The African Swine Fever Isolate ASFV-Kenya-IX-1033 Is Highly Virulent and Stable after Propagation in the Wild Boar Cell Line WSL

Viruses. 2022 Aug 29;14(9):1912. doi: 10.3390/v14091912.

Abstract

We describe the characterization of an African swine fever genotype IX virus (ASFV-Kenya-IX-1033), which was isolated from a domestic pig in western Kenya during a reported outbreak. This includes the efficiency of virus replication and in vivo virulence, together with genome stability and virulence, following passage in blood macrophages and in a wild boar lung cell line (WSL). The ASFV-Kenya-IX-1033 stock retained its ability to replicate in primary macrophages and retained virulence in vivo, following more than 20 passages in a WSL. At the whole genome level, a few single-nucleotide differences were observed between the macrophage and WSL-propagated viruses. Thus, we propose that the WSL is suitable for the production of live-attenuated ASFV vaccine candidates based on the modification of this wild-type isolate. The genome sequences for ASFV-Kenya-IX-1033 propagated in macrophages and in WSL cells were submitted to GenBank, and a challenge model based on the isolate was developed. This will aid the development of vaccines against the genotype IX ASFV circulating in eastern and central Africa.

Keywords: African swine fever virus; Kenyan isolate; genotype IX; virulence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • African Swine Fever Virus*
  • African Swine Fever*
  • Animals
  • Cell Line
  • Kenya
  • Nucleotides
  • Sus scrofa
  • Swine
  • Vaccines, Attenuated

Substances

  • Nucleotides
  • Vaccines, Attenuated

Grants and funding

This research was funded by the Canadian International Development Research Centre (IDRC) Livestock Vaccine Innovation Fund (LVIF), grant no. 108514-002 (phase I), no. 109212-001 (phase II), the CGIAR Research Program on Livestock, and the CGIAR Consortium. In-kind contribution from GALVMED grant no. ILR-R39A0752S4 was also provided.