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Serological diagnosis of Toxoplasma gondii: analysis of false-positive IgG results and implications

Background: Primary infection by Toxoplasma gondii in pregnant women can result in serious outcomes for the foetus. A false-positive IgG result during pregnancy can lead to a misdiagnosis of past infection and to stopping preventive measures. We collected 189 sera with positive Architect(®) Toxo IgG...

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Autores principales: Simon, Loïc, Fillaux, Judith, Guigon, Aurélie, Lavergne, Rose-Anne, Villard, Odile, Villena, Isabelle, Marty, Pierre, Pomares, Christelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: EDP Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006501/
https://www.ncbi.nlm.nih.gov/pubmed/32031519
http://dx.doi.org/10.1051/parasite/2020006
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author Simon, Loïc
Fillaux, Judith
Guigon, Aurélie
Lavergne, Rose-Anne
Villard, Odile
Villena, Isabelle
Marty, Pierre
Pomares, Christelle
author_facet Simon, Loïc
Fillaux, Judith
Guigon, Aurélie
Lavergne, Rose-Anne
Villard, Odile
Villena, Isabelle
Marty, Pierre
Pomares, Christelle
author_sort Simon, Loïc
collection PubMed
description Background: Primary infection by Toxoplasma gondii in pregnant women can result in serious outcomes for the foetus. A false-positive IgG result during pregnancy can lead to a misdiagnosis of past infection and to stopping preventive measures. We collected 189 sera with positive Architect(®) Toxo IgG assay (Abbott Laboratories) and negative IgG results with at least two other serological tests, in order to find an explanation for the suspected false-positive IgG results. We used the recomLine Toxoplasma IgG(®) immunoblot (Mikrogen Diagnostik) to search for specific antigenic reactivities of the sera, and the LDBio Toxo II IgG(®) immunoblot (LDBio Diagnostics) as a confirmatory test. Results: The bands GRA8 and/or GRA7 were positive for 148 samples (78.3%). GRA8 was the most frequent band, appearing in 133 patterns (70.4%), whereas GRA7 was present for 49 samples (25.9%). Of the 81 samples tested with LDBio(®), 23 (28.4%) turned out to be positive. Of the 58 negative LDBio(®) tests (71.6%) (real false-positive Architect(®) IgG), 23 samples (39.6%) did not show either a GRA8 or p30 band by recomLine(®). Their false positivity with Architect(®) remains unexplained since Abbott uses these two recombinant antigens for their assay. Conclusions: The Architect(®) IgG false positivity for T. gondii seems to be due to reactivity against GRA8 for the majority of the sera and GRA7 to a lesser extent. The hypothesis of past contact with parasites genetically close to T. gondii such as Hammondia hammondi or Neospora caninum seems promising and should be assessed further.
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spelling pubmed-70065012020-02-13 Serological diagnosis of Toxoplasma gondii: analysis of false-positive IgG results and implications Simon, Loïc Fillaux, Judith Guigon, Aurélie Lavergne, Rose-Anne Villard, Odile Villena, Isabelle Marty, Pierre Pomares, Christelle Parasite Research Article Background: Primary infection by Toxoplasma gondii in pregnant women can result in serious outcomes for the foetus. A false-positive IgG result during pregnancy can lead to a misdiagnosis of past infection and to stopping preventive measures. We collected 189 sera with positive Architect(®) Toxo IgG assay (Abbott Laboratories) and negative IgG results with at least two other serological tests, in order to find an explanation for the suspected false-positive IgG results. We used the recomLine Toxoplasma IgG(®) immunoblot (Mikrogen Diagnostik) to search for specific antigenic reactivities of the sera, and the LDBio Toxo II IgG(®) immunoblot (LDBio Diagnostics) as a confirmatory test. Results: The bands GRA8 and/or GRA7 were positive for 148 samples (78.3%). GRA8 was the most frequent band, appearing in 133 patterns (70.4%), whereas GRA7 was present for 49 samples (25.9%). Of the 81 samples tested with LDBio(®), 23 (28.4%) turned out to be positive. Of the 58 negative LDBio(®) tests (71.6%) (real false-positive Architect(®) IgG), 23 samples (39.6%) did not show either a GRA8 or p30 band by recomLine(®). Their false positivity with Architect(®) remains unexplained since Abbott uses these two recombinant antigens for their assay. Conclusions: The Architect(®) IgG false positivity for T. gondii seems to be due to reactivity against GRA8 for the majority of the sera and GRA7 to a lesser extent. The hypothesis of past contact with parasites genetically close to T. gondii such as Hammondia hammondi or Neospora caninum seems promising and should be assessed further. EDP Sciences 2020-02-07 /pmc/articles/PMC7006501/ /pubmed/32031519 http://dx.doi.org/10.1051/parasite/2020006 Text en © L. Simon et al., published by EDP Sciences, 2020 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Simon, Loïc
Fillaux, Judith
Guigon, Aurélie
Lavergne, Rose-Anne
Villard, Odile
Villena, Isabelle
Marty, Pierre
Pomares, Christelle
Serological diagnosis of Toxoplasma gondii: analysis of false-positive IgG results and implications
title Serological diagnosis of Toxoplasma gondii: analysis of false-positive IgG results and implications
title_full Serological diagnosis of Toxoplasma gondii: analysis of false-positive IgG results and implications
title_fullStr Serological diagnosis of Toxoplasma gondii: analysis of false-positive IgG results and implications
title_full_unstemmed Serological diagnosis of Toxoplasma gondii: analysis of false-positive IgG results and implications
title_short Serological diagnosis of Toxoplasma gondii: analysis of false-positive IgG results and implications
title_sort serological diagnosis of toxoplasma gondii: analysis of false-positive igg results and implications
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006501/
https://www.ncbi.nlm.nih.gov/pubmed/32031519
http://dx.doi.org/10.1051/parasite/2020006
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