scholarly journals African Horse Sickness Virus Serotype 1 on Horse Farm, Thailand, 2020

2021 ◽  
Vol 27 (8) ◽  
pp. 2208-2211
Author(s):  
Napawan Bunpapong ◽  
Kamonpan Charoenkul ◽  
Chanakarn Nasamran ◽  
Ekkapat Chamsai ◽  
Kitikhun Udom ◽  
...  
2008 ◽  
Vol 89 (5) ◽  
pp. 1159-1168 ◽  
Author(s):  
Melvyn Quan ◽  
Moritz van Vuuren ◽  
Peter G. Howell ◽  
Daleen Groenewald ◽  
Alan J. Guthrie

Between 2004 and 2006, 145 African horse sickness viruses (AHSV) were isolated from blood and organ samples submitted from South Africa to the Faculty of Veterinary Science, University of Pretoria. All nine serotypes were represented, with a range of 3–60 isolates per serotype. The RNA small segment 10 (S10) nucleotide sequences of these isolates were determined and the phylogeny investigated. AHSV, bluetongue virus (BTV) and equine encephalosis virus (EEV) all formed monophyletic groups and BTV was genetically closer to AHSV than EEV. This study confirmed the presence of three distinct S10 phylogenetic clades (α, β and γ). Some serotypes (6, 8 and 9 in α; 3 and 7 in β; 2 in γ) were restricted to a single clade, while other serotypes (1, 4 and 5) clustered into both the α and γ clades. Strong purifying selection was evident and a constant molecular clock was inappropriate. The S10 gene is the second most variable gene of the AHSV genome and the use of S10 in molecular epidemiology was illustrated by an AHS outbreak in the Western Cape in 2004. It was shown that two separate AHSV were circulating in the area, even though AHSV serotype 1 was the only isolate from the outbreak. The small size of the gene (755–764 bp) and conserved terminal regions facilitate easy and quick sequencing. The establishment of an S10 sequence database is important for characterizing outbreaks of AHS. It will be an essential resource for elucidating the epidemiology of AHS.


2011 ◽  
Vol 140 (3) ◽  
pp. 462-465 ◽  
Author(s):  
C. A. L. OURA ◽  
P. A. S. IVENS ◽  
K. BACHANEK-BANKOWSKA ◽  
A. BIN-TARIF ◽  
D. B. JALLOW ◽  
...  

SUMMARYAfrican horse sickness virus serotype 9 (AHSV-9) has been known for some time to be circulating amongst equids in West Africa without causing any clinical disease in indigenous horse populations. Whether this is due to local breeds of horses being resistant to disease or whether the AHSV-9 strains circulating are avirulent is currently unknown. This study shows that the majority (96%) of horses and donkeys sampled across The Gambia were seropositive for AHS, despite most being unvaccinated and having no previous history of showing clinical signs of AHS. Most young horses (<3 years) were seropositive with neutralizing antibodies specific to AHSV-9. Eight young equids (<3 years) were positive for AHSV-9 by serotype-specific RT–PCR and live AHSV-9 was isolated from two of these horses. Sequence analysis revealed the presence of an AHSV-9 strain showing 100% identity to Seg-2 of the AHSV-9 reference strain, indicating that the virus circulating in The Gambia was highly likely to have been derived from a live-attenuated AHSV-9 vaccine strain.


2016 ◽  
Vol 53 ◽  
pp. 65
Author(s):  
N.D. Diouf ◽  
E. Etter ◽  
S. Lecollinet ◽  
S. Zientara ◽  
D. Klinkenberg ◽  
...  

Author(s):  
Evans M. Mathebula ◽  
Frederika E. Faber ◽  
Wouter Van Wyngaardt ◽  
Antoinette Van Schalkwyk ◽  
Alri Pretorius ◽  
...  

Identifying antigenic proteins and mapping their epitopes is important for the development of diagnostic reagents and recombinant vaccines. B-cell epitopes of African horse sickness virus (AHSV) have previously been mapped on VP2, VP5, VP7 and NS1, using mouse, rabbit and chicken monoclonal antibodies. A comprehensive study of the humoral immune response of five vaccinated horses to AHSV-4 antigenic peptides was undertaken. A fragmented-genome phage display library expressing a repertoire of AHSV-4 peptides spanning the entire genome was constructed. The library was affinity selected for binders on immobilised polyclonal immunoglobulin G (IgG) isolated from horse sera collected pre- and post-immunisation with an attenuated AHSV-4 monovalent vaccine. The DNA inserts of binding phages were sequenced with Illumina high-throughput sequencing. The data were normalised using preimmune IgG-selected sequences. More sequences mapped to the genes coding for NS3, VP6 and VP5 than to the other genes. However, VP2 and VP5 each had more antigenic regions than each of the other proteins. This study identified a number of epitopes to which the horse’s humoral immune system responds during immunisation with AHSV-4.


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