Oral immunoprophylaxis of finfish using alginate microencapsulation

Oral delivery is a potential solution to constraints associated with the immunoprophylaxismethods most prevalent in aquaculture: injection and immersion. However, oral immunogendelivery has produced inconsistent outcomes in fish. This is primarily attributed to antigendegradation, solutions to which...

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Main Authors: Ghosh, B, Cain, KD, Nowak, BF, Bridle, AR
Format: Conference Object
Language:English
Published: . 2014
Subjects:
Online Access:http://ecite.utas.edu.au/105000
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spelling ftunivtasecite:oai:ecite.utas.edu.au:105000 2023-05-15T18:09:54+02:00 Oral immunoprophylaxis of finfish using alginate microencapsulation Ghosh, B Cain, KD Nowak, BF Bridle, AR 2014 application/pdf http://ecite.utas.edu.au/105000 en eng . http://ecite.utas.edu.au/105000/1/Proceedings isaah7-24b.pdf Ghosh, B and Cain, KD and Nowak, BF and Bridle, AR, Oral immunoprophylaxis of finfish using alginate microencapsulation, Proceedings of the Seventh International Symposium on Aquatic Animal Health, 31 August - 4 September 2014, Portland, Oregon, USA, pp. 174. (2014) [Conference Extract] http://ecite.utas.edu.au/105000 Agricultural and Veterinary Sciences Fisheries Sciences Aquaculture Conference Extract NonPeerReviewed 2014 ftunivtasecite 2019-12-13T22:06:15Z Oral delivery is a potential solution to constraints associated with the immunoprophylaxismethods most prevalent in aquaculture: injection and immersion. However, oral immunogendelivery has produced inconsistent outcomes in fish. This is primarily attributed to antigendegradation, solutions to which are typically complex and expensive. Here, we developed andvalidated a method for oral fish immunoprophylaxis using alginate microcapsules (aMCs). Anemulsion/internal-gelation protocol was adapted to minimize impact on the material beingencapsulated. Microcapsules were characterized in vitro using lysozyme and bovine serumalbumin (BSA). Post-encapsulation change in bioactivity of lysozyme was used to determineprotocol impacts on the encapsulated substance. aMC release dynamics were tested at differentpH levels and temperatures using BSA. Uptake and systemic distribution was verified usingFITC-labeled BSA-aMCs ex vivo in intestinal explants, and combined in feed for in vivo administration to Salmo salar fry. Oncorhynchus mykiss fry were immunized against Flavobacterium psychrophilum infection with microencapsulated live attenuated oral vaccine.Microencapsulation did not significantly reduce lysozyme bioactivity. BSA release from aMCswas pH- and temperature-responsive. Uptake and translocation of aMCs was visible ex vivo and in vivo . Oral immunization significantly increased survival against bacterial challenge (F=11.4;p=0.01), and was comparable to IP immunization. Our findings indicate this method could be aconvenient, effective alternative to prevalent finfish immunoprophylaxis strategies. Conference Object Salmo salar eCite UTAS (University of Tasmania)
institution Open Polar
collection eCite UTAS (University of Tasmania)
op_collection_id ftunivtasecite
language English
topic Agricultural and Veterinary Sciences
Fisheries Sciences
Aquaculture
spellingShingle Agricultural and Veterinary Sciences
Fisheries Sciences
Aquaculture
Ghosh, B
Cain, KD
Nowak, BF
Bridle, AR
Oral immunoprophylaxis of finfish using alginate microencapsulation
topic_facet Agricultural and Veterinary Sciences
Fisheries Sciences
Aquaculture
description Oral delivery is a potential solution to constraints associated with the immunoprophylaxismethods most prevalent in aquaculture: injection and immersion. However, oral immunogendelivery has produced inconsistent outcomes in fish. This is primarily attributed to antigendegradation, solutions to which are typically complex and expensive. Here, we developed andvalidated a method for oral fish immunoprophylaxis using alginate microcapsules (aMCs). Anemulsion/internal-gelation protocol was adapted to minimize impact on the material beingencapsulated. Microcapsules were characterized in vitro using lysozyme and bovine serumalbumin (BSA). Post-encapsulation change in bioactivity of lysozyme was used to determineprotocol impacts on the encapsulated substance. aMC release dynamics were tested at differentpH levels and temperatures using BSA. Uptake and systemic distribution was verified usingFITC-labeled BSA-aMCs ex vivo in intestinal explants, and combined in feed for in vivo administration to Salmo salar fry. Oncorhynchus mykiss fry were immunized against Flavobacterium psychrophilum infection with microencapsulated live attenuated oral vaccine.Microencapsulation did not significantly reduce lysozyme bioactivity. BSA release from aMCswas pH- and temperature-responsive. Uptake and translocation of aMCs was visible ex vivo and in vivo . Oral immunization significantly increased survival against bacterial challenge (F=11.4;p=0.01), and was comparable to IP immunization. Our findings indicate this method could be aconvenient, effective alternative to prevalent finfish immunoprophylaxis strategies.
format Conference Object
author Ghosh, B
Cain, KD
Nowak, BF
Bridle, AR
author_facet Ghosh, B
Cain, KD
Nowak, BF
Bridle, AR
author_sort Ghosh, B
title Oral immunoprophylaxis of finfish using alginate microencapsulation
title_short Oral immunoprophylaxis of finfish using alginate microencapsulation
title_full Oral immunoprophylaxis of finfish using alginate microencapsulation
title_fullStr Oral immunoprophylaxis of finfish using alginate microencapsulation
title_full_unstemmed Oral immunoprophylaxis of finfish using alginate microencapsulation
title_sort oral immunoprophylaxis of finfish using alginate microencapsulation
publisher .
publishDate 2014
url http://ecite.utas.edu.au/105000
genre Salmo salar
genre_facet Salmo salar
op_relation http://ecite.utas.edu.au/105000/1/Proceedings isaah7-24b.pdf
Ghosh, B and Cain, KD and Nowak, BF and Bridle, AR, Oral immunoprophylaxis of finfish using alginate microencapsulation, Proceedings of the Seventh International Symposium on Aquatic Animal Health, 31 August - 4 September 2014, Portland, Oregon, USA, pp. 174. (2014) [Conference Extract]
http://ecite.utas.edu.au/105000
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