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Development of live attenuated Enterovirus 71 vaccine strains that confer protection against lethal challenge in mice

Besides causing mild hand, foot and mouth infections, Enterovirus A71 (EV-A71) is associated with neurological complications and fatality. With concerns about rising EV-A71 virulence, there is an urgency for more effective vaccines. The live attenuated vaccine (LAV) is a more valuable vaccine as it...

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Autores principales: Yee, Pinn Tsin Isabel, Tan, Soon Hao, Ong, Kien Chai, Tan, Kuan Onn, Wong, Kum Thong, Hassan, Sharifah Syed, Poh, Chit Laa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423319/
https://www.ncbi.nlm.nih.gov/pubmed/30886246
http://dx.doi.org/10.1038/s41598-019-41285-z
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author Yee, Pinn Tsin Isabel
Tan, Soon Hao
Ong, Kien Chai
Tan, Kuan Onn
Wong, Kum Thong
Hassan, Sharifah Syed
Poh, Chit Laa
author_facet Yee, Pinn Tsin Isabel
Tan, Soon Hao
Ong, Kien Chai
Tan, Kuan Onn
Wong, Kum Thong
Hassan, Sharifah Syed
Poh, Chit Laa
author_sort Yee, Pinn Tsin Isabel
collection PubMed
description Besides causing mild hand, foot and mouth infections, Enterovirus A71 (EV-A71) is associated with neurological complications and fatality. With concerns about rising EV-A71 virulence, there is an urgency for more effective vaccines. The live attenuated vaccine (LAV) is a more valuable vaccine as it can elicit both humoral and cellular immune responses. A miRNA-based vaccine strain (pIY) carrying let-7a and miR-124a target genes in the EV-A71 genome which has a partial deletion in the 5′NTR (∆11 bp) and G64R mutation (3D(p)°(l)) was designed. The viral RNA copy number and viral titers of the pIY strain were significantly lower in SHSY-5Y cells that expressed both let-7a and miR-124a. Inhibition of the cognate miRNAs expressed in RD and SHSY-5Y cells demonstrated de-repression of viral mRNA translation. A previously constructed multiply mutated strain, MMS and the pIY vaccine strain were assessed in their ability to protect 4-week old mice from hind limb paralysis. The MMS showed higher amounts of IFN-γ ex vivo than the pIY vaccine strain. There was absence of EV-A71 antigen in the skeletal muscles and spinal cord micrographs of mice vaccinated with the MMS and pIY strains. The MMS and pIY strains are promising LAV candidates developed against severe EV-A71 infections.
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spelling pubmed-64233192019-03-26 Development of live attenuated Enterovirus 71 vaccine strains that confer protection against lethal challenge in mice Yee, Pinn Tsin Isabel Tan, Soon Hao Ong, Kien Chai Tan, Kuan Onn Wong, Kum Thong Hassan, Sharifah Syed Poh, Chit Laa Sci Rep Article Besides causing mild hand, foot and mouth infections, Enterovirus A71 (EV-A71) is associated with neurological complications and fatality. With concerns about rising EV-A71 virulence, there is an urgency for more effective vaccines. The live attenuated vaccine (LAV) is a more valuable vaccine as it can elicit both humoral and cellular immune responses. A miRNA-based vaccine strain (pIY) carrying let-7a and miR-124a target genes in the EV-A71 genome which has a partial deletion in the 5′NTR (∆11 bp) and G64R mutation (3D(p)°(l)) was designed. The viral RNA copy number and viral titers of the pIY strain were significantly lower in SHSY-5Y cells that expressed both let-7a and miR-124a. Inhibition of the cognate miRNAs expressed in RD and SHSY-5Y cells demonstrated de-repression of viral mRNA translation. A previously constructed multiply mutated strain, MMS and the pIY vaccine strain were assessed in their ability to protect 4-week old mice from hind limb paralysis. The MMS showed higher amounts of IFN-γ ex vivo than the pIY vaccine strain. There was absence of EV-A71 antigen in the skeletal muscles and spinal cord micrographs of mice vaccinated with the MMS and pIY strains. The MMS and pIY strains are promising LAV candidates developed against severe EV-A71 infections. Nature Publishing Group UK 2019-03-18 /pmc/articles/PMC6423319/ /pubmed/30886246 http://dx.doi.org/10.1038/s41598-019-41285-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yee, Pinn Tsin Isabel
Tan, Soon Hao
Ong, Kien Chai
Tan, Kuan Onn
Wong, Kum Thong
Hassan, Sharifah Syed
Poh, Chit Laa
Development of live attenuated Enterovirus 71 vaccine strains that confer protection against lethal challenge in mice
title Development of live attenuated Enterovirus 71 vaccine strains that confer protection against lethal challenge in mice
title_full Development of live attenuated Enterovirus 71 vaccine strains that confer protection against lethal challenge in mice
title_fullStr Development of live attenuated Enterovirus 71 vaccine strains that confer protection against lethal challenge in mice
title_full_unstemmed Development of live attenuated Enterovirus 71 vaccine strains that confer protection against lethal challenge in mice
title_short Development of live attenuated Enterovirus 71 vaccine strains that confer protection against lethal challenge in mice
title_sort development of live attenuated enterovirus 71 vaccine strains that confer protection against lethal challenge in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423319/
https://www.ncbi.nlm.nih.gov/pubmed/30886246
http://dx.doi.org/10.1038/s41598-019-41285-z
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