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Cloning and expression of a 16-kDa recombinant protein from Angiostrongylus cantonensis for use in immunoblot diagnosis of human angiostrongyliasis

dc.contributor.authorApichat Vittaen_US
dc.contributor.authorParon Dekumyoyen_US
dc.contributor.authorChalit Komalamisraen_US
dc.contributor.authorThareerat Kalambahetien_US
dc.contributor.authorTimothy P. Yoshinoen_US
dc.contributor.otherNaresuan Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of Wisconsin Madison, School of Veterinary Medicineen_US
dc.date.accessioned2018-12-11T01:55:44Z
dc.date.accessioned2019-03-14T08:03:56Z
dc.date.available2018-12-11T01:55:44Z
dc.date.available2019-03-14T08:03:56Z
dc.date.issued2016-11-01en_US
dc.description.abstract© 2016, Springer-Verlag Berlin Heidelberg. Angistrongylus cantonensis is a zoonotic nematode parasite and causative agent of human angiostrongyliasis, which clinically presents as eosinophilic meningitis or meningoencephalitis. Diagnosis of the disease is problematic since parasitologic findings are infrequent, and infection determinations must be based on the clinical symptoms and serological tests with limited specificities and sensitivities. The aim of the present study was to identify and generate a novel recombinant protein from A. cantonensis and evaluate its efficacy in the diagnosis of human angiostrongyliasis when incorporated into a Western blot serodiagnostic system. A cDNA protein expression library from adult A. cantonensis was constructed, followed by immunoscreening with serum from confirmed infected patients to identify and isolate immunoreactive clones. One clone, designated fAC40, possessed a partial sequence encoding a LisH protein domain with a predicted molecular weight of 16 kDa and containing four predicted antigenic peptides. By incorporating recombinant fAC40 in Western immunoblot tests using a serum panel consisting of confirmed and clinically diagnosed cases of human angiostrongyliasis and other helminthic infections, fAC40 exhibited a sensitivity and specificity of 91.8 and 100 %, respectively, and a positive and negative predictive value of 100 and 97.19 %, respectively, in the diagnosis of angiostrongyliasis. Importantly, it was not reactive with antibodies from serum of patients infected with Gnathostoma spinigerum and Cysticercus cellulosae, infections that clinically present neurological symptoms similar to angiostrongyliasis. These data demonstrate that the 16-kDa recombinant protein from A. cantonensis possesses high potential as a candidate antigen for a more sensitive and specific serodiagnosis of human angiostrongyliasis.en_US
dc.identifier.citationParasitology Research. Vol.115, No.11 (2016), 4115-4122en_US
dc.identifier.doi10.1007/s00436-016-5184-1en_US
dc.identifier.issn14321955en_US
dc.identifier.issn09320113en_US
dc.identifier.other2-s2.0-84978044110en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/42888
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84978044110&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleCloning and expression of a 16-kDa recombinant protein from Angiostrongylus cantonensis for use in immunoblot diagnosis of human angiostrongyliasisen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84978044110&origin=inwarden_US

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