ArticleViruses2025
Assessing Virus Survival in African Swine Fever Virus-Contaminated Materials-Implications for Indirect Virus Transmission.
Article in Viruses, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
4 citing papers in PubMed.
- Temperature-dependent Persistence of African Swine Fever Virus.International journal of veterinary science and medicine · 2026Article
- Comparative epidemiology and preparedness for African swine fever and porcine reproductive and respiratory syndrome in four major Asian swine industries.Frontiers in veterinary science · 2026Review
- Spatial prediction of wild boar distribution in Thailand applications for African swine fever prevention and control.Scientific reports · 2025Article
- Mitigation Strategies for African Swine Fever Virus Biosecurity: From Virus Inactivation to Pig Health.Transboundary and emerging diseases · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
Introduction of African swine fever virus (ASFV) into pig herds can occur via virus-contaminated feed or other objects. Knowledge about ASFV survival in different matrices and under different conditions is required to understand indirect virus transmission. Maintenance of ASFV infectivity can occur for extended periods outside pigs. Current assays detecting ASFV have inherent disadvantages. Cell culture-based assays are labor-intensive and sensitive to contaminants while methods using qPCR detect ASFV DNA with high sensitivity and specificity, but this may not correspond to infectious virus. Here, we have combined the use of these assays to assess the replication of ASFV within cells and determined the effect of pig feces, straw, wood shavings, and mixed feed on ASFV infectivity. In porcine serum, infectious ASFV survived for at least 60 days at 4 °C, 22 °C, and 37 °C; for two days at 50 °C; one day at 60 °C; and ≤5 min at 70 °C. In the presence of feed, straw, or wood shavings, the survival of the virus wasmarkedly shortened. Samples remained positive in the qPCR assay despite the loss of virus infectivity. Thus, it was possible to distinguish between the presence of ASFV DNA and the survival of the infectious virus.
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Registered trials
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