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Characterizing Enterovirus 71 and Coxsackievirus A16 virus-like particles production in insect cells.

作者信息

Somasundaram Balaji, Chang Cindy, Fan Yuan Y, Lim Pei-Yin, Cardosa Jane, Lua Linda

机构信息

The University of Queensland, Protein Expression Facility, Brisbane, QLD 4072, Australia.

The University of Queensland, Australian Institute for Bioengineering and Nanotechnology, Brisbane, QLD 4072, Australia.

出版信息

Methods. 2016 Feb 15;95:38-45. doi: 10.1016/j.ymeth.2015.09.023. Epub 2015 Sep 26.


DOI:10.1016/j.ymeth.2015.09.023
PMID:26410190
Abstract

Enterovirus 71 (EV71) and Coxsackievirus A16 (CVA16) are two viruses commonly responsible for hand, foot and mouth disease (HFMD) in children. The lack of prophylactic or therapeutic measures against HFMD is a major public health concern. Insect cell-based EV71 and CVA16 virus-like particles (VLPs) are promising vaccine candidates against HFMD and are currently under development. In this paper, the influence of insect cell line, incubation temperature, and serial passaging effect and stability of budded virus (BV) stocks on EV71 and CVA16 VLP production was investigated. Enhanced EV71 and CVA16 VLP production was observed in Sf9 cells compared to High Five™ cells. Lowering the incubation temperature from the standard 27°C to 21°C increased the production of both VLPs in Sf9 cells. Serial passaging of CVA16 BV stocks in cell culture had a detrimental effect on the productivity of the structural proteins and the effect was observed with only 5 passages of BV stocks. A 2.7× higher production yield was achieved with EV71 compared to CVA16. High-resolution asymmetric flow field-flow fractionation couple with multi-angle light scattering (AF4-MALS) was used for the first time to characterize EV71 and CVA16 VLPs, displaying an average root mean square radius of 15±1nm and 15.3±5.8 nm respectively. This study highlights the need for different approaches in the design of production process to develop a bivalent EV71 and CVA16 vaccine.

摘要

相似文献

[1]
Characterizing Enterovirus 71 and Coxsackievirus A16 virus-like particles production in insect cells.

Methods. 2016-2-15

[2]
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J Virol. 2015-6

[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Adaptive Laboratory Evolution to Improve Recombinant Protein Production Using Insect Cells.

Methods Mol Biol. 2024

[2]
Non-Polio Enterovirus Surveillance in the Ural Federal District and Western Siberia, 2022: Is There a Need for a Vaccine?

Vaccines (Basel). 2023-10-12

[3]
Asexual Blood-Stage Malaria Vaccine Candidate PfRipr5: Enhanced Production in Insect Cells.

Front Bioeng Biotechnol. 2022-6-30

[4]
Scalable Process for High-Yield Production of CyRPA Using Insect Cells for Inclusion in a Malaria Virosome-Based Vaccine Candidate.

Front Bioeng Biotechnol. 2022-5-20

[5]
A Versatile Processing Workflow to Enable Pathogen Detection in Clinical Samples from Organs Using VIDISCA.

Diagnostics (Basel). 2021-4-27

[6]
From Monovalent to Multivalent Vaccines, the Exploration for Potential Preventive Strategies Against Hand, Foot, and Mouth Disease (HFMD).

Virol Sin. 2021-4

[7]
Integrated Process for Capture and Purification of Virus-Like Particles: Enhancing Process Performance by Cross-Flow Filtration.

Front Bioeng Biotechnol. 2020-5-25

[8]
Asymmetrical Flow Field-Flow Fractionation on Virus and Virus-Like Particle Applications.

Microorganisms. 2019-11-12

[9]
Development and characterization of an enterovirus 71 (EV71) virus-like particles (VLPs) vaccine produced in .

Hum Vaccin Immunother. 2020-7-2

[10]
Halophilic viruses with varying biochemical and biophysical properties are amenable to purification with asymmetrical flow field-flow fractionation.

Extremophiles. 2017-11

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