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Comparison of total immunoglobulin G antibody responses to different protein fragments of Plasmodium vivax Reticulocyte binding protein 2b

BACKGROUND: Plasmodium vivax is emerging as the dominant and prevalent species causing malaria in near-elimination settings outside of Africa. Hypnozoites, the dormant liver stage parasite of P. vivax, are undetectable to any currently available diagnostic test, yet are a major reservoir for transmi...

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Autores principales: Bourke, Caitlin, Takashima, Eizo, Chan, Li-Jin, Dietrich, Melanie H., Mazhari, Ramin, White, Michael, Sattabongkot, Jetsumon, Tham, Wai-Hong, Tsuboi, Takafumi, Mueller, Ivo, Longley, Rhea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896302/
https://www.ncbi.nlm.nih.gov/pubmed/35246142
http://dx.doi.org/10.1186/s12936-022-04085-x
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author Bourke, Caitlin
Takashima, Eizo
Chan, Li-Jin
Dietrich, Melanie H.
Mazhari, Ramin
White, Michael
Sattabongkot, Jetsumon
Tham, Wai-Hong
Tsuboi, Takafumi
Mueller, Ivo
Longley, Rhea
author_facet Bourke, Caitlin
Takashima, Eizo
Chan, Li-Jin
Dietrich, Melanie H.
Mazhari, Ramin
White, Michael
Sattabongkot, Jetsumon
Tham, Wai-Hong
Tsuboi, Takafumi
Mueller, Ivo
Longley, Rhea
author_sort Bourke, Caitlin
collection PubMed
description BACKGROUND: Plasmodium vivax is emerging as the dominant and prevalent species causing malaria in near-elimination settings outside of Africa. Hypnozoites, the dormant liver stage parasite of P. vivax, are undetectable to any currently available diagnostic test, yet are a major reservoir for transmission. Advances have been made to harness the naturally acquired immune response to identify recent exposure to P. vivax blood-stage parasites and, therefore, infer the presence of hypnozoites. This in-development diagnostic is currently able to detect infections within the last 9-months with 80% sensitivity and 80% specificity. Further work is required to optimize protein expression and protein constructs used for antibody detection. METHODS: The antibody response against the top performing predictor of recent infection, P. vivax reticulocyte binding protein 2b (PvRBP2b), was tested against multiple fragments of different sizes and from different expression systems. The IgG induced against the recombinant PvRBP2b fragments in P. vivax infected individuals was measured at the time of infection and in a year-long observational cohort; both conducted in Thailand. RESULTS: The antibody responses to some but not all different sized fragments of PvRBP2b protein are highly correlated with each other, significantly higher 1-week post-P. vivax infection, and show potential for use as predictors of recent P. vivax infection. CONCLUSIONS: To achieve P. vivax elimination goals, novel diagnostics are required to aid in detection of hidden parasite reservoirs. PvRBP2b was previously shown to be the top candidate for single-antigen classification of recent P. vivax exposure and here, it is concluded that several alternative recombinant PvRBP2b fragments can achieve equal sensitivity and specificity at predicting recent P. vivax exposure. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04085-x.
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spelling pubmed-88963022022-03-14 Comparison of total immunoglobulin G antibody responses to different protein fragments of Plasmodium vivax Reticulocyte binding protein 2b Bourke, Caitlin Takashima, Eizo Chan, Li-Jin Dietrich, Melanie H. Mazhari, Ramin White, Michael Sattabongkot, Jetsumon Tham, Wai-Hong Tsuboi, Takafumi Mueller, Ivo Longley, Rhea Malar J Research BACKGROUND: Plasmodium vivax is emerging as the dominant and prevalent species causing malaria in near-elimination settings outside of Africa. Hypnozoites, the dormant liver stage parasite of P. vivax, are undetectable to any currently available diagnostic test, yet are a major reservoir for transmission. Advances have been made to harness the naturally acquired immune response to identify recent exposure to P. vivax blood-stage parasites and, therefore, infer the presence of hypnozoites. This in-development diagnostic is currently able to detect infections within the last 9-months with 80% sensitivity and 80% specificity. Further work is required to optimize protein expression and protein constructs used for antibody detection. METHODS: The antibody response against the top performing predictor of recent infection, P. vivax reticulocyte binding protein 2b (PvRBP2b), was tested against multiple fragments of different sizes and from different expression systems. The IgG induced against the recombinant PvRBP2b fragments in P. vivax infected individuals was measured at the time of infection and in a year-long observational cohort; both conducted in Thailand. RESULTS: The antibody responses to some but not all different sized fragments of PvRBP2b protein are highly correlated with each other, significantly higher 1-week post-P. vivax infection, and show potential for use as predictors of recent P. vivax infection. CONCLUSIONS: To achieve P. vivax elimination goals, novel diagnostics are required to aid in detection of hidden parasite reservoirs. PvRBP2b was previously shown to be the top candidate for single-antigen classification of recent P. vivax exposure and here, it is concluded that several alternative recombinant PvRBP2b fragments can achieve equal sensitivity and specificity at predicting recent P. vivax exposure. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04085-x. BioMed Central 2022-03-04 /pmc/articles/PMC8896302/ /pubmed/35246142 http://dx.doi.org/10.1186/s12936-022-04085-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Bourke, Caitlin
Takashima, Eizo
Chan, Li-Jin
Dietrich, Melanie H.
Mazhari, Ramin
White, Michael
Sattabongkot, Jetsumon
Tham, Wai-Hong
Tsuboi, Takafumi
Mueller, Ivo
Longley, Rhea
Comparison of total immunoglobulin G antibody responses to different protein fragments of Plasmodium vivax Reticulocyte binding protein 2b
title Comparison of total immunoglobulin G antibody responses to different protein fragments of Plasmodium vivax Reticulocyte binding protein 2b
title_full Comparison of total immunoglobulin G antibody responses to different protein fragments of Plasmodium vivax Reticulocyte binding protein 2b
title_fullStr Comparison of total immunoglobulin G antibody responses to different protein fragments of Plasmodium vivax Reticulocyte binding protein 2b
title_full_unstemmed Comparison of total immunoglobulin G antibody responses to different protein fragments of Plasmodium vivax Reticulocyte binding protein 2b
title_short Comparison of total immunoglobulin G antibody responses to different protein fragments of Plasmodium vivax Reticulocyte binding protein 2b
title_sort comparison of total immunoglobulin g antibody responses to different protein fragments of plasmodium vivax reticulocyte binding protein 2b
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896302/
https://www.ncbi.nlm.nih.gov/pubmed/35246142
http://dx.doi.org/10.1186/s12936-022-04085-x
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