213 Volume 46, Number 4, December 2013 Research Report Prevotella intermedia and Porphyromonas gingivalis in dental caries with periapical granuloma Risya Cilmiaty,1 Afiono Agung Prasetyo,2,3,4 Khilyat Ulin Nur Zaini,3,4 Mandojo Rukmo,5 Suhartono Taat Putra6 and Widya Asmara7 1Department of Dental and Oral Disease, Faculty of Medicine, Universitas Sebelas Maret, Surakarta-Indonesia 2Department of Microbiology, Faculty of Medicine Universitas Sebelas Maret, Surakarta- Indonesia 3A-IGIC Research Group, Universitas Sebelas Maret, Surakarta-Indonesia 4Center of Biotechnology and Biodiversity Research and Development, Universitas Sebelas Maret, Surakarta-Indonesia 5Department of Conservative Dentistry, Faculty of Dentistry Universitas Airlangga, Surabaya-Indonesia 6Department of Pathobiology, Faculty of Medicine Universitas Airlangga, Surabaya-Indonesia 7 Department of Microbiology, Faculty of Veterinary Medicine Universitas Gadjah Mada, Yogyakarta-Indonesia abstract Background: Dental caries with necrotic pulp is a multifactorial disease that attacks enamel involving tooth pulp. The anaerobic bacteria infection in the pulp chamber could induce the formation of periapical granuloma. However, the presence of the most frequently anaerobic bacteria identified in apical periodontitis, Porphyromonas gingivalis and Prevotella intermedia, in periapical granuloma have not been confirmed. Purpose: The aims of study were to determine the presence of Porphyromonas gingivalis and Prevotella intermedia in dental caries with necrotic pulp and to determine its relation to periapical granuloma. Methods: Thirty-six patients of dental caries with necrotic pulp in Dr. Moewardi General Hospital in Surakarta, Indonesia were involved and classified into two groups, the group of patients with periapical granuloma and the group of patients without periapical granuloma. The caries tooth was extracted, and the chronic periapical tissue was swabbed and cultured on blood agar medium in anaerobic condition. The bacterial DNA was extracted from the positive cultures and subjected for Polymerase Chain Reaction (PCR). Results: Periapical granuloma was more likely found in women (OR 5.5, 95% CI=1.277-23.693; RR 2.5, 95% CI= 1.025-6.100). Black colonies bacteria were associated with periapical granuloma (OR 2.2, 95% CI=0.517-9.594; RR 1.5, 95% CI=0.655-3.623). Porphyromonas gingivalis and Prevotella intermedia were detected in group with or without periapical granuloma, however, only Prevotella intermedia was associated with periapical granuloma (OR 1.6, 95% CI=0.418-5.903; RR 1.3, 95% CI=0.653-2.393). Conclusion: The presence of Porphyromonas gingivalis and Prevotella intermedia in periapical granuloma were confirmed, however, only Prevotella intermedia were associated with periapical granuloma. Key words: Dental caries, necrotic pulp, periapical granuloma, Prevotella intermedia, Porphyromonas gingivalis abstrak Latar belakang: Karies gigi dengan pulpa nekrosis adalah penyakit multifaktorial yang menyerang enamel hingga ruang pulpa gigi. Infeksi bakteri anaerob di pulpa nekrosis dapat menginduksi pembentukan granuloma periapikal. Namun, keberadaan bakteri anaerob yang paling banyak ditemukan di periodontitis apikal, Porphyromonas gingivalis dan Prevotella intermedia, di granuloma periapikal masih perlu diteliti . Tujuan: Penelitian ini bertujuan meneliti keberadaan bakteri Porphyromonas gingivalis dan Prevotella intermedia, di karies gigi dengan pulpa nekrosis dan menganalisis kaitannya dengan granuloma periapikal. Metode: Tiga puluh enam pasien karies gigi dengan pulpa nekrosis di Rumah Sakit Umum Dr. Moewardi di Surakarta Indonesia dilibatkan dan diklasifikasikan dalam dua kelompok yaitu kelompok pasien dengan granuloma periapikal dan kelompok pasien tanpa granuloma periapikal. Gigi karies diekstraksi dan jaringan periapikal kronis diusap dan dikultur di media agar darah dalam kondisi anaerob. DNA bakteri diekstrak dari kultur yang positif dan dilakukan pemeriksaan dengan Polymerase Chain Reaction (PCR). Hasil: Granuloma periapikal lebih banyak ditemukan pada wanita (OR 5,5, 95% CI= 1,277-23,693; RR 2,5, 95% CI= 1,025-6,100). Koloni bakteri berwarna hitam diasosiasikan dengan granuloma periapikal (OR 2,2, 95% CI= 0,517-9,594; RR 1,5, 95% CI= 0,655-3,623). Porphyromonas gingivalis dan Prevotella 214 Dent. J. (Maj. Ked. Gigi), Volume 46, Number 4, December 2013: 213–217 Figure 1. The radiographic of tooth (A) without periapical granuloma, (B) with periapical granuloma (radiolucent). intermedia terdeteksi di jaringan karies dental dengan atau tanpa granuloma periapikal, namun hanya Prevotella intermedia yang diasosiasikan dengan granuloma periapikal (OR 1,6, 95% CI= 0,418-5,903; RR 1,3, 95% CI= 0,653-2,393). Simpulan: Porphyromonas gingivalis dan Prevotella intermedia ditemukan di granuloma periapikal, namun hanya Prevotella intermedia yang terkait langsung dengan granuloma periapikal. Kata kunci: Karies gigi, pulpa nekrosis, granuloma periapikal, Prevotella intermedia, Porphyromonas gingivalis Correspondence: Afiono Agung Prasetyo, c/o: Laboratorium Mikrobiologi Fakultas Kedokteran Universitas Sebelas Maret. Jl. Ir. Sutami 36 A Surakarta 57126, Indonesia. Email: afie.agp.la@gmail.com atau afieagp@yahoo.com introduction Dental caries is characterized by the progressive demineralization of enamel, following acid metabolism by the bacteria.1 The Indonesian population in range of age 15 years old or older, 71.2% had caries and 52.3% cases are untreated.2 The untreated dental caries could lead into necrotic pulp, and infection of the root canal system resulting a disruption at the apical.3-5 In some case, the tooth become sensitive that is caused by hyperemia, edema and inflammation of the apical periodontal.6 Endodontic and periodontal infections are commonly found preceded by caries process and associated with anaerobic bacteria, including that of the black-pigmented bacteria, Porphyromonas spp. and Prevotella spp.7-9 The most frequently identified in acute and chronic apical periodontitis are Porphyromonas gingivalis and Prevotella intermedia.9,10As gram-negative bacteria, both bacteria have lipopolysaccharide (LPS) in the cell wall, which can induce macrophage to release pro-inflammatory cytokines such as interleukin-8 (IL-8), IL-1β, interferon gamma (IFN-γ) and tumor necrosis factor alpha (TNF-α), causing tissue inflammation and bone resorption.7,11 The bacteria also have exopolysaccharides (EPS) which can enhance their virulence.12 Porphyromonas gingivalis (P. gingivalis) has occurred between family members13 and the bacteria presentation in periodontitis tissue also indicative of alveolar bone loss.14 Prevotella intermedia (P. intermedia) has ability to invade and evade the host innate response, so the possibility of infection will be increased.14 However, the role of both bacteria in periapical granuloma have not been elucidated. The presence of periodontal pathogen may affected by ethnic and geography.13 In Indonesia, the presence of P. gingivalis and P. intermedia are quite high in oral cavity, but there is lack information concerning the bacteria of chronic periapical tissue due to dental caries. The aims of study were to determine the presence of Porphyromonas gingivalis and Prevotella intermedia in dental caries with necrotic pulp and to determine its relation to periapical granuloma. materials and methods Chronic periapical tissue of permanent teeth from dental caries patients aged 17-57 years old with normal albumin levels and no anemia at Dr. Moewardi General Hospital, in Surakarta, Indonesia were assayed in the study. All patients had no antibiotic and or immunosuppressant therapy prior the tooth extraction. None patient had systemic disease. The sample size was 9 in every group, calculated as previously published.16 The sample used was doubled for each group. Finally, the total sample used was 36, were classified into two groups, with and without periapical granuloma, based on following dental radiographic criteria: well-circumscribed radiolucent periapical lesion attached to the root apex and measured less than 1 cm6,17 (Figure 1A and 1B). 9 Table 1. Age, gender, dental element and radiographic of dental caries patients in General Hospital Dr. Moewardi in Surakarta. With periapical granuloma (n= 18) Without periapical granuloma (n= 18) N % N % Age <21 5 27.8 4 22.2 21-30 1 5.6 2 11.1 31-40 8 44.4 2 11.1 41-50 2 11.1 8 44.4 >50 2 11.1 2 11.1 Gender Men 4 22.2 11 61.1 Women 14 77.8 7 38.9 Element Quadrant 1 0 - 1 5.6 Quadrant 2 4 22.2 7 38.9 Quadrant 3 7 38.9 3 16.7 Quadrant 4 7 38.9 7 38.9 Figure 1. The radiographic of tooth (A) without periapical granuloma, (B) with periapical granuloma (radiolucent). Periapical granuloma A B 215Cilmiaty, et al.: Prevotella intermedia and porphyromonas gingivalis in dental caries Figure 2. A sample of electrophoresis result from PCR assay to detect the presentation of P.. gingivalis’s DNA. PCR results from sample no. 19-25 were shown. M= VC 100bp Plus DNA Ladder (Vivantis, Selangor, Malaysia). P. gingivalis’s DNA was detected in sample no. 19-22 and 24-25. igure 3. A sample of electrophoresis result from PCR assay to detect the presentation of P. intermedia’s DNA. PCR results from sample no. 19-25 were shown. M= VC 100bp Plus DNA Ladder (Vivantis). P. intermedia’s DNA was detected in sample no. 19-22 and 24-25. Table 1. Age, gender, dental element and radiographic of dental caries patients in General Hospital Dr. Moewardi in Surakarta. With periapical granuloma (n= 18) Without periapical granuloma (n= 18) N % N % Age <21 5 27.8 4 22.2 21-30 1 5.6 2 11.1 31-40 8 44.4 2 11.1 41-50 2 11.1 8 44.4 >50 2 11.1 2 11.1 Gender Men 4 22.2 11 61.1 Women 14 77.8 7 38.9 Element Quadrant 1 0 - 1 5.6 Quadrant 2 4 22.2 7 38.9 Quadrant 3 7 38.9 3 16.7 Quadrant 4 7 38.9 7 38.9 10 Figure 2. A sample of electrophoresis result from PCR assay to detect the presentation of P.. gingivalis’s DNA. PCR results from sample no. 19-25 were shown. M= VC 100bp Plus DNA Ladder (Vivantis, Selangor, Malaysia). P. gingivalis’s DNA was detected in sample no. 19-22 and 24-25. Figure 3. A sample of electrophoresis result from PCR assay to detect the presentation of P. intermedia’s DNA. PCR results from sample no. 19-25 were shown. M= VC 100bp Plus DNA Ladder (Vivantis). P. intermedia’s DNA was detected in sample no. 19-22 and 24- 25. 600 bp M 19 20 21 22 23 24 25 M 19 20 21 22 23 24 25 400 bp 10 Figure 2. A sample of electrophoresis result from PCR assay to detect the presentation of P.. gingivalis’s DNA. PCR results from sample no. 19-25 were shown. M= VC 100bp Plus DNA Ladder (Vivantis, Selangor, Malaysia). P. gingivalis’s DNA was detected in sample no. 19-22 and 24-25. Figure 3. A sample of electrophoresis result from PCR assay to detect the presentation of P. intermedia’s DNA. PCR results from sample no. 19-25 were shown. M= VC 100bp Plus DNA Ladder (Vivantis). P. intermedia’s DNA was detected in sample no. 19-22 and 24- 25. 600 bp M 19 20 21 22 23 24 25 M 19 20 21 22 23 24 25 400 bp 216 Dent. J. (Maj. Ked. Gigi), Volume 46, Number 4, December 2013: 213–217 Approval was obtained from institutional ethical committee review boards of the Faculty of Medicine of Universitas Sebelas Maret and Dr. Moewardi General Hospital in Surakarta, Indonesia. Informed consent was obtained from all patients involved in the study. Data including age, gender, dental elements and dental radiographic were obtained from all patients. The caries tooth from each patient was extracted and the chronic periapical tissue was swabbed. The swab was then smeared on blood agar medium and incorporated into anaerobic jar with Gas generating kit (Thermo Scientific, Hampshire, United Kingdom) at 37° C for 7-14 days. The present study was focused on P. gingivalis and P. intermedia, so only the black-pigmented bacteria colonies’ DNA were extracted using a High Pure PCR Template Preparation Kit (Roche Molecular Diagnostics, Mannheim, Germany), according to the manufacturer’s instructions. The P. gingivalis’ DNA was detected using 5’ - AGG CTT CAG GCC ATA CTG CG - 3’ and 5’ - ACT GTT AGC AAC TAC CGA TGT - 3’ set primer. Briefly, the PCR reaction was performed by initial denaturation at 94°C for 5 minutes, 40 cycles of 94° C for 45 seconds, 66°C for 1 minute and 72° C for 2 minutes, followed by a final extension at 72° C for 10 minutes. The P. intermedia’s DNA was detected using 5’ - TTT GTT GGG GGG GAG TAA AGC - 3’ and 5’ - TCA ACA TCT CTG TAT CCT GCG T - 3’ set primer. The PCR reaction was performed by initial denaturation at 94° C for 5 minutes, 40 cycles of 94° C for 45 seconds, 62°C for 1 minute and 72° C for 2 minutes followed by a final extension at 72° C for 10 minutes. All PCR reaction was performed using Ready To Go PCR Bead (Promega, Buckinghamshire, United Kingdom). The PCR products were then subjected to electrophoresis in 1% agarose gels, stained with Ethidium Bromide, and visualized under ultraviolet illumination. The data was analyzed by SPSS version 16 software (SPSS, Chicago, IL). A 95% confidence interval (CI) was used for all data analysis. results Thirty-six dental caries patients (19 women and 17 men) with necrotic pulp were agreed to participate. The mean age of the patients studied was 35.7 years old (in range of 17 to 57 years old) and the most frequent element was derived from 4th quadrant (38.9%, 14/36). Periapical granuloma was found in 77.8% (14/18) women (OR 5.5, 95% CI= 1.277- 23.693; RR 2.5, 95% CI= 1.025-6.100) and 22.2% (4/18) men (OR 0.2; 95% CI= 0.042-0.783; RR 0.400; 95% CI= 0.164-0.976) (Table 1). Twenty-five of the 36 (69.4%) samples had black- pigmented bacteria. These bacteria were identified in 77.8% (14/18) periapical granuloma’s samples (OR 2.2, 95% CI= 0.517-9.594; RR 1.3, 95% CI=0.817-1.983) and 61.1% (11/18) of non periapical granuloma’s samples (OR 0.4, 95% CI= 0.104-1.934; RR 0.8, 95% CI= 0.504-1.224). P. gingivalis’s DNA was detected (Figure 2) in 64.3% (9/14) of black colonies from periapical granuloma’s samples and 63.6% (7/11) of black colonies from non periapical granuloma’s samples (p= 1.00) and had no association with periapical granuloma formation (OR 1.0, 95% CI= 0.271- 3.694). P. intermedia’s DNA was detected (Figure 3) in 57.1% (8/14) of black colonies from periapical granuloma’s samples (OR 1.6, 95%CI= 0.418-5.903; RR 1.3, 95% CI=0.653-2.393). Co-infection of P. gingivalis and P. intermedia was detected only in 33.3% (6/18) periapical granuloma’s samples (OR 1.0, 95% CI= 0.250-3.999; RR 1.0, 95% CI= 0.500-1.999). discussion Dental caries with necrotic pulp is a multi-causal disease that attacks the enamel and reach tooth pulp chamber, causing destruction structure of the tooth, and open the door to bacterial infection.1,4 The bacterial infection can activate host immune response to isolate and eradicate microorganisms or chronic irritants, causing periapical granuloma, an inflammatory reaction in the apex of non-vital tooth. The inflammatory tissue of periapical granuloma (containing macrophages, polymorphonuclear leukocytes and lymphocytes) is covered by epithelial cells and ultimately results in destruction of the alveolar bone surrounding the tooth.7,8 The P. gingivalis and P. intermedia already known dominant in primary endodontic infection due to its content, LPS.8 LPS induces pulp fibroblast and osteoblast to produce IL-8. The IL-8 then attracts and activates polymorphonuclear leukocytes to surround and kills the bacteria, stimulates osteoclast activity and causes pain symptom in periapical lesion. The LPS also activates macrophages through CD14 receptor to produce pro-inflammatory mediators, IL-1 and TNF-α. IL-1 then induces the production of IL-12, TNF-α, IFN-γ and IL-1 itself. In human periapical lesion, IL-1β, one variant of IL-1, is predominant and stimulates T-lymphocytes; enhances bone resorption and inhibits bone formation. The macrophages and T-lymphocytes in the inflammatory tissue also produce TNF-α. The TNF-α activates the macrophages, T-lymphocytes and natural killer cells and also stimulates bone resorption. However, if the bacteria (P. gingivalis and or P. intermedia) are difficult to be eliminated, T-lymphocyte would lead B-lymphocyte activation, to synthesize the antibody to bacterial antigen. The bacterial-antibody formation will attract activated- macrophages to surround and phagocyte the formation. Finally, all reaction will causes periapical granuloma formation in the root of the tooth.7,18-20 P. gingivalis and P. intermedia are frequently detected in intraoral7-9 and the numbers of these bacteria are increase in the disease site compared with healthy site.9 In the present study, P. gingivalis and P. intermedia could be isolated from dental caries tissue, both of with and without periapical granuloma, consistent with previous reports,7,8,21 217Cilmiaty, et al.: Prevotella intermedia and porphyromonas gingivalis in dental caries however, only P. intermedia was associated with periapical granuloma. In the present study, periapical granuloma was more likely found in women than in men. LPS of bacteria induces production of IL-1β and TNF-α.11 These pro- inflammatory cytokines could be influenced by sex hormone. Sex hormone, especially estrogen, already known significantly reduces P. gingivalis bacteria compared with P. intermedia.21 Testosterone also could reduce the expression of TNF-α and IL-1β, so reduce the inflammation process.9,21-23 The study revealed that the presence of P. gingivalis and P. intermedia were confirmed in periapical granuloma and could be isolated in dental caries tissue; however, only P. intermedia had association with periapical granuloma. Further studies are needed to confirm and extend our findings. acknowledgement This work was supported partially by grants from the APBN/DIPA UNS (No. 159a/UN27.11/PN/2013) and BOPTN UNS (No. 165/UN27.11/PN/2013). references 1. Deljo E, Cavaljuga S, Mescovic B. Prevalence of dental caries in the municipality gorazde during the period 2007-2012. Mater Sociomed 2013; 25(3): 163-6. 2. The Indonesian household heath survey. Health profile of Indonesian 2004. Jakarta: Ministry of health republic of Indonesia; 2006. p. 19. 3. Bjørndal L. 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