Epidemiology and ecology of the sylvatic cycle of African Swine Fever Virus in Kenya

•Detection of African Swine Fever Virus (ASFV) in Ornithodoros porcinus in Kenya.•Ornithodoros porcinus is a vector of Genotype IX ASFV.•Common warthogs have a high exposure to ASFV.•Twist Comprehensive Viral Research Panel (TCVRP) can be used for detection of DNA viruses as well as barcoding of. ti...

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Veröffentlicht in:Virus research 2024-10, Vol.348, p.199434, Article 199434
Hauptverfasser: Obanda, Vincent, Akinyi, Mercy, King'ori, Edward, Nyakundi, Ruth, Ochola, Griphin, Oreng, Purity, Mugambi, Kevin, Waiguchu, Grace Mwihaki, Chege, Mary, Rosenbaum, William, Ylitalo, Erik Bovinder, Bäck, Anne Tuiskunen, Pettersson, Lisa, Mukunzi, Opanda Silvanos, Agwanda, Bernard, Stenberg-Lewerin, Susanna, Lwande, Olivia Wesula
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Sprache:eng
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Zusammenfassung:•Detection of African Swine Fever Virus (ASFV) in Ornithodoros porcinus in Kenya.•Ornithodoros porcinus is a vector of Genotype IX ASFV.•Common warthogs have a high exposure to ASFV.•Twist Comprehensive Viral Research Panel (TCVRP) can be used for detection of DNA viruses as well as barcoding of. tick species•Ornithodoros porcinus seems to have a rich virome, which is yet to be explored but could be exploited to inform ASF control in Africa. African Swine Fever (ASF) is caused by a DNA virus (AFSV) maintained and transmitted by the Argasid ticks. The re-emergence of the disease in Africa coupled with its rapid spread globally is a threat to the pig industry, food security and livelihoods. The ecology and epidemiology of the ASFV sylvatic cycle, especially in the face of changing land use and land cover, further compounds the menace and impacts of this disease in Kenya. The study aimed to determine the occurrence and distribution of ASFV seroprevalence in warthog populations, the tick vectors and extent of tick infestation of warthog burrows, and the genotypes of ASFV in soft ticks in Kenya. Warthogs from different parts of Kenya were captured and venous blood was centrifuged to harvest sera. Warthog burrows were examined for their conditions and to extract ticks. Sera were analyzed for antibodies against ASFV using a commercial ELISA kit coated with p32 ASFV recombinant protein. Ticks were pooled, DNA extracted and the p72 gene of the ASFV was amplified by qPCR and conventional PCR. The overall seroprevalence of ASFV in warthogs was 87.5 %. A total of 228 warthog burrows were examined and 2154 argasid ticks were extracted from the burrows. Tick pools from Kigio Farm and Lewa Wildlife Conservancies were ASFV-positive by qPCR and conventional PCR. ASFV was further confirmed by the Twist Comprehensive Viral Research Panel (TCVRP), which also identified the argasid ticks as Ornithodoros porcinus. The ticks were infected with virus genotype IX, and their occurrence overlaps with regions of previous ASF outbreaks in domestic pigs. Further, Viruses that could be tick endosymbionts/commensals or due to bloodmeal were detected in ticks by TCVRP; Porcine type-C oncovirus; Pandoravirus neocaledonia; Choristoneura fumiferana granulovirus; Enterobacteria phage p7; Leporid herpesvirus 4 isolate; 5; Human Lymphotropic virus; Human herpesvirus 5. In conclusion, our results suggest that infected Ornithodoros spp. seems to have a rich virome, which has not been explored but
ISSN:0168-1702
1872-7492
1872-7492
DOI:10.1016/j.virusres.2024.199434