Abstract

African swine fever (ASF) caused by the African swine fever virus (ASFV) is ranked by OIE as the most important source of mortality in domestic pigs globally and is indigenous to African wild suids and soft ticks. Despite two ASFV genotypes causing economically devastating epidemics outside the continent since 1961, there have been no genome-level analyses of virus evolution in Africa. The virus was recently transported from south-eastern Africa to Georgia in 2007 and has subsequently spread to Russia, eastern Europe, China, and south-east Asia with devastating socioeconomic consequences. To date, two of the 24 currently described ASFV genotypes defined by sequencing of the p72 gene, namely genotype I and II, have been reported outside Africa, with genotype II being responsible for the ongoing pig pandemic. Multiple complete genotype II genome sequences have been reported from European, Russian and Chinese virus isolates but no complete genome sequences have yet been reported from Africa. We report herein the complete genome of a Tanzanian genotype II isolate, Tanzania/Rukwa/2017/1, collected in 2017 and determined using an Illumina short read strategy. The Tanzania/Rukwa/2017/1 sequence is 183,186 bp in length (in a single contig) and contains 188 open reading frames. Considering only un-gapped sites in the pairwise alignments, the new sequence has 99.961% identity with the updated Georgia 2007/1 reference isolate (FR682468.2), 99.960% identity with Polish isolate Pol16_29413_o23 (MG939586) and 99.957% identity with Chinese isolate ASFV-wbBS01 (MK645909.1). This represents 73 single nucleotide polymorphisms (SNPs) relative to the Polish isolate and 78 SNPs with the Chinese genome. Phylogenetic analysis indicated that Tanzania/Rukwa/2017/1 clusters most closely with Georgia 2007/1. The majority of the differences between Tanzania/Rukwa/2017/1 and Georgia 2007/1 genotype II genomes are insertions/deletions (indels) as is typical for ASFV. The indels included differences in the length and copy number of the terminal multicopy gene families, MGF 360 and 110. The Rukwa2017/1 sequence is the first complete genotype II genome from a precisely mapped locality in Africa, since the exact origin of Georgia2007/1 is unknown. It therefore provides baseline information for future analyses of the diversity and phylogeography of this globally important genetic sub-group of ASF viruses.

Highlights

  • According to the World Organization for Animal Health (OIE), African swine fever virus (ASF) is the most important disease-causing pathogen affecting the domestic swine population g­ lobally[1]

  • As a result of the recent introduction to Georgia and rapid subsequent dissemination North to the Russian Federation and subsequently East to China and Southeast Asia and West as far as East Germany, genotype II p72 group ASF virus (ASFV) represents by far the most geographically widespread of the twenty-four viral genotypes that are currently ­known[37,38]. This virus group is of major concern as the cause of a serious on-going pig pandemic, our study provides the first full genome sequence of a genotype II ASFV from Africa

  • Our analyses demonstrate close similarity of the Tanzanian sequence to viral sequences from Georgia (2007), Poland (2017) and China (2018), consistent with widespread dissemination of genotype II ASFV following its introduction into Georgia from southeastern Africa in 2007

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Summary

Introduction

According to the World Organization for Animal Health (OIE), African swine fever virus (ASF) is the most important disease-causing pathogen affecting the domestic swine population g­ lobally[1]. The first occurrence outside Africa, of a virus classified in p72 genotype I, was reported in 1958 and again in 1961 from Lisbon Portugal, with subsequent spread to other regions of Europe and Latin America (reviewed ­by[6,7]). In 2007, an ASF virus (ASFV) within p72 genotype ­II8 was again exported through a human agency outside sub-Saharan Africa into Georgia. Between mid-2007 to date, ASF genotype II viruses, derived from the Georgia introduction, have been reported throughout the Caucasus, Russia, the Baltic republics, Czech Republic, Romania, Hungary, Bulgaria, Poland, Belgium, and most recently ­China[18] and South-east Asia. Despite significant efforts by FAO and others to control its spread, numbers of ASFV infected animals are increasing rapidly in domestic pigs and wild boar populations, with movements of the latter facilitating the rapid geographical spread of the virus (reviewed i­n2). Multiple approaches have been used to characterize the v­ irus[20], with genotyping of the virus by full length or partial sequencing of the genes encoding the p72, p54, p30 proteins and the Central variable region widely applied

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