Evidence map›Paper›PMID 40264120›Full record

ArticleBMC veterinary research2025

Detection of African swine fever virus in archived Formalin fixed Paraffin embedded swine tissue sections in Uganda using Immunohistochemistry (IHC) and Polymerase chain reaction (PCR).

Mathias Afayoa, Lonzy Ojok, Julius Boniface Okuni

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Article in BMC veterinary research, 2025. 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Mathias AfayoaSection of Veterinary Pathology, Department of Pharmacy Clinical and Comparative Veterinary Medicine, College of Veterinary Medicine, Animal Resources and Biosecurity, Makerere University, Kampala City, Uganda. mafayoa@gmail.com.
Lonzy OjokDepartment of Pathology, Faculty of Medicine, Gulu University, Gulu City, Uganda.
Julius Boniface OkuniSection of Veterinary Pathology, Department of Pharmacy Clinical and Comparative Veterinary Medicine, College of Veterinary Medicine, Animal Resources and Biosecurity, Makerere University, Kampala City, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAfrican swine fever (ASF), a devastating viral disease of pigs, is one of the main hindrances to pig farming in sub-Saharan Africa. Sporadic outbreaks of the disease occur annually in various regions of Uganda most of which remain undocumented. Confirmatory diagnosis of ASF is vital for instituting the disease prevention and control measures. Unfortunately, laboratory confirmatory diagnosis of ASF in Uganda is limited due to the high costs and expertise required. The aim of this study was to compare the level of agreement for positive detection of ASF virus by PCR and immunohistochemistry in archived formalin fixed, paraffin-embedded pig tissues from clinically suspected ASF cases in Uganda.

resultsMore than a third of the archived pig lymphoid tissues, (lymph nodes 33.3%, 95/285 and spleen; 42.8%, 120/280) had lesions suggestive of ASF. On average, 17% and 15% of the archived samples had ASF viral DNA and antigen respectively. The positivity rate for ASF in the tested tissue samples was higher in spleen (PCR, 17.5% and IHC, 16.1%) than in other tissues. More than half (51.1%, 48/94) of the lymph nodes and 41.9% (49/117) of spleen tissues that had lesions suggestive of ASF tested positive for ASF using conventional PCR. There was a strong agreement (kappa = 0.93913 at 95% CI; 0.88634-0.99193) between IHC and PCR in diagnosis of ASF in formalin fixed paraffin embedded pig tissue samples examined.

conclusionASF is still wide spread in Uganda and is one of the major threats to pig production in the country. PCR remain the most effective and reliable technique for diagnosing ASF in tissues even after a long period of archiving.

Indexed as

African Swine FeverAfrican Swine Fever VirusImmunohistochemistryPolymerase Chain ReactionAnimalsDNA, ViralFormaldehydeLymph NodesParaffin EmbeddingSpleenSwineUgandaDNA, ViralFormaldehydeAfrican swine feverArchived tissuesDiagnosisImmunohistochemistryPCRPigs

Identifiers

PMID40264120
PMCPMC12012999

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