Malassezia spp. Infection: Malasseziasis
Malassezia spp. (formerly Pityrosporum spp.) is rarely associated with disease in rabbits. Opportunistic overgrowth of Malassezia spp. yeast forms has been reported in an outbreak of sarcoptic mange involving 4% of rabbits in a rabbitry.
Malessezia cuniculi has been validated as a new species and appears to be present as a component of the lipophilic microbiota of rabbit skin. The zoonotic significance of rabbit Malassezia is not known.Pneumocystis oryctolagi sp. nov. Infection
Pneumocystis spp. are obligate extracellular yeast-like organisms that are now classified as members of the fungal kingdom. There is high genetic divergence among Pneumocystis species resulting from coevolution within their various mammalian hosts. Each species is host-specific, including P. jirovecii in humans, P. carinii and P. wakefieldae in rats, P. murina in mice, and P. oryctolagi in rabbits. The list of genetically distinct Pneumocystis species is likely to grow with genetic analysis of Pneumocystis from other host species.
Epizootiology and Pathogenesis
Pneumocystis oryctolagi organisms are typically restricted to the alveoli of the lung, and rabbits appear to become infected as neonates, presumably by inhalation or maternal grooming. The life cycle of Pneumocystis includes a trophic form, which replicates asexually by binary fission, and sexual replication through formation of an ascus (cyst) containing 8 ascospores, plus several intermediate forms. Aerosol transmission is mediated by ascospores. Unlike other yeasts, Pneumocystis does not undergo budding. Trophic forms attach to type I pneu- mocytes. Pneumocystis spp. generally exist within their immunocompetent hosts as commensal organisms with minimal consequence. Infection becomes clinically significant under conditions in which the host is immune- compromised.
Pathology
Based on studies in Europe, subclinical pulmonary disease is very common in rabbits during the postweaning period.
Rabbits have extensive diffuse pulmonary lesions that arise abruptly at weaning, evolve over the next 7-10 days, and then slowly resolve, with complete resolution within 3-4 weeks, corresponding to decline in pathogen levels. There is some evidence that intrauterine infections occur, and as early as the 10th day of pregnancy. Lesions described include pulmonary edema, congestion of alveolar vessels, thickening and hypercellularity of alveolar septa with infiltration of mononuclear and polymorphonuclear leukocytes, and exudation into alveolar lumina. During the early stages of infection, organisms can be demonstrated lining alveolar spaces in tissue sections using silver stains. Infection can also be confirmed by PCR and serology.Deep Mycoses
Aside from pulmonary aspergillosis, deep mycoses are quite rare in domestic rabbits. A single case of adiaspir- omycosis in a rabbit with pulmonary granulomata caused by Emmonsia spp. has been reported. Histoplasmosis has also been reported in 2 domestic rabbits. Affected animals had nodular cutaneous lesions. One case had disseminated disease, with multiple periocular, nasal, perioral, and prepucial alopecic nodules upon clinical presentation. Necropsy revealed additional involvement of other cutaneous sites, lymph node, and small intestine. Lesions featured dense infiltration of macrophages, with fewer numbers of heterophils and multinucleated giant cells. Both intracellular and extracellular yeast forms were apparent.
More on the topic Malassezia spp. Infection: Malasseziasis:
- Bacterial Enteric Infections Brachyspira spp. Infection
- Aspergillus spp. Infection: Aspergillosis
- Actinobacillus spp. Infection
- Actinomyces spp. Infection
- Leptospira spp. Infection
- Brucella spp. Infection: Brucellosis
- Chlamydophlla spp. Infection
- Helicobacter spp. Infection
- Mycobacterium spp. Infection: Tuberculosis, Paratuberculosis
- Enterococcus spp. Infection: Enterococcal Enteropathy
- Salmonella spp. Infection: Salmonellosis
- Klebsiella spp. Infection