Advancements in the Growth and Construction of Recombinant Lumpy Skin Disease Virus (LSDV) for Use as a Vaccine Vector

dc.contributor.authorvan Diepen, Michiel
dc.contributor.authorChapman, Rosamund
dc.contributor.authorDouglass, Nicola
dc.contributor.authorWhittle, Leah
dc.contributor.authorChineka, Nicole
dc.contributor.authorGalant, Shireen
dc.contributor.authorCotchobos, Christian
dc.contributor.authorSuzuki, Akiko
dc.contributor.authorWilliamson, Anna-Lise
dc.date.accessioned2021-10-25T11:20:17Z
dc.date.available2021-10-25T11:20:17Z
dc.date.issued2021-10-04
dc.date.updated2021-10-22T13:55:44Z
dc.description.abstractAttenuated vaccine strains of lumpy skin disease virus (LSDV) have become increasingly popular as recombinant vaccine vectors, to target both LSDV, as well as other pathogens, including human infectious agents. Historically, these vaccine strains and recombinants were generated in primary (lamb) testis (LT) cells, Madin–Darby bovine kidney (MDBK) cells or in eggs. Growth in eggs is a laborious process, the use of primary cells has the potential to introduce pathogens and MDBK cells are known to harbor bovine viral diarrhea virus (BVDV). In this study, data is presented to show the growth of an attenuated LSDV strain in baby hamster kidney (BHK-21) cells. Subsequently, a recombinant LSDV vaccine was generated in BHK-21 cells. Partial growth was also observed in rabbit kidney cells (RK13), but only when the vaccinia virus host range gene K1L was expressed. Despite the limited growth, the expression of K1L was enough to serve as a positive selection marker for the generation of recombinant LSDV vaccines in RK13 cells. The simplification of generating (recombinant) LSDV vaccines shown here should increase the interest for this platform for future livestock vaccine development and, with BHK-21 cells approved for current good manufacturing practice, this can be expanded to human vaccines as well.en_US
dc.identifier10.3390/vaccines9101131
dc.identifier.apacitationvan Diepen, M., Chapman, R., Douglass, N., Whittle, L., Chineka, N., Galant, S., ... Williamson, A. (2021). Advancements in the Growth and Construction of Recombinant Lumpy Skin Disease Virus (LSDV) for Use as a Vaccine Vector. <i>Vaccines</i>, 9(10), 1131. http://hdl.handle.net/11427/35287en_ZA
dc.identifier.chicagocitationvan Diepen, Michiel, Rosamund Chapman, Nicola Douglass, Leah Whittle, Nicole Chineka, Shireen Galant, Christian Cotchobos, Akiko Suzuki, and Anna-Lise Williamson "Advancements in the Growth and Construction of Recombinant Lumpy Skin Disease Virus (LSDV) for Use as a Vaccine Vector." <i>Vaccines</i> 9, 10. (2021): 1131. http://hdl.handle.net/11427/35287en_ZA
dc.identifier.citationvan Diepen, M., Chapman, R., Douglass, N., Whittle, L., Chineka, N., Galant, S., Cotchobos, C. & Suzuki, A. et al. 2021. Advancements in the Growth and Construction of Recombinant Lumpy Skin Disease Virus (LSDV) for Use as a Vaccine Vector. <i>Vaccines.</i> 9(10):1131. http://hdl.handle.net/11427/35287en_ZA
dc.identifier.ris TY - Journal Article AU - van Diepen, Michiel AU - Chapman, Rosamund AU - Douglass, Nicola AU - Whittle, Leah AU - Chineka, Nicole AU - Galant, Shireen AU - Cotchobos, Christian AU - Suzuki, Akiko AU - Williamson, Anna-Lise AB - Attenuated vaccine strains of lumpy skin disease virus (LSDV) have become increasingly popular as recombinant vaccine vectors, to target both LSDV, as well as other pathogens, including human infectious agents. Historically, these vaccine strains and recombinants were generated in primary (lamb) testis (LT) cells, Madin–Darby bovine kidney (MDBK) cells or in eggs. Growth in eggs is a laborious process, the use of primary cells has the potential to introduce pathogens and MDBK cells are known to harbor bovine viral diarrhea virus (BVDV). In this study, data is presented to show the growth of an attenuated LSDV strain in baby hamster kidney (BHK-21) cells. Subsequently, a recombinant LSDV vaccine was generated in BHK-21 cells. Partial growth was also observed in rabbit kidney cells (RK13), but only when the vaccinia virus host range gene K1L was expressed. Despite the limited growth, the expression of K1L was enough to serve as a positive selection marker for the generation of recombinant LSDV vaccines in RK13 cells. The simplification of generating (recombinant) LSDV vaccines shown here should increase the interest for this platform for future livestock vaccine development and, with BHK-21 cells approved for current good manufacturing practice, this can be expanded to human vaccines as well. DA - 2021-10-04 DB - OpenUCT DP - University of Cape Town IS - 10 J1 - Vaccines LK - https://open.uct.ac.za PY - 2021 T1 - Advancements in the Growth and Construction of Recombinant Lumpy Skin Disease Virus (LSDV) for Use as a Vaccine Vector TI - Advancements in the Growth and Construction of Recombinant Lumpy Skin Disease Virus (LSDV) for Use as a Vaccine Vector UR - http://hdl.handle.net/11427/35287 ER - en_ZA
dc.identifier.urihttp://hdl.handle.net/11427/35287
dc.identifier.vancouvercitationvan Diepen M, Chapman R, Douglass N, Whittle L, Chineka N, Galant S, et al. Advancements in the Growth and Construction of Recombinant Lumpy Skin Disease Virus (LSDV) for Use as a Vaccine Vector. Vaccines. 2021;9(10):1131. http://hdl.handle.net/11427/35287.en_ZA
dc.language.isoenen_US
dc.publisher.departmentDepartment of Pathologyen_US
dc.publisher.facultyFaculty of Health Sciencesen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceVaccinesen_US
dc.source.journalissue10en_US
dc.source.journalvolume9en_US
dc.source.pagination1131en_US
dc.source.urihttps://www.mdpi.com/journal/vaccines
dc.titleAdvancements in the Growth and Construction of Recombinant Lumpy Skin Disease Virus (LSDV) for Use as a Vaccine Vectoren_US
dc.typeJournal Articleen_US
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