Fungal microbiota isolated from healthy pig skin

Authors

  • Fabiano Bonfim Carregaro UFRGS
  • Andréia Spanamberg UFRGS
  • Edna Maria Cavallini Sanches UFRGS
  • Juliana Siqueira Argenta UFRGS
  • Daniela Isabel Brayer Pereira UFRGS
  • Régis Zanette UFRGS
  • Janio Morais Santurio UFSM
  • David Emílio Santos Neves de Barcellos UFRGS
  • Laerte Ferreiro UFRGS

DOI:

https://doi.org/10.22456/1679-9216.16613

Keywords:

Microbiota fúngica, Pele de suínos, Leveduras, Hialohifomicetos, Feohifomicetos, Zigomicetos, Scopulariopsis brevicaulis, Dermatite Pustular Psoriaforme

Abstract

Background:

 

 

 

Researches have been developed to observe the normal microbiota of different animal species. This subject is of major importance for the control of potential infection risks. Fungi can be found in various substrates, foodstuffs (cereals, meat, milk, vegetables) and also in the skin, mucosae, respiratory and gastrointestinal tracts of animals. With the dissemination of immunosuppressive diseases in swine herds over the last years, the number of concomitant diseases caused by opportunist microorganisms is gradually increasing in literature. The objective of this study was to determine the microbiota of pig skin with no apparent lesions. Materials, Methods and Results: A number of 261 pigs from 11 swine farms located in six municipalities of the State of Rio Grande do Sul, in Southern Brazil, were used for the study, in the period from April 2005 to April 2006. After being cleaned with water and 70% ethanol, skin samples were collected by friction of circular and sterile hair brushes against the posterior ventral region of the animals, on an area of no more than 10 cm. After sample collection, the brushes were wrapped with the same aluminium foil used in the sterilization process. Within the next 24 hours, the material was streaked onto agar and incubated at 25°C to 30ºC for up to four weeks. Micromorphology was used for mold identification purposes, and the process employed lactophenol cotton blue staining. Whenever an initial identification was not possible due to the absence of characteristic structures, the isolate would be picked onto Potato agar to stimulate the development of reproductive structures. Yeasts and yeast-like fungi were characterized by physiological routine assays and differential tests, such as chlamydoconidia production and germ tube tests, and also by cultivation in HiCrome Agar. Isolates that produced arthroconidia were classified into the genera Geotrichum or Trichosporon. A number of 501 isolates were obtained, of which 297 were molds and 204 yeasts. Among the molds, the hyalohyphomycetes prevailed with 211 isolates, followed by 53 pheohyphomycetes and 33 zygomycetes. Two hundred and four yeast samples were identified as Candida albicans and Trichosporon spp., in addition to other far less frequent species, such as C. glabrata. Discussion: The varied range of species isolated from the skin of pigs in this study can be explained by a number of factors, such as type of management, swine farm installations and environmental variations. The diversity of the microbiota found in relation to other studies demonstrates the necessity of this kind of research, because knowledge of the prevailing microbiota in a determined region facilitates the evaluation of potential impacts of sporadic or emerging new fungal diseases in herds, particularly in immunosuppressed animals. The observation of 17 Scopulariopsis brevicaulis isolates is worth pointing out, as its presence, associated with environmental and host factors, may favor the infection of pigs and the clinical development of the Dermatitis in the species. Knowledge of the diversity of mycological agents that are in direct contact with healthy animals may assist the diagnosis of exotic etiologies, particularly in animals with immunosuppressive diseases, considering that these are being diagnosed in swine with an increasing frequency.

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Author Biographies

Fabiano Bonfim Carregaro, UFRGS

Andréia Spanamberg, UFRGS

 

 

 

Setor de Micologia, Faculdade de Veterinária (FaVet) & Programa de Pósgraduação em Ciências Veterinárias (PPGCV), Universidade Federal do Rio Grande do Sul (UFRGS)

Edna Maria Cavallini Sanches, UFRGS

 

 

 

Setor de Micologia, Faculdade de Veterinária (FaVet) & Programa de Pósgraduação em Ciências Veterinárias (PPGCV), Universidade Federal do Rio Grande do Sul (UFRGS)

Juliana Siqueira Argenta, UFRGS

 

 

 

Setor de Micologia, Faculdade de Veterinária (FaVet) & Programa de Pósgraduação em Ciências Veterinárias (PPGCV), Universidade Federal do Rio Grande do Sul (UFRGS)

Daniela Isabel Brayer Pereira, UFRGS

 

 

 

Setor de Micologia, Faculdade de Veterinária (FaVet) & Programa de Pósgraduação em Ciências Veterinárias (PPGCV), Universidade Federal do Rio Grande do Sul (UFRGS)

Régis Zanette, UFRGS

 

 

 

Setor de Micologia, Faculdade de Veterinária (FaVet) & Programa de Pósgraduação em Ciências Veterinárias (PPGCV), Universidade Federal do Rio Grande do Sul (UFRGS)

Janio Morais Santurio, UFSM

 

 

 

LAPEMI (Laboratório de Pesquisas Micológicas), Departamento de Microbiologia e Parasitologia, Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brasil.

David Emílio Santos Neves de Barcellos, UFRGS

 

 

 

Setor de Suínos, FaVet & PPGCV-UFRGS.

Laerte Ferreiro, UFRGS

 

 

 

Setor de Micologia, Faculdade de Veterinária (FaVet) & Programa de Pósgraduação em Ciências Veterinárias (PPGCV), Universidade Federal do Rio Grande do Sul (UFRGS)

Published

2018-06-27

How to Cite

Carregaro, F. B., Spanamberg, A., Sanches, E. M. C., Argenta, J. S., Pereira, D. I. B., Zanette, R., Santurio, J. M., Barcellos, D. E. S. N. de, & Ferreiro, L. (2018). Fungal microbiota isolated from healthy pig skin. Acta Scientiae Veterinariae, 38(2), 147–153. https://doi.org/10.22456/1679-9216.16613

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