Cargando…

Toxoplasma gondii Recombinant antigen AMA1: Diagnostic Utility of Protein Fragments for the Detection of IgG and IgM Antibodies

Toxoplasma gondii is an important zoonotic protozoan that infects a wide variety of vertebrates as intermediate hosts. For this reason, the diagnosis of this disease is very important and requires continuous improvement. One possibility is to use recombinant antigens in serological tests. Apical mem...

Descripción completa

Detalles Bibliográficos
Autores principales: Ferra, Bartłomiej, Holec-Gąsior, Lucyna, Gatkowska, Justyna, Dziadek, Bożena, Dzitko, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168680/
https://www.ncbi.nlm.nih.gov/pubmed/31948063
http://dx.doi.org/10.3390/pathogens9010043
_version_ 1783523694638792704
author Ferra, Bartłomiej
Holec-Gąsior, Lucyna
Gatkowska, Justyna
Dziadek, Bożena
Dzitko, Katarzyna
author_facet Ferra, Bartłomiej
Holec-Gąsior, Lucyna
Gatkowska, Justyna
Dziadek, Bożena
Dzitko, Katarzyna
author_sort Ferra, Bartłomiej
collection PubMed
description Toxoplasma gondii is an important zoonotic protozoan that infects a wide variety of vertebrates as intermediate hosts. For this reason, the diagnosis of this disease is very important and requires continuous improvement. One possibility is to use recombinant antigens in serological tests. Apical membrane antigen 1 (AMA1), a protein located in specific secretory organelles (micronemes) of T. gondii, is very interesting in regard to its potential diagnostic utility. In the present study, we attempted to identify a fragment of the AMA1 protein with a high sensitivity and specificity for the serological diagnosis of human toxoplasmosis. The full-length AMA1 and two different fragments (AMA1N and AMA1C) were produced using an Escherichia coli expression system. After purification by metal affinity chromatography, recombinant proteins were tested for their utility as antigens in enzyme-linked immunosorbent assays (ELISAs) for the detection of IgG and IgM anti-T. gondii antibodies in human and mouse immune sera. Our data demonstrate that the full-length AMA1 recombinant antigen (corresponding to amino acid residues 67–569 of the native protein) has a better diagnostic potential than its N- or C-terminal fragments. This recombinant protein strongly interacts with specific anti-T. gondii IgG (99.4%) and IgM (80.0%) antibodies, and may be used for developing new tools for diagnostics of toxoplasmosis.
format Online
Article
Text
id pubmed-7168680
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-71686802020-04-20 Toxoplasma gondii Recombinant antigen AMA1: Diagnostic Utility of Protein Fragments for the Detection of IgG and IgM Antibodies Ferra, Bartłomiej Holec-Gąsior, Lucyna Gatkowska, Justyna Dziadek, Bożena Dzitko, Katarzyna Pathogens Article Toxoplasma gondii is an important zoonotic protozoan that infects a wide variety of vertebrates as intermediate hosts. For this reason, the diagnosis of this disease is very important and requires continuous improvement. One possibility is to use recombinant antigens in serological tests. Apical membrane antigen 1 (AMA1), a protein located in specific secretory organelles (micronemes) of T. gondii, is very interesting in regard to its potential diagnostic utility. In the present study, we attempted to identify a fragment of the AMA1 protein with a high sensitivity and specificity for the serological diagnosis of human toxoplasmosis. The full-length AMA1 and two different fragments (AMA1N and AMA1C) were produced using an Escherichia coli expression system. After purification by metal affinity chromatography, recombinant proteins were tested for their utility as antigens in enzyme-linked immunosorbent assays (ELISAs) for the detection of IgG and IgM anti-T. gondii antibodies in human and mouse immune sera. Our data demonstrate that the full-length AMA1 recombinant antigen (corresponding to amino acid residues 67–569 of the native protein) has a better diagnostic potential than its N- or C-terminal fragments. This recombinant protein strongly interacts with specific anti-T. gondii IgG (99.4%) and IgM (80.0%) antibodies, and may be used for developing new tools for diagnostics of toxoplasmosis. MDPI 2020-01-05 /pmc/articles/PMC7168680/ /pubmed/31948063 http://dx.doi.org/10.3390/pathogens9010043 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ferra, Bartłomiej
Holec-Gąsior, Lucyna
Gatkowska, Justyna
Dziadek, Bożena
Dzitko, Katarzyna
Toxoplasma gondii Recombinant antigen AMA1: Diagnostic Utility of Protein Fragments for the Detection of IgG and IgM Antibodies
title Toxoplasma gondii Recombinant antigen AMA1: Diagnostic Utility of Protein Fragments for the Detection of IgG and IgM Antibodies
title_full Toxoplasma gondii Recombinant antigen AMA1: Diagnostic Utility of Protein Fragments for the Detection of IgG and IgM Antibodies
title_fullStr Toxoplasma gondii Recombinant antigen AMA1: Diagnostic Utility of Protein Fragments for the Detection of IgG and IgM Antibodies
title_full_unstemmed Toxoplasma gondii Recombinant antigen AMA1: Diagnostic Utility of Protein Fragments for the Detection of IgG and IgM Antibodies
title_short Toxoplasma gondii Recombinant antigen AMA1: Diagnostic Utility of Protein Fragments for the Detection of IgG and IgM Antibodies
title_sort toxoplasma gondii recombinant antigen ama1: diagnostic utility of protein fragments for the detection of igg and igm antibodies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168680/
https://www.ncbi.nlm.nih.gov/pubmed/31948063
http://dx.doi.org/10.3390/pathogens9010043
work_keys_str_mv AT ferrabartłomiej toxoplasmagondiirecombinantantigenama1diagnosticutilityofproteinfragmentsforthedetectionofiggandigmantibodies
AT holecgasiorlucyna toxoplasmagondiirecombinantantigenama1diagnosticutilityofproteinfragmentsforthedetectionofiggandigmantibodies
AT gatkowskajustyna toxoplasmagondiirecombinantantigenama1diagnosticutilityofproteinfragmentsforthedetectionofiggandigmantibodies
AT dziadekbozena toxoplasmagondiirecombinantantigenama1diagnosticutilityofproteinfragmentsforthedetectionofiggandigmantibodies
AT dzitkokatarzyna toxoplasmagondiirecombinantantigenama1diagnosticutilityofproteinfragmentsforthedetectionofiggandigmantibodies