Evidence map›Paper›PMID 42569661›Full record

ArticleVeterinary and animal science2026

Molecular detection of African horse sickness virus from selected areas in Ethiopia.

Degu Fhetanegest Esey, Hika Waktole, Esayas Gelaye, Dessalew Habte Alene, Habtamu Addis Minale

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Article in Veterinary and animal science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Degu Fhetanegest EseyDepartment of Veterinary Laboratory Technology, Injibara University, Injibara, Ethiopia.
Hika WaktoleCollege of Veterinary Medicine and Agriculture, Addis Ababa University, Bishoftu, Ethiopia.
Esayas GelayeFood and Agriculture Organization of the United Nations (FAO), Addis Ababa, Ethiopia.
Dessalew Habte AleneDepartment of Clinical Medicine, School of Veterinary Medicine, Bahir Dar University, Bahir Dar, Ethiopia.
Habtamu Addis MinaleDepartment of Veterinary Laboratory Technology, Injibara University, Injibara, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Equines are vital to global economies and support millions of livelihoods. However, their productivity and welfare are severely hindered by infectious diseases such as African Horse Sickness, which causes major socio-economic losses in Ethiopia. A cross-sectional study was conducted from November 2022 to May 2023 to isolate and detect African horse sickness virus in equines across epidemic areas of Ethiopia. In total, 30 blood samples and 2 tissue representative specimens were aseptically collected from clinically sick and recently dead animals and transported under cold chain to the National Veterinary Institute, Bishoftu. A total of 32 samples were analyzed using conventional Reverse Transcriptase Polymerase Chain Reaction (RT-PCR), targeting the Viral Protein 7 (VP7) gene to amplify segment 7 fragments of all serotypes with serogroup-specific primers. Of these, 7 samples (21.88%) produced 102bp fragments on 2% agarose gel electrophoresis. For serotyping, the 7 PCR-positive samples were further tested by targeting the gene encoding Viral Protein 2 (VP2) with serotype-specific primers, and serotype 9 was identified from tissue samples with a 228bp band. Only tissue samples were cultured on Vero cells, which exhibited cytopathic effects characterized by cell aggregation, rounding, and detachment. In conclusion, African horse sickness caused by serotype 9 severely impacts equines and leads to high mortality in horses. Strategic disease control through vaccination is essential, and further studies are needed to assess outbreak potential and conduct genotypic characterization of the virus in both equines and insect vectors.

Indexed as

AHSHorseMolecular detectionRT-PCRSerotype – 9

Identifiers

PMID42569661
PMCPMC13450614

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