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High Throughput Selection of Effective Serodiagnostics for Trypanosoma cruzi infection

BACKGROUND: Diagnosis of Trypanosoma cruzi infection by direct pathogen detection is complicated by the low parasite burden in subjects persistently infected with this agent of human Chagas disease. Determination of infection status by serological analysis has also been faulty, largely due to the la...

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Autores principales: Cooley, Gretchen, Etheridge, R. Drew, Boehlke, Courtney, Bundy, Becky, Weatherly, D. Brent, Minning, Todd, Haney, Matthew, Postan, Miriam, Laucella, Susana, Tarleton, Rick L.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556098/
https://www.ncbi.nlm.nih.gov/pubmed/18841200
http://dx.doi.org/10.1371/journal.pntd.0000316
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author Cooley, Gretchen
Etheridge, R. Drew
Boehlke, Courtney
Bundy, Becky
Weatherly, D. Brent
Minning, Todd
Haney, Matthew
Postan, Miriam
Laucella, Susana
Tarleton, Rick L.
author_facet Cooley, Gretchen
Etheridge, R. Drew
Boehlke, Courtney
Bundy, Becky
Weatherly, D. Brent
Minning, Todd
Haney, Matthew
Postan, Miriam
Laucella, Susana
Tarleton, Rick L.
author_sort Cooley, Gretchen
collection PubMed
description BACKGROUND: Diagnosis of Trypanosoma cruzi infection by direct pathogen detection is complicated by the low parasite burden in subjects persistently infected with this agent of human Chagas disease. Determination of infection status by serological analysis has also been faulty, largely due to the lack of well-characterized parasite reagents for the detection of anti-parasite antibodies. METHODS: In this study, we screened more than 400 recombinant proteins of T. cruzi, including randomly selected and those known to be highly expressed in the parasite stages present in mammalian hosts, for the ability to detect anti-parasite antibodies in the sera of subjects with confirmed or suspected T. cruzi infection. FINDINGS: A set of 16 protein groups were identified and incorporated into a multiplex bead array format which detected 100% of >100 confirmed positive sera and also documented consistent, strong and broad responses in samples undetected or discordant using conventional serologic tests. Each serum had a distinct but highly stable reaction pattern. This diagnostic panel was also useful for monitoring drug treatment efficacy in chronic Chagas disease. CONCLUSIONS: These results substantially extend the variety and quality of diagnostic targets for Chagas disease and offer a useful tool for determining treatment success or failure.
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spelling pubmed-25560982008-10-08 High Throughput Selection of Effective Serodiagnostics for Trypanosoma cruzi infection Cooley, Gretchen Etheridge, R. Drew Boehlke, Courtney Bundy, Becky Weatherly, D. Brent Minning, Todd Haney, Matthew Postan, Miriam Laucella, Susana Tarleton, Rick L. PLoS Negl Trop Dis Research Article BACKGROUND: Diagnosis of Trypanosoma cruzi infection by direct pathogen detection is complicated by the low parasite burden in subjects persistently infected with this agent of human Chagas disease. Determination of infection status by serological analysis has also been faulty, largely due to the lack of well-characterized parasite reagents for the detection of anti-parasite antibodies. METHODS: In this study, we screened more than 400 recombinant proteins of T. cruzi, including randomly selected and those known to be highly expressed in the parasite stages present in mammalian hosts, for the ability to detect anti-parasite antibodies in the sera of subjects with confirmed or suspected T. cruzi infection. FINDINGS: A set of 16 protein groups were identified and incorporated into a multiplex bead array format which detected 100% of >100 confirmed positive sera and also documented consistent, strong and broad responses in samples undetected or discordant using conventional serologic tests. Each serum had a distinct but highly stable reaction pattern. This diagnostic panel was also useful for monitoring drug treatment efficacy in chronic Chagas disease. CONCLUSIONS: These results substantially extend the variety and quality of diagnostic targets for Chagas disease and offer a useful tool for determining treatment success or failure. Public Library of Science 2008-10-08 /pmc/articles/PMC2556098/ /pubmed/18841200 http://dx.doi.org/10.1371/journal.pntd.0000316 Text en Cooley et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cooley, Gretchen
Etheridge, R. Drew
Boehlke, Courtney
Bundy, Becky
Weatherly, D. Brent
Minning, Todd
Haney, Matthew
Postan, Miriam
Laucella, Susana
Tarleton, Rick L.
High Throughput Selection of Effective Serodiagnostics for Trypanosoma cruzi infection
title High Throughput Selection of Effective Serodiagnostics for Trypanosoma cruzi infection
title_full High Throughput Selection of Effective Serodiagnostics for Trypanosoma cruzi infection
title_fullStr High Throughput Selection of Effective Serodiagnostics for Trypanosoma cruzi infection
title_full_unstemmed High Throughput Selection of Effective Serodiagnostics for Trypanosoma cruzi infection
title_short High Throughput Selection of Effective Serodiagnostics for Trypanosoma cruzi infection
title_sort high throughput selection of effective serodiagnostics for trypanosoma cruzi infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556098/
https://www.ncbi.nlm.nih.gov/pubmed/18841200
http://dx.doi.org/10.1371/journal.pntd.0000316
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