Melissa
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Inclusion Body Disease in Boa ConstrictorCase II-165 or 96N165 (AFIP 2548995) Armed
Forces Institute of Pathology Conference,
September 11, 1996
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Signalment: History: Gross
Pathology: Laboratory Results:
Contributor's
Diagnosis and Comments: Intra-cytoplasmic eosinophilic inclusion bodies in most cell types - Boid inclusion body disease. Inclusion body disease (IBD) affects various species of boid snakes and usually manifests as progressive debilitation, anorexia, weight loss, regurgitation, and neurologic signs. The presence of the typical, well-defined intracytoplasmic eosinophilic inclusion bodies is often associated with cellular degeneration in various tissues, most commonly in the CNS, where a non-suppurative encephalomyelitis can also be observed. Various secondary infections are frequently associated with IBD, such as pneumonia and nephritis. In this boa, encephalitis was not noted, although inclusions were numerous in the brain, and were associated with degeneration. The animal also had a mycotic enteritis affecting a focal segment of distal small intestine. The morphology of the fungal elements (pleomorphic hyphae, yeast forms) was compatible with both the Aspergillus clavatus and Trichosporon beigelii organisms obtained by fungal culture of the intestinal contents. The boa probably developed fungal enteritis from the changes in gut flora induced by prolonged antibiotic treatment; IBD may have been a predisposing factor. Electron microscopy of liver tissue revealed that the inclusions contained granular homogenous osmiophilic material. Lined around the periphery, and occasionally inside the inclusions were numerous clathrin-coated pinocytotic vesicles. A few particles consistent with type C retroviruses, measuring 95-110 nm, were observed in the intercellular spaces, sometimes budding from the cell membrane. The particles were similar to those previously reported in snakes with IBD (see reference). AFIP
Diagnosis: Intestinal epithelium; lymphocytes; intestinal ganglion cells of myenteric plexi: Eosinophilic intracytoplasmic inclusion bodies. Conference
Note: Inclusion body disease of boid snakes has been recognized for over 20 years in private and zoological collections in the United States. The disease affects only snakes of the Family Boidae including both boa constrictors and pythons. The disease is characterized by the formation of intracytoplasmic inclusions in the epithelial cells of all major organs and neurons in the central nervous system. Clinical symptoms include head tremors, disorientation, incoordination, and regurgitation. Ultrastructurally, a type C retrovirus has been associated with the lesions. The presence of a retrovirus is supported by demonstration of reverse transcriptase activity in the plasma and within the supernatant from primary kidney cell cultures of affected snakes. Major histologic lesions include a nonsuppurative meningoencephalitis with neuronal degeneration, gliosis, and demyelinization. Intracytoplasmic inclusions are noted within degenerating neurons of the gray matter and ependymal cells. Inflammation in the central nervous system is more severe in pythons; however, intracytoplasmic inclusions are more numerous in boa constrictors. In the experience of pathologists at the National Zoological Park, Washington D.C., inclusion body disease has been found not only as a primary disease but also in association with secondary infections or as an incidental finding. In fact, many lesions within visceral organs of affected snakes have been attributed to secondary infections. Contributor: Reference:
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