Development of a miniaturized protein microarray as a new serological IgG screening test for zoonotic agents and production diseases in pigs

dc.bibliographicCitation.firstPagee0217290eng
dc.bibliographicCitation.issue5eng
dc.bibliographicCitation.volume14eng
dc.contributor.authorLoreck, Katharina
dc.contributor.authorMitrenga, Sylvia
dc.contributor.authorMeemken, Diana
dc.contributor.authorHeinze, Regina
dc.contributor.authorReissig, Annett
dc.contributor.authorMueller, Elke
dc.contributor.authorEhricht, Ralf
dc.contributor.authorEngemann, Claudia
dc.contributor.authorGreiner, Matthias
dc.date.accessioned2021-12-13T05:38:16Z
dc.date.available2021-12-13T05:38:16Z
dc.date.issued2019
dc.description.abstractIn order to monitor the occurrence of zoonotic agents in pig herds as well as to improve herd health management, the development of new cost-effective diagnostic methods for pigs is necessary. In this study, a protein microarray-based assay for the simultaneous detection of immunoglobulin G (IgG) antibodies against different zoonotic agents and pathogens causing production diseases in pigs was developed. Therefore, antigens of ten different important swine pathogens (Toxoplasma gondii, Yersinia enterocolitica, Salmonella spp., Trichinella spp., Mycobacterium avium, Hepatitis E virus, Mycoplasma hyopneumoniae, Actinobacillus pleuropneumoniae, the porcine reproductive and respiratory syndrome virus, Influenza A virus) were spotted and covalently immobilized as ‘antigen-spots’ on microarray chips in order to test pig serum for the occurrence of antibodies. Pig serum was sampled at three German abattoirs and ELISA tests for the different pathogens were conducted with the purpose of creating a panel of reference samples for microarray analysis. To evaluate the accuracy of the antigens on the microarray, receiver operating characteristic (ROC) curve analysis using the ELISA test results as reference was performed for the different antigens. High area under curve values were achieved for the antigens of two zoonotic agents: Toxoplasma gondii (0.91), Yersinia enterocolitica (0.97) and for three production diseases: Actinobacillus pleuropneumoniae (0.77), Mycoplasma hyopneumoniae (0.94) and the porcine reproductive and respiratory syndrome virus (0.87). With the help of the newly developed microarray assay, collecting data on the occurrence of antibodies against zoonotic agents and production diseases in pig herds could be minimized to one measurement, resulting in an efficient screening test.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/7682
dc.identifier.urihttps://doi.org/10.34657/6729
dc.language.isoengeng
dc.publisherSan Francisco, California, US : PLOSeng
dc.relation.doihttps://doi.org/10.1371/journal.pone.0217290
dc.relation.essn1932-6203
dc.relation.ispartofseriesPLOS ONE 14 (2019), Nr. 5eng
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subjectzoonotic agentseng
dc.subjectdiagnostic methodeng
dc.subjectimmunoglobulin G (IgG) antibodieseng
dc.subjectbacterium antibodyeng
dc.subjectprotozoon antibodyeng
dc.subjectvirus antibodyeng
dc.subject.ddc500eng
dc.subject.ddc610eng
dc.titleDevelopment of a miniaturized protein microarray as a new serological IgG screening test for zoonotic agents and production diseases in pigseng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitlePLOS ONEeng
tib.accessRightsopenAccesseng
wgl.contributorIPHTeng
wgl.subjectMedizin, Gesundheiteng
wgl.typeZeitschriftenartikeleng
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