Chronic Subcutaneous Sporotrichosis (S. schenckii) in T. truncatus Dolphin: Differentials, Diagnostics, Identification and Treatment
IAAAM 2014
Jaime A. Bernal1*; Robert T. Braun1; Martin Haulena4; Wayne F. Phillips1,2; Gloria M. González5; José A. Rueda3; Roberto A. Real1; Alejandro R. Garcia2; Ricardo C. Santos2; Marcos H. Cancino2; Hector R. Ramirez6; David A. Espinosa7
1Laboratory, Research and Veterinary, and 2Operation, Training and Husbandry, Cabo Dolphins, Los Cabos, México; 3Departamento de Microbiología, UPC, Guadalajara Jalisco, México; 4Renaissance Group Diversified, Point Roberts, WA, USA; 5Departamento de Microbiología, F.M. Universidad Autónoma de Nuevo León, México; 6Departamento de Biomedicina Molecular, CINVESTAV, DF, México; 7Centro de Patología Veterinaria Guadalajara, Jal. C.P., México

Abstract

In 2006, a bottlenose dolphin Tursiops truncatus maintained in a natural sea water tank with 4 million liters water, develop macroscopic skin lesions on the right flank and abdominal area. Initially diagnosed as lymphoplasmacytic perivascular dermatitis, the lesions they were not pathognomonics; however, they showed local suppurative ulcers and/or subcutaneous nodules without a specific microorganism or cause identified. Hematology and serum chemistry results were consistent with a nonspecific inflammatory response and included leukocytosis, neutrophilia, increased erythrocyte sedimentation rate, low serum iron and low alkaline phosphatase. No changes in behavior, appetite or energy were associated with the development of lesions. However and based on hematology and chemistry parameters, metrics of inflammation were linked to newly developing areas. Multiple diagnostic tests were performed on samples from the lesions including; PCR, cultures, histopathology, Immunohistochemistry and serology. Two samples were collected one year apart each. The samples were collected from different areas and from different lesions, using a 16 gauge x 16 cm biopsy Instrument guided by ultrasound. The samples were submitted for culture and histopathology and after 14 days on Sabouraud dextrose agar, PAS and blue cotton stains revealed a filamentous fungal growth. Histopathological sections show severe pyogranulomatous inflammation of deep dermis and subcutaneous tissue, with intralesional oval to elongate-shaped budding yeast-like structures. These forms were compatible with Sporothrix schenckii and they were confirmed by phenotypic characterization and DNA sequencing. Different antifungal approaches and treatments were implemented, with no obvious resolution; however, during the last 7 months oral terbinafine (2 mg/kg SID) plus local hyperthermia had positive local and systemic effects.

Acknowledgements

The authors wish to thank Michael G Rinaldi, Fungus Testing Laboratory, Leopoldo S Argumedo, Centro de Investigación y de Estudios Avanzados del IPN, Gerardo Salas, Universidad Nacional Autonoma de Mexico, Stephen Raverty, Provincial Animal Health Centre, Gregory D. Bossart, Animal Care, Research and Conservation Georgia Aquarium, Nathan P. Wiederhold, Fungus Testing Laboratory. Michael Kinsel Zoological Pathology Program University of Illinois.

* Presenting author

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Speaker Information
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Jaime A. Bernal
Laboratory, Research and Veterinary, Cabo Dolphins
Los Cabos, México


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