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dc.contributor.authorWalczak, Marek
dc.contributor.authorSzymankiewicz, Krzesimir
dc.contributor.authorRodriguez, Fernando
dc.contributor.authorArgilaguet, Jordi
dc.contributor.authorGavrilov, Boris
dc.contributor.authorŻmudzki, Jacek
dc.contributor.authorKochanowski, Maciej
dc.contributor.authorJuszkiewicz, Małgorzata
dc.contributor.authorSzczotka-Bochniarz, Anna
dc.contributor.otherProducció Animalca
dc.date.accessioned2024-01-17T15:52:07Z
dc.date.available2024-01-17T15:52:07Z
dc.date.issued2023-12-19
dc.identifier.citationWalczak, Marek, Krzesimir Szymankiewicz, Fernando Rodriguez, Jordi Argilaguet, Boris Gavrilov, Jacek Żmudzki, Maciej Kochanowski, Małgorzata Juszkiewicz, and Anna Szczotka-Bochniarz. 2023. “Molecular contamination of an animal facility during and after African swine fever virus infection”. Journal of Veterinary Research 67 (4): 503–8. doi:10.2478/jvetres-2023-0065.ca
dc.identifier.issn2450-8608ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/2722
dc.description.abstractThe molecular contamination of an animal facility was investigated during and after an infection with highly pathogenic African swine fever virus (ASFV) among domestic pigs. The investigation evaluated the risk of indirect transmission of the disease and indicated points that may facilitate cleaning and disinfection processes. Material and Methods: Six domestic pigs were infected oronasally with the highly pathogenic Georgia 2007 strain. Environmental samples from the floors, walls, rubber floor mats, feeders, drinkers, high-efficiency particulate-absorbing filter covers and doors were collected 7 days post infection (dpi), 7 days later and 24 h after disinfection of the facility. The samples were investigated by real-time PCR and in vitro assays to find genetic traces of ASFV and infectious virus. Results: Typical clinical outcomes for ASF (i.e. fever, apathy, recumbency and bloody diarrhoea) were observed, and all animals died or required euthanasia before or at 9 dpi. No infectious virus was found in environmental samples at the sampling time points. Genetic traces of ASFV were found in all locations except the doors. The initial virus load was calculated using real-time PCR threshold cycle values and was the highest at the drain. A statistically significant decrease of virus load over time was found on non-porous surfaces mechanically cleaned by water (the floor and drain). Conclusion: The gathered data confirmed different routes of virus excretion (oral and nasal, faeces and urine, and aerosol) and showed virus locations and different initial concentrations in the animal facility. Maintaining the facility with mechanical cleaning and using personal protection (gloves) and hand disinfection may efficiently minimise the risk of further virus spread. Together with the results of previously published studies, the present investigations’ failure to isolate infectious virus may suggest that if stable environmental conditions are assured, the time needed before the introduction of new herds into previously ASF-affected farm facilities could be shortened and in this way the economic losses caused by the disease outbreak mitigated.ca
dc.format.extent6ca
dc.language.isoengca
dc.publisherSciendoca
dc.relation.ispartofJournal of Veterinary Researchca
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalca
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleMolecular contamination of an animal facility during and after African swine fever virus infectionca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc619ca
dc.identifier.doihttps://doi.org/10.2478/jvetres-2023-0065ca
dc.contributor.groupSanitat Animalca


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Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by-nc-nd/4.0/
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