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ASF -survivors’ Sera Do Not Inhibit African Swine Fever Virus Replication in Vitro

INTRODUCTION: African swine fever virus (ASFV) causes one of the most dangerous diseases of pigs and wild boar – African swine fever (ASF). Since its second introduction into Europe (in 2007), the disease has been spreading consistently, and now ASF-free European countries are at risk. Complex inter...

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Autores principales: Walczak, Marek, Juszkiewicz, Małgorzata, Szymankiewicz, Krzesimir, Szczotka-Bochniarz, Anna, Woźniakowski, Grzegorz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959686/
https://www.ncbi.nlm.nih.gov/pubmed/35582480
http://dx.doi.org/10.2478/jvetres-2022-0016
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author Walczak, Marek
Juszkiewicz, Małgorzata
Szymankiewicz, Krzesimir
Szczotka-Bochniarz, Anna
Woźniakowski, Grzegorz
author_facet Walczak, Marek
Juszkiewicz, Małgorzata
Szymankiewicz, Krzesimir
Szczotka-Bochniarz, Anna
Woźniakowski, Grzegorz
author_sort Walczak, Marek
collection PubMed
description INTRODUCTION: African swine fever virus (ASFV) causes one of the most dangerous diseases of pigs and wild boar – African swine fever (ASF). Since its second introduction into Europe (in 2007), the disease has been spreading consistently, and now ASF-free European countries are at risk. Complex interactions between the host’s immune system and the virus have long prevented the development of a safe vaccine against ASF. This study analysed the possibility of neutralisation of the ASFV in vitro by sera collected from ASF-survivor animals. MATERIAL AND METHODS: Two pig and three wild boar serum samples were collected from previously selected potential ASF survivors. All sera presented high antibody titres (>5 log(10)/mL). Primary alveolar macrophages were cultured in growth medium containing 10% and 20% concentrations of selected sera and infected with a haemadsorbing ASFV strain (Pol18_28298_O111, genotype II). The progress of infection was investigated under a light microscope by observing the cytopathic effect (CPE) and the haemadsorption phenomenon. Growth kinetics were investigated using a real-time PCR assay. RESULTS: Haemadsorption inhibition was detected in the presence of almost all selected sera; however, the inhibition of virus replication in vitro was excluded. In all samples, a CPE and decreasing quantification cycle values of the viral DNA were found. CONCLUSION: Anti-ASFV antibodies alone are not able to inhibit virus replication. Interactions between the humoral and cellular immune response which effectively combat the disease are implicated in an ASF-survivor’s organism.
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spelling pubmed-89596862022-05-16 ASF -survivors’ Sera Do Not Inhibit African Swine Fever Virus Replication in Vitro Walczak, Marek Juszkiewicz, Małgorzata Szymankiewicz, Krzesimir Szczotka-Bochniarz, Anna Woźniakowski, Grzegorz J Vet Res Research Article INTRODUCTION: African swine fever virus (ASFV) causes one of the most dangerous diseases of pigs and wild boar – African swine fever (ASF). Since its second introduction into Europe (in 2007), the disease has been spreading consistently, and now ASF-free European countries are at risk. Complex interactions between the host’s immune system and the virus have long prevented the development of a safe vaccine against ASF. This study analysed the possibility of neutralisation of the ASFV in vitro by sera collected from ASF-survivor animals. MATERIAL AND METHODS: Two pig and three wild boar serum samples were collected from previously selected potential ASF survivors. All sera presented high antibody titres (>5 log(10)/mL). Primary alveolar macrophages were cultured in growth medium containing 10% and 20% concentrations of selected sera and infected with a haemadsorbing ASFV strain (Pol18_28298_O111, genotype II). The progress of infection was investigated under a light microscope by observing the cytopathic effect (CPE) and the haemadsorption phenomenon. Growth kinetics were investigated using a real-time PCR assay. RESULTS: Haemadsorption inhibition was detected in the presence of almost all selected sera; however, the inhibition of virus replication in vitro was excluded. In all samples, a CPE and decreasing quantification cycle values of the viral DNA were found. CONCLUSION: Anti-ASFV antibodies alone are not able to inhibit virus replication. Interactions between the humoral and cellular immune response which effectively combat the disease are implicated in an ASF-survivor’s organism. Sciendo 2022-03-25 /pmc/articles/PMC8959686/ /pubmed/35582480 http://dx.doi.org/10.2478/jvetres-2022-0016 Text en © 2022 M. Walczak et al. published by Sciendo https://creativecommons.org/licenses/by-nc-nd/3.0/This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
spellingShingle Research Article
Walczak, Marek
Juszkiewicz, Małgorzata
Szymankiewicz, Krzesimir
Szczotka-Bochniarz, Anna
Woźniakowski, Grzegorz
ASF -survivors’ Sera Do Not Inhibit African Swine Fever Virus Replication in Vitro
title ASF -survivors’ Sera Do Not Inhibit African Swine Fever Virus Replication in Vitro
title_full ASF -survivors’ Sera Do Not Inhibit African Swine Fever Virus Replication in Vitro
title_fullStr ASF -survivors’ Sera Do Not Inhibit African Swine Fever Virus Replication in Vitro
title_full_unstemmed ASF -survivors’ Sera Do Not Inhibit African Swine Fever Virus Replication in Vitro
title_short ASF -survivors’ Sera Do Not Inhibit African Swine Fever Virus Replication in Vitro
title_sort asf -survivors’ sera do not inhibit african swine fever virus replication in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959686/
https://www.ncbi.nlm.nih.gov/pubmed/35582480
http://dx.doi.org/10.2478/jvetres-2022-0016
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