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Assessment of florfenicol as a possible treatment for chlamydiosis in koalas ( Phascolarctos cinereus )
Author(s) -
Budd C,
Flanagan C,
Gillett A,
Hanger J,
Loader JJ,
Govendir M
Publication year - 2017
Publication title -
australian veterinary journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.382
H-Index - 59
eISSN - 1751-0813
pISSN - 0005-0423
DOI - 10.1111/avj.12617
Subject(s) - florfenicol , dose , chlamydia , pharmacokinetics , pharmacology , antibiotics , chloramphenicol , biology , medicine , immunology , microbiology and biotechnology
Objective Because of limited availability of chloramphenicol to veterinary suppliers, a preliminary study was performed to predict whether an analogue, florfenicol, is an efficacious treatment for chlamydiosis in koalas. Methods Florfenicol was administered to koalas with naturally occurring chlamydiosis at 20 mg/kg SC (n = 3) and at 5 mg/kg (n = 3) and 10 mg/kg (n = 3) IV. The estimated areas under the plasma concentration versus time curves (AUC) were compared with the minimum inhibitory concentration to inhibit Chlamydia pecorum . Clinical data were also examined from field trials conducted on koalas (n = 19) with naturally occurring chlamydiosis and treated with florfenicol at a range of dosages (5–20 mg/kg SC and 6–15 mg/kg IV). Florfenicol binding to proteins in plasma was also determined. Results Florfenicol was not detectable in plasma 24 h post‐administration at 20 mg/kg SC. The estimated AUC 0–24 h following administration at 10 mg/kg IV suggests florfenicol might be effective against Chlamydia spp. via this route. Florfenicol binding to plasma proteins was 13.0% (± 0.30 SEM). After treatment with florfenicol in field trials, 5 of 19 koalas (26%) were released without further treatment, 4 with no long‐term follow‐up; 6 (32%) required additional treatment with chloramphenicol to resolve chlamydiosis; 7 (36%) failed to clinically improve, of which 3 had clinical signs and/or necropsy findings suggestive of antibiotic‐related gastrointestinal dysbiosis; another koala died within minutes of florfenicol administered IV at 7 mg/kg. Conclusion When administered at dosages tolerable in the field, florfenicol is a problematic treatment for chlamydiosis based on equivocal outcomes and plasma concentrations below those that inhibit the pathogen.