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Evaluation of Crude and Recombinant Antigens of Schistosoma japonicum for the Detection of Schistosoma mekongi Human Infection

Asian schistosomiasis caused by the blood fluke Schistosoma mekongi is endemic in northern Cambodia and Southern Lao People’s Democratic Republic. The disease is mainly diagnosed by stool microscopy. However, serodiagnosis such as enzyme-linked immunosorbent assay (ELISA) with soluble egg antigen (S...

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Autores principales: Angeles, Jose Ma. M., Wanlop, Atcharaphan, Dang-Trinh, Minh-Anh, Kirinoki, Masashi, Kawazu, Shin-ichiro, Yajima, Aya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9857461/
https://www.ncbi.nlm.nih.gov/pubmed/36672994
http://dx.doi.org/10.3390/diagnostics13020184
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author Angeles, Jose Ma. M.
Wanlop, Atcharaphan
Dang-Trinh, Minh-Anh
Kirinoki, Masashi
Kawazu, Shin-ichiro
Yajima, Aya
author_facet Angeles, Jose Ma. M.
Wanlop, Atcharaphan
Dang-Trinh, Minh-Anh
Kirinoki, Masashi
Kawazu, Shin-ichiro
Yajima, Aya
author_sort Angeles, Jose Ma. M.
collection PubMed
description Asian schistosomiasis caused by the blood fluke Schistosoma mekongi is endemic in northern Cambodia and Southern Lao People’s Democratic Republic. The disease is mainly diagnosed by stool microscopy. However, serodiagnosis such as enzyme-linked immunosorbent assay (ELISA) with soluble egg antigen (SEA), has been shown to have better sensitivity compared to the stool examination, especially in the settings with a low intensity of infection. To date, no recombinant antigen has been assessed using ELISA for the detection of S. mekongi infection, due to the lack of genome information for this schistosome species. Thus, the objective of this study is to evaluate several recombinant S. japonicum antigens that have been developed in our laboratory for the detection of S. mekongi infection. The crude antigen SjSEA and recombinant antigens Sj7TR, SjPCS, SjPRx-4, and SjChi-3 were evaluated in ELISA using serum samples positive for S. mekongi infection. The cross-reaction was checked using sera positive for Ophistorchis viverrini. ELISA results showed that S. japonicum SEA at low concentrations showed better diagnostic performance than the recombinant antigens tested using the archived serum samples from Cambodia. However, further optimization of the recombinant antigens should be conducted in future studies to improve their diagnostic performance for S. mekongi detection.
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spelling pubmed-98574612023-01-21 Evaluation of Crude and Recombinant Antigens of Schistosoma japonicum for the Detection of Schistosoma mekongi Human Infection Angeles, Jose Ma. M. Wanlop, Atcharaphan Dang-Trinh, Minh-Anh Kirinoki, Masashi Kawazu, Shin-ichiro Yajima, Aya Diagnostics (Basel) Communication Asian schistosomiasis caused by the blood fluke Schistosoma mekongi is endemic in northern Cambodia and Southern Lao People’s Democratic Republic. The disease is mainly diagnosed by stool microscopy. However, serodiagnosis such as enzyme-linked immunosorbent assay (ELISA) with soluble egg antigen (SEA), has been shown to have better sensitivity compared to the stool examination, especially in the settings with a low intensity of infection. To date, no recombinant antigen has been assessed using ELISA for the detection of S. mekongi infection, due to the lack of genome information for this schistosome species. Thus, the objective of this study is to evaluate several recombinant S. japonicum antigens that have been developed in our laboratory for the detection of S. mekongi infection. The crude antigen SjSEA and recombinant antigens Sj7TR, SjPCS, SjPRx-4, and SjChi-3 were evaluated in ELISA using serum samples positive for S. mekongi infection. The cross-reaction was checked using sera positive for Ophistorchis viverrini. ELISA results showed that S. japonicum SEA at low concentrations showed better diagnostic performance than the recombinant antigens tested using the archived serum samples from Cambodia. However, further optimization of the recombinant antigens should be conducted in future studies to improve their diagnostic performance for S. mekongi detection. MDPI 2023-01-04 /pmc/articles/PMC9857461/ /pubmed/36672994 http://dx.doi.org/10.3390/diagnostics13020184 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Angeles, Jose Ma. M.
Wanlop, Atcharaphan
Dang-Trinh, Minh-Anh
Kirinoki, Masashi
Kawazu, Shin-ichiro
Yajima, Aya
Evaluation of Crude and Recombinant Antigens of Schistosoma japonicum for the Detection of Schistosoma mekongi Human Infection
title Evaluation of Crude and Recombinant Antigens of Schistosoma japonicum for the Detection of Schistosoma mekongi Human Infection
title_full Evaluation of Crude and Recombinant Antigens of Schistosoma japonicum for the Detection of Schistosoma mekongi Human Infection
title_fullStr Evaluation of Crude and Recombinant Antigens of Schistosoma japonicum for the Detection of Schistosoma mekongi Human Infection
title_full_unstemmed Evaluation of Crude and Recombinant Antigens of Schistosoma japonicum for the Detection of Schistosoma mekongi Human Infection
title_short Evaluation of Crude and Recombinant Antigens of Schistosoma japonicum for the Detection of Schistosoma mekongi Human Infection
title_sort evaluation of crude and recombinant antigens of schistosoma japonicum for the detection of schistosoma mekongi human infection
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9857461/
https://www.ncbi.nlm.nih.gov/pubmed/36672994
http://dx.doi.org/10.3390/diagnostics13020184
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