Analysis of the biological diversity of the skin and oropharyngeal microbiota depending on various treatment methods for psoriasis

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Abstract

Introduction. Psoriasis is a chronic inflammatory systemic disorder of a multifactorial origin, characterized by accelerated keratinocyte proliferation and impaired differentiation. Recently, the potential role of the human microbiota in the emergence of various chronic conditions, including psoriasis, has become a popular area of research. At the same time, no specific microbiological markers have been identified that could be used to accurately evaluate treatment effectiveness. The aim of the study was to assess the biological diversity of microbial communities of the skin and oropharynx in patients receiving different psoriasis treatment regimens, and to investigate an association between the incidence of isolated individual microorganisms and the applied treatment method. Materials and methods. The study included 155 male and female patients, aged > 18 years old, with psoriasis vulgaris of varying severity. All patients were divided into three groups. Group 1 — patients receiving topical corticosteroids (N = 52); group 2 — patients receiving methotrexate (N = 51); Group 3 — patients receiving IL-17 inhibitors (N = 52). Microbiological examination of skin and oropharynx swabs was conducted for all patients. The identification of microorganisms was performed using MALDI-ToF mass spectrometry. Results. In general, 109 and 139 individual species were isolated from oropharynx and skin, respectively. Analyzing biological diversity of the oropharyngeal microbiota revealed that the following microbial species are referred to resident microbiota in patients from all three groups: Streptococcus salivarius, Neisseria subflava, Streptococcus vestibularis. Differences in the microbiological diversity between the studied groups were only revealed due to an additional oropharyngeal microbiota. Analysis of the microbial diversity of the skin microbiota showed, that none of the isolated microorganisms was a resident part of the microbiota in all patients. Statistically significant differences were obtained for skin microorganisms, such as Staphylococcus hominis (p = 0.047) and Enterococcus faecalis (p = 0.013), as well as oropharyngeal microorganisms, including Neisseria flavescens (p = 0.022), Micrococcus luteus (p = 0.048) and Acinetobacter ursingii (p = 0.040). Conclusion. Thus, there has been revealed significant differences between studied groups in isolating individual microorganisms, which may potentially show varying effectiveness for different approaches to manage psoriatic patients.

About the authors

A. A. Arsenyeva

FSBEI HE “Samara State Medical University” of Ministry of Healthсare of Russian Federation

Email: a.a.arseneva@samsmu.ru
ORCID iD: 0000-0002-7933-3515
SPIN-code: 4320-1196

PhD (Medicine), Associate Professor, Head of the Department of Dermatovenerology and Cosmetology of Post-Graduate Education Institute

Russian Federation, Samara

A. V. Lyamin

FSBEI HE “Samara State Medical University” of Ministry of Healthсare of Russian Federation

Email: a.v.lyamin@samsmu.ru
ORCID iD: 0000-0002-5905-1895
SPIN-code: 6607-8990

DSc (Medicine), Associate Professor, Director of Research and Educational Professional Center for Genetic and Laboratory Technologies

Russian Federation, Samara

N. B. Migacheva

FSBEI HE “Samara State Medical University” of Ministry of Healthсare of Russian Federation

Email: n.b.migacheva@samsmu.ru
ORCID iD: 0000-0003-0941-9871
SPIN-code: 1313-9021

PhD (Medicine), Associate Professor, Head of the Department of Pediatrics of Post-Graduate Education Institute

Russian Federation, Samara

A. D. Prokopenko

FSBEI HE “Samara State Medical University” of Ministry of Healthсare of Russian Federation

Email: nastya205945@yandex.ru
ORCID iD: 0009-0008-2418-5253

Student of the Institute of Clinical Medicine

Russian Federation, Samara

S. T. Gritsenko

FSBEI HE “Samara State Medical University” of Ministry of Healthсare of Russian Federation

Email: s.t.gricenko@samsmu.ru
ORCID iD: 0009-0008-6164-675X

Specialist of the Laboratory of Culturomic and Proteomic Research in Microbiology of Professional Center for Education and Research in Genetic and Laboratory Technologies

Russian Federation, Samara

Dmitriy V. Alekseev

FSBEI HE “Samara State Medical University” of Ministry of Healthсare of Russian Federation

Author for correspondence.
Email: d.v.alekseev@samsmu.ru
ORCID iD: 0000-0002-8864-4956
SPIN-code: 6991-8918

Specialist of Laboratory of Cultural and Proteomic Research in Microbiology, Research and Educational Professional Center for Genetic and Laboratory Technologies

Russian Federation, Samara

References

  1. Суханова Е.В., Орлов Е.В., Арнольдов С.В. Распространенность патологии ЛОР-органов у больных псориазом // Известия Самарского научного центра РАН. Социальные, гуманитарные, медико-биологические науки. 2015. Т. 17, № 2-2. С. 389–391. [Sukhanova E.V., Orlov E.V., Arnoldov S.V. Prevalence of pathology of ENT organs in patients with psoriasis. Izvestiya Samarskogo nauchnogo tsentra RAN. Sotsial’nye, gumanitarnye, mediko-biologicheskie nauki = Izvestiya of the Samara Russian Academy of Sciences Scientific Center. Social, Humanitarian, Medicobiological Sciences, 2015, vol. 17, no. 2-2, pp. 389–391. (In Russ.)]
  2. Belstrøm D., Eiberg J.M., Enevold C., Grande M.A., Jensen C.A.J., Skov L., Hansen P.R. Salivary microbiota and inflammation-related proteins in patients with psoriasis. Oral Dis., 2020, vol. 26, no. 3, pp. 677–687. doi: 10.1111/odi.13277
  3. D’Argenio V., Casaburi G., Precone V., Pagliuca C., Colicchio R., Sarnataro D., Discepolo V., Kim S.M., Russo I., Del Vecchio Blanco G., Horner D.S., Chiara M., Pesole G., Salvatore P., Monteleone G., Ciacci C., Caporaso G.J., Jabri B., Salvatore F., Sacchetti L. Metagenomics Reveals Dysbiosis and a Potentially Pathogenic N. flavescens Strain in Duodenum of Adult Celiac Patients. Am. J. Gastroenterol., 2016, vol. 111, no. 6, pp. 879–890. doi: 10.1038/ajg.2016.95
  4. Griffiths C.E.M., Armstrong A.W., Gudjonsson J.E., Barker J.N.W.N. Psoriasis. Lancet, 2021, vol. 397, no. 10281, pp. 1301–1315. doi: 10.1016/S0140-6736(20)32549-6
  5. Iaffaldano L., Granata I., Pagliuca C., Esposito M.V., Casaburi G., Salerno G., Colicchio R., Piccirillo M., Ciacci C., Del Vecchio Blanco G., Salvatore P., D’Argenio V., Sacchetti L. Oropharyngeal microbiome evaluation highlights Neisseria abundance in active celiac patients. Sci. Rep., 2018, vol. 8, no. 1: 11047. doi: 10.1038/s41598-018-29443-1
  6. Langan E.A., Künstner A., Miodovnik M., Zillikens D., Thaçi D., Baines J.F., Ibrahim S.M., Haneke A., Lüscher B., Buer J., Böer-Auer A. Combined culture and metagenomic analyses reveal significant shifts in the composition of the cutaneous microbiome in psoriasis. Br. J. Dermatol., 2019, vol. 181, no. 6, pp. 1254–1264. doi: 10.1111/bjd.17989
  7. Lee H.J., Kim M. Challenges and Future Trends in the Treatment of Psoriasis. Int. J. Mol. Sci., 2023, vol. 24, no. 17: 13313. doi: 10.3390/ijms241713313
  8. Lewis D.J., Chan W.H., Hinojosa T., Hsu S., Feldman S.R. Mechanisms of microbial pathogenesis and the role of the skin microbiome in psoriasis: A review. Clin. Dermatol., 2019, vol. 37, no. 2, pp. 160–166. doi: 10.1016/j.clindermatol.2019.01.011
  9. Liu S., He M., Jiang J., Duan X., Chai B., Zhang J., Deng H., Wu Y., Cen B., Long F. Triggers for the onset and recurrence of psoriasis: a review and update. Cell Commun. Signal., 2024, vol. 22, no. 1: 108. doi: 10.1186/s12964-023-01381-0
  10. Maronese C.A., Valenti M., Moltrasio C., Romagnuolo M., Ferrucci S.M., Gilliet M., Costanzo A., Marzano A.V. Paradoxical Psoriasis: An Updated Review of Clinical Features, Pathogenesis, and Treatment Options. J. Investig. Dermatol., 2024, vol. 144, no. 11, pp. 2364–2376. doi: 10.1016/j.jid.2024.05.015
  11. Nakatsuji T., Chen T.H., Narala S., Chun K.A., Two A.M., Yun T., Shafiq F., Kotol P.F., Bouslimani A., Melnik A.V., Latif H., Kim J.N., Lockhart A., Artis K., David G., Taylor P., Streib J., Dorrestein P.C., Grier A., Gill S.R., Zengler K., Hata T.R., Leung D.Y.M., Gallo R.L. Antimicrobials from human skin commensal bacteria protect against Staphylococcus aureus and are deficient in atopic dermatitis. Sci. Transl. Med., 2017, vol. 9, no. 378: eaah4680. doi: 10.1126/scitranslmed.aah4680
  12. Shemesh S., Marom T., Vaknine H., Tamir S.O. Neisseria flavescens Infection in Atypical Multiple Vallecular Cysts. Indian J. Otolaryngol. Head Neck Surg., 2019, vol. 71, suppl. 1, pp. 11–13. doi: 10.1007/s12070-015-0871-2
  13. Yan D., Issa N., Afifi L., Jeon C., Chang H.W., Liao W. The Role of the Skin and Gut Microbiome in Psoriatic Disease. Curr. Dermatol. Rep., 2017, vol. 6, no. 2, pp. 94–103. doi: 10.1007/s13671-017-0178-5
  14. Yeh N.L., Hsu C.Y., Tsai T.F., Chiu H.Y. Gut Microbiome in Psoriasis is Perturbed Differently During Secukinumab and Ustekinumab Therapy and Associated with Response to Treatment. Clin. Drug Investig., 2019, vol. 39, no. 12, pp. 1195–1203. doi: 10.1007/s40261-019-00849-7
  15. Zhao K., Zhao Y., Guo A., Xiao S., Tu C. Oral Microbiota Variations in Psoriasis Patients Without Comorbidity. Clin. Cosmet. Investig. Dermatol., 2024, vol. 17, pp. 2231–2241. doi: 10.2147/CCID.S473237

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Copyright (c) 2025 Arsenyeva A.A., Lyamin A.V., Migacheva N.B., Prokopenko A.D., Gritsenko S.T., Alekseev D.V.

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