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Flavobacterium psychrophilum, cause of ... - cop.eXtension.org

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Treatment<br />

Although many treatments are discussed within this section, licensed procedures vary<br />

within different countries. An individual must, therefore, become familiar with and<br />

utilize only those treatments, which have been <strong>of</strong>ficially sanctioned or licensed by the<br />

appropriate regulatory authority for use within a specific geographic region.<br />

Chemical baths have limited impact against F. <strong>psychrophilum</strong> be<strong>cause</strong> the bacterium<br />

generally establishes systemic infections. Furanace, (generic name for this compound is<br />

nifurpirinol) however, is a nitr<strong>of</strong>uran that is rapidly absorbed from the water into fish<br />

tissues. Be<strong>cause</strong> therapeutic levels <strong>of</strong> this compound are readily absorbed within the fish,<br />

furanace has provided effective control <strong>of</strong> BCWD when administered to fry as a 60-<br />

minute bath repeated at three day intervals at 0.5 µg <strong>of</strong> drug mL -1 <strong>of</strong> water (Holt et al.<br />

1975). Control was also achieved among fingerlings by application <strong>of</strong> similar baths<br />

administered twice weekly. Even just a single 60-minute bath treatment in furanace at<br />

10-15 mg L -1 has been effective (Wood 1974). In another study, single 60-minute bath<br />

applications <strong>of</strong> nifurpirinol at 1 mg mL -1 also provided favorable control <strong>of</strong> F.<br />

<strong>psychrophilum</strong>, but the compound was even more effective when fish were treated with<br />

two baths, 24 hours apart (Amend 1972). Be<strong>cause</strong> nitr<strong>of</strong>urans are carcinogenic, these<br />

compounds are not approved for use on food fish within the United States.<br />

In early stages <strong>of</strong> external infections, bath treatments with either water-soluble<br />

oxytetracycline at 10-50 mg L -1 or quaternary ammonium compounds at 2 mg L -1 have<br />

been recommended (Snieszko 1964; Schachte 1983). Such treatments are generally

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