Publication:
Expression and characterization of glutathione peroxidase of the liver fluke, Fasciola gigantica

dc.contributor.authorNarin Changklungmoaen_US
dc.contributor.authorKulathida Chaithirayanonen_US
dc.contributor.authorWerachon Cheukamuden_US
dc.contributor.authorAthit Chaiwichienen_US
dc.contributor.authorSupawadee Osotprasiten_US
dc.contributor.authorTepparit Samriten_US
dc.contributor.authorPrasert Sobhonen_US
dc.contributor.authorPornanan Kueakhaien_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherBurapha Universityen_US
dc.date.accessioned2019-08-23T10:13:41Z
dc.date.available2019-08-23T10:13:41Z
dc.date.issued2018-11-01en_US
dc.description.abstract© 2018, Springer-Verlag GmbH Germany, part of Springer Nature. Glutathione peroxidase (GPx) is a key member of the family of antioxidant enzymes in trematode parasites including Fasciola spp. Because of its abundance and central role as an anti-oxidant that helps to protect parasites from damage by free radicals released from the host immune cells, it has both diagnostic as well as vaccine potential against fasciolosis. In this study, we have cloned, characterized, and detected the expression of the GPx protein in Fasciola gigantica (Fg). FgGPx (582 bp) was cloned by polymerase chain reaction (PCR) from complementary DNA (cDNA) from an adult fluke. Its putative peptide has no signal sequence and is composed of 168 amino acids, with a molecular weight of 19.1 kDa, and conserved sequences at NVACKUG, FPCNQFGGQ, and WNF. Phylogenetic analysis showed that GPx is present from protozoa to mammals and FgGPx was closely related to Fasciola hepatica GPx. A recombinant FgGPx (rFgGPx) was expressed in Escherichia coli BL21 (DE3) and used for immunizing mice to obtain polyclonal antibodies (anti-rFgGPx) for immunoblotting and immunolocalization. In immunoblotting analysis, the FgGPx was expressed in all stages of F. gigantica (eggs, metacercariae, newly excysted juveniles (NEJ), 4-week-old juveniles, and adults). This mouse anti-rFgGPx reacted with the native FgGPx at a molecular weight of 19.1 kDa in adult whole body (WB) and tegumental antigens (TA) as detected by immunoblotting. The FgGPx protein was expressed at a high level in the tegument, vitelline glands, and eggs of the parasite. Anti-rFgGPx exhibited no cross-reactivity with the other parasite antigens, including Eurytrema pancreaticum, Cotylophoron cotylophorum, Fischoederius cobboldi, Gastrothylax crumenifer, Paramphistomum cervi, and Setaria labiato papillosa. The possibility of using rFgGPx for immunodiagnosis and/or as a vaccine for fasciolosis in animals of economic importance will be explored in the future.en_US
dc.identifier.citationParasitology Research. Vol.117, No.11 (2018), 3487-3495en_US
dc.identifier.doi10.1007/s00436-018-6046-9en_US
dc.identifier.issn14321955en_US
dc.identifier.issn09320113en_US
dc.identifier.other2-s2.0-85052638006en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/44653
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052638006&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.subjectVeterinaryen_US
dc.titleExpression and characterization of glutathione peroxidase of the liver fluke, Fasciola giganticaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052638006&origin=inwarden_US

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