The state of microbiocenosis in patients with bullous lesions of the oral mucosa according to the PCR diagnostic method

Authors

  • O.F. Rabinovich 1, PhD in Medical Sciences, head of the Oral mucosa diseases Department
    ORCID ID: 0000-0002-1018-9017
  • I.M. Rabinovich 1, PhD in Medical Sciences, full professor of the Therapeutic dentistry Division and the Caries and endodontics Department
    ORCID ID: 0000-0001-8539-814X
  • E.S. Abramova 1, PhD in Medical Sciences, senior researcher of the Oral mucosa diseases Group
  • K.V. Umarova 1, PhD in Medical Sciences, researcher of the Oral mucosa diseases Group
    ORCID ID: 0000-0003-3985-8058
  • 1 Central research institute of dental and maxillofacial surgery, 119021, Moscow, Russia

Abstract

Autoimmune bullous lesions are a group of inflammatory diseases affecting the skin and mucous membranes, with a severe chronic course. Microorganisms that colonize the skin and mucous membranes and make up the microbiome can influence the course of inflammatory diseases. The purpose of this study was to investigate the oral mucosal microbiome in patients with bullous lesions by polymerase chain reaction (PCR).
Materials and methods.
We studied scrapings from the surface of lesions of the oral mucosa in 25 patients with pemphigus vulgaris, 35 patients with pemphigoid bullosa and 40 people with bullous form of ruber lichen planus. Fusobacterium, Str. pneumoniae, Candida albicans, Ureaplasma, and 3 types of viruses: human papilloma virus 16, Epstein-Barr virus, and cytomegalovirus were determined.
Results.
Str. pneumoniae was detected most frequently in patients with bullous lesions: in 42.5% of cases in patients with pemphigus vulgaris, in 58.3% of cases in patients with pemphigoid bullosa and in 68.8% of cases in patients with bullous form of ruber lichen planus. Candida albicans was second most frequently detected: in 33.0% of patients with pemphigoid bullosa, in 28.6% of patients with pemphigus vulgaris, and in 25.0% of patients with bullous form of ruber lichen planus. Among viruses, Epstein—Barr virus was most frequently detected in patients with bullous lesions of oral mucosa (in 66.7, 75, and 50% of patients with pemphigus vulgaris, pemphigoid bullosa, and bullous form of ruber lichen planus, respectively). However, cytomegalovirus was practically undetectable in scrapes in patients with pemphigoid bullosa and ruber lichen planus. The frequency of detection of associations of bacteria, fungi and viruses in scrapes in patients with pemphigoid bullosa reached 38.5%.
Conclusions.
The obtained data indicate a pronounced violation of oral microbiocenosis and microbial dysbiosis of the oral mucosa in patients with bullous lesions.

Key words:

oral mucosa, bullous lesions, microbiocenosis, microbiota, microbiome, polymerase chain reaction

For Citation

[1]
Rabinovich O.F., Rabinovich I.M., Abramova E.S., Umarova K.V. The state of microbiocenosis in patients with bullous lesions of the oral mucosa according to the PCR diagnostic method. Clinical Dentistry (Russia).  2021; 24 (3): 47—51

References

  1. Rashid H., Lamberts A., Diercks G.F.H., Pas H.H., Meijer J.M., Bolling M.C., Horváth B. Oral lesions in autoimmune bullous diseases: An overview of clinical characteristics and diagnostic algorithm. Am J Clin Dermatol. 2019; 20 (6): 847—861. PMID: 31313078
  2. Schmidt E., Zillikens D. Pemphigoid diseases. Lancet. 2013; 381 (9863): 320—32. PMID: 23237497
  3. Mustafa M.B., Porter S.R., Smoller B.R., Sitaru C. Oral mucosal manifestations of autoimmune skin diseases. Autoimmun Rev. 2015; 14 (10): 930—51. PMID: 26117595
  4. Sadik C.D., Schmidt E. Resolution in bullous pemphigoid. Semin Immunopathol. 2019; 41 (6): 645—654. PMID: 31732776
  5. Bystryn J.C., Rudolph J.L. Pemphigus. Lancet. 2005; 366 (9479): 61—73. PMID: 15993235
  6. Kridin K. Subepidermal autoimmune bullous diseases: overview, epidemiology, and associations. Immunol Res. 2018; 66 (1): 6—17. PMID: 29159697
  7. Hübner F., Langan E.A., Recke A. Lichen planus pemphigoides: From lichenoid inflammation to autoantibody-mediated blistering. Front Immunol. 2019; 10: 1389. PMID: 31312198
  8. Kubanov A.A., Znamenskaya L.F., Abramova T.V., Svishchenko S.I. Revisited diagnostics of true (acantholytic) pemphigus. Vestnik Dermatologii i Venerologii. 2014; 6: 121—130 (In Russ.). eLIBRARY ID: 22842757
  9. Bertram F., Bröcker E.B., Zillikens D., Schmidt E. Prospective analysis of the incidence of autoimmune bullous disorders in Lower Franconia, Germany. J Dtsch Dermatol Ges. 2009; 7 (5): 434—440. PMID: 19170813
  10. Bernard P., Vaillant L., Labeille B., Bedane C., Arbeille B., Denoeux J.P., Lorette G., Bonnetblanc J.M., Prost C. Incidence and distribution of subepidermal autoimmune bullous skin diseases in three French regions. Bullous Diseases French Study Group. Arch Dermatol. 1995; 131 (1): 48—52. PMID: 7826096
  11. Wong S.N., Chua S.H. Spectrum of subepidermal immunobullous disorders seen at the National Skin Centre, Singapore: a 2-year review. Br J Dermatol. 2002; 147 (3): 476—480. PMID: 12207586
  12. Zillikens D., Wever S., Roth A., Weidenthaler-Barth B., Hashimoto T., Bröcker E.B. Incidence of autoimmune subepidermal blistering dermatoses in a region of central Germany. Arch Dermatol. 1995; 131 (8): 957—958. PMID: 7669112
  13. Bulgakova A.I., Hismatullina Z.R., Gabidullina G.F. Prevalence, etiology and clinical manifestations of blistering disease. Bashkortostan Medical Journal. 2016; 11 (6): 86—90 (In Russ.). eLIBRARY ID: 27508497
  14. Miyamoto D., Santi C.G., Aoki V., Maruta C.W. Bullous pemphigoid. An Bras Dermatol. 2019; 94 (2): 133—146. PMID: 31090818
  15. Huang Y.H., Kuo C.F., Chen Y.H., Yang Y.W. Incidence, mortality, and causes of death of patients with pemphigus in Taiwan: a nationwide population-based study. J Invest Dermatol. 2012; 132 (1): 92—7. PMID: 21850023
  16. Chen J., Mao X., Zhao W., Zhang B., Chen X., Yu C., Zheng Z., Jin H., Li L. Assessment of the characteristics and associated factors of infectious complications in bullous pemphigoid. Front Immunol. 2020; 11: 1607. PMID: 32793235
  17. Rabinovich O.F., Rabinovich I.M., Abramova E.S. Epidemiology, etiology, pathogenesis of oral mucosa bullous lesions. Stomatology. 2019; 98 (2): 71—5 (In Russ.). eLIBRARY ID: 37785554
  18. Kilian M., Chapple I.L., Hannig M., Marsh P.D., Meuric V., Pedersen A.M., Tonetti M.S., Wade W.G., Zaura E. The oral microbiome an update for oral healthcare professionals. Br Dent J. 2016; 221 (10): 657—666. PMID: 27857087
  19. Sharma N., Bhatia S., Sodhi A.S., Batra N. Oral microbiome and health. AIMS Microbiol. 2018; 4 (1): 42—66. PMID: 31294203
  20. Lamont R.J., Koo H., Hajishengallis G. The oral microbiota: dynamic communities and host interactions. Nat Rev Microbiol. 2018; 16 (12): 745—759. PMID: 30301974
  21. Rabinovich O.F., Rabinovich I.M., Abramova E.S. Appearance of disbacteriosis and candidosis in different diseases of oral mucosa. Clinical Dentistry (Russia). 2011; 3 (59): 48—51 (In Russ.). eLIBRARY ID: 22625365
  22. Petruchina N.B., Rabinovich I.M., Zorina O.A. Violation of the microbiocenosis of the oral cavity in patients with metabolic syndrome (part I). The Dental Institute. 2014; 1 (62): 54—57 (In Russ.). eLIBRARY ID: 22133903
  23. Gordeev A.V., Galushko E.A., Savushkina N.M. Disbiosis of upper digestive tract a harbinger of rheumatoid arthritis? Experimental and Clinical Gastroenterology Journal. 2019; 3 (163): 10—15 (In Russ.). eLIBRARY ID: 40457778
  24. Mark Welch J.L., Rossetti B.J., Rieken C.W., Dewhirst F.E., Borisy G.G. Biogeography of a human oral microbiome at the micron scale. Proc Natl Acad Sci U S A. 2016; 113 (6): E791—800. PMID: 26811460
  25. Berg G., Rybakova D., Fischer D., Cernava T., Vergès M.C., Charles T., Chen X., Cocolin L., Eversole K., Corral G.H., Kazou M., Kinkel L., Lange L., Lima N., Loy A., Macklin J.A., Maguin E., Mauchline T., McClure R., Mitter B., Ryan M., Sarand I., Smidt H., Schelkle B., Roume H., Kiran G.S., Selvin J., Souza R.S.C., van Overbeek L., Singh B.K., Wagner M., Walsh A., Sessitsch A., Schloter M. Microbiome definition re-visited: old concepts and new challenges. Microbiome. 2020; 8 (1): 103. PMID: 32605663
  26. Deo P.N., Deshmukh R. Oral microbiome: Unveiling the fundamentals. J Oral Maxillofac Pathol. 2019; 23 (1): 122—128. PMID: 31110428
  27. Galimova I.A., Usmanova I.N., Gerasimova L.P., Khusnarizanova R.F., Usmanov I.R., Kotova Y.B. The study of the state of the micribiome and local immunity in patients with chronic recurrent atami mouth. Ural Medical Journal. 2019; 9 (177): 11—14 (In Russ.). eLIBRARY ID: 39539115
  28. Chervinets V.M., Chervinets Yu.V., Serova N.E., Stulov N.M., Voevodina V.A., Belyaev V.S., Yakovleva M.V. Microbiom of oral cavity and intestine in patients with arterial hypertension. Bulletin of the Orenburg Scientific Center of the Russian Academy of Sciences Ural Branch. 2019; 3: 27 (In Russ.). eLIBRARY ID: 41746621
  29. Tsarev V.N., Makeyeva I.M., Yagodina E.A., Sudarikova N.V., Tsareva T.V., Nikolaeva E.N., Fomicheva E.M. Herpes and papillomaviruses as components of microbiome in diseases of oral mucosa and periodontium. Dental Forum. 2017; 3: 46—49 (In Russ.). eLIBRARY ID: 30059961
  30. Katola V.M., Komogortseva V.E. The role of oral microbiome in the development of inflammation and somatic pathology. Bulletin Physiology and Pathology of Respiration. 2018; 68: 117—122 (In Russ.). eLIBRARY ID: 35110819
  31. Zorba M., Melidou A., Patsatsi A., Ioannou E., Kolokotronis A. The possible role of oral microbiome in autoimmunity. Int J Womens Dermatol. 2020; 6 (5): 357—364. PMID: 33898698
  32. Drago F., Nozza P., Casazza S., Brusati C., Bandelloni R., Rebora A. Human herpesviruses in bullous pemphigoid lesions. Br J Dermatol. 2005; 152 (2): 375—376. PMID: 15727661
  33. He Y., Gong D., Shi C., Shao F., Shi J., Fei J. Dysbiosis of oral buccal mucosa microbiota in patients with oral lichen planus. Oral Dis. 2017; 23 (5): 674—682. PMID: 28199766
  34. Villa T.G., Sánchez-Pérez Á., Sieiro C. Oral lichen planus: a microbiologist point of view. Int Microbiol. 2021; 24 (3): 275—289. PMID: 33751292

Received

July 2, 2021

Accepted

September 4, 2021

Published on

September 1, 2021