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2020-07-31Zeitschriftenartikel DOI: 10.1186/s13071-020-04244-6
Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens
dc.contributor.authorFabian, Benedikt T.
dc.contributor.authorHedar, Fatima
dc.contributor.authorKoethe, Martin
dc.contributor.authorBangoura, Berit
dc.contributor.authorMaksimov, Pavlo
dc.contributor.authorConraths, Franz J.
dc.contributor.authorVillena, Isabelle
dc.contributor.authorAubert, Dominique
dc.contributor.authorSeeber, Frank
dc.contributor.authorSchares, Gereon
dc.date.accessioned2026-09-29T15:10:11Z
dc.date.available2026-09-29T15:10:11Z
dc.date.issued2020-07-31none
dc.identifier.urihttp://edoc.rki.de/176904/13985
dc.description.abstractBackground Free-ranging chickens are often infected with Toxoplasma gondii and seroconvert upon infection. This indicates environmental contamination with T. gondii. Methods Here, we established a bead-based multiplex assay (BBMA) using the Luminex technology for the detection of T. gondii infections in chickens. Recombinant biotinylated T. gondii surface antigen 1 (TgSAG1bio) bound to streptavidin-conjugated magnetic Luminex beads served as antigen. Serum antibodies were detected by a fluorophore-coupled secondary antibody. Beads of differing color codes were conjugated with anti-chicken IgY or chicken serum albumin and served for each sample as an internal positive or negative control, respectively. The assay was validated with sera from experimentally and naturally infected chickens. The results were compared to those from reference methods, including other serological tests, PCRs and bioassay in mice. Results In experimentally infected chickens, the vast majority (98.5%, n = 65/66) of birds tested seropositive in the BBMA. This included all chickens positive by magnetic-capture PCR (100%, n = 45/45). Most, but not all inoculated and TgSAG1bio-BBMA-positive chickens were also positive in two previously established TgSAG1-ELISAs (TgSAG1-ELISASL, n = 61/65; or TgSAG1-ELISASH, n = 60/65), or positive in an immunofluorescence assay (IFAT, n = 64/65) and in a modified agglutination test (MAT, n = 61/65). All non-inoculated control animals (n = 28/28, 100%) tested negative. In naturally exposed chickens, the TgSAG1bio-BBMA showed a high sensitivity (98.5%; 95% confidence interval, CI: 90.7–99.9%) and specificity (100%; 95% CI: 85.0–100%) relative to a reference standard established using ELISA, IFAT and MAT. Almost all naturally exposed chickens that were positive in bioassay or by PCR tested positive in the TgSAG1bio-BBMA (93.5%; 95% CI: 77.1–98.9%), while all bioassay- or PCR-negative chickens remained negative (100%; 95% CI: 85.0–100%). Conclusions The TgSAG1bio-BBMA represents a suitable method for the detection of T. gondii infections in chickens with high sensitivity and specificity, which is comparable or even superior to other tests. Since assays based on this methodology allow for the simultaneous analysis of a single biological sample with respect to multiple analytes, the described assay may represent a component in future multiplex assays for broad serological monitoring of poultry and other farm animals for various pathogens.eng
dc.language.isoengnone
dc.publisherRobert Koch-Institut
dc.rights(CC BY 3.0 DE) Namensnennung 3.0 Deutschlandger
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/de/
dc.subject.ddc610 Medizin und Gesundheitnone
dc.titleFluorescent bead-based serological detection of Toxoplasma gondii infection in chickensnone
dc.typearticle
dc.identifier.urnurn:nbn:de:0257-176904/13985-9
dc.identifier.doi10.1186/s13071-020-04244-6
dc.type.versionpublishedVersionnone
local.edoc.container-titleParasites & Vectorsnone
local.edoc.container-issn1756-3305none
local.edoc.pages11none
local.edoc.type-nameZeitschriftenartikel
local.edoc.container-typeperiodical
local.edoc.container-type-nameZeitschrift
local.edoc.container-urlhttps://link.springer.com/journal/13071none
local.edoc.container-publisher-nameSpringer Naturenone
local.edoc.container-volume13none
local.edoc.container-reportyear2020none
dc.description.versionPeer Reviewednone

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