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dc.contributor.authorAli, Shimaa Elsayed
dc.contributor.authorThoen, Even
dc.contributor.authorEvensen, Øystein
dc.contributor.authorSkaar, Ida
dc.date.accessioned2015-03-01T11:10:57Z
dc.date.accessioned2015-04-24T15:19:11Z
dc.date.available2015-03-01T11:10:57Z
dc.date.available2015-04-24T15:19:11Z
dc.date.issued2014
dc.identifier.citationPLoS ONE 2014, 9(4)nb_NO
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/11250/282455
dc.description-nb_NO
dc.description.abstractSaprolegnia infections cause severe economic losses among freshwater fish and their eggs. The banning of malachite green increased the demand for finding effective alternative treatments to control the disease. In the present study, we investigated the ability of boric acid to control saprolegniosis in salmon eggs and yolk sac fry. Under in vitro conditions, boric acid was able to decrease Saprolegnia spore activity and mycelial growth in all tested concentrations above 0.2 g/L, while complete inhibition of germination and growth was observed at a concentration of 0.8 g/L. In in vivo experiments using Atlantic salmon eyed eggs, saprolegniosis was controlled by boric acid at concentrations ranging from 0.2–1.4 g/L during continuous exposure, and at 1.0–4.0 g/L during intermittent exposure. The same effect was observed on salmon yolk sac fry exposed continuously to 0.5 g/L boric acid during the natural outbreak of saprolegniosis. During the experiments no negative impact with regard to hatchability and viability was observed in either eggs or fry, which indicate safety of use at all tested concentrations. The high hatchability and survival rates recorded following the in vivo testing suggest that boric acid is a candidate for prophylaxis and control of saprolegniosis.
dc.language.isoengnb_NO
dc.rightsNavngivelse 3.0 Norge*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/no/*
dc.titleBoric acid inhibits germination and colonization of Saprolegnia spores in vitro and in vivonb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.date.updated2015-03-01T11:10:57Z
dc.identifier.doi10.1371/journal.pone.0091878
dc.identifier.cristin1147984


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