Development of a Gaussia luciferase immunoprecipitation assay for detecting Schistosoma japonicum infection

Timely and accurate diagnosis of Schistosoma infection is important to adopt effective strategies for schistosomiasis control. Previously, we demonstrated that Schistosoma japonicum can secret extracellular vesicles and their cargos may serve as a novel type of biomarkers for diagnosing schistosomia...

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Veröffentlicht in:Experimental parasitology 2024-07, Vol.262, p.108776, Article 108776
Hauptverfasser: Wang, Xiaoxu, Giri, Bikash R., Cui, Zhoukai, Munkhjargal, Tserendorj, Wang, Chunren, Fontanilla, Ian Kendrich C., Cheng, Guofeng
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Sprache:eng
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Zusammenfassung:Timely and accurate diagnosis of Schistosoma infection is important to adopt effective strategies for schistosomiasis control. Previously, we demonstrated that Schistosoma japonicum can secret extracellular vesicles and their cargos may serve as a novel type of biomarkers for diagnosing schistosomiasis. Here, we developed a Gaussia luciferase immunoprecipitation assay combined with S. japonicum extracellular vesicle (SjEV) protein to evaluate its potential for diagnosing schistosomiasis. A saposin-like protein (SjSLP) identified from SjEVs was fused to the Gaussia luciferase as the diagnostic antigen. The developed method showed good capability for detecting S. japonicum infection in mice and human patients. We also observed that the method could detect Schistosoma infection in mice as early as 7 days of post-infection, which showed better sensitivity than that of indirect ELISA method. Overall, the developed method showed a good potential for detecting Schistosoma infection particularly for early stage, which may provide an alternative strategy for identify Schistosoma infection for disease control. [Display omitted] •A LIPS method using the saposin-like protein as the antigen was developed.•This method showed better sensitivity for diagnosing schistosomiasis than the indirect ELISA method.•The method showed a potential for detecting Schistosoma infection at early stage.
ISSN:0014-4894
1090-2449
1090-2449
DOI:10.1016/j.exppara.2024.108776