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Serodiagnostic antigens of Clonorchis sinensis identified and evaluated by high-throughput proteogenomics.

Pyo Yun ChoJi-Yun LeeTae Im KimJin-Ho SongSung-Jong HongWon Gi YooTakafumi TsuboiKwon-Soo HaJae-Wan JungSatoru TakeoEun-Taek HanBanchob SripaSung-Tae HongJong-Yil ChaiHo-Woo NamJhang Ho PakTong-Soo Kim
Published in: PLoS neglected tropical diseases (2020)
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.
Keyphrases
  • high throughput
  • small molecule
  • high resolution
  • protein protein
  • high density
  • pluripotent stem cells