Systemic Nocardiosis in an Adult Female Leopard Seal (Hydrurga leptonyx), in a Zoological Facility
IAAAM 2010
Alana Shrubsole-Cockwill1; Cheryl Sangster2; Larry Vogelnest2
1North Shore Veterinary Specialist Centre, Crows Nest, NSW, Australia; 2Taronga Conservation Society Australia, Mosman, NSW, Australia

Abstract

Leopard seals (Hydrurga leptonyx) are widely distributed and primarily inhabit the Antarctic pack ice and sub-Antarctic islands, ranging between 50-80°S.4 Vagrant leopard seals occasionally haul out in regions of the world remote from Antarctica. These animals are frequently debilitated. On August 5th 1999, a juvenile (estimated age of 8 months), female leopard seal was found hauled out at Garie Beach (151.06839E 34.17015S) in Royal National Park, New South Wales, Australia. The animal was weak and emaciated with skin wounds consistent with cookie cutter shark (Isistius brasiliensis) bites. She was taken to Taronga Zoo, Sydney for assessment and care. The animal was deemed unsuitable for rehabilitation and release and held in permanent care at Taronga Zoo.

In 2008 the leopard seal presented with a 6 month history of intermittent inappetence, lethargy and depression. Various treatments were administered including non-steroidal anti-inflammatories, H2 blockers, and antibiotics. The seal would make dramatic improvements only to become inappetant again with no apparent instigating factor. Further diagnostics were impeded because of the risk of physical restraint and anaesthesia when dealing with this species. Despite medical management and continued supportive care, the animal continued to deteriorate and died in May 2008.

On post mortem examination, there was a pyogranulomatous and necrotizing, multifocal to coalescing, subacute and severe pneumonia with pulmonary congestion, edema and focal fibrosis surrounding a firm mass. Other notable gross findings included serosanguineous and fibrinous hydrothorax, serous hydropericardium, renal papillary necrosis and small nodules in the cortex of the kidneys. Histologically, gram-positive long, branching, filamentous bacteria were present throughout the neutrophilic foci of the lung and granulation tissue surrounding a necrotic portion of the lung, corresponding to the firm mass noted grossly. These filamentous bacteria were partially acid fast on a modified Ziehl Neelsen stain but not on a Kinyoun stain. Nocardia otitidiscavarium were isolated on bacterial culture from the kidney, lung and pleural fluid demonstrating a septicemia. The infection had disseminated to multiple tissues including liver, kidney and brain, manifesting as pyogranulomatous foci.

Nocardia are soil saphrophytes with a worldwide distribution which degrade organic matter and are found in soil, water and on plants.3,4,6,7 Nocardia are gram-positive, partially acid fast, rods that are branched and filamentous in tissue and culture. Nocardia can gain access to its host following contamination of wounds and inhalation.

Nocardia spp. have been reported to cause pyogranulomatous lesions in free-ranging and captive cetaceans and pinnipeds.1,2,8,9 There have been two reported cases of pulmonary lesions in leopard seals,1,8 both of which were males found in Hawke's Bay on the south east coast of the North Island of New Zealand.

Potential sources of Nocardia in this case are aerosolization of the organism from soil due to construction taking place near the enclosure or the presence of an underlying Nocardia infection when the animal was initially taken into care. Nocardiosis should be considered as a differential for pulmonary disease in leopard seals and other pinnipeds.

Acknowledgements

The authors thank Dr Kimberly Vinette Herrin, Dr Frances Hulst, Kaye Humphreys and the marine mammal keepers at Taronga Zoo for their assistance with the management of this case.

References

1.  Davis GB, Stevenson BJ, Kyle RJ, Price MC 1977. Isolation of an actinomycete from a sea leopard (Hydrurga leptonyx). N Z Vet J 25:274.

2.  Dunn JL, Buck JD, Robeck TR 2001. Bacterial diseases of cetaceans and pinnipeds (Ch. 16). Dierauf LA and FMD Gulland, ed. In: CRC Handbook of Marine Mammal Medicine, 2nd ed. pp. 321-325. CRC Press, New York, NY, USA. ISBN 0-8493-0839-9.

3.  Edwards DF 2009. Actinomycosis and nocardiosis (Ch. 49). CE Greene, ed. In: Infectious Disease of the Dog and Cat. 3rd ed. pp.456-461 Saunders Elsevier. St. Louis, Missouri, USA. ISBN-10: 1-4160-3600-8.

4.  Goodfellow M, Williams ST 1983. Ecology of actinomycetes. Ann Rev Microbiol 37:189-216.

5.  Hofman RJ, Reichle RA, Siniff DB, Müller-Schwarze D 1977. The leopard seal (Hydrurga leptonyx) at Palmer Station, Antarctica. Adaptations within Antarctic ecosystems. G.A. Llano, ed. In: Proc Third SCAR Symp on Antarctic Biol:769-783.

6.  Murray PR, Rosenthal KS, Pfaller M 2009. Nocardia and related bacterial (Ch. 27). Murray PR, Rosenthal KS, and M Pfaller. eds. 6th ed. Medical Microbiology. Mosby Elsevier. Philadelphia, PA, USA; pp 269-273. USBN 978-0-323-05470-6.

7.  Orchard VA, Goodfellow M, Williams ST 1977. Selective isolation and occurrence of nocardiae in soil. Soil Biol Biochem 9:233-238.

8.  St. Leger JA, Begeman L, Fleetwood M, Frasca Jr. S, Garner MM, Lair S, Trembley S, Linn MJ, Terio KA 2009. Comparative pathology of nocardiosis in marine mammals. Vet Pathol 46:299-308.

9.  Sweeney JC, Migaki G, Vainik PM, Conklin RH. 1976. Systemic mycoses in marine mammals. J Am Vet Med Assoc 169:946-948.

 

Speaker Information
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Alana Shrubsole-Cockwill
North Shore Veterinary Specialist Centre
Crows Nest, NSW, Australia


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