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Detection and identification of Malassezia species in domestic animals and aquatic birds by PCR-RFLP.

Abstract: The present study aimed at detection and species-level identification of the Malassezia yeasts in domestic animals and aquatic birds by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Samples were collected using tape strips and swabs from 471 animals including 97 horses, 102 cattle, 105 sheep, 20 camels, 60 dogs, 30 cats, 1 hamster, 1 squirrel, 50 aquatic birds and 5 turkeys. Tape-strip samples were examined by direct microscopy. All samples were inoculated on modified Leeming and Notman agar medium. DNA extracted from the yeast colonies was amplified by PCR using primers specific for 26S rDNA. RFLP of the PCR products was performed using Hin6I enzyme, and PCR and RFLP products were visualized by agarose gel electrophoresis. Malassezia yeasts were detected at the following frequencies: 15.46% in horses, 12.74% in cattle, 12.38% in sheep, 28.33% in dogs, 26.66% in cats and 26% in aquatic birds. Eighty colonies of 6 species were isolated: Malassezia globosa 41.25%, Malassezia furfur 22.5%, Malassezia restricta 15%, Malassezia sympodialis 15%, Malassezia pachydermatis 5% and Malassezia slooffiae 1.25%. Therefore different lipophilic Malassezia species are found in a wide diversity of animals and aquatic birds. PCR-RFLP is a suitable technique for identification of different Malassezia species.
Publication Date: 2015-01-01 PubMed ID: 27175148PubMed Central: PMC4789237
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  • Journal Article

Summary

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This research looked at how to effectively detect and identify different species of the yeast, Malassezia, in domestic animals and aquatic birds using PCR-RFLP – a specific laboratory technique.

Detailed Explanation

The study’s main goal was to identify and determine the prevalence of Malassezia yeast species in a wide variety of animals, including domestic animals like horses, cattle, dogs, cats and others, as well as aquatic birds. This was done by using a method called polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).

  • The researchers collected samples using tape strips and swabs from 471 animals. The range of animals was very diverse, from horses and dogs to a hamster and a squirrel.
  • After collection, the samples were examined under a microscope and cultured on modified Leeming and Notman agar, a media often used to grow and isolate these types of yeast.
  • Next, they extracted DNA from these yeast colonies and amplified (or made copies of) the DNA using a technique called polymerase chain reaction (PCR), with specific markers for 26S rDNA, a component of the yeast’s genetic material.
  • They then used another technique called restriction fragment length polymorphism (RFLP) on these PCR products. In RFLP, a specific enzyme (in this case Hin6I) is used to cut the DNA at specific sequences, creating fragments of varying lengths.
  • These fragments were then separated and visualized using agarose gel electrophoresis, which sorts DNA fragments by length. By comparing these patterns of DNA fragments, the researchers could distinguish between different yeast species.
  • The results showed that Malassezia yeasts were present on a number of animals at varying frequencies, including in 15.46% of horses, 12.74% of cattle, 12.38% of sheep, 28.33% of dogs, 26.66% of cats, and 26% of aquatic birds.
  • The researchers were able to isolate six different species of Malassezia, with Malassezia globosa being the most common, found in 41.25% of the samples.

In conclusion, the researchers found evidence of various Malassezia yeast species present in a wide diversity of domestic animals and aquatic birds. The PCR-RFLP method was found to be suitable for the purpose of identifying these different yeast species.

Cite This Article

APA
Zia M, Mirhendi H, Toghyani M. (2015). Detection and identification of Malassezia species in domestic animals and aquatic birds by PCR-RFLP. Iran J Vet Res, 16(1), 36-41.

Publication

ISSN: 1728-1997
NlmUniqueID: 101660030
Country: Iran
Language: English
Volume: 16
Issue: 1
Pages: 36-41

Researcher Affiliations

Zia, M
  • Department of Basic Sciences, Khorasgan (Isfahan) Branch, Islamic Azad University, Isfahan, Iran;
Mirhendi, H
  • Department of Medical Parasitology and Mycology, School of Public Health and Institute of Public Health Researches (Isfahan Center), Tehran University of Medical Sciences, Tehran, Iran;
Toghyani, M
  • Department of Animal Sciences, Khorasgan (Isfahan) Branch, Islamic Azad University, Isfahan, Iran.

References

This article includes 33 references
  1. Ashbee HR. Update on the genus Malassezia.. Med Mycol 2007 Jun;45(4):287-303.
    pubmed: 17510854doi: 10.1080/13693780701191373google scholar: lookup
  2. Bensignor E, Jankowski F, Seewald W, Touati F, Deville M, Guillot J. Comparison of two sampling techniques to assess quantity and distribution of Malassezia yeasts on the skin of Basset Hounds.. Vet Dermatol 2002 Oct;13(5):237-41.
  3. Cabañes FJ, Theelen B, Castellá G, Boekhout T. Two new lipid-dependent Malassezia species from domestic animals.. FEMS Yeast Res 2007 Sep;7(6):1064-76.
  4. Cabañes FJ, Vega S, Castellá G. Malassezia cuniculi sp. nov., a novel yeast species isolated from rabbit skin.. Med Mycol 2011 Jan;49(1):40-8.
    pubmed: 20560865doi: 10.3109/13693786.2010.493562google scholar: lookup
  5. Cafarchia C, Gallo S, Romito D, Capelli G, Otranto D. New insights into the diagnosis and patho-genicity of Malassezia yeasts.. Vet. Res. Commun. 2006;30:231–234.
    pubmed: 0
  6. Castellá G, Hernández JJ, Cabañes FJ. Genetic typing of Malassezia pachydermatis from different domestic animals.. Vet Microbiol 2005 Jul 1;108(3-4):291-6.
    pubmed: 15922521doi: 10.1016/j.vetmic.2005.04.016google scholar: lookup
  7. Crespo MJ, Abarca ML, Cabañes FJ. Atypical lipid-dependent Malassezia species isolated from dogs with otitis externa.. J Clin Microbiol 2000 Jun;38(6):2383-5.
  8. Crespo MJ, Abarca ML, Cabañes FJ. Occurrence of Malassezia spp. in the external ear canals of dogs and cats with and without otitis externa.. Med Mycol 2002 Apr;40(2):115-21.
    pubmed: 12058723doi: 10.1080/mmy.40.2.115.121google scholar: lookup
  9. Crespo MJ, Abarca ML, Cabañes FJ. Occurrence of Malassezia spp. in horses and domestic ruminants.. Mycoses 2002 Oct;45(8):333-7.
  10. Dokos C, Pana ZD, Tragiannidis A. Malassezia species: a rare cause of invasive fungal infections in immunocompromised patients.. Curr. Fungal Infect. Rep. 2012;5:18–22.
  11. Duarte EP, Melo MM, Hahn RC, Hamdan JS. Prevalence of Malassezia spp. in the ears of asymptomatic cattle and cattle with otitis in Brazil.. Med Mycol 1999 Jun;37(3):159-62.
    pubmed: 10498444
  12. Eidi S, Khosravi AR, Jamshidi SH, Soltani M. Molecular characterization of Malassezia species isolated from dog with and without otitis and seborrhoeic dermatitis.. World J. Zool. 2011;6:134–141.
  13. Gaitanis G, Magiatis P, Hantschke M, Bassukas ID, Velegraki A. The Malassezia genus in skin and systemic diseases.. Clin Microbiol Rev 2012 Jan;25(1):106-41.
    pmc: PMC3255962pubmed: 22232373doi: 10.1128/cmr.00021-11google scholar: lookup
  14. Gaitanis G, Robert V, Velegraki A. Verifiable single nucleotide polymorphisms of the internal transcribed spacer 2 region for the identification of 11 Malassezia species.. J Dermatol Sci 2006 Sep;43(3):214-7.
  15. Gaitanis G, Velegraki A, Frangoulis E, Mitroussia A, Tsigonia A, Tzimogianni A, Katsambas A, Legakis NJ. Identification of Malassezia species from patient skin scales by PCR-RFLP.. Clin Microbiol Infect 2002 Mar;8(3):162-73.
  16. Garau M, del Palacio A, García J. Prevalence of Malassezia spp. in healthy pigs.. Mycoses 2005 Jan;48(1):17-20.
  17. Giusiano G, Sosa Mde L, Rojas F, Vanacore ST, Mangiaterra M. Prevalence of Malassezia species in pityriasis versicolor lesions in northeast Argentina.. Rev Iberoam Micol 2010 Jun 30;27(2):71-4.
    pubmed: 20346299doi: 10.1016/j.riam.2009.12.005google scholar: lookup
  18. Gupta AK, Kohli Y, Faergemann J, Summerbell RC. Epidemiology of Malassezia yeasts associated with pityriasis versicolor in Ontario, Canada.. Med Mycol 2001 Apr;39(2):199-206.
    pubmed: 11346269doi: 10.1080/mmy.39.2.199.206google scholar: lookup
  19. Hirai A, Kano R, Makimura K, Yasuda K, Konishi K, Yamaguchi H, Hasegawa A. A unique isolate of Malassezia from a cat.. J Vet Med Sci 2002 Oct;64(10):957-9.
    pubmed: 12419877doi: 10.1292/jvms.64.957google scholar: lookup
  20. Hort W, Mayser P. Malassezia virulence determinants.. Curr Opin Infect Dis 2011 Apr;24(2):100-5.
    pubmed: 21192258doi: 10.1097/qco.0b013e328342f787google scholar: lookup
  21. Hort W, Nilles M, Mayser P. [Malassezia yeasts and their significance in dermatology].. Hautarzt 2006 Jul;57(7):633-43; quiz 644-5.
    pubmed: 16758222doi: 10.1007/s00105-006-1170-3google scholar: lookup
  22. Jang SJ, Lim SH, Ko JH, Oh BH, Kim SM, Song YC, Yim SM, Lee YW, Choe YB, Ahn KJ. The Investigation on the Distribution of Malassezia Yeasts on the Normal Korean Skin by 26S rDNA PCR-RFLP.. Ann Dermatol 2009 Feb;21(1):18-26.
    pmc: PMC2883363pubmed: 20548850doi: 10.5021/ad.2009.21.1.18google scholar: lookup
  23. Ko JH, Lee YW, Choe YB, Ahn KJ. Epidemiologic Study of Malassezia Yeasts in Patients with Malassezia Folliculitis by 26S rDNA PCR-RFLP Analysis.. Ann Dermatol 2011 May;23(2):177-84.
    pmc: PMC3130860pubmed: 21747616doi: 10.5021/ad.2011.23.2.177google scholar: lookup
  24. Mirhendi H, Makimura K, Zomorodian K, Yamada T, Sugita T, Yamaguchi H. A simple PCR-RFLP method for identification and differentiation of 11 Malassezia species.. J Microbiol Methods 2005 May;61(2):281-4.
    pubmed: 15722156doi: 10.1016/j.mimet.2004.11.016google scholar: lookup
  25. Morishita N, Sei Y, Sugita T. Molecular analysis of malassezia microflora from patients with pityriasis versicolor.. Mycopathologia 2006 Feb;161(2):61-5.
    pubmed: 16463088doi: 10.1007/s11046-005-0149-4google scholar: lookup
  26. Morris DO. Malassezia pachydermatis carriage in dog owners.. Emerg Infect Dis 2005 Jan;11(1):83-8.
    pmc: PMC3294355pubmed: 15705327doi: 10.3201/eid1101.040882google scholar: lookup
  27. Nardoni S, Dini M, Taccini F, Mancianti F. Occurrence, distribution and population size of Malassezia pachydermatis on skin and mucosae of atopic dogs.. Vet Microbiol 2007 May 16;122(1-2):172-7.
    pubmed: 17257784doi: 10.1016/j.vetmic.2006.12.023google scholar: lookup
  28. Raabe P, Mayser P, Weiss R. Demonstration of Malassezia furfur and M. sympodialis together with M. pachydermatis in veterinary specimens.. Mycoses 1998 Dec;41(11-12):493-500.
  29. Rincón S, Celis A, Sopó L, Motta A, Cepero de García MC. Malassezia yeast species isolated from patients with dermatologic lesions.. Biomedica 2005 Jun;25(2):189-95.
    pubmed: 16022373
  30. Sei Y. [Malassezia infections].. Med Mycol J 2012;53(1):7-11.
    pubmed: 22467125doi: 10.3314/mmj.53.7google scholar: lookup
  31. Sugita T, Suzuki M, Goto S, Nishikawa A, Hiruma M, Yamazaki T, Makimura K. Quantitative analysis of the cutaneous Malassezia microbiota in 770 healthy Japanese by age and gender using a real-time PCR assay.. Med Mycol 2010 Mar;48(2):229-33.
    pubmed: 19462267doi: 10.1080/13693780902977976google scholar: lookup
  32. Yamada Y, Makimura K, Merhendi H, Ueda K, Nishiyama Y, Yamaguchi H, Osumi M. Comparison of different methods for extraction of mitochondrial DNA from human pathogenic yeasts.. Jpn J Infect Dis 2002 Aug;55(4):122-5.
    pubmed: 12403909
  33. Zomorodain K, Mirhendi H, Tarazooie B, Kordbacheh P, Zeraati H, Nayeri F. Molecular analysis of Malassezia species isolated from hospitalized neonates.. Pediatr Dermatol 2008 May-Jun;25(3):312-6.

Citations

This article has been cited 5 times.
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  2. Vidal S, Brandt BW, Dettwiler M, Abril C, Bressan J, Greub G, Frey CF, Perreten V, Rodriguez-Campos S. Limited added value of fungal ITS amplicon sequencing in the study of bovine abortion. Heliyon 2018 Nov;4(11):e00915.
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  3. Meister SL, Soto S, Rüttener M, Wenker C, Kittl S. Yeast-associated skin disease in captive king penguins (Aptenodytes patagonicus) caused by an undescribed Malassezia species in a Swiss zoological garden. BMC Vet Res 2025 Dec 23;22(1):74.
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  4. Moskaluk AE. Fungus in the Fur: An Overview of Fungal Infections in Cats, Dogs, and Exotic Small Mammals. Curr Top Microbiol Immunol 2025;446:137-178.
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