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In Vitro and In Vivo Evaluation of Potassium Permanganate Treatment Efficacy for the Control of Acute Experimental Infection by Flavobacterium columnare in Channel Catfish
Author(s) -
Darwish Ahmed M.,
Mitchell Andrew J.,
Hobbs Melissa S.
Publication year - 2008
Publication title -
north american journal of aquaculture
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 41
eISSN - 1548-8454
pISSN - 1522-2055
DOI - 10.1577/a06-081.1
Subject(s) - catfish , biology , in vivo , microbiology and biotechnology , potassium permanganate , mucus , gill , ictalurus , pathology , chemistry , fish <actinopterygii> , fishery , medicine , ecology , organic chemistry
An experiment was performed to evaluate the in vitro and in vivo efficacy of potassium permanganate (KMnO 4 ) against Flavobacterium columnare. In vitro, F. columnare treated with KMnO 4 at 2 mg/L for 8 h exhibited a 70% reduction in colony‐forming units (CFU). A minimum KMnO 4 concentration of 10 mg/L was needed to inhibit bacterial growth. An acute and systemic experimental infection was produced in channel catfish Ictalurus punctatus by waterborne exposure to the bacteria after mechanical cutaneous abrasion to remove mucus and epithelium. At 22 h postchallenge, an 8‐h treatment with KMnO 4 at 2.3 mg/L (2.0 mg/L above the average KMnO 4 demand of 0.3 mg/L) was initiated. This did not reduce mortality in experimentally infected fish. The infection model utilized in the experiment was evaluated by examining the clinical signs and histopathology of infected fish. Fish in the model showed columnaris signs similar to those of a natural infection, including skin depigmentation and ulceration and gill necrosis. Histologically, the skin had severe ulcerative necrotizing dermatitis and the muscles had severe necrotizing myositis. The gills had severe multifocal necrotizing branchitis involving the lamellar and filament epithelium, pillar cells, and central venous sinus. Heavy bacterial aggregates of long rods were associated with the necrotic cellular debris. The identity of the bacteria isolated from the challenged fish was confirmed by polymerase chain reaction. The results suggest that KMnO 4 is beneficial for reducing F. columnare load in the water column and possibly on fish, but the therapeutic value of KMnO 4 is limited in fish with an acute and systemic columnaris infection. Further research is warranted to investigate the value of KMnO 4 as a therapeutic agent for fish with a milder columnaris infection and as a treatment to prevent further spread of columnaris in a fish population.