This study describes clinical, histologic, immunohistochemical and electron microscopic features of amyloid A amyloidosis occurring in black-footed ferrets (Mustela nigripes) from eight U.S. zoological institutions. Ferrets had nonregenerative anemia, serum chemistries consistent with chronic renal disease, and proteinuria. Amyloid was present in a variety of tissues, but it was most severe in renal glomeruli and associated with tubular protein loss and emaciation. Congo red/potassium permanganate (KMnO4) and immunohistochemical stains revealed that the amyloid was of the AA type. Concurrent diseases and genetic predisposition were considered the most important contributing factors to development of amyloidosis. Analysis of the genetic tree did not reveal convincing evidence of a common ancestor in the affected ferrets, but a genetic predisposition is likely because all the captive black-footed ferrets are related.
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http://dx.doi.org/10.1638/06-023.1 | DOI Listing |
J Mammal
December 2024
USDA National Wildlife Research Center, 4101 Laporte Avenue, Fort Collins, CO 80521, United States.
The consequences of intraguild predation on vulnerable subordinate species are an important consideration in the recovery of endangered species. In prairie ecosystems, coyotes () are the primary predator of endangered black-footed ferrets (; hereafter, ferrets) and presumably compete for prairie dog ( spp.) prey.
View Article and Find Full Text PDFCommun Biol
September 2024
Center for Conservation Genomics, Smithsonian's National Zoo & Conservation Biology Institute, Washington, DC, USA.
Sci Rep
March 2024
Department of Integrative Biology, University of California, Berkeley, USA.
J Zoo Wildl Med
March 2024
Department of Pathology, Midwestern University, College of Veterinary Medicine, Glendale, AZ 85308, USA.
Renal disease is an important cause of morbidity and mortality in managed black-footed ferrets (BFF; ). The objectives of this study were to establish reference intervals for blood analytes of clinically normal BFF (1-2 yr old), summarize the frequency of various renal histopathologic findings in a managed population of BFF, assess the diagnostic performance of blood analytes and urine specific gravity (USG) for the diagnosis of renal disease, and assess if comorbidities or age affects the performance of these analytes in diagnosing renal disease. Reference intervals were established using a cohort (n = 35) of clinically normal, young adult BFF.
View Article and Find Full Text PDFCommun Biol
February 2024
Center for Conservation Genomics, Smithsonian's National Zoo & Conservation Biology Institute, Washington, DC, USA.
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