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A Novel Rotavirus Reverse Genetics Platform Supports Flexible Insertion of Exogenous Genes and Enables Rapid Development of a High-Throughput Neutralization Assay
Despite the success of rotavirus vaccines, rotaviruses remain one of the leading causes of diarrheal diseases, resulting in significant childhood morbidity and mortality, especially in low- and middle-income countries. The reverse genetics system enables the manipulation of the rotavirus genome and...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10611407/ https://www.ncbi.nlm.nih.gov/pubmed/37896813 http://dx.doi.org/10.3390/v15102034 |
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author | Wei, Jiajie Radcliffe, Scott Pirrone, Amanda Lu, Meiqing Li, Yuan Cassaday, Jason Newhard, William Heidecker, Gwendolyn J. Rose II, William A. He, Xi Freed, Daniel Citron, Michael Espeseth, Amy Wang, Dai |
author_facet | Wei, Jiajie Radcliffe, Scott Pirrone, Amanda Lu, Meiqing Li, Yuan Cassaday, Jason Newhard, William Heidecker, Gwendolyn J. Rose II, William A. He, Xi Freed, Daniel Citron, Michael Espeseth, Amy Wang, Dai |
author_sort | Wei, Jiajie |
collection | PubMed |
description | Despite the success of rotavirus vaccines, rotaviruses remain one of the leading causes of diarrheal diseases, resulting in significant childhood morbidity and mortality, especially in low- and middle-income countries. The reverse genetics system enables the manipulation of the rotavirus genome and opens the possibility of using rotavirus as an expression vector for heterologous proteins, such as vaccine antigens and therapeutic payloads. Here, we demonstrate that three positions in rotavirus genome—the C terminus of NSP1, NSP3 and NSP5—can tolerate the insertion of reporter genes. By using rotavirus expressing GFP, we develop a high-throughput neutralization assay and reveal the pre-existing immunity against rotavirus in humans and other animal species. Our work shows the plasticity of the rotavirus genome and establishes a high-throughput assay for interrogating humoral immune responses, benefiting the design of next-generation rotavirus vaccines and the development of rotavirus-based expression platforms. |
format | Online Article Text |
id | pubmed-10611407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106114072023-10-28 A Novel Rotavirus Reverse Genetics Platform Supports Flexible Insertion of Exogenous Genes and Enables Rapid Development of a High-Throughput Neutralization Assay Wei, Jiajie Radcliffe, Scott Pirrone, Amanda Lu, Meiqing Li, Yuan Cassaday, Jason Newhard, William Heidecker, Gwendolyn J. Rose II, William A. He, Xi Freed, Daniel Citron, Michael Espeseth, Amy Wang, Dai Viruses Article Despite the success of rotavirus vaccines, rotaviruses remain one of the leading causes of diarrheal diseases, resulting in significant childhood morbidity and mortality, especially in low- and middle-income countries. The reverse genetics system enables the manipulation of the rotavirus genome and opens the possibility of using rotavirus as an expression vector for heterologous proteins, such as vaccine antigens and therapeutic payloads. Here, we demonstrate that three positions in rotavirus genome—the C terminus of NSP1, NSP3 and NSP5—can tolerate the insertion of reporter genes. By using rotavirus expressing GFP, we develop a high-throughput neutralization assay and reveal the pre-existing immunity against rotavirus in humans and other animal species. Our work shows the plasticity of the rotavirus genome and establishes a high-throughput assay for interrogating humoral immune responses, benefiting the design of next-generation rotavirus vaccines and the development of rotavirus-based expression platforms. MDPI 2023-09-30 /pmc/articles/PMC10611407/ /pubmed/37896813 http://dx.doi.org/10.3390/v15102034 Text en © 2023 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 Wei, Jiajie Radcliffe, Scott Pirrone, Amanda Lu, Meiqing Li, Yuan Cassaday, Jason Newhard, William Heidecker, Gwendolyn J. Rose II, William A. He, Xi Freed, Daniel Citron, Michael Espeseth, Amy Wang, Dai A Novel Rotavirus Reverse Genetics Platform Supports Flexible Insertion of Exogenous Genes and Enables Rapid Development of a High-Throughput Neutralization Assay |
title | A Novel Rotavirus Reverse Genetics Platform Supports Flexible Insertion of Exogenous Genes and Enables Rapid Development of a High-Throughput Neutralization Assay |
title_full | A Novel Rotavirus Reverse Genetics Platform Supports Flexible Insertion of Exogenous Genes and Enables Rapid Development of a High-Throughput Neutralization Assay |
title_fullStr | A Novel Rotavirus Reverse Genetics Platform Supports Flexible Insertion of Exogenous Genes and Enables Rapid Development of a High-Throughput Neutralization Assay |
title_full_unstemmed | A Novel Rotavirus Reverse Genetics Platform Supports Flexible Insertion of Exogenous Genes and Enables Rapid Development of a High-Throughput Neutralization Assay |
title_short | A Novel Rotavirus Reverse Genetics Platform Supports Flexible Insertion of Exogenous Genes and Enables Rapid Development of a High-Throughput Neutralization Assay |
title_sort | novel rotavirus reverse genetics platform supports flexible insertion of exogenous genes and enables rapid development of a high-throughput neutralization assay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10611407/ https://www.ncbi.nlm.nih.gov/pubmed/37896813 http://dx.doi.org/10.3390/v15102034 |
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