Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)

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Tilapia Lake Virus (TiLV) is a pathogen that causes massive mortalities in both cultured and wild tilapia populations around the world. The development of an effective vaccine against this emerging pathogen is imperative to prevent economic losses. In this work an expression vector was designed and...

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Detalles Bibliográficos
Autores: Criollo Joaquin, Mónica Paola, Motte, Emmerik, Salvatierra, Max, Medina, Jorge, Diringer, Benoit, Sandoval, Gustavo, Mialhe, Eric
Formato: artículo
Fecha de Publicación:2019
Institución:Universidad Nacional Mayor de San Marcos
Repositorio:Revistas - Universidad Nacional Mayor de San Marcos
Lenguaje:español
OAI Identifier:oai:ojs.csi.unmsm:article/15516
Enlace del recurso:https://revistasinvestigacion.unmsm.edu.pe/index.php/rpb/article/view/15516
Nivel de acceso:acceso abierto
Materia:aquaculture
tilapia
structural homology
gene expression
neuraminidase
acuicultura
homología estructural
expresión génica
neuraminidasa
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network_acronym_str REVUNMSM
network_name_str Revistas - Universidad Nacional Mayor de San Marcos
repository_id_str
dc.title.none.fl_str_mv Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)
Diseño y evaluación de la expresión de una potencial vacuna de ADN contra el virus de la Tilapia de Lago (TiLV)
title Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)
spellingShingle Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)
Criollo Joaquin, Mónica Paola
aquaculture
tilapia
structural homology
gene expression
neuraminidase
tilapia
acuicultura
homología estructural
expresión génica
neuraminidasa
title_short Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)
title_full Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)
title_fullStr Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)
title_full_unstemmed Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)
title_sort Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)
dc.creator.none.fl_str_mv Criollo Joaquin, Mónica Paola
Motte, Emmerik
Salvatierra, Max
Medina, Jorge
Diringer, Benoit
Sandoval, Gustavo
Mialhe, Eric
author Criollo Joaquin, Mónica Paola
author_facet Criollo Joaquin, Mónica Paola
Motte, Emmerik
Salvatierra, Max
Medina, Jorge
Diringer, Benoit
Sandoval, Gustavo
Mialhe, Eric
author_role author
author2 Motte, Emmerik
Salvatierra, Max
Medina, Jorge
Diringer, Benoit
Sandoval, Gustavo
Mialhe, Eric
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv aquaculture
tilapia
structural homology
gene expression
neuraminidase
tilapia
acuicultura
homología estructural
expresión génica
neuraminidasa
topic aquaculture
tilapia
structural homology
gene expression
neuraminidase
tilapia
acuicultura
homología estructural
expresión génica
neuraminidasa
description Tilapia Lake Virus (TiLV) is a pathogen that causes massive mortalities in both cultured and wild tilapia populations around the world. The development of an effective vaccine against this emerging pathogen is imperative to prevent economic losses. In this work an expression vector was designed and evaluated as a potential DNA vaccine against this virus. Initially, a threading analysis was done to predict the three-dimensional structures and functions of the TiLV proteins. Structural homologies were found between the TiLV proteins corresponding to the genomic segment 1 and the genomic segment 4, with the RNA-dependent RNA polymerase proteins of the influenza B virus (56%) and the neuraminidase protein belonging to the influenza A virus capsid (12%), respectively. The PCR product of the viral neuraminidase gene was inserted into the expression plasmid vector pCMV. Finally, the plasmid construct was injected into juveniles of the Nile tilapia Oreochromis niloticus and its expression was measured by real time RT-PCR at 8h, 16h, 24h, and 72h after the second immunizing injection. It was possible to detect gene expression in the four evaluated times and greater expression at 16 hours post injection. These results are the first step in the development of an effective vaccine for the protection of tilapia stocks around the world.
publishDate 2019
dc.date.none.fl_str_mv 2019-09-29
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://revistasinvestigacion.unmsm.edu.pe/index.php/rpb/article/view/15516
10.15381/rpb.v26i3.15516
url https://revistasinvestigacion.unmsm.edu.pe/index.php/rpb/article/view/15516
identifier_str_mv 10.15381/rpb.v26i3.15516
dc.language.none.fl_str_mv spa
language spa
dc.relation.none.fl_str_mv https://revistasinvestigacion.unmsm.edu.pe/index.php/rpb/article/view/15516/14282
dc.rights.none.fl_str_mv https://creativecommons.org/licenses/by-nc-sa/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidad Nacional Mayor de San Marcos, Facultad de Ciencias Biológicas
publisher.none.fl_str_mv Universidad Nacional Mayor de San Marcos, Facultad de Ciencias Biológicas
dc.source.none.fl_str_mv Revista Peruana de Biología; Vol. 26 Núm. 3 (2019); 301-310
Revista Peruana de Biología; Vol. 26 No. 3 (2019); 301-310
1727-9933
1561-0837
10.15381/rpb.v26i3
reponame:Revistas - Universidad Nacional Mayor de San Marcos
instname:Universidad Nacional Mayor de San Marcos
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instname_str Universidad Nacional Mayor de San Marcos
instacron_str UNMSM
institution UNMSM
reponame_str Revistas - Universidad Nacional Mayor de San Marcos
collection Revistas - Universidad Nacional Mayor de San Marcos
repository.name.fl_str_mv
repository.mail.fl_str_mv
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spelling Design and evaluation of the expression of a potential DNA vaccine against Tilapia lake virus (TiLV)Diseño y evaluación de la expresión de una potencial vacuna de ADN contra el virus de la Tilapia de Lago (TiLV)Criollo Joaquin, Mónica PaolaMotte, EmmerikSalvatierra, MaxMedina, JorgeDiringer, BenoitSandoval, GustavoMialhe, Ericaquaculturetilapiastructural homologygene expressionneuraminidasetilapiaacuiculturahomología estructuralexpresión génicaneuraminidasaTilapia Lake Virus (TiLV) is a pathogen that causes massive mortalities in both cultured and wild tilapia populations around the world. The development of an effective vaccine against this emerging pathogen is imperative to prevent economic losses. In this work an expression vector was designed and evaluated as a potential DNA vaccine against this virus. Initially, a threading analysis was done to predict the three-dimensional structures and functions of the TiLV proteins. Structural homologies were found between the TiLV proteins corresponding to the genomic segment 1 and the genomic segment 4, with the RNA-dependent RNA polymerase proteins of the influenza B virus (56%) and the neuraminidase protein belonging to the influenza A virus capsid (12%), respectively. The PCR product of the viral neuraminidase gene was inserted into the expression plasmid vector pCMV. Finally, the plasmid construct was injected into juveniles of the Nile tilapia Oreochromis niloticus and its expression was measured by real time RT-PCR at 8h, 16h, 24h, and 72h after the second immunizing injection. It was possible to detect gene expression in the four evaluated times and greater expression at 16 hours post injection. These results are the first step in the development of an effective vaccine for the protection of tilapia stocks around the world.El Virus de la Tilapia del Lago (TiLV), es un patógeno causante de mortalidades masivas tanto en poblaciones de tilapias cultivadas y silvestres alrededor del mundo. El desarrollo de una vacuna efectiva contra este patógeno emergente es imperativo para prevenir pérdidas económicas. En este trabajo se diseñó y evaluó un vector de expresión como una potencial vacuna de ADN contra este virus. Inicialmente, se realizó un análisis de enhebramiento para predecir las estructuras tridimensionales y las funciones de las proteínas del TiLV. Se encontraron homologías estructurales entre las proteínas correspondientes al segmento genómico 1 y al segmento genómico 4 del TiLV, con las proteínas de ARN polimerasa dependiente de ARN del virus de la influenza B (56%) y la proteína neuraminidasa que pertenece a la cápside del virus de la influenza A (12%), respectivamente. Se insertó el producto de PCR del gen neuraminidasa viral en el vector plasmídico de expresión pCMV. Finalmente, se inyectó el constructo plasmídico en juveniles de la tilapia del Nilo Oreochromis niloticus y se midió su expresión mediante RT-PCR en tiempo real a las 8h, 16h, 24h, 72h después de la segunda inyección inmunizante. Se logró detectar expresión génica en los cuatro tiempos evaluados, con mayor expresión a las 16 horas post inyección. Estos resultados constituyen el primer paso para el desarrollo de una vacuna efectiva para la protección de los stocks de tilapias alrededor del mundo.Universidad Nacional Mayor de San Marcos, Facultad de Ciencias Biológicas2019-09-29info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://revistasinvestigacion.unmsm.edu.pe/index.php/rpb/article/view/1551610.15381/rpb.v26i3.15516Revista Peruana de Biología; Vol. 26 Núm. 3 (2019); 301-310Revista Peruana de Biología; Vol. 26 No. 3 (2019); 301-3101727-99331561-083710.15381/rpb.v26i3reponame:Revistas - Universidad Nacional Mayor de San Marcosinstname:Universidad Nacional Mayor de San Marcosinstacron:UNMSMspahttps://revistasinvestigacion.unmsm.edu.pe/index.php/rpb/article/view/15516/14282Derechos de autor 2019 Mónica Criollo-Joaquin; Emmerik Motte; Max Salvatierra; Jorge Medina; Benoit Diringer; Gustavo Sandoval; Eric Mialhehttps://creativecommons.org/licenses/by-nc-sa/4.0info:eu-repo/semantics/openAccessoai:ojs.csi.unmsm:article/155162019-10-01T01:07:59Z
score 13.95948
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