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Development of an in vivo-mimic silkworm infection model with Mycobacterium avium complex
- Source :
- Drug Discoveries & Therapeutics. 14:287-295
- Publication Year :
- 2020
- Publisher :
- International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA), 2020.
-
Abstract
- In vivo-mimic silkworm infection models with Mycobacterium avium and Mycobacterium intracellulare were newly established to evaluate the therapeutic effects of anti-M. avium complex (MAC) antibiotics. Silkworms raised at 37°C died within 72 hours of an injection of M. avium or M.intracellulare (2.5 × 107 colony-forming unit (CFU)/larva·g) into the hemolymph. Clinical anti-mycobacterial (tuberculosis) antibiotics were evaluated under these conditions. Clarithromycin, kanamycin, streptomycin, amikacin, and ciprofloxacin exerted therapeutic effects in a dose-dependent manner, which was consistent with those in the mouse model. Furthermore, three effective actinomycete culture broths were selected in the screening program of our microbial broth library using the silkworm model, and four active metabolites, ohmyungsamycins A and B (1 and 2), chartreusin (3), and griseoviridin (4), were identified. Among these compounds, 1 showed the lowest 50% effective dose (ED50) value (8.5 µg/larva·g), while 3 had the best ED50/minimum inhibitory concentration (MIC) ratio (7.4). These results indicate that silkworm models are a useful tool for identifying anti-MAC antibiotics candidates with veritable therapeutic effects.
- Subjects :
- biology
010405 organic chemistry
medicine.drug_class
Chartreusin
fungi
Antibiotics
Kanamycin
General Medicine
010402 general chemistry
biology.organism_classification
01 natural sciences
0104 chemical sciences
Microbiology
Minimum inhibitory concentration
Amikacin
Streptomycin
Clarithromycin
medicine
Pharmacology (medical)
General Pharmacology, Toxicology and Pharmaceutics
medicine.drug
Mycobacterium
Subjects
Details
- ISSN :
- 1881784X and 18817831
- Volume :
- 14
- Database :
- OpenAIRE
- Journal :
- Drug Discoveries & Therapeutics
- Accession number :
- edsair.doi...........de9471de98902e06d862927ea70048f3
- Full Text :
- https://doi.org/10.5582/ddt.2020.03099