High incidence of Mycobacterium avium subspecies hominissuis infection in a zoo population of bongo antelopes (Tragelaphus eurycerus)
Language English Country United States Media print-electronic
Document type Case Reports, Journal Article, Research Support, Non-U.S. Gov't
PubMed
23780935
DOI
10.1177/1040638713490689
PII: 1040638713490689
Knihovny.cz E-resources
- Keywords
- Antelopes, Mycobacterium avium complex, genotyping, mycobacteriosis, zoonosis,
- MeSH
- Antelopes microbiology MeSH
- DNA, Bacterial chemistry genetics MeSH
- Fatal Outcome MeSH
- Feces microbiology MeSH
- Genotype MeSH
- Incidence MeSH
- Mycobacterium avium genetics isolation & purification MeSH
- Lung Diseases epidemiology microbiology veterinary MeSH
- Polymerase Chain Reaction veterinary MeSH
- Soil Microbiology MeSH
- DNA Transposable Elements genetics MeSH
- Tuberculosis epidemiology microbiology veterinary MeSH
- Animals, Zoo MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA, Bacterial MeSH
- DNA Transposable Elements MeSH
Mycobacterium avium subsp. hominissuis (Mah) infection was diagnosed in 5 captive bongo antelopes (Tragelaphus eurycerus) originating from a collection in a zoological garden. The animals suffered from emaciation. Postmortem examination revealed nodular lesions in the lungs of all 5 examined animals. Acid-fast bacilli were observed in the lungs of 4 animals. Culture and polymerase chain reaction identification based on IS901 negativity and IS1245 positivity confirmed Mah infection in the lungs of all 5 antelopes. In 3 animals, Mah was also isolated from other organs (liver, spleen, and kidney). Molecular analysis of these isolates using IS1245 restriction fragment length polymorphism and/or mycobacterial interspersed repetitive units-variable number tandem repeat revealed that the studied antelopes were infected by 1 identical genotype. Furthermore, in 2 antelopes, other genotypes were also detected. This shows the possibility of either genetic modifications occurring during infection or polyclonal infection. Culture examination of environmental samples from the enclosures holding the bongos revealed Mah in mulch bark, peat, and soil. Genotyping of these environmental isolates determined several genotypes with 1 dominant genotype that was identical to the dominant genotype detected in antelopes.
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