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Discovery of Schistosoma mekongi circulating proteins and antigens in infected mouse sera.
Uthailak, Naphatsamon; Adisakwattana, Poom; Thiangtrongjit, Tipparat; Limpanont, Yanin; Chusongsang, Phiraphol; Chusongsang, Yupa; Tanasarnprasert, Kanthi; Reamtong, Onrapak.
Affiliation
  • Uthailak N; Department of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Adisakwattana P; Department of Helminthology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Thiangtrongjit T; Department of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Limpanont Y; Department of Social and Environmental Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Chusongsang P; Department of Social and Environmental Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Chusongsang Y; Department of Social and Environmental Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Tanasarnprasert K; Department of Social and Environmental Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Reamtong O; Department of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
PLoS One ; 17(10): e0275992, 2022.
Article in En | MEDLINE | ID: mdl-36227939
ABSTRACT
Schistosomiasis is a neglected tropical disease caused by an infection of the parasitic flatworms schistosomes. Schistosoma mekongi is a restricted Schistosoma species found near the Mekong River, mainly in southern Laos and northern Cambodia. Because there is no vaccine or effective early diagnosis available for S. mekongi, additional biomarkers are required. In this study, serum biomarkers associated with S. mekongi-infected mice were identified at 14-, 28-, 42-, and 56-days post-infection. Circulating proteins and antigens of S. mekongi in mouse sera were analyzed using mass spectrometry-based proteomics. Serine protease inhibitors and macrophage erythroblast attacher were down-regulated in mouse sera at all infection timepoints. In addition, 54 circulating proteins and 55 antigens of S. mekongi were identified. Notable circulating proteins included kyphoscoliosis peptidase and putative tuberin, and antigens were detected at all four infection timepoints, particularly in the early stages (12 days). The putative tuberin sequence of S. mekongi was highly similar to homologs found in other members of the genus Schistosoma and less similar to human and murine sequences. Our study provided the identity of promising diagnostic biomarkers that could be applicable in early schistosomiasis diagnosis and vaccine development.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Schistosoma / Schistosomiasis Type of study: Screening_studies Limits: Animals / Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2022 Document type: Article Affiliation country: Tailandia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Schistosoma / Schistosomiasis Type of study: Screening_studies Limits: Animals / Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2022 Document type: Article Affiliation country: Tailandia