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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Uncommon mandibular osteomyelitis in a cat caused by Nocardia africana

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Autor(es):
de Farias, Marconi Rodrigues [1] ; Werner, Juliana [1] ; Ribeiro, Marcio Garcia [2, 3] ; Rodigheri, Sabrina Marin [4] ; Cavalcante, Carolina Zaghi [1] ; Chi, Kung Darh [1] ; Zeni Condas, Larissa Anuska [2] ; Gonoi, Tohru [5] ; Matsuzama, Tetsuhiro [5] ; Yazama, Katsukiyo [5]
Número total de Autores: 10
Afiliação do(s) autor(es):
[1] Pontificia Univ Catolica, Coll Vet Med, Compan Vet Hosp, Sao Jose Dos Pinhais, Parana - Brazil
[2] Univ Estadual Paulista UNESP, Sch Vet Med & Anim Sci, Dept Vet Hyg & Publ Hlth, Botucatu, SP - Brazil
[3] Univ Estadual Paulista UNESP, Sch Vet Med & Anim Sci, Dept Vet Hyg & Publ Hlth, BR-18618970 Botucatu, SP - Brazil
[4] FEPAR, Curitiba, Parana - Brazil
[5] Chiba Univ, Med Mycol Res Ctr, Chiba - Japan
Número total de Afiliações: 5
Tipo de documento: Artigo Científico
Fonte: BMC Veterinary Research; v. 8, DEC 6 2012.
Citações Web of Science: 3
Resumo

Background: Nocardiosis is an unusual infection in companion animals characterized by suppurative to pyogranulomatous lesions, localized or disseminated. Cutaneous-subcutaneous, pulmonary and systemic signs are observed in feline nocardiosis. However, osteomyelitis is a rare clinical manifestation in cats. Nocardia cyriacigeorgica (formerly N. asteroides sensu stricto), Nocardia brasiliensis, Nocardia otitidiscaviarum, and Nocardia nova are the most common pathogenic species identified in cats, based on recent molecular classification (16S rRNA gene). The present report is, to our knowledge, the first case of mandibular osteomyelitis in a cat caused by Nocardia africana, diagnosed based upon a combination of methods, including molecular techniques. Case presentation: A one-year-old non-neutered female cat, raised in a rural area, was admitted to the Companion Animal Hospital-PUCPR, Sao Jose dos Pinhais, State of Parana, Brazil, with a history a progressive facial lesion, difficulty apprehending food, loss of appetite, apathy and emaciation. Clinical examination showed fever, submandibular lymphadenitis, and a painless, 8 cm diameter mass, which was irregularly-shaped, of firm consistency, and located in the region of the left mandible. The skin around the lesion was friable, with diffuse inflammation (cellulitis), multiple draining sinuses, and exudation of serosanguinous material containing whitish ``sulfur{''} granules. Diagnosis was based initially in clinical signs, microbiological culture, cytological, and histopathological findings, and radiographic images. Molecular sequencing of 16S rRNA of isolate allowed diagnosis of Nocardia africana. Despite supportive care and antimicrobial therapy based on in vitro susceptibility testing the animal died. Conclusion: The present report describes a rare clinical case of feline osteomyelitis caused by Nocardia africana, diagnosed based upon a combination of clinical signs, microbiological culture, cytological and histopathological findings, radiographic images, and molecular methods. The use of modern molecular techniques constitutes a quick and reliable method for Nocardia species identification, and may contribute to identification to new species of Nocardia that are virulent in cats. (AU)

Processo FAPESP: 08/56037-1 - Caracterização fenotípica, genotípica e de fatores de virulência em linhagens do gênero Nocardia isoladas de mastite bovina, afecções em animais de companhia e de pacientes humanos, com e sem imunossupressão, acometidos de nocardiose
Beneficiário:Larissa Anuska Zeni Condas
Modalidade de apoio: Bolsas no Brasil - Mestrado
Processo FAPESP: 09/53494-5 - Caracterização fenotípica, genotípica e de fatores de virulência em linhagens do gênero Nocardia isoladas de mastite bovina, afecções em animais de companhia e de pacientes humanos, com e sem imunossupressão, acometidos de nocardiose
Beneficiário:Marcio Garcia Ribeiro
Modalidade de apoio: Auxílio à Pesquisa - Regular