Cargando…

Microencapsulation of Piscirickettsia salmonis Antigens for Fish Oral Immunization: Optimization and Stability Studies

The development of fish oral vaccines is of great interest to the aquaculture industry due to the possibility of rapid vaccination of a large number of animals at reduced cost. In a previous study, we evaluated the effect of alginate-encapsulated Piscirickettsia salmonis antigens (AEPSA) incorporate...

Descripción completa

Detalles Bibliográficos
Autores principales: Sotomayor-Gerding, Daniela, Troncoso, José Miguel, Díaz-Riquelme, Katherine, Torres-Obreque, Karin Mariana, Cumilaf, Juan, Yañez, Alejandro J., Rubilar, Mónica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741032/
https://www.ncbi.nlm.nih.gov/pubmed/36501507
http://dx.doi.org/10.3390/polym14235115
_version_ 1784848216345280512
author Sotomayor-Gerding, Daniela
Troncoso, José Miguel
Díaz-Riquelme, Katherine
Torres-Obreque, Karin Mariana
Cumilaf, Juan
Yañez, Alejandro J.
Rubilar, Mónica
author_facet Sotomayor-Gerding, Daniela
Troncoso, José Miguel
Díaz-Riquelme, Katherine
Torres-Obreque, Karin Mariana
Cumilaf, Juan
Yañez, Alejandro J.
Rubilar, Mónica
author_sort Sotomayor-Gerding, Daniela
collection PubMed
description The development of fish oral vaccines is of great interest to the aquaculture industry due to the possibility of rapid vaccination of a large number of animals at reduced cost. In a previous study, we evaluated the effect of alginate-encapsulated Piscirickettsia salmonis antigens (AEPSA) incorporated in feed, effectively enhancing the immune response in Atlantic salmon (Salmo salar). In this study, we seek to characterize AEPSA produced by ionic gelation using an aerodynamically assisted jetting (AAJ) system, to optimize microencapsulation efficiency (EE%), to assess microparticle stability against environmental (pH, salinity and temperature) and gastrointestinal conditions, and to evaluate microparticle incorporation in fish feed pellets through micro-CT-scanning. The AAJ system was effective in obtaining small microparticles (d < 20 μm) with a high EE% (97.92%). Environmental conditions (pH, salinity and temperature) generated instability in the microparticles, triggering protein release. 62.42% of the protein content was delivered at the intestinal level after in vitro digestion. Finally, micro-CT-scanning images confirmed microparticle incorporation in fish feed pellets. In conclusion, the AAJ system is effective at encapsulating P. salmonis antigens in alginate with a high EE% and a size small enough to be incorporated in fish feed and produce an oral vaccine.
format Online
Article
Text
id pubmed-9741032
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-97410322022-12-11 Microencapsulation of Piscirickettsia salmonis Antigens for Fish Oral Immunization: Optimization and Stability Studies Sotomayor-Gerding, Daniela Troncoso, José Miguel Díaz-Riquelme, Katherine Torres-Obreque, Karin Mariana Cumilaf, Juan Yañez, Alejandro J. Rubilar, Mónica Polymers (Basel) Article The development of fish oral vaccines is of great interest to the aquaculture industry due to the possibility of rapid vaccination of a large number of animals at reduced cost. In a previous study, we evaluated the effect of alginate-encapsulated Piscirickettsia salmonis antigens (AEPSA) incorporated in feed, effectively enhancing the immune response in Atlantic salmon (Salmo salar). In this study, we seek to characterize AEPSA produced by ionic gelation using an aerodynamically assisted jetting (AAJ) system, to optimize microencapsulation efficiency (EE%), to assess microparticle stability against environmental (pH, salinity and temperature) and gastrointestinal conditions, and to evaluate microparticle incorporation in fish feed pellets through micro-CT-scanning. The AAJ system was effective in obtaining small microparticles (d < 20 μm) with a high EE% (97.92%). Environmental conditions (pH, salinity and temperature) generated instability in the microparticles, triggering protein release. 62.42% of the protein content was delivered at the intestinal level after in vitro digestion. Finally, micro-CT-scanning images confirmed microparticle incorporation in fish feed pellets. In conclusion, the AAJ system is effective at encapsulating P. salmonis antigens in alginate with a high EE% and a size small enough to be incorporated in fish feed and produce an oral vaccine. MDPI 2022-11-24 /pmc/articles/PMC9741032/ /pubmed/36501507 http://dx.doi.org/10.3390/polym14235115 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sotomayor-Gerding, Daniela
Troncoso, José Miguel
Díaz-Riquelme, Katherine
Torres-Obreque, Karin Mariana
Cumilaf, Juan
Yañez, Alejandro J.
Rubilar, Mónica
Microencapsulation of Piscirickettsia salmonis Antigens for Fish Oral Immunization: Optimization and Stability Studies
title Microencapsulation of Piscirickettsia salmonis Antigens for Fish Oral Immunization: Optimization and Stability Studies
title_full Microencapsulation of Piscirickettsia salmonis Antigens for Fish Oral Immunization: Optimization and Stability Studies
title_fullStr Microencapsulation of Piscirickettsia salmonis Antigens for Fish Oral Immunization: Optimization and Stability Studies
title_full_unstemmed Microencapsulation of Piscirickettsia salmonis Antigens for Fish Oral Immunization: Optimization and Stability Studies
title_short Microencapsulation of Piscirickettsia salmonis Antigens for Fish Oral Immunization: Optimization and Stability Studies
title_sort microencapsulation of piscirickettsia salmonis antigens for fish oral immunization: optimization and stability studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741032/
https://www.ncbi.nlm.nih.gov/pubmed/36501507
http://dx.doi.org/10.3390/polym14235115
work_keys_str_mv AT sotomayorgerdingdaniela microencapsulationofpiscirickettsiasalmonisantigensforfishoralimmunizationoptimizationandstabilitystudies
AT troncosojosemiguel microencapsulationofpiscirickettsiasalmonisantigensforfishoralimmunizationoptimizationandstabilitystudies
AT diazriquelmekatherine microencapsulationofpiscirickettsiasalmonisantigensforfishoralimmunizationoptimizationandstabilitystudies
AT torresobrequekarinmariana microencapsulationofpiscirickettsiasalmonisantigensforfishoralimmunizationoptimizationandstabilitystudies
AT cumilafjuan microencapsulationofpiscirickettsiasalmonisantigensforfishoralimmunizationoptimizationandstabilitystudies
AT yanezalejandroj microencapsulationofpiscirickettsiasalmonisantigensforfishoralimmunizationoptimizationandstabilitystudies
AT rubilarmonica microencapsulationofpiscirickettsiasalmonisantigensforfishoralimmunizationoptimizationandstabilitystudies