Immunopathological studies on feline cutaneous and (muco)cutaneous mycobacteriosis
A Kipar1, I Schiller, W Baumgärtner
1Institut für Veterinär-Pathologie, Universität Giessen, Frankfurter Strasse 96, 35392 Giessen, Germany. akipar@liverpool.ac.uk
Insights
Feline mycobacteriosis cases were caused by Mycobacterium tuberculosis or M. avium complex. Inflammatory cells showed cytokine and iNOS expression, indicating low virulence and successful infection control in cats.
Area of Science:
- Veterinary Pathology
- Infectious Diseases
- Immunology
Background:
- Feline (muco)cutaneous mycobacteriosis is a rare condition.
- Identifying causative agents and inflammatory responses is crucial for understanding disease pathogenesis.
Purpose of the Study:
- To identify the causative agents of feline mycobacteriosis.
- To characterize the phenotype and functional characteristics of inflammatory cells involved in the lesions.
Main Methods:
- Polymerase chain reaction (PCR) and sequencing for agent identification.
- Histopathological examination of lesions.
- Immunohistochemistry for inflammatory cell markers and cytokine expression (IL-1beta, IL-6, IL-12, TNF-alpha, iNOS).
Main Results:
- Mycobacterium tuberculosis or M. avium complex identified in equal proportions.
- Lesions showed pyogranulomatous inflammation with varying necrosis and giant cell formation.
- Macrophages expressed myeloid/histiocyte antigen (calprotectin), decreasing with differentiation.
- Cytokines and iNOS were expressed by macrophages, epithelioid cells, and giant cells, particularly in heavily infected cells.
- M. tuberculosis complex showed extracellular bacilli, while M. avium complex showed intracellular bacilli.
Conclusions:
- The intense inflammatory response suggests relatively low virulence of these mycobacterial agents in cats.
- Confinement of bacilli to lesions indicates an effective host response controlling infection spread.
Abstract:
Eight cases of feline (muco)cutaneous mycobacteriosis were studied to identify the causative agent and examine for phenotype and functional characteristics (expression of interleukin (IL)-1beta, IL-6, IL-12, tumour necrosis factor-alpha and inducible nitric oxide synthase) of the inflammatory cells. Polymerase chain reaction and sequencing identified the causative agents as Mycobacterium tuberculosis or M. avium complex in each four cases. Lesions were characterised by pyogranulomatous infiltration, with variability in the presence and size of necrotic areas, the presence of multinucleated giant cells and the degree of lymphocyte infiltration. Macrophages were positive for myeloid/histiocyte antigen (calprotectin), suggesting they represented freshly recruited monocytes; further differentiation to epithelioid cells and multinucleated giant cells was associated with loss of the myeloid/histiocyte antigen. Lymphocytes were found disseminated in the infiltrate (predominantly T cells) and as B cell-dominated accumulations mainly in the periphery of the lesions. Acid-fast bacilli were numerous. In M. tuberculosis complex infection, extracellular bacilli were most prominent, whereas in M. avium complex infection, bacilli were mainly located intracellularly. All cytokines examined as well as inducible nitric oxide synthase (iNOS) were variably expressed by macrophages, epithelioid cells and multinucleated giant cells. Expression was most intense in degenerating macrophages loaded with intracellular bacilli, but was also seen cell-free within necrotic areas. The intense induction of cytokine and iNOS expression especially in infected macrophages suggests a relatively low virulence for these infectious agents in cats. Furthermore, the confinement of the bacilli to lesions indicates a successful response to infection.
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