Determinasi Jumlah Bakteri Porphyromonas Gingivalis ATCC 33277 pada Saliva Anak Stunting

Authors

  • Nadhifah Salsabila Universitas Andalas
  • Nila Kasuma Universitas Andalas
  • Eti Yerizel Universitas Andalas

DOI:

https://doi.org/10.35790/eg.v12i1.47864

Abstract

Abstract: Nutrition affects the immune system and the development of oral health, including periodontal tissue health. Stunted children experience decreased salivary flow rate causing the growth of microorganisms that cause periodontal disease. Porphyromonas gingivalis is referred to one of the keystone pathogens in the development of periodontal disease. This study aimed to identify the number of Porphyromonas gingivalis ATCC 33277 bacteria in stunted child saliva. This was a descriptive study with a cross sectional design. Prior to collection, subjects were instructed to rinse their mouth for 30 seconds using distilled water, saliva was collected with draining method, then 2 mL of saliva was taken, and DNA was isolated from Porphyromonas gingivalis ATCC 33277. DNA amplification and DNA calculation of Porphyromonas gingivalis ATCC 33277 were performed by using Real-time PCR. The results obtained 23 stunted children age 6-12 years as subjects. The average number of Porphyromonas gingivalis ATCC 33277 bacteria in stunting child saliva was 230.8 x 106 ± 320.1 x 106 CFU/ml. In conclusion, the number of Porphyromonas gingivalis ATCC 33277 is higher in stunted children saliva than in normal child saliva.

Keywords: stunted children; Porphyromonas gingivalis ATCC 33277 bacteria; periodontal diseases

 

Abstrak: Gizi memengaruhi sistem pertahanan dan perkembangan kesehatan rongga mulut termasuk kesehatan jaringan periodontal. Anak stunting mengalami penurunan laju alir saliva yang menyebabkan pertumbuhan mikroorganisme penyebab penyakit periodontal, antara lain Porphyromonas gingivalis sebagai salah satu keystone pathogens dalam perkembangan penyakit periodontal. Penelitian ini bertujuan untuk menentukan jumlah bakteri Porphyromonas gingivalis ATCC 33277 pada saliva anak stunting. Jenis penelitian ialah deskriptif dengan desain potong lintang. Sebelum pengambilan saliva, subjek diinstruksikan berkumur selama 30 detik menggunakan akuades. Pengambilan saliva dengan metode draining selama 10 menit, saliva terkumpul sebanyak 2 mL, dan dilakukan isolasi DNA bakteri Porphyromonas gingivalis ATCC 33277. Amplifikasi DNA dan perhitungan jumlah DNA bakteri Porphyromonas gingivalis ATCC 33277 dilakukan menggunakan Real-time PCR. Hasil penelitian mendapatkan 23 anak stunting dengan usia 6-12 tahun.  Rerata jumlah bakteri Porphyromonas gingivalis ATCC 33277 pada saliva anak stunting 230,8x106±320,1x106 CFU/ml yang lebih tinggi daripada anak sehat yaitu 180,8x106±201,8x106 CFU/mL Simpulan penelitian ini ialah rerata jumlah bakteri Porphyromonas  gingivalis ATCC 33277 pada saliva anak stunting lebih tinggi daripada saliva anak  normal.

Kata kunci: anak stunting; bakteri Porphyromonas gingivalis ATCC 33277; penyakit periodontal

Author Biographies

Nadhifah Salsabila, Universitas Andalas

Program Magister Ilmu Biomedis Fakultas Kedokteran Universitas Andalas, Padang, Indonesia

Nila Kasuma, Universitas Andalas

Fakultas Kedokteran Gigi Universitas Andalas, Padang, Indonesia

Eti Yerizel, Universitas Andalas

Departemen Biokimia Fakultas Kedokteran Universitas Andalas, Padang, Indonesia

References

Vilcins D, Sly PD, Jagals P. Environmental risk factors associated with child stunting: A systematic review of the literature. Ann Glob Heal. 2018;84(4):551–62. Doi: 10.29024/aogh.2361

Sjarif DR, Yuliarti K, Iskandar WJ. Daily consumption of growing-up milk is associated with less stunting among indonesian toddlers. Med J Indones. 2019;28(1):70–6. Doi: 10.13181/mji.v28i1.2607

Yustisia Y, Anmaru R, Laksono B. The influencing factor analysis of stunting incidence in children aged 24-59 months at Kedung Jati Village. Public Heal Perspect J. 2019;4(2):116–21. Available from: http://journal.unnes.ac.id/sju/index.php/phpj.

Raiten DJ, Bremer AA. Exploring the nutritional ecology of stunting: new approaches to an old problem. Nutrients. 2020;12(2):371. Doi: 10.3390/nu12020371.

Bourke CD, Berkley JA, Prendergast AJ. Immune dysfunction as a cause and consequence of malnutrition. Trends Immunol. 2016;37(6):386–98. Doi: 10.1016/j.it.2016.04.003.

Akbar HF, Pratiwi R, Hardiana SNAN. Oral hygiene and oral health related quality of life of children with stunting in Indonesia. Int J Dent Oral Sci (IJDOS). 2020;7(1):711–7. Doi: 10.19070/2377-8075-20000140.

Madhusudhan KS, Madhusudhan PMR. Malnutrition -a risk for oral health. Internatioal J Sci Res. 2019;8(4):74-6. Doi: 10.13140/RG.2.2.24176.10249

Hashem DS, El-Bayoumy SY, Fahmy WA, El Malt MA. Effect of childhood malnutrition on salivary flow and pH. ADJ-for Grils. 2016;3(2):141–5.

Rytter MJH, Kolte L, Briend A, Friis H, Christensen VB. The immune system in children with malnutrition - a systematic review. PLoS One. 2014;9(8):e105017. Doi: 10.1371/journal.pone.0105017

Popova C, Dosseva-Panova V, Panov V. Microbiology of periodontal diseases. A review. Biotechnol Biotechnol Equip. 2013;27(3):3754–9. Doi: 10.5504/BBEQ.2013.0027

Reddy S. Essentials of Clinical Periodontology and Periodontics. 2018. New Delhi: The Health Sciences Publisher. Doi:10.5005/jp/books/18042.

Newman MG, Takei H, Klokkevold PR, Carranza FA. Newman and Carranza’s Clinical Periodontology (13th ed). Elsevier Inc.; 2017.

Nakano K, Ooshima T, Amano A. Periodontal Diseases in Children and Adolescents. New York: Nova Science Publisher; 2011

Lakshmi A, Rekha V, Sharmin D, Annamalai S, Baghkomeh PN. Periodontal diseases in children – a literature review. Int J Curr Res. 2017;9(5):51269–75.

Aydin K, Ekinci FY, Korachi M. Expression profiles of TGF-β and TLR pathways in porphyromonas gingivalis and prevotella intermedia challenged osteoblasts. Jundishapur J Microbiol. 2015;8(4):0–7. Doi: 10.5812/jjm.8(4)2015.17920.

Bengtsson T, Khalaf A, Khalaf H. Secreted gingipains from Porphyromonas gingivalis colonies exert potent immunomodulatory effects on human gingival fibroblasts. Microbiol Res. 2015;178:18–26. Doi: 10.1016/j.micres.2015.05.008.

Romero-Lastra P, Sánchez MC, Llama-Palacios A, Figuero E, Herrera D, Sanz M. Gene expression of Porphyromonas gingivalis ATCC 33277 when growing in an in vitro multispecies biofilm. PLoS One. 2019;14(8):1–18. Doi: 10.1371/journal.pone.0221234

Tribble GD, Kerr JE, Wang BY. Genetic diversity in the oral pathogen Porphyromonas gingivalis: Molecular mechanisms and biological consequences. Future Microbiol. 2013;8(5):607–20. Doi: 10.2217/fmb.13.30.

Al-Ghuitaimel H, Riba H, Al-Kahtani S, Al-Duhaimi S. Common Periodontal diseases of children and adolescents. Int J Dent. 2014;2014:850674. Doi: 10.1155/2014/850674

Reddy S. Essentials of Clinical Periodontology and Periodontics.; 2011. Jaypee Brothers Medical Publishers Pvt. Doi: 10.5005/jp/books/11392

Tada A, Miura H. The relationship between vitamin C and periodontal diseases: A systematic review. Int J Environ Res Public Health. 2019;16(14):2472. Doi: 10.3390/ijerph16142472.

Olsen I, Yamazaki K. Can oral bacteria affect the microbiome of the gut? J Oral Microbiol. 2019;11(1):1586422. Doi: 10.1080/20002297.2019.1586422.

Kato T, Yamazaki K, Nakajima M, Date Y, Kikuchi J, Hase K. Oral administration of Porphyromonas gingivalis alters the gut microbiome and serum metabolome . mSphere. 2018;3(5):e00460-18. Doi: 10.1128/msphere.00460-18.

Costalonga M, Herzberg MC. The oral microbiome and the immunobiology of periodontal disease and caries. Immunol Lett. 2014;162(2):22–38. Doi: 10.1016/j.imlet.2014.08.017.

Bourke CD, Jones KDJ, Prendergast AJ. Current understanding of innate immune cell dysfunction in childhood undernutrition. Front Immunol. 2019;10(July):1728. Doi: 10.3389/fimmu.2019.01728.

Sakanaka A, Takeuchi H, Kuboniwa M, Amano A. Dual lifestyle of Porphyromonas gingivalis in biofilm and gingival cells. Microb Pathog. 2016;94:42–7. Doi: 10.1016/j.micpath.2015.10.003.

Cornejo Ulloa P, van der Veen MH, Krom BP. Review: modulation of the oral microbiome by the host to promote ecological balance. Odontology. 2019;107(4):437–48. Doi: 10.1007/s10266-019-00413-x.

Darout IA, Albandar JM, Skaug N. Correlations between bacterial levels in autologous subgingival plaque and saliva of adult Sudanese. Clin Oral Investig. 2002;6(4):210-6. Doi:10.1007/s00784-002-0177-0.

Downloads

Published

2023-08-05

How to Cite

Nadhifah Salsabila, Kasuma, N., & Yerizel, E. (2023). Determinasi Jumlah Bakteri Porphyromonas Gingivalis ATCC 33277 pada Saliva Anak Stunting. E-GiGi, 12(1), 26–31. https://doi.org/10.35790/eg.v12i1.47864

Issue

Section

Articles