Complete genome analysis of African swine fever virus genotypes II, IX and XV from domestic pigs in Tanzania

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作者
Jean N. Hakizimana
Clara Yona
Mariam R. Makange
Ester A. Kasisi
Christopher L. Netherton
Hans Nauwynck
Gerald Misinzo
机构
[1] Sokoine University of Agriculture,OR Tambo Africa Research Chair for Viral Epidemics, SACIDS Foundation for One Health
[2] Sokoine University of Agriculture,Department of Biosciences, Solomon Mahlangu College of Natural and Applied Sciences
[3] Sokoine University of Agriculture,SACIDS Africa Centre of Excellence for Infectious Diseases, SACIDS Foundation for One Health
[4] The Pirbright Institute,African Swine Fever Vaccinology Group
[5] Ghent University,Laboratory of Virology, Faculty of Veterinary Medicine
[6] Sokoine University of Agriculture,Department of Veterinary Microbiology, Parasitology and Biotechnology, College of Veterinary Medicine and Biomedical Sciences
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摘要
African swine fever (ASF) caused by ASF virus (ASFV) is an infectious transboundary animal disease notifiable to the World Organization for Animal Health causing high mortality in domestic pigs and wild boars threatening the global domestic pig industry. To date, twenty-four ASFV genotypes have been described and currently genotypes II, IX, X, XV and XVI are known to be circulating in Tanzania. Despite the endemic status of ASF in Tanzania, only one complete genome of ASFV from the country has been described. This study describes the first complete genome sequence of ASFV genotype XV. In addition, the first Tanzanian complete genome of ASFV genotype IX and three ASFV strains belonging to genotype II collected during ASF outbreaks in domestic pigs in Tanzania were determined in this study using Illumina sequencing and comparative genomics analysis. The generated ASFV complete genome sequences ranged from 171,004 to 184,521 base pairs in length with an average GC content of 38.53% and encoded 152 to 187 open reading frames. The results of this study provide insights into the genomic structure of ASFV and can be used to monitor changes within the ASFV genome and improve our understanding of ASF transmission dynamics.
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