COMPARISON OF MALASSEZIA SPP. PROPORTIONS IN INFLAMMATORY AND NON-INFLAMMATORY FACIAL ACNE VULGARIS LESIONS

Authors

  • AGASSI SUSENO SUTARJO Department of Dermatology and Venerology, Faculty of Medicine, Universitas Indonesia–Cipto Mangunkusumo Hospital, Jakarta, Indonesia
  • IRMA BERNADETTE S. SITOHANG Department of Dermatology and Venerology, Faculty of Medicine, Universitas Indonesia–Cipto Mangunkusumo Hospital, Jakarta, Indonesia
  • MARDIASTUTI H. WAHID Department of Clinical Microbiology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia
  • SANDRA WIDATY Department of Dermatology and Venerology, Faculty of Medicine, Universitas Indonesia–Cipto Mangunkusumo Hospital, Jakarta, Indonesia

DOI:

https://doi.org/10.22159/ijap.2020.v12s3.39454

Keywords:

Acne lesion, Malassezia spp, Skin microbiome

Abstract

Objective: The skin microbiome plays a role in the pathogenesis of acne vulgaris (AV). Among other species, Malassezia spp. can be found in the pilosebaceous follicle. However, its role on the pathogenesis of AV has not yet been described. The objective of this study was to identify the presence and the distribution of Malassezia spp. in facial AV lesions and also to compare the distribution of Malassezia spp. between inflammatory and non-inflammatory lesions.

Methods: One hundred and twenty subjects were allocated into two groups: inflammatory lesions and non-inflammatory lesions. Samples were taken from hair follicles and examined by microscopy using 20% potassium hydroxide and Parker ink and cultured for species identification.

Results: There was no difference in the spore load between the two groups (p=0.142). Malassezia spp. were isolated from 64.2% of subjects and consisted of M. dermatis (43%), M. sympodialis (18%), M. slooffiae (16%), M. japonica (5%), M. furfur (5%), M. pachydermatis (3%), and M. restricta (1%). There was a higher Malassezia spp. proportion in non-inflammatory lesions (p=0.019). The predominant species in inflammatory AV lesions was M. dermatis (45,8%), followed by M. sympodialis (17.1%), and M. slooffiae (11.4%).

Conclusion: Malassezia spp. were found in facial acne lesions. M. dermatis was the predominant species found in facial AV, followed by M. sympodialis, and M. slooffiae. A higher proportion of Malassezia spp. was found in non-inflammatory lesions.

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References

Bhate K, Williams H. Epidemiology of acne vulgaris. Br J Dermatol 2016;74:945–73.

Dreno B. What is new in the pathophysiology of acne, an overview. J Eur Acad Dermatol Venereol 2017;31:8–12.

Knutsen Larson S, Dawson AL, Dunnick CA, Dellavalle RP. Acne vulgaris: Pathogenesis, treatment, and needs assessment. Dermatol Clin 2012;30:99–106.

Tanghetti EA. The role of inflammation in the pathology of acne. J Clin Aesthet Dermatol 2013;6:27–35.

Till AE, Goulden V, Cunliffe WJ, Holland KT. The cutaneous microflora of adolescent, persistent and late-onset acne patients does not differ. Br J Dermatol 2000;142:885–92.

Ljubojevic S, Skerlev M, Lipozencic J, Basta Juzbasic A. The role of Malassezia furfur in dermatology. Clin Dermatol 2002;22:1529–47.

Numata S, Akamatsu H, Akaza N, Yagami A, Nakata S, Matsunaga K. Analysis of facial skin-resident microbiota in Japanese acne patients. Dermatology 2014;228:86–92.

Akaza N, Akamatsu H, Numata S, Yamada S, Yagami A, Nakata S, et al. Microorganisms inhabiting follicular contents of facial acne are not only propionibacterium but also Malassezia spp. J Dermatol 2016;43:906–11.

Prindaville B, Belazarian L, Levin NA, Wiss K. Pityrosporum folliculitis: a retrospective review of 110 cases. J Am Acad Dermatol 2018;78:511-4.

Kang S, Kim H. The isolation of Malassezia yeasts in the comedones of acne vulgaris. Korean J Med Mycol 1999;4:33–9.

Gaitanis G, Velegraki A, Mayser P, Bassukas ID. Skin diseases associated with Malassezia yeasts: facts and controversies. Clin Dermatol 2013;31:455–63.

Jacinto Jamora S, Tamesis J, Katigbak ML. Pityrosporum folliculitis in the philippines: diagnosis, prevalence, and management. J Am Acad Dermatol 1991;24:693–6.

Gaitanis G, Magiatis P, Hantschke M, Bassukas ID, Velegraki A. The Malassezia genus in skin and systemic diseases. Clin Microbiol Rev 2012;25:106–41.

Guelho Kellermann E, Boekhout T, Begerow D. Biodiversity, phylogeny, and ultrastucture. In: Boekhout T, Gueho E, Mayser PA, Velegraki A. editors. Malassezia and the skin. Berlin, Heiderlberg: Springer; 2010. p. 17–64.

Kaneko T, Makimura K, Abe M, Shiota R, Nakamura Y, Kano R, et al. Revised culture-based system for identification of Malassezia species. J Clin Microbiol 2007;45:3737–42.

Song Y, Hanh H, Ko J, Lee Y. Epidemiologic study of Malassezia yeast in acne patients by analysis of 26SrDNA PCR-RFLP. Ann Dermatol 2011;23:321–9.

Zoulba EN, Widaty S, Krisanty RIA, Wahid M. Identification of Malassezia species and the severity of seborrheic dermatitis on scalp in Dr. Cipto Mangunkusumo ospital Jakarta. J Comput Theor Nanosci 2018;24:6649-52.

Prohic A, Simic D, Sadikovic TJ, Krupalija Fazlic M. Distribution of Malassezia species on healthy human skin in bosnia and herzegovina: correlation with the body part, age and gender. Iran J Microbiol 2014;6:253–62.

Barac A, Arsenijevic V, Pekmezovic M, Milobratovic D, Otrasevic Tasic S, Radunovic M. Presence, species distribution, and density of Malassezia yeast in a patient with seborrheic dermatitis-a community-based case-control study and review of the literature. Mycoses 2015;58:69–75.

Karakaş M, Turac Bicer A, Ilkit M, Durdu M, Seydaolu G. Epidemiology of pityriasis versicolor in Adana, Turkey. J Dermatol 2009;36:377–82.

Kaneko T, Shiota R, Shibuya S, Watanabe S, Umeda Y, Takeshita K, et al. Human external ear canal as the specific reservoir of Malassezia slooffiae. Med Mycol 2010;48:824–7.

Prohic A, Sadikovic TJ, Kuskunovic Vlahovljak S, Baljic R. Distribution of Malassezia species in patients with different dermatological disorders and healthy Individuals. Acta Dermatovenerol Croat 2016;24:274–81.

Akaza N, Akamatsu H, Sasaki Y, Kishi M, Mizutani H, Sano A, et al. Malassezia folliculitis is caused by cutaneous resident Malassezia species. Med Mycol 2009;47:618–24.

Akaza N, Akamatsu H, Takeoka S, Mizutani H, Nakata S, Matsunaga K. Increased hydrophobicity in Malassezia species correlates with increased proinflammatory cytokine expression in human keratinocytes. Med Mycol 2012;87:802–10.

Jeremy AHT, Holland DB, Roberts SG, Thomson KF, Cunli WJ. Inflammatory events are involved in acne lesion initiation. J Invest Dermatol 2003;121:20-7.

Published

15-10-2020

How to Cite

SUTARJO, A. S., SITOHANG, I. B. S., WAHID, M. H., & WIDATY, S. (2020). COMPARISON OF MALASSEZIA SPP. PROPORTIONS IN INFLAMMATORY AND NON-INFLAMMATORY FACIAL ACNE VULGARIS LESIONS. International Journal of Applied Pharmaceutics, 12(3), 7–11. https://doi.org/10.22159/ijap.2020.v12s3.39454

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