An Improved αvβ6-Receptor-Expressing Suspension Cell Line for Foot-and-Mouth Disease Vaccine Production

Foot-and-mouth disease (FMD) is endemic in large parts of sub-Saharan Africa, Asia and South America, where outbreaks in cloven-hooved livestock threaten food security and have severe economic impacts. Vaccination in endemic regions remains the most effective control strategy. Current FMD vaccines a...

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Main Authors: Yongjie Harvey, Ben Jackson, Brigid Veronica Carr, Kay Childs, Katy Moffat, Graham Freimanis, Chandana Tennakoon, Nicholas Juleff, Julian Seago
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/14/3/621
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author Yongjie Harvey
Ben Jackson
Brigid Veronica Carr
Kay Childs
Katy Moffat
Graham Freimanis
Chandana Tennakoon
Nicholas Juleff
Julian Seago
author_facet Yongjie Harvey
Ben Jackson
Brigid Veronica Carr
Kay Childs
Katy Moffat
Graham Freimanis
Chandana Tennakoon
Nicholas Juleff
Julian Seago
author_sort Yongjie Harvey
collection DOAJ
description Foot-and-mouth disease (FMD) is endemic in large parts of sub-Saharan Africa, Asia and South America, where outbreaks in cloven-hooved livestock threaten food security and have severe economic impacts. Vaccination in endemic regions remains the most effective control strategy. Current FMD vaccines are produced from chemically inactivated foot-and-mouth disease virus (FMDV) grown in suspension cultures of baby hamster kidney 21 cells (BHK-21). Strain diversity means vaccines produced from one subtype may not fully protect against circulating disparate subtypes, necessitating the development of new vaccine strains that “antigenically match”. However, some viruses have proven difficult to adapt to cell culture, slowing the manufacturing process, reducing vaccine yield and limiting the availability of effective vaccines, as well as potentiating the selection of undesired antigenic changes. To circumvent the need to cell culture adapt FMDV, we have used a systematic approach to develop recombinant suspension BHK-21 that stably express the key FMDV receptor integrin αvβ6. We show that αvβ6 expression is retained at consistently high levels as a mixed cell population and as a clonal cell line. Following exposure to field strains of FMDV, these recombinant BHK-21 facilitated higher virus yields compared to both parental and control BHK-21, whilst demonstrating comparable growth kinetics. The presented data supports the application of these recombinant αvβ6-expressing BHK-21 in future FMD vaccine production.
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spelling doaj.art-161ac1e7c2514d2abfe65db5364147192023-11-30T22:47:13ZengMDPI AGViruses1999-49152022-03-0114362110.3390/v14030621An Improved αvβ6-Receptor-Expressing Suspension Cell Line for Foot-and-Mouth Disease Vaccine ProductionYongjie Harvey0Ben Jackson1Brigid Veronica Carr2Kay Childs3Katy Moffat4Graham Freimanis5Chandana Tennakoon6Nicholas Juleff7Julian Seago8The Pirbright Institute, Ash Road, Woking GU24 0NF, UKThe Pirbright Institute, Ash Road, Woking GU24 0NF, UKThe Pirbright Institute, Ash Road, Woking GU24 0NF, UKThe Pirbright Institute, Ash Road, Woking GU24 0NF, UKThe Pirbright Institute, Ash Road, Woking GU24 0NF, UKThe Pirbright Institute, Ash Road, Woking GU24 0NF, UKThe Pirbright Institute, Ash Road, Woking GU24 0NF, UKBill & Melinda Gates Foundation, 500 5th Ave. N, Seattle, WA 98109, USAThe Pirbright Institute, Ash Road, Woking GU24 0NF, UKFoot-and-mouth disease (FMD) is endemic in large parts of sub-Saharan Africa, Asia and South America, where outbreaks in cloven-hooved livestock threaten food security and have severe economic impacts. Vaccination in endemic regions remains the most effective control strategy. Current FMD vaccines are produced from chemically inactivated foot-and-mouth disease virus (FMDV) grown in suspension cultures of baby hamster kidney 21 cells (BHK-21). Strain diversity means vaccines produced from one subtype may not fully protect against circulating disparate subtypes, necessitating the development of new vaccine strains that “antigenically match”. However, some viruses have proven difficult to adapt to cell culture, slowing the manufacturing process, reducing vaccine yield and limiting the availability of effective vaccines, as well as potentiating the selection of undesired antigenic changes. To circumvent the need to cell culture adapt FMDV, we have used a systematic approach to develop recombinant suspension BHK-21 that stably express the key FMDV receptor integrin αvβ6. We show that αvβ6 expression is retained at consistently high levels as a mixed cell population and as a clonal cell line. Following exposure to field strains of FMDV, these recombinant BHK-21 facilitated higher virus yields compared to both parental and control BHK-21, whilst demonstrating comparable growth kinetics. The presented data supports the application of these recombinant αvβ6-expressing BHK-21 in future FMD vaccine production.https://www.mdpi.com/1999-4915/14/3/621foot-and-mouth diseaseFMDVvaccinesuspension BHK-21
spellingShingle Yongjie Harvey
Ben Jackson
Brigid Veronica Carr
Kay Childs
Katy Moffat
Graham Freimanis
Chandana Tennakoon
Nicholas Juleff
Julian Seago
An Improved αvβ6-Receptor-Expressing Suspension Cell Line for Foot-and-Mouth Disease Vaccine Production
Viruses
foot-and-mouth disease
FMDV
vaccine
suspension BHK-21
title An Improved αvβ6-Receptor-Expressing Suspension Cell Line for Foot-and-Mouth Disease Vaccine Production
title_full An Improved αvβ6-Receptor-Expressing Suspension Cell Line for Foot-and-Mouth Disease Vaccine Production
title_fullStr An Improved αvβ6-Receptor-Expressing Suspension Cell Line for Foot-and-Mouth Disease Vaccine Production
title_full_unstemmed An Improved αvβ6-Receptor-Expressing Suspension Cell Line for Foot-and-Mouth Disease Vaccine Production
title_short An Improved αvβ6-Receptor-Expressing Suspension Cell Line for Foot-and-Mouth Disease Vaccine Production
title_sort improved αvβ6 receptor expressing suspension cell line for foot and mouth disease vaccine production
topic foot-and-mouth disease
FMDV
vaccine
suspension BHK-21
url https://www.mdpi.com/1999-4915/14/3/621
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