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Production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice
To develop monovalent dengue virus-like particle for serotype 3 (DENV-LP/3), we prepared and expressed two structural polyprotein constructs using silkworm and Bm5 cells: DENV-3 Capsid-premembrane-envelope (DENV-3CprME) and premembrane-envelope (DENV-3prME). The expressed PA-tagged 3CprME and 3prME...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431508/ https://www.ncbi.nlm.nih.gov/pubmed/32804287 http://dx.doi.org/10.1186/s13568-020-01087-3 |
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author | Utomo, Doddy Irawan Setyo Pambudi, Sabar Sjatha, Fithriyah Kato, Tatsuya Park, Enoch Y. |
author_facet | Utomo, Doddy Irawan Setyo Pambudi, Sabar Sjatha, Fithriyah Kato, Tatsuya Park, Enoch Y. |
author_sort | Utomo, Doddy Irawan Setyo |
collection | PubMed |
description | To develop monovalent dengue virus-like particle for serotype 3 (DENV-LP/3), we prepared and expressed two structural polyprotein constructs using silkworm and Bm5 cells: DENV-3 Capsid-premembrane-envelope (DENV-3CprME) and premembrane-envelope (DENV-3prME). The expressed PA-tagged 3CprME and 3prME polypeptides were partially purified by PA-tag affinity chromatography and had molecular weights of 85 and 75 kDa, respectively. Expressed proteins were separately verified using the following primary antibodies: the anti-PA tag antibody, DENV premembrane polyclonal antibody, and DENV envelope polyclonal antibody. Transmission electron microscopy revealed that these DENV-3CprME and 3prME formed rough, spherical DENV-LPs (DENV-LP/3CprME and DENV-LP/3prME), respectively, with a diameter of 30–55 nm. The heparin-binding assay demonstrated that these DENV-LPs contained the envelope protein domain III on their surfaces. Both DENV-LPs showed an affinity to sera from human dengue patients and immunized mice. Immunization of mice with DENV-LP/3prME significantly induced the level of antibodies compared with DENV-LP/3CprME. These results indicate that DENV-LP/3prME is suitable as a vaccine candidate compared with DENV-LP/3CprME. |
format | Online Article Text |
id | pubmed-7431508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-74315082020-08-20 Production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice Utomo, Doddy Irawan Setyo Pambudi, Sabar Sjatha, Fithriyah Kato, Tatsuya Park, Enoch Y. AMB Express Original Article To develop monovalent dengue virus-like particle for serotype 3 (DENV-LP/3), we prepared and expressed two structural polyprotein constructs using silkworm and Bm5 cells: DENV-3 Capsid-premembrane-envelope (DENV-3CprME) and premembrane-envelope (DENV-3prME). The expressed PA-tagged 3CprME and 3prME polypeptides were partially purified by PA-tag affinity chromatography and had molecular weights of 85 and 75 kDa, respectively. Expressed proteins were separately verified using the following primary antibodies: the anti-PA tag antibody, DENV premembrane polyclonal antibody, and DENV envelope polyclonal antibody. Transmission electron microscopy revealed that these DENV-3CprME and 3prME formed rough, spherical DENV-LPs (DENV-LP/3CprME and DENV-LP/3prME), respectively, with a diameter of 30–55 nm. The heparin-binding assay demonstrated that these DENV-LPs contained the envelope protein domain III on their surfaces. Both DENV-LPs showed an affinity to sera from human dengue patients and immunized mice. Immunization of mice with DENV-LP/3prME significantly induced the level of antibodies compared with DENV-LP/3CprME. These results indicate that DENV-LP/3prME is suitable as a vaccine candidate compared with DENV-LP/3CprME. Springer Berlin Heidelberg 2020-08-17 /pmc/articles/PMC7431508/ /pubmed/32804287 http://dx.doi.org/10.1186/s13568-020-01087-3 Text en © The Author(s) 2020 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/. |
spellingShingle | Original Article Utomo, Doddy Irawan Setyo Pambudi, Sabar Sjatha, Fithriyah Kato, Tatsuya Park, Enoch Y. Production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice |
title | Production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice |
title_full | Production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice |
title_fullStr | Production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice |
title_full_unstemmed | Production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice |
title_short | Production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice |
title_sort | production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431508/ https://www.ncbi.nlm.nih.gov/pubmed/32804287 http://dx.doi.org/10.1186/s13568-020-01087-3 |
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