with a remaining pocket depth of ≥ 4 mm was selected for microbiological sampling with the paper point technique. Two paper points (one point delivered from the PadoTest 4.5 kit and one sterilized medium size paperpoint (size 45, Roeko, Coltène/Whaledent, Langenau, Germany) were concomitantly inserted in the periodontal pocket and kept in place for 10 secs. The 4 PadoTest 4.5 points (green marked at the top) taken from the same patients were pooled for the PadoTest 4.5. The samples were sent for analysis to the Institute fur Angewandte Immunologie (IAI, Zuchwil, Switzerland). The other 4 points from the same patients were pooled into 150 µl TE buffer for analysis with the checkerboard methodology and sent to the laboratory of Oral Microbiology, Institute of Odontology, Sahlgrenska Academy at University of Gothenburg, Sweden. The samples were handled in the routine outline of the two laboratories and they did not know they participated in a comparative study.
IAI PadoTest 4.5 (a DNA/RNA Probe Method)
The procedures are based on oligonucleotid probe technology according to standard procedures . According to their protocol the samples were hybridized for the 16S rRNA gene of A. actinomycetemcomitans, P. gingivalis, T. forsythia, T. denticola and to an universal bacterial probe (IAI and MicroProbe Corporation, Bothwell, WA, USA).
Checkerboard Technique (a DNA/DNA Probe Method)
The presence and level of the four species A. actinomycetemcomitans, P. gingivalis, T. forsythia, T. denticola were determined with the aid of the checkerboard DNA-DNA hybridization methodology according to Dahlén and Leonhardt, . In the routine setting in the laboratory the checkerboard panel contains additional 8 species, Campylobacter rectus, Filifactor alocis, Fusobacterium nucleatum, Parvimonas micra, Porphyromonas endodontalis, Prevotella intermedia, Prevotella nigrescens and Prevotella tannerae. In brief, whole genomic DNA probes were prepared from the panel of bacterial species using a digoxygenin labelling kit (Roche, Mannheim, Germany). The plaque samples were denaturated with 0.5 M NaOH, freezed and thawed 5 times and finally the bacterial cells were mechanically disrupted of by vortexing with glass beads. The samples were then boiled for 5 min, neutralized with ammonium acetate, transferred onto nylon membranes (Minislot device, Immunetics, Cambridge, MA) and fixed by UV-light. After 2h of pre-hybridisation at 42ºC, the DNA probes were allowed to hybridize over night in lanes vertically to the plaque and saliva samples using a Miniblotter device (Immunetics) at 42ºC. After a series of stringency washes at 70ºC, hybrids were detected using phosphatase-conjugated anti-digoxygenin antibodies and the signals were visualised with a chemiluminescent substrate (CDP-Star, Roche). Evaluation of the number of bacteria in the samples was performed by comparing the obtained signals with the ones generated by pooled standard samples containing 106 and 105 cells of each species. The results were transferred to a scoring system (0-5), where 0 indicated no signals, score 1 visible signals corresponding to <105 and score 3 signals corresponding between 105-106 cells.
A series of control samples were prepared from plaque sampled with curette from 5 periodontally healthy students, who had abstained from tooth brushing for one day. The plaque from each student was suspended into 100 µl TE-buffer and 106 cells of each target bacteria were then added to make a positive control sample with a mixed microbial population. From these suspensions paper point samples were taken, one for PadoTest 4.5 and one for checkerboard analysis mimicking true samples taken directly from periodontal pockets. The control samples were also blinded for the two laboratories.
Agreement (%) between the two methods was calculated (statistical package SAS 8.2) for the 4 target bacterial species and a kappa coefficient was calculated for each target bacteria using score > 1 or score >3 for checkerboard results versus PadoTest 4.5.
The 30 patients had a mean age 57 (SD ±11, range 39-81). They had 23.7±4.2 remaining teeth (range 16-28), 75.5±12.0 % sites ≥4mm and 5.5± 9.2 % sites with PPD ≥7mm. Full mouth PlI, BoP, and PPD recordings are shown in Table 1. The mean probing pocket depth of sampling sites were 5.54 ±0.71 mm and mean BoP at sampling sites 77.5±17.7 %. All sampling sites were clinically defined as diseased.
Clinical Parameters Full Mouth and in Sample Sites of 30 Patients with Periodontitis Used for Comparison Between Two Microbiological Tests
|Clinical Parameters||Full Mouth Recordings||Recordings at Sample Sites|
|BoP % (mean±SD)||60.9+16.3||77.5±17.7|
|PlI % (mean±SD)||60.6+15.7||62.9±17.7|
Bacterial Marker Frequency
The 3 red complex bacteria (P. gingivalis, T.denticola, T. forsythia) were frequently found with the checkerboard method at the score 1 and more and considerably less at score ≥ 3 (Table 2). The PadoTest 4.5 identified the 3 red complex bacteria in a lower frequency. A. actinomycetemcomitans was detected with the checkerboard technique in 11 of the 30 patients (36.7%) at score 1 while in no case it was identified using the Pado test 4.5. In all, 16 patients (53.3%) indicated a disease associated flora in the checkerboard analysis while 11 (36.7%) was indicated with the PradoTest 4.5 (Table 2). Table 3 showing the extended panel of bacterial species in the checkerboard method shows that other bacterial species also were quite frequent in the samples. Thus P. tannerae and F. alocis were present in around 50% of the cases and any of the 12 bacterial markers at score 3 or more was found in 83.3%.
Comparison Checkerboard and PadoTest 4.5
|Bacterial Markers||Checkerboard Score >1 No of samples (%)||Checkerboard Score >3 No of samples (%)||PadoTest 4.5 Presence of Marker No of samples (%)|
|A. actinomycetemcomitans||10 (33.3)||0 (0)||0 (0)|
|P. gingivalis||16 (53.3)||5 (16.5)||9 (30.0)|
|T. denticola||29 (96.7)||11 (36.7)||5 (16.7)|
|T. forsythia||18 (60.0)||10 (33.3)||3 (10.0)|
|Any of the 4 markers||30 (100)||16 (53.3)||11 (36.7)|
|Total bacterial load (TBL)||nd||nd||34.1+14.8*|
nd =not determined
* TBL according to PadoTest protocol (Unknown sort)
Presence (Score Frequency) in Samples Analysed with the Checkerboard Method
|Bacterial Markers||Checkerboard Score >1 No of Samples (%)||Checkerboard Score >3 No of Samples (%)|
|P. intermedia||14 (46.7)||8 (26.7)|
|P. nigrescens||14 (46.7)||9 (30.0)|
|F. nucleatum||16 (53.3)||2 (6.7)|
|P. micra||25 (83.3)||10 (33.3)|
|C. rectus||24 (80.0)||1 (3.3)|
|E. corrodens||18 (60.0)||9 (30.0)|
|P. tannerae||30 (100)||15 (50.0)|
|F. alocis||29 (96.7)||16 (53.3)|
|P. endodontalis||17 (56.7)||8 (26.7)|
|1-12 of the markers||30 (100)||25 (83.3)|
Correlation (Agreement) Between Pado test 4.5 and Checkerboard Technique
The agreement (%) between the two methods was seemingly high (agreement >50%) for 3 of the marker bacteria (except T. denticola with an agreement of 19%), when score 1 was used as cut off point for the checkerboard method (Table 4). When score ≥ 3 was used, the agreement was even higher, explained by the increase of negative samples with both methods. In 17 (57%) samples the checkerboard was positive and the Pado test was negative and 4 of the samples were positive for more than 1 species (Table 4). The kappa statistics showed that this agreement was not at an acceptable level. The agreement for A. actinomycetemcomitans was 100% due to all samples were negative with both methods.
Agreement of Bacterial Markers with the Use of Prado Test 4.5 Versus Checkerboard in Pooled Samples (4 Sites) from 30 Patients with Chronic Periodontitis
|Bacterial species Score ≥1 Checkerboard||PadoTest + Checkerboard +||PadoTest + Checkerboard â€“||PadoTest â€“ Checkerboard +||PadoTest â€“ Checkerboard â€“||Aggreement %||Kappa Coefficient|
|Score ≥3 checkerboard|
* Kappa statistics calculated for checkerboard score 1 and higher
The five control samples in which 106 cells of the 4 target species were added to plaque samples from periodontally healthy students showed no agreement between the PadoTest 4.5 (Table 5). The PadoTest 4.5 identified the added P. gingivalis only and as present in low number (score 1) in one sample. The checkerboard showed score 5 for all 4 target species in all 5 samples.
Number of Positive Control Samples with Target Cells Added to Plaque Samples and Analyzed with PadoTest 4.5 and Checkerboard (Score ≥ 3)
|Bacterial Species||PadoTest 4.5||Checkerboard|
|No cells added||0||0|
The agreement for a positive outcome of 4 bacterial periodontal markers between the PadoTest 4.5 and the checkerboard DNA-DNA hybridization method was found to be low. When the score 3 (corresponding to 106 cells) was used as cut off level for the checkerboard this method disclosed more positive (53.3 %) samples than the PadoTest 4.5 (36.7 %) (Table 2). For each of the individual markers (target bacteria) the discrepancy between the two methods was even more pronounced. Only in two cases the two methods concomitantly disclosed the same bacteria (T.denticola). PadoTest 4.5 showed a negative outcome in 17 samples (57%) for which the checkerboard showed a positive outcome using the higher cut off level. This indicates a lower detection sensitivity of the PadoTest 4.5. On the other hand in 2 samples a higher score was found with PadoTest 4.5 than the checkerboard indicating methodological shortcomings may prevail with both methods.
For this study, patients were selected with moderate to advanced chronic periodontitis and with an expected high frequency of marker bacteria. The detection frequencies found indicated a low sensitivity of the PadoTest 4.5 method compared to the checkerboard method. The PadoTest 4.5 thus seems to underestimate the number of positive sites/individuals suggested by a high number of false negatives. From the control experiment where cells of the target bacteria were added to plaque samples taken from students it was obvious that the PadoTest 4.5 did not detect the marker bacteria to the same extent as the checkerboard method. It is possible that the difference in transport time and the time lapse of several days before analysis may explain some of the discrepancy between the methods. Presence of bacterial DNAses in the sample may degrade bacterial DNA leading to a lower level of target DNA. The checkerboard sample was processed immediately. PadoTest 4.5 has been compared with a similar DNA/RNA oligoprobe method MERDI  and showed a good agreement for three of the species P. gingivalis, T. forsythia and T. denticola. It was claimed  that the sensitivity of DNA/RNA oligonucleotide probes has a slightly lower sensitivity (104-105 cells) compared to whole genomic DNA/DNA hybridization methods such as the used checkerboard technique. The checkerboard has been calculated to have a detection level of 104 which can explain the higher detection rate of the marker bacteria . On the other hand, the specificity in the PadoTest 4.5 is supposed to be higher due to the risk for cross-hybridizations between related species using the checkerboard method and whole genomic probes . Cross-reactions lower the specificity and increase a risk for a higher frequency of false positives  when using the lower threshold level (Score 1) for detection. Consequently, using Score 3 as a more reliable level for a biological cut off gives a higher specificity. The number of diseased patients, which should be treated as indicated microbiologically was 16 (53.3%) using the checkerboard method. On the other hand, the remaining 14 patients are maybe false negatives at this cut off if the 4 marker bacteria are used. At the lower score (score 1) all 30 patients indicated a diseased flora. If the entire checkerboard panel of 12 bacteria is used, 25 patients were positives at score 3. This shows the necessity to expand the number of marker bacteria associated with disease. Clinically all 30 patients were untreated and defined as periodontally diseased. Consequently, chronic periodontitis should be regarded as a polymicrobial infection with a rather limited specificity if the red complex and A. actinomycetemcomitans are used as markers.
There is a risk for false negatives using only one test occasion. A repeated evaluation of each patient would probably ncrease the number of positives with both methods due to methodological variations in sampling, handling, and transportation and in the laboratory process. On the other hand repeated sampling and analyzing will extend the diagnostic period and become too expensive and will not be an option in the clinical practice.
No method is ideal for detecting periodontitis associated bacteria. The lack of a gold standard method makes it difficult to evaluate the best method for a reliable detection of the microflora and bacterial markers of deep periodontal pockets. That would speak for a more sensitive methodology such as a PCR based method with detection below 102 cells. On the other hand such sensitive method may certainly increase the number positives also in non-diseased pockets and patients. Thus a higher sensitivity leads to an increased number of false positives, a misguidance of diagnosis and maybe an overtreatment of the patient. If there is a certain threshold for which the true positives are high and false positives are low is not known.
The importance of various microorganisms in periodontitis progression has changed from the specific plaque hypothesis in the 80´s over clusters and complexes to the ecological plaque hypothesis proposed by Marsh . With this hypothesis as a basis for the choice of an appropriate method to disclose a diseased related microflora should include a panel of bacteria to cover the differences in the microbiological pattern from one patient to another. The checkerboard method with an extended panel would be more ideal and clinically useful .
Microbiological diagnosis was used in this study on untreated patients with chronic periodontitis with the purpose of disclosing many positives in order to get an appropriate comparison between the two methods. On the other hand, microbiological analysis has little to add for patients and sites that already by clinical criteria are diagnosed as diseased. Microbiological analysis would be more informative to perform as an adjunct to clinical diagnosis after treatment to evaluate whether site/patients has been sufficiently treated. Then a presence of markers at high scores would indicate a remaining disease associated flora and these sites should be retreated with the aim of changing the ecology of the periodontal pocket (pocket elimination by surgery and/or antibiotics). The Pado test 4.5 could not detect the bacteria placed in the control samples. We therefore challenge the utility of the test. A method for microbiological analysis that is cheap and convenient and that allow sampling of many sites and detecting many relevant markers but not necessarily be very sensitive should be used. The checkerboard methodology would fulfill many of these requirements.
This study was supported by the Public Dental Health Service, Västra Götaland, Sweden.