The oral microbiota of patients with recurrent aphthous stomatitis

Journal of Oral Microbiology

Volumn 6, Issue , 2014, Pages 1-11

  Bankvall, Maria ^a   Sjöberg, Fei ^a   Gale, Gita ^a   Wold, Agnes ^a   Jontell, Mats ^a   Östman, Sofia ^a  

^a UNIVERSITY OF GOTHENBURG   (Sweden)

Author keywords

Oral bacteria; Oral cavity; Oral mucosa; Oral mucosal disease; Oral ulceration; Terminal restriction fragment length polymorphism

Indexed keywords

RNA 16S;

ADOLESCENT; ADULT; AGED; ANIMAL TISSUE; APHTHOUS STOMATITIS; ARTICLE; CASE CONTROL STUDY; CHILD; CONTROLLED STUDY; DISCRIMINANT ANALYSIS; DNA EXTRACTION; ENZYME METABOLISM; FEMALE; GENE AMPLIFICATION; GENE SEQUENCE; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MOUTH FLORA; NONHUMAN; ORAL BIOPSY; PATHOGENESIS; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SPECIES RICHNESS;

EID: 84930658510     PISSN: None     EISSN: 20002297     Source Type: Journal    
DOI: 10.3402/jom.v6.25739     Document Type: Article

References (42)

1. Jurge S, Kuffer R, Scully C, Porter SR. Mucosal disease series. Number VI. Recurrent aphthous stomatitis. Oral Dis 2006; 12: 1-21.
2. Barile MF, Graykowski EA, Driscoll EJ, Riggs DB. L Form of bacteria isolated from recurrent aphthous stomatitis lesions. Oral Surg Oral Med Oral Pathol 1963; 16: 1395-402.
3. Ship II. Inheritance of aphthous ulcers of the mouth. J Dent Res 1965; 44: 837-44.
4. Hoover CI, Greenspan JS. Immunochemical comparison of cellwall antigens of various viridans streptococci, including strain 2A2_3 hot from recurrent oral aphthous ulceration in man. Arch Oral Biol 1983; 28: 917-22.
5. Narikawa S, Suzuki Y, Takahashi M, Furukawa A, Sakane T, Mizushima Y. Streptococcus oralis previously identified as uncommon Streptococcus sanguis in Behcet's disease. Arch Oral Biol 1995; 40: 685-90.
6. Lehner T, Lavery E, Smith R, van der Zee R, Mizushima Y, Shinnick T. Association between the 65-kilodalton heat shock protein, Streptococcus sanguis, and the corresponding antibodies in Behcet's syndrome. Infect Immun 1991; 59: 1434-41.
7. Leimola-Virtanen R, Happonen RP, Syrjanen S. Cytomegalovirus (CMV) and Helicobacter pylori (HP) found in oral mucosal ulcers. J Oral Pathol Med 1995; 24: 14-17.
8. Greenspan JS, Gadol N, Olson JA, Hoover CI, Jacobsen PL, Shillitoe EJ, et al. Lymphocyte function in recurrent aphthous ulceration. J Oral Pathol 1985; 14: 592-602.
9. Khor B, Gardet A, Xavier RJ. Genetics and pathogenesis of inflammatory bowel disease. Nature 2011; 474: 307-17.
10. Berry D, Reinisch W. Intestinal microbiota: a source of novel biomarkers in inflammatory bowel diseases? Best Pract Res Clin Gastroenterol 2013; 27: 47-58.
11. Liu WT, Marsh TL, Cheng H, Forney LJ. Characterization of microbial diversity by determining terminal restriction fragment length polymorphisms of genes encoding 16S rRNA. Appl Environ Microbiol 1997; 63: 4516-22.
12. Donatsky O, Justesen T, Lind K, Vestergaard BF. Microorganisms in recurrent aphthous ulcerations. Scand J Dent Res 1977; 85: 426-33.
13. Marchini L, Campos MS, Silva AM, Paulino LC, Nobrega FG. Bacterial diversity in aphthous ulcers. Oral Microbiol Immunol 2007; 22: 225-31.
14. Jontell M, Mattsson U, Torgersson O. MedView: an instrument for clinical research and education in oral medicine. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2005; 99: 55-63.
15. Sjoberg F, Nowrouzian F, Rangel I, Hannoun C, Moore E, Adlerberth I, et al. Comparison between Terminal-Restriction Fragment Length Polymorphism (T-RFLP) and quantitative culture for analysis of infants' gut microbiota. J Microbiol Methods 2013; 94: 37-46.
16. Gutell RR. Collection of small subunit (16S- and 16S-like) ribosomal RNA structures: 1994. Nucleic Acids Res 1994; 22: 3502-7.
17. Bikandi J, San Millan R, Rementeria A, Garaizar J. In silico analysis of complete bacterial genomes: PCR, AFLP-PCR and endonuclease restriction. Bioinformatics 2004; 20: 798-9.
18. Abdo Z, Schuette UM, Bent SJ, Williams CJ, Forney LJ, Joyce P. Statistical methods for characterizing diversity of microbial communities by analysis of terminal restriction fragment length polymorphisms of 16S rRNA genes. Environ Microbiol 2006; 8: 929-38.
19. Westerhuis JA, van Velzen EJ, Hoefsloot HC, Smilde AK. Multivariate paired data analysis: multilevel PLSDA versus OPLSDA. Metabolomics 2010; 6: 119-28.
20. Tuomisto H. A consistent terminology for quantifying species diversity? Yes, it does exist. Oecologia 2010; 164: 853-60.
21. Baccaglini L, Lalla RV, Bruce AJ, Sartori-Valinotti JC, Latortue MC, Carrozzo M, et al. Urban legends: recurrent aphthous stomatitis. Oral Dis 2011; 17: 755-70.
22. Sakamoto M, Takeuchi Y, Umeda M, Ishikawa I, Benno Y. Application of terminal RFLP analysis to characterize oral bacterial flora in saliva of healthy subjects and patients with periodontitis. J Med Microbiol 2003; 52: 79-89.
23. Aas JA, Paster BJ, Stokes LN, Olsen I, Dewhirst FE. Defining the normal bacterial flora of the oral cavity. J Clin Microbiol 2005; 43: 5721-32.
24. Kang JG, Kim SH, Ahn TY. Bacterial diversity in the human saliva from different ages. J Microbiol 2006; 44: 572-6.
25. Nasidze I, Li J, Quinque D, Tang K, Stoneking M. Global diversity in the human salivary microbiome. Genome Res 2009; 19: 636-43.
26. Wade WG. The oral microbiome in health and disease. Pharmacol Res 2013; 69: 137-43.
27. Costello EK, Lauber CL, Hamady M, Fierer N, Gordon JI, Knight R. Bacterial community variation in human body habitats across space and time. Science 2009; 326: 1694-7.
28. Graykowski EA, Barile MF, Lee WB, Stanley HR, Jr. Recurrent aphthous stomatitis. Clinical, therapeutic, histopathologic, and hypersensitivity aspects. JAMA 1966; 196: 637-44.
29. Donatsky O, Bendixen G. In vitro demonstration of cellular hypersensitivity to strep 2A in recurrent aphthous stomatitis by means of the leucocyte migration test. Acta Allergol 1972; 27: 137-44.
30. Donatsky O, Dabelsteen E. An immunofluorescence study on the humoral immunity to Strep. 2A in recurrent aphthous stomatitis. Acta Pathol Microbiol Scand Section B: Microbiol Immunol 1974; 82: 107-12.
31. Oppenheim JJ, Francis TC. The role of delayed hypersensitivity in immunological processes and its relationship to aphthous stomatitis. J Periodontol 1970; 41: 205-9.
32. Martin DK, Nelms DC, Mackler BF, Peavy DL. Lymphoproliferative responses induced by streptococcal antigens in recurrent aphthous stomatitis and Behcet's syndrome. Clin Immunol Immunopathol 1979; 13: 146-55.
33. Birek C, Grandhi R, McNeill K, Singer D, Ficarra G, Bowden G. Detection of Helicobacter pylori in oral aphthous ulcers. J Oral Pathol Med 1999; 28: 197-203.
34. Albanidou-Farmaki E, Giannoulis L, Markopoulos A, Fotiades S, Aggouridaki X, Farmakis K, et al. Outcome following treatment for Helicobacter pylori in patients with recurrent aphthous stomatitis. Oral Dis 2005; 11: 22-6.
35. Tas DA, Yakar T, Sakalli H, Serin E. Impact of Helicobacter pylori on the clinical course of recurrent aphthous stomatitis. J Oral Pathol Med 2013; 42: 89-94.
36. Porter SR, Barker GR, Scully C, Macfarlane G, Bain L. Serum IgG antibodies to Helicobacter pylori in patients with recurrent aphthous stomatitis and other oral disorders. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1997; 83: 325-8.
37. Mravak-Stipetic M, Gall-Troselj K, Lukac J, Kusic Z, Pavelic K, Pavelic J. Detection of Helicobacter pylori in various oral lesions by nested polymerase chain reaction (PCR). J Oral Pathol Med 1998; 27: 1-3.
38. Mansour-Ghanaei F, Asmar M, Bagherzadeh AH, Ekbataninezhad S. Helicobacter pylori infection in oral lesions of patients with recurrent aphthous stomatitis. Med Sci Monit 2005; 11: CR576-9.
39. Wang M, Karlsson C, Olsson C, Adlerberth I, Wold AE, Strachan DP, et al. Reduced diversity in the early fecal microbiota of infants with atopic eczema. J Allergy Clin Immunol 2008; 121: 129-34.
40. Abrahamsson TR, Jakobsson HE, Andersson AF, Bjorksten B, Engstrand L, Jenmalm MC. Low diversity of the gut microbiota in infants with atopic eczema. J Allergy Clin Immunol 2012; 129: 434-40, 440. e1-2.
41. Ismail IH, Oppedisano F, Joseph SJ, Boyle RJ, Licciardi PV, Robins-Browne RM, et al. Reduced gut microbial diversity in early life is associated with later development of eczema but not atopy in high-risk infants. Pediatr Allergy Immunol 2012; 23: 674-81.
42. Pandey J, Ganesan K, Jain RK. Variations in T-RFLP profiles with differing chemistries of fluorescent dyes used for labeling the PCR primers. J Microbiol Methods 2007; 68: 633-8.