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Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens

BACKGROUND: 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 infecti...

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Autores principales: Fabian, Benedikt T., Hedar, Fatima, Koethe, Martin, Bangoura, Berit, Maksimov, Pavlo, Conraths, Franz J., Villena, Isabelle, Aubert, Dominique, Seeber, Frank, Schares, Gereon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393333/
https://www.ncbi.nlm.nih.gov/pubmed/32736581
http://dx.doi.org/10.1186/s13071-020-04244-6
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author Fabian, Benedikt T.
Hedar, Fatima
Koethe, Martin
Bangoura, Berit
Maksimov, Pavlo
Conraths, Franz J.
Villena, Isabelle
Aubert, Dominique
Seeber, Frank
Schares, Gereon
author_facet Fabian, Benedikt T.
Hedar, Fatima
Koethe, Martin
Bangoura, Berit
Maksimov, Pavlo
Conraths, Franz J.
Villena, Isabelle
Aubert, Dominique
Seeber, Frank
Schares, Gereon
author_sort Fabian, Benedikt T.
collection PubMed
description BACKGROUND: 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 (TgSAG1(bio)) 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 TgSAG1(bio)-BBMA-positive chickens were also positive in two previously established TgSAG1-ELISAs (TgSAG1-ELISA(SL), n = 61/65; or TgSAG1-ELISA(SH), 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 TgSAG1(bio)-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 TgSAG1(bio)-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 TgSAG1(bio)-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. [Image: see text]
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spelling pubmed-73933332020-07-31 Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens Fabian, Benedikt T. Hedar, Fatima Koethe, Martin Bangoura, Berit Maksimov, Pavlo Conraths, Franz J. Villena, Isabelle Aubert, Dominique Seeber, Frank Schares, Gereon Parasit Vectors Research BACKGROUND: 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 (TgSAG1(bio)) 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 TgSAG1(bio)-BBMA-positive chickens were also positive in two previously established TgSAG1-ELISAs (TgSAG1-ELISA(SL), n = 61/65; or TgSAG1-ELISA(SH), 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 TgSAG1(bio)-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 TgSAG1(bio)-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 TgSAG1(bio)-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. [Image: see text] BioMed Central 2020-07-31 /pmc/articles/PMC7393333/ /pubmed/32736581 http://dx.doi.org/10.1186/s13071-020-04244-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Fabian, Benedikt T.
Hedar, Fatima
Koethe, Martin
Bangoura, Berit
Maksimov, Pavlo
Conraths, Franz J.
Villena, Isabelle
Aubert, Dominique
Seeber, Frank
Schares, Gereon
Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens
title Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens
title_full Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens
title_fullStr Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens
title_full_unstemmed Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens
title_short Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens
title_sort fluorescent bead-based serological detection of toxoplasma gondii infection in chickens
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393333/
https://www.ncbi.nlm.nih.gov/pubmed/32736581
http://dx.doi.org/10.1186/s13071-020-04244-6
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