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Screening of a Library of Recombinant Schistosoma mansoni Proteins With Sera From Murine and Human Controlled Infections Identifies Early Serological Markers

BACKGROUND: Schistosomiasis is a major global health problem caused by blood-dwelling parasitic worms, which is currently tackled primarily by mass administration of the drug praziquantel. Appropriate drug treatment strategies are informed by diagnostics that establish the prevalence and intensity o...

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Autores principales: Crosnier, Cécile, Hokke, Cornelis H, Protasio, Anna V, Brandt, Cordelia, Rinaldi, Gabriel, Langenberg, Marijke C C, Clare, Simon, Janse, Jacqueline J, Wilson, Shona, Berriman, Matthew, Roestenberg, Meta, Wright, Gavin J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016452/
https://www.ncbi.nlm.nih.gov/pubmed/32524140
http://dx.doi.org/10.1093/infdis/jiaa329
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author Crosnier, Cécile
Hokke, Cornelis H
Protasio, Anna V
Brandt, Cordelia
Rinaldi, Gabriel
Langenberg, Marijke C C
Clare, Simon
Janse, Jacqueline J
Wilson, Shona
Berriman, Matthew
Roestenberg, Meta
Wright, Gavin J
author_facet Crosnier, Cécile
Hokke, Cornelis H
Protasio, Anna V
Brandt, Cordelia
Rinaldi, Gabriel
Langenberg, Marijke C C
Clare, Simon
Janse, Jacqueline J
Wilson, Shona
Berriman, Matthew
Roestenberg, Meta
Wright, Gavin J
author_sort Crosnier, Cécile
collection PubMed
description BACKGROUND: Schistosomiasis is a major global health problem caused by blood-dwelling parasitic worms, which is currently tackled primarily by mass administration of the drug praziquantel. Appropriate drug treatment strategies are informed by diagnostics that establish the prevalence and intensity of infection, which, in regions of low transmission, should be highly sensitive. METHODS: To identify sensitive new serological markers of Schistosoma mansoni infections, we have compiled a recombinant protein library of parasite cell-surface and secreted proteins expressed in mammalian cells. RESULTS: Together with a time series of sera samples from volunteers experimentally infected with a defined number of male parasites, we probed this protein library to identify several markers that can detect primary infections with as low as 10 parasites and as early as 5 weeks postinfection. CONCLUSIONS: These new markers could be further explored as valuable tools to detect ongoing and previous S mansoni infections, including in endemic regions where transmission is low.
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spelling pubmed-90164522022-04-20 Screening of a Library of Recombinant Schistosoma mansoni Proteins With Sera From Murine and Human Controlled Infections Identifies Early Serological Markers Crosnier, Cécile Hokke, Cornelis H Protasio, Anna V Brandt, Cordelia Rinaldi, Gabriel Langenberg, Marijke C C Clare, Simon Janse, Jacqueline J Wilson, Shona Berriman, Matthew Roestenberg, Meta Wright, Gavin J J Infect Dis Major Articles and Brief Reports BACKGROUND: Schistosomiasis is a major global health problem caused by blood-dwelling parasitic worms, which is currently tackled primarily by mass administration of the drug praziquantel. Appropriate drug treatment strategies are informed by diagnostics that establish the prevalence and intensity of infection, which, in regions of low transmission, should be highly sensitive. METHODS: To identify sensitive new serological markers of Schistosoma mansoni infections, we have compiled a recombinant protein library of parasite cell-surface and secreted proteins expressed in mammalian cells. RESULTS: Together with a time series of sera samples from volunteers experimentally infected with a defined number of male parasites, we probed this protein library to identify several markers that can detect primary infections with as low as 10 parasites and as early as 5 weeks postinfection. CONCLUSIONS: These new markers could be further explored as valuable tools to detect ongoing and previous S mansoni infections, including in endemic regions where transmission is low. Oxford University Press 2020-06-10 /pmc/articles/PMC9016452/ /pubmed/32524140 http://dx.doi.org/10.1093/infdis/jiaa329 Text en © The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Major Articles and Brief Reports
Crosnier, Cécile
Hokke, Cornelis H
Protasio, Anna V
Brandt, Cordelia
Rinaldi, Gabriel
Langenberg, Marijke C C
Clare, Simon
Janse, Jacqueline J
Wilson, Shona
Berriman, Matthew
Roestenberg, Meta
Wright, Gavin J
Screening of a Library of Recombinant Schistosoma mansoni Proteins With Sera From Murine and Human Controlled Infections Identifies Early Serological Markers
title Screening of a Library of Recombinant Schistosoma mansoni Proteins With Sera From Murine and Human Controlled Infections Identifies Early Serological Markers
title_full Screening of a Library of Recombinant Schistosoma mansoni Proteins With Sera From Murine and Human Controlled Infections Identifies Early Serological Markers
title_fullStr Screening of a Library of Recombinant Schistosoma mansoni Proteins With Sera From Murine and Human Controlled Infections Identifies Early Serological Markers
title_full_unstemmed Screening of a Library of Recombinant Schistosoma mansoni Proteins With Sera From Murine and Human Controlled Infections Identifies Early Serological Markers
title_short Screening of a Library of Recombinant Schistosoma mansoni Proteins With Sera From Murine and Human Controlled Infections Identifies Early Serological Markers
title_sort screening of a library of recombinant schistosoma mansoni proteins with sera from murine and human controlled infections identifies early serological markers
topic Major Articles and Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016452/
https://www.ncbi.nlm.nih.gov/pubmed/32524140
http://dx.doi.org/10.1093/infdis/jiaa329
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