Deletion of B125R increases protection induced by a genotype II African swine fever vaccine candidate

A modified live attenuated African swine fever genotype II virus, GΔDKE-CmutQ96R/K108D, with deletions of three genes, DP148R, EP153R, and K145R and expressing a mutated CD2v protein with a non-haemadsorbing phenotype, was further modified by first removing two reporter gene cassettes expressing fluorescent proteins. The B125R gene was then deleted and one reporter cassette was reinserted as a marker. Groups of pigs were immunised with this virus using a range of doses from 100 to 10,000 infectious particles. One pig immunised with the lowest dose reached a moderate severity humane endpoint. The other pigs showed mild or no clinical signs. Low levels of the virus used for immunisation were detected post-immunisation. After challenge with virulent virus, all pigs were protected, and few clinical signs were observed. Low levels of replication of the challenge virus were detected in seven from the twenty-three challenged pigs and no virus in the remaining pigs.

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Publication Details

Journal
npj Vaccines
Published
2025-03-19
DOI
https://doi.org/10.1038/s41541-025-01101-4
Citations
3
Primary Topic
Animal Disease Management and Epidemiology
Type
article
Field-Weighted Citation Impact
5.71

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article

Deletion of B125R increases protection induced by a genotype II African swine fever vaccine candidate

Elisenda Viaplana, Ana Luísa Reis, Alicia Urniza, Katy Moffat et al.
3 citations
npj Vaccines
Animal Disease Management and Epidemiology
5.71
article

Deletion of B125R increases protection induced by a genotype II African swine fever vaccine candidate

Elisenda Viaplana, Ana Luísa Reis, Alicia Urniza, Katy Moffat, Anusyah Rathakrishnan, Lynnette C. Goatley, Linda K. Dixon, Jose Carlos Mancera
article en
3 citations

Abstract

A modified live attenuated African swine fever genotype II virus, GΔDKE-CmutQ96R/K108D, with deletions of three genes, DP148R, EP153R, and K145R and expressing a mutated CD2v protein with a non-haemadsorbing phenotype, was further modified by first removing two reporter gene cassettes expressing fluorescent proteins. The B125R gene was then deleted and one reporter cassette was reinserted as a marker. Groups of pigs were immunised with this virus using a range of doses from 100 to 10,000 infectious particles. One pig immunised with the lowest dose reached a moderate severity humane endpoint. The other pigs showed mild or no clinical signs. Low levels of the virus used for immunisation were detected post-immunisation. After challenge with virulent virus, all pigs were protected, and few clinical signs were observed. Low levels of replication of the challenge virus were detected in seven from the twenty-three challenged pigs and no virus in the remaining pigs.

npj VaccinesVol. 10(1)
The Pirbright Institute (GB), Zoetis (Belgium) (BE)
Biotechnology and Biological Sciences Research Council
Good health and well-being
Openalex Percentile: Top 5%
Animal Disease Management and Epidemiology
5.71
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