Disseminated Mycobacterium avium infection in young cats: overrepresentation of Abyssinian cats

Author:

Baral Randolph M.1,Metcalfe Steven S.2,Krockenberger Mark B.3,Catt Melissa J.1,Barrs Vanessa R.4,McWhirter Carol5,Hutson Christina A.6,Wigney Denise I.7,Martin Patricia8,Chen Sharon C.A.8,Mitchell David H.8,Malik Richard9

Affiliation:

1. Paddington Cat Hospital, 183 Glenmore Road, Paddington, NSW 2021, Australia

2. Applecross Veterinary Centre, 9 Sleat Road, Applecross, WA 6153, Australia

3. Faculty of Veterinary Science, University of Sydney, NSW 2006, Australia

4. University of Veterinary Centre, University of Sydney, NSW 2006, Australia

5. Chatswood Veterinary Clinic, 80 Sydney Street, Willoughby, NSW 2068, Australia

6. Animal Hospital of Redondo Beach, 820 Torrance Blvd, Redondo Beach, CA 90277, USA

7. Veterinary Pathology Diagnostic Services Laboratory, University Veterinary Centre, The University of Sydney, NSW 2006, Australia

8. Centre for Infectious Diseases and Microbiology, Institute for Clinical Pathology and Infectious Diseases, Westmead Hospital, Westmead, NSW 2145, Australia

9. Post Graduate Foundation in Veterinary Science, University of Sydney, NSW 2006, Australia

Abstract

Disseminated Mycobacterium avium-intracellulare complex (MAC) infection was diagnosed in 10 young cats (1–5 years of age) from Australia or North America between 1995 and 2004. A further two cats with disseminated mycobacteriosis (precise agent not identified) were recognised during this period. Of the 12, 10 were Abyssinian cats, one was a Somali cat and one was a domestic shorthair cat. None of the cats tested positive for either FeLV antigen or FIV antibody. The clinical course of these infections was indolent, with cats typically presenting for weight loss, initially in the face of polyphagia, with a chronicity of up to several months. Additional clinical features included lower respiratory tract signs and peripheral lymphadenomegaly. A marked diffuse interstitial pattern was evident in thoracic radiographs, even in cats without overt respiratory involvement. Hair clipped to perform diagnostic procedures tended to regrow slowly, if at all. Diagnosis was generally made by obtaining representative tissue specimens from mesenteric lymph nodes, liver or kidney at laparotomy, or from a popliteal lymph node. The primary antecedent event was most likely colonisation of either the alimentary or respiratory tract, followed by local invasion and eventual lymphatic and haematogenous dissemination. Nine cases were treated using combination therapy with agents effective for MAC infection in human patients. Two cats are still undergoing initial therapy and have responded. Of the remaining seven, all responded during long courses (5–14 months) of clarithromycin combined with either clofazimine or rifampicin, and a fluoroquinolone or doxycycline. Of these, three cats remain well (with durations between 2 months and 2 years following therapy); two developed recurrent disease (at 3 months and 2 years, respectively, following therapy) and have restarted therapy. The remaining two cats improved 1 year and 5 months, respectively, after diagnosis but ultimately succumbed. The two cats in which therapy was restarted have improved dramatically. Certain lines of Abyssinian and Somali cats likely suffer from a familial immunodeficiency that predisposes them to infection with slow-growing mycobacteria such as MAC.

Publisher

SAGE Publications

Subject

Small Animals

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