Chapter 39 Mycobacteriosis
Mycobacteria are gram-positive organisms that cause sporadic disease in human beings and in animals. All mycobacterial organisms contain a lipid-rich cell wall that inhibits host defense mechanisms and imparts a characteristic staining property in the laboratory. This staining property involves the retention of carbolfuchsin after acid and alcohol decolorization. Thus mycobacteria are classified as acid-fast staining organisms.
2. Localized disease caused by saprophytic mycobacteria in immunocompetent hosts
a. Where the infection is self-limiting and the immune response eventually eliminates the organisms (e.g., canine leproid granuloma syndrome)
FELINE LEPROSY SYNDROMES
Feline Leprosy Caused by Mycobacterium Lepraemurium
Etiology
• Caused by M. lepraemurium, the rat leprosy organism. Although the rat leprosy organism had been suspected for many years, it was only in the 1980s that sophisticated culture techniques and biochemical analysis could identify M. lepraemurium as the etiologic agent.
• The mode of transmission is unknown, although cats are thought to become infected following bite injuries from infected rats.
Clinical Signs
• Young adult cats are affected, predominantly males living in either suburban or rural environments.
• Lesions are painless, raised, fleshy, freely movable nodules of a few millimeters up to 4 cm in diameter. They may develop rapidly, and some ulcerate when large.
• Nodules are usually multiple (but may be single), tend to initially concentrate in one body region, and may spread to adjacent areas and regional lymph nodes.
• Nodules may occur anywhere on the body, but the head and limbs are more frequently affected. Additionally, lesions may occur on the lips, oral mucosa, tongue, and nasal mucosa. The condition disseminates rarely to the spleen, bone marrow, liver, kidney, lung, or adjacent muscle. Cats with disseminated disease usually show signs of systemic illness, which are not seen in cats with localized infection.
Diagnosis
• The diagnosis is achieved primarily through histologic evaluation of biopsy samples in conjunction with compatible history, physical examination, cytology, culture, and laboratory animal inoculation findings.
• The differential diagnoses for feline leprosy include atypical mycobacteriosis, tuberculosis, foreign body dermatitis, deep mycotic infections, mycetomas, dermatophyte pseudomycetomas, chronic bacterial infections, eosinophilic granuloma complex, and neoplastic diseases.
Cytology
• Cytology of needle aspirates or lesional impression smears reveals mixed inflammatory cells with macrophages and histiocytes containing variable numbers (often many) of acid-fast bacilli (long slender rods). In Diff-Quik–stained preparations, negative-staining organisms are seen within macrophages. Ziehl-Neelsen stain and a modified Fite’s stain are the acid-fast stains most commonly used.
Biopsy
• Biopsy specimens of lesions are fixed in 10% buffered formalin and evaluated histologically, using both hematoxylin-eosin and acid-fast stains (Ziehl-Neelsen and modified Fite’s stains). (See Chapter 37 for skin biopsy technique.)
• Histologically, two forms are seen: tuberculoid and lepromatous forms. The tuberculoid form (most common in the United States and Canada) consists primarily of non-encapsulated epithelioid granulomas that are interspersed with neutrophils and surrounded by a zone of lymphocytes with low numbers of organisms. The lepromatous form is composed of sheets of large foamy macrophages that contain large numbers of acid-fast bacilli. The tuberculoid form is associated with a more competent host immune response.
Polymerase Chain Reaction
• Polymerase chain reaction (PCR) amplification of gene fragments from tissue samples provides a rapid and accurate diagnosis and identification of the causative organisms. Fresh (frozen) tissue or freeze-dried tissue is best, although PCR can also be performed on formalin-fixed, paraffin-embedded samples. (PCR for mycobacterial organisms is performed at the School of Veterinary Medicine, University of California, Davis, CA.)
Laboratory Animal Inoculation
• Laboratory animal inoculation is used primarily in research to propagate and investigate the feline leprosy organism. This procedure is of greatest value for differentiating feline leprosy from tuberculosis. Only tuberculosis-producing mycobacteria routinely kill guinea pigs within 6 to 8 weeks after inoculation.
Treatment
• Clofazimine may cause a reversible hepatopathy, and regular biochemical monitoring of cats is mandatory. Vomiting and inappetence are strong indications to reduce the dose and to perform a biochemical evaluation of the patient. Photosensitivity and pitting corneal edema have also been noted in cats.