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dc.contributor.authorBohorquez, Jose Alejandro
dc.contributor.authorLanka, Saraswathi
dc.contributor.authorRosell, Rosa
dc.contributor.authorPérez-Simó, Marta
dc.contributor.authorAlberch, Mònica
dc.contributor.authorRodriguez, Fernando
dc.contributor.authorGanges, Llilianne
dc.contributor.authorMaddox, Carol W
dc.contributor.otherProducció Animalca
dc.date.accessioned2023-06-29T08:58:50Z
dc.date.available2023-06-29T08:58:50Z
dc.date.issued2023-01-27
dc.identifier.citationBohorquez, Jose Alejandro, Saraswathi Lanka, Rosa Rosell, Marta Pérez-Simó, Mònica Alberch, Fernando Rodriguez, Llilianne Ganges, and Carol W. Maddox. 2023. "Efficient Detection Of African Swine Fever Virus Using Minimal Equipment Through A LAMP PCR Method". Frontiers In Cellular And Infection Microbiology 13. doi:10.3389/fcimb.2023.1114772.ca
dc.identifier.issn2235-2988ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/2285
dc.description.abstractAfrican swine fever virus (ASFV) currently represents the biggest threat to the porcine industry worldwide, with high economic impact and severe animal health and welfare concerns. Outbreaks have occurred in Europe and Asia since ASFV was reintroduced into the continent in 2007 and, in 2021, ASFV was detected in the Caribbean, raising alarm about the reemergence of the virus in the Americas. Given the lack of vaccines against ASFV, control of the virus relies on molecular surveillance, which can be delayed due to the need for sample shipment to specialized laboratories. Isothermal PCR techniques, such as LAMP, have become increasingly attractive as point-of-care diagnostic tools given the minimal material expense, equipment, and training required. The present study aimed to develop a LAMP assay for the detection of ASFV. Four LAMP primer sets were designed, based on a consensus sequence for the ASFV p72 gene, and were tested using a synthetic plasmid containing the cloned ASFV p72 target gene as a positive control. Two primer sets, were selected for further validation, given their very short time for amplification. Both primer sets showed thermal stability, amplifying the ASFV DNA at temperatures between 60-70°C and proved to have an analytical limit of detection as low as one ASFV-plasmid DNA copy/µL, using both fluorometric and colorimetric methods. The selected primers did not yield false positive or cross reactive results with other common swine pathogens, showing high specificity. Testing of DNA-spiked samples showed that LAMP amplification was not affected by the nature of the matrices, including oral fluids, tonsils, blood, or rectal swabs. The primer sets were able to detect the two more prevalent ASFV genotypes in the field. Taken together, the results show that ASFV-LAMP-BG2 and ASFV-LAMP-BG3 would be a useful tool for rapid, highly sensitive on-site diagnostic testing.ca
dc.format.extent13ca
dc.language.isoengca
dc.publisherFrontiers Mediaca
dc.relation.ispartofFrontiers in Cellular and Infection Microbiologyca
dc.rightsAttribution 4.0 Internationalca
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleEfficient detection of African Swine Fever Virus using minimal equipment through a LAMP PCR methodca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.relation.projectIDMICIU/Programa Estatal de generación del conocimiento y fortalecimiento científico y tecnológico del sistema I+D+I y Programa Estatal de I+D+I orientada a los retos de la sociedad/PID2019-107616RB-I00/ES/Peste porcina africana; de la emergencia a evitar el endemismo/ca
dc.subject.udc619ca
dc.identifier.doihttps://doi.org/10.3389/fcimb.2023.1114772ca
dc.contributor.groupSanitat Animalca


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