Virus adaptation and selection following challenge of animals vaccinated against classical swine fever virus
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Virus adaptation and selection following challenge of animals vaccinated against classical swine fever virus. / Fahnøe, Ulrik; Pedersen, Anders Gorm; Johnston, Camille Melissa; Orton, Richard J.; Höper, Dirk; Beer, Martin; Bukh, Jens; Belsham, Graham J.; Rasmussen, Thomas Bruun.
In: Viruses, Vol. 11, No. 10, 932, 2019.Research output: Contribution to journal › Journal article › peer-review
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TY - JOUR
T1 - Virus adaptation and selection following challenge of animals vaccinated against classical swine fever virus
AU - Fahnøe, Ulrik
AU - Pedersen, Anders Gorm
AU - Johnston, Camille Melissa
AU - Orton, Richard J.
AU - Höper, Dirk
AU - Beer, Martin
AU - Bukh, Jens
AU - Belsham, Graham J.
AU - Rasmussen, Thomas Bruun
PY - 2019
Y1 - 2019
N2 - Vaccines against classical swine fever have proven very effective in protecting pigs from this deadly disease. However, little is known about how vaccination impacts the selective pressures acting on the classical swine fever virus (CSFV). Here we use high-throughput sequencing of viral genomes to investigate evolutionary changes in virus populations following the challenge of naïve and vaccinated pigs with the highly virulent CSFV strain "Koslov". The challenge inoculum contained an ensemble of closely related viral sequences, with three major haplotypes being present, termed A, B, and C. After the challenge, the viral haplotype A was preferentially located within the tonsils of naïve animals but was highly prevalent in the sera of all vaccinated animals. We find that the viral population structure in naïve pigs after infection is very similar to that in the original inoculum. In contrast, the viral population in vaccinated pigs, which only underwent transient low-level viremia, displayed several distinct changes including the emergence of 16 unique non-synonymous single nucleotide polymorphisms (SNPs) that were not detectable in the challenge inoculum. Further analysis showed a significant loss of heterogeneity and an increasing positive selection acting on the virus populations in the vaccinated pigs. We conclude that vaccination imposes a strong selective pressure on viruses that subsequently replicate within the vaccinated animal.
AB - Vaccines against classical swine fever have proven very effective in protecting pigs from this deadly disease. However, little is known about how vaccination impacts the selective pressures acting on the classical swine fever virus (CSFV). Here we use high-throughput sequencing of viral genomes to investigate evolutionary changes in virus populations following the challenge of naïve and vaccinated pigs with the highly virulent CSFV strain "Koslov". The challenge inoculum contained an ensemble of closely related viral sequences, with three major haplotypes being present, termed A, B, and C. After the challenge, the viral haplotype A was preferentially located within the tonsils of naïve animals but was highly prevalent in the sera of all vaccinated animals. We find that the viral population structure in naïve pigs after infection is very similar to that in the original inoculum. In contrast, the viral population in vaccinated pigs, which only underwent transient low-level viremia, displayed several distinct changes including the emergence of 16 unique non-synonymous single nucleotide polymorphisms (SNPs) that were not detectable in the challenge inoculum. Further analysis showed a significant loss of heterogeneity and an increasing positive selection acting on the virus populations in the vaccinated pigs. We conclude that vaccination imposes a strong selective pressure on viruses that subsequently replicate within the vaccinated animal.
KW - Classical swine fever virus
KW - CSFV
KW - Deep sequencing
KW - Haplotype selection
KW - Vaccination
KW - Viral populations
KW - Virulence
KW - Virus evolution
U2 - 10.3390/v11100932
DO - 10.3390/v11100932
M3 - Journal article
C2 - 31658773
AN - SCOPUS:85074240212
VL - 11
JO - Viruses
JF - Viruses
SN - 1999-4915
IS - 10
M1 - 932
ER -
ID: 230148686