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African Swine Fever Laboratory Diagnosis—Lessons Learned from Recent Animal Trials

African swine fever virus (ASFV) causes a hemorrhagic disease in pigs with high socio-economic consequences. To lower the impact of disease incursions, early detection is crucial. In the context of experimental animal trials, we evaluated diagnostic workflows for a high sample throughput in active s...

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Autores principales: Pikalo, Jutta, Deutschmann, Paul, Fischer, Melina, Roszyk, Hanna, Beer, Martin, Blome, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915929/
https://www.ncbi.nlm.nih.gov/pubmed/33562103
http://dx.doi.org/10.3390/pathogens10020177
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author Pikalo, Jutta
Deutschmann, Paul
Fischer, Melina
Roszyk, Hanna
Beer, Martin
Blome, Sandra
author_facet Pikalo, Jutta
Deutschmann, Paul
Fischer, Melina
Roszyk, Hanna
Beer, Martin
Blome, Sandra
author_sort Pikalo, Jutta
collection PubMed
description African swine fever virus (ASFV) causes a hemorrhagic disease in pigs with high socio-economic consequences. To lower the impact of disease incursions, early detection is crucial. In the context of experimental animal trials, we evaluated diagnostic workflows for a high sample throughput in active surveillance, alternative sample matrices for passive surveillance, and lateral flow devices (LFD) for rapid testing. We could demonstrate that EDTA blood is significantly better suited for early ASFV detection than serum. Tissues recommended by the respective diagnostic manuals were in general comparable in their performance, with spleen samples giving best results. Superficial lymph nodes, ear punches, and different blood swabs were also evaluated as potential alternatives. In summary, all matrices yielded positive results at the peak of clinical signs and could be fit for purpose in passive surveillance. However, weaknesses were discovered for some matrices when it comes to the early phase of infection or recovery. The antigen LFD showed variable results with best performance in the clinical phase. The antibody LFD was quite comparable with ELISA systems. Concluding, alternative approaches are feasible but have to be embedded in control strategies selecting test methods and sample materials following a “fit-for-purpose” approach.
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spelling pubmed-79159292021-03-01 African Swine Fever Laboratory Diagnosis—Lessons Learned from Recent Animal Trials Pikalo, Jutta Deutschmann, Paul Fischer, Melina Roszyk, Hanna Beer, Martin Blome, Sandra Pathogens Article African swine fever virus (ASFV) causes a hemorrhagic disease in pigs with high socio-economic consequences. To lower the impact of disease incursions, early detection is crucial. In the context of experimental animal trials, we evaluated diagnostic workflows for a high sample throughput in active surveillance, alternative sample matrices for passive surveillance, and lateral flow devices (LFD) for rapid testing. We could demonstrate that EDTA blood is significantly better suited for early ASFV detection than serum. Tissues recommended by the respective diagnostic manuals were in general comparable in their performance, with spleen samples giving best results. Superficial lymph nodes, ear punches, and different blood swabs were also evaluated as potential alternatives. In summary, all matrices yielded positive results at the peak of clinical signs and could be fit for purpose in passive surveillance. However, weaknesses were discovered for some matrices when it comes to the early phase of infection or recovery. The antigen LFD showed variable results with best performance in the clinical phase. The antibody LFD was quite comparable with ELISA systems. Concluding, alternative approaches are feasible but have to be embedded in control strategies selecting test methods and sample materials following a “fit-for-purpose” approach. MDPI 2021-02-06 /pmc/articles/PMC7915929/ /pubmed/33562103 http://dx.doi.org/10.3390/pathogens10020177 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pikalo, Jutta
Deutschmann, Paul
Fischer, Melina
Roszyk, Hanna
Beer, Martin
Blome, Sandra
African Swine Fever Laboratory Diagnosis—Lessons Learned from Recent Animal Trials
title African Swine Fever Laboratory Diagnosis—Lessons Learned from Recent Animal Trials
title_full African Swine Fever Laboratory Diagnosis—Lessons Learned from Recent Animal Trials
title_fullStr African Swine Fever Laboratory Diagnosis—Lessons Learned from Recent Animal Trials
title_full_unstemmed African Swine Fever Laboratory Diagnosis—Lessons Learned from Recent Animal Trials
title_short African Swine Fever Laboratory Diagnosis—Lessons Learned from Recent Animal Trials
title_sort african swine fever laboratory diagnosis—lessons learned from recent animal trials
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915929/
https://www.ncbi.nlm.nih.gov/pubmed/33562103
http://dx.doi.org/10.3390/pathogens10020177
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