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Concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column

BACKGROUND: Enterovirus 71 (EV-71) is a neurotropic virus causing Hand, Foot and Mouth Disease (HFMD) in infants and children under the age of five. It is a major concern for public health issues across Asia-Pacific region. The most effective way to control the disease caused by EV-71 is by vaccinat...

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Autores principales: Kattur Venkatachalam, Ashok Raj, Szyporta, Milene, Kiener, Tanja Kristin, Balraj, Premanand, Kwang, Jimmy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042139/
https://www.ncbi.nlm.nih.gov/pubmed/24884895
http://dx.doi.org/10.1186/1743-422X-11-99
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author Kattur Venkatachalam, Ashok Raj
Szyporta, Milene
Kiener, Tanja Kristin
Balraj, Premanand
Kwang, Jimmy
author_facet Kattur Venkatachalam, Ashok Raj
Szyporta, Milene
Kiener, Tanja Kristin
Balraj, Premanand
Kwang, Jimmy
author_sort Kattur Venkatachalam, Ashok Raj
collection PubMed
description BACKGROUND: Enterovirus 71 (EV-71) is a neurotropic virus causing Hand, Foot and Mouth Disease (HFMD) in infants and children under the age of five. It is a major concern for public health issues across Asia-Pacific region. The most effective way to control the disease caused by EV-71 is by vaccination thus a novel vaccine is urgently needed. Inactivated EV-71 induces a strong, virus-neutralizing antibody response in animal models, protecting them against a lethal EV-71 challenge and it has been shown to elicit cross-neutralizing antibodies in human trials. Hence, the large-scale production of purified EV-71 is required for vaccine development, diagnosis and clinical trials. METHODS: CIM(®) Monolith columns are single-piece columns made up of poly(glycidyl methacrylate co-ethylene dimethacrylate) as support matrix. They are designed as porous channels rather than beads with different chemistries for different requirements. As monolithic columns have a high binding capacity, flow rate and resolution, a CIM(®) DEAE-8f tube monolithic column was selected for purification in this study. The EV-71 infected Rhabdomyosarcoma (RD) cell supernatant was concentrated using 8% PEG 8000 in the presence of 400 mM sodium chloride. The concentrated virus was purified by weak anion exchange column using 50 mM HEPES + 1 M sodium chloride as elution buffer. RESULTS: Highly pure viral particles were obtained at a concentration of 350 mM sodium chloride as confirmed by SDS-PAGE and electron microscopy. Presence of viral proteins VP1, VP2 and VP3 was validated by western blotting. The overall process achieved a recovery of 55%. CONCLUSIONS: EV-71 viral particles of up to 95% purity can be recovered by a single step ion-exchange chromatography using CIM-DEAE monolithic columns and 1 M sodium chloride as elution buffer. Moreover, this method is scalable to purify several litres of virus-containing supernatant, using industrial monolithic columns with a capacity of up to 8 L such as CIM(®) cGMP tube monolithic columns.
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spelling pubmed-40421392014-06-04 Concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column Kattur Venkatachalam, Ashok Raj Szyporta, Milene Kiener, Tanja Kristin Balraj, Premanand Kwang, Jimmy Virol J Methodology BACKGROUND: Enterovirus 71 (EV-71) is a neurotropic virus causing Hand, Foot and Mouth Disease (HFMD) in infants and children under the age of five. It is a major concern for public health issues across Asia-Pacific region. The most effective way to control the disease caused by EV-71 is by vaccination thus a novel vaccine is urgently needed. Inactivated EV-71 induces a strong, virus-neutralizing antibody response in animal models, protecting them against a lethal EV-71 challenge and it has been shown to elicit cross-neutralizing antibodies in human trials. Hence, the large-scale production of purified EV-71 is required for vaccine development, diagnosis and clinical trials. METHODS: CIM(®) Monolith columns are single-piece columns made up of poly(glycidyl methacrylate co-ethylene dimethacrylate) as support matrix. They are designed as porous channels rather than beads with different chemistries for different requirements. As monolithic columns have a high binding capacity, flow rate and resolution, a CIM(®) DEAE-8f tube monolithic column was selected for purification in this study. The EV-71 infected Rhabdomyosarcoma (RD) cell supernatant was concentrated using 8% PEG 8000 in the presence of 400 mM sodium chloride. The concentrated virus was purified by weak anion exchange column using 50 mM HEPES + 1 M sodium chloride as elution buffer. RESULTS: Highly pure viral particles were obtained at a concentration of 350 mM sodium chloride as confirmed by SDS-PAGE and electron microscopy. Presence of viral proteins VP1, VP2 and VP3 was validated by western blotting. The overall process achieved a recovery of 55%. CONCLUSIONS: EV-71 viral particles of up to 95% purity can be recovered by a single step ion-exchange chromatography using CIM-DEAE monolithic columns and 1 M sodium chloride as elution buffer. Moreover, this method is scalable to purify several litres of virus-containing supernatant, using industrial monolithic columns with a capacity of up to 8 L such as CIM(®) cGMP tube monolithic columns. BioMed Central 2014-05-27 /pmc/articles/PMC4042139/ /pubmed/24884895 http://dx.doi.org/10.1186/1743-422X-11-99 Text en Copyright © 2014 Kattur Venkatachalam et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology
Kattur Venkatachalam, Ashok Raj
Szyporta, Milene
Kiener, Tanja Kristin
Balraj, Premanand
Kwang, Jimmy
Concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column
title Concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column
title_full Concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column
title_fullStr Concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column
title_full_unstemmed Concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column
title_short Concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column
title_sort concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042139/
https://www.ncbi.nlm.nih.gov/pubmed/24884895
http://dx.doi.org/10.1186/1743-422X-11-99
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