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Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm

Dengue is an arboviral disease, which threatens almost half the global population, and has emerged as the most significant of current global public health challenges. In this study, we prepared dengue virus-like particles (DENV-LPs) consisting of Capsid-premembrane-envelope (CprME) and premembrane-e...

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Autores principales: Utomo, Doddy Irawan Setyo, Pambudi, Sabar, Park, Enoch Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802989/
https://www.ncbi.nlm.nih.gov/pubmed/35102445
http://dx.doi.org/10.1186/s13568-022-01353-6
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author Utomo, Doddy Irawan Setyo
Pambudi, Sabar
Park, Enoch Y.
author_facet Utomo, Doddy Irawan Setyo
Pambudi, Sabar
Park, Enoch Y.
author_sort Utomo, Doddy Irawan Setyo
collection PubMed
description Dengue is an arboviral disease, which threatens almost half the global population, and has emerged as the most significant of current global public health challenges. In this study, we prepared dengue virus-like particles (DENV-LPs) consisting of Capsid-premembrane-envelope (CprME) and premembrane-envelope (prME) polypeptides from serotype 1 and 4, which were expressed in the silkworms using Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid. 1CprME, 1prME, 4CprME, and 4prME expressed proteins in hemolymph, and the molecular weight of the purified proteins was 55 kDa, respectively. The purified polypeptides formed spherical Dengue virus-like particles (DENV-LPs) with ~ 30–55 nm in diameter. The immunoelectron microscopy (IEM) images revealed antigens to the surface of a lipid bilayer of DENV-LPs. The heparin-binding assay shows a positive relationship between absorbance and E protein domain III (EDIII) quantity, which is supported by the isothermal titration calorimetry assay. This indicates a moderate binding affinity between heparin and DENV-LP. The high correlation between patient sera and DENV-LP reactivities revealed that these DENV-LPs shared similar epitopes with the natural dengue virus. IgG elicitation studies in mice have demonstrated that DENV-LPs/CPrMEs elicit a stronger immune response than DENV-LP/prMEs, which lends credence to this claim. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-022-01353-6.
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spelling pubmed-88029892022-02-01 Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm Utomo, Doddy Irawan Setyo Pambudi, Sabar Park, Enoch Y. AMB Express Original Article Dengue is an arboviral disease, which threatens almost half the global population, and has emerged as the most significant of current global public health challenges. In this study, we prepared dengue virus-like particles (DENV-LPs) consisting of Capsid-premembrane-envelope (CprME) and premembrane-envelope (prME) polypeptides from serotype 1 and 4, which were expressed in the silkworms using Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid. 1CprME, 1prME, 4CprME, and 4prME expressed proteins in hemolymph, and the molecular weight of the purified proteins was 55 kDa, respectively. The purified polypeptides formed spherical Dengue virus-like particles (DENV-LPs) with ~ 30–55 nm in diameter. The immunoelectron microscopy (IEM) images revealed antigens to the surface of a lipid bilayer of DENV-LPs. The heparin-binding assay shows a positive relationship between absorbance and E protein domain III (EDIII) quantity, which is supported by the isothermal titration calorimetry assay. This indicates a moderate binding affinity between heparin and DENV-LP. The high correlation between patient sera and DENV-LP reactivities revealed that these DENV-LPs shared similar epitopes with the natural dengue virus. IgG elicitation studies in mice have demonstrated that DENV-LPs/CPrMEs elicit a stronger immune response than DENV-LP/prMEs, which lends credence to this claim. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-022-01353-6. Springer Berlin Heidelberg 2022-01-31 /pmc/articles/PMC8802989/ /pubmed/35102445 http://dx.doi.org/10.1186/s13568-022-01353-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Utomo, Doddy Irawan Setyo
Pambudi, Sabar
Park, Enoch Y.
Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm
title Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm
title_full Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm
title_fullStr Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm
title_full_unstemmed Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm
title_short Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm
title_sort humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802989/
https://www.ncbi.nlm.nih.gov/pubmed/35102445
http://dx.doi.org/10.1186/s13568-022-01353-6
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