| Literature DB >> 33370333 |
Pyo Yun Cho1,2, Ji-Yun Lee1, Tae Im Kim1,2, Jin-Ho Song3, Sung-Jong Hong1, Won Gi Yoo1, Takafumi Tsuboi4, Kwon-Soo Ha5, Jae-Wan Jung5, Satoru Takeo6, Eun-Taek Han7, Banchob Sripa8, Sung-Tae Hong9, Jong-Yil Chai9,10, Ho-Woo Nam11, Jhang Ho Pak12, Tong-Soo Kim13.
Abstract
Clonorchiasis caused by Clonorchis sinensis is endemic in East Asia; approximately 15 million people have been infected thus far. To diagnose the infection, serodiagnostic tests with excellent functionality should be performed. First, 607 expressed sequence tags encoding polypeptides with a secretory signal were expressed into recombinant proteins using an in vitro translation system. By protein array-based screening using C. sinensis-infected sera, 18 antigen candidate proteins were selected and assayed for cross-reactivity against Opisthorchis viverrini-infected sera. Of the six antigenic proteins selected, four were synthesized on large scale in vitro and evaluated for antigenicity against the flukes-infected human sera using ELISA. CsAg17 antigen showed the highest sensitivity (77.1%) and specificity (71.2%). The sensitivity and specificity of the bacterially produced CsAg17-28GST fusion antigen was similar to those of CsAg17 antigen. CsAg17 antigen can be used to develop point-of-care serodiagnostic tests for clonorchiasis.Entities:
Mesh:
Substances:
Year: 2020 PMID: 33370333 PMCID: PMC7793300 DOI: 10.1371/journal.pntd.0008998
Source DB: PubMed Journal: PLoS Negl Trop Dis ISSN: 1935-2727