Journal of Microbiology and Biotechnology

  • 제30권11호
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  • Pages.1760-1768
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  • 2020
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  • 1017-7825(pISSN)
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  • 1738-8872(eISSN)
한국미생물·생명공학회 (The Korean Society for Microbiology and Biotechnology)
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Generation and Characterization of Monoclonal Antibodies to the Ogawa Lipopolysaccharide of Vibrio cholerae O1 from Phage-Displayed Human Synthetic Fab Library

  • Kim, Dain (Department of Systems Immunology, College of Biomedical Science, Kangwon National University) ;
  • Hong, Jisu (Department of Systems Immunology, College of Biomedical Science, Kangwon National University) ;
  • Choi, Yoonjoo (Medical Research Center, Chonnam National University Medical School) ;
  • Han, Jemin (Eubiologics Co., Ltd.) ;
  • Kim, Sangkyu (Department of Systems Immunology, College of Biomedical Science, Kangwon National University) ;
  • Jo, Gyunghee (Department of Systems Immunology, College of Biomedical Science, Kangwon National University) ;
  • Yoon, Jun-Yeol (Department of Systems Immunology, College of Biomedical Science, Kangwon National University) ;
  • Chae, Heesu (Department of Systems Immunology, College of Biomedical Science, Kangwon National University) ;
  • Yoon, Hyeseon (Eubiologics Co., Ltd.) ;
  • Lee, Chankyu (Eubiologics Co., Ltd.) ;
  • Hong, Hyo Jeong (Department of Systems Immunology, College of Biomedical Science, Kangwon National University)
  • 투고 : 2020.05.29
  • 심사 : 2020.08.22
  • 발행 : 2020.11.28
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초록

Vibrio cholerae, cause of the life-threatening diarrheal disease cholera, can be divided into different serogroups based on the structure of its lipopolysaccharide (LPS), which consists of lipid-A, core-polysaccharide and O-antigen polysaccharide (O-PS). The O1 serogroup, the predominant cause of cholera, includes two major serotypes, Inaba and Ogawa. These serotypes are differentiated by the presence of a single 2-O-methyl group in the upstream terminal perosamine of the Ogawa O-PS, which is absent in the Inaba O-PS. To ensure the consistent quality and efficacy of the current cholera vaccines, accurate measurement and characterization of each of these two serotypes is highly important. In this study, we efficiently screened a phage-displayed human synthetic Fab library by bio-panning against Ogawa LPS and finally selected three unique mAbs (D9, E11, and F7) that specifically react with Ogawa LPS. The mAbs bound to Vibrio cholerae vaccine in a dose-dependent fashion. Sequence and structure analyses of antibody paratopes suggest that IgG D9 might have the same fine specificity as that of the murine mAbs, which were shown to bind to the upstream terminal perosamine of Ogawa O-PS, whereas IgGs F7 and E11 showed some different characteristics in the paratopes. To our knowledge, this study is the first to demonstrate the generation of Ogawa-specific mAbs using phage display technology. The mAbs will be useful for identification and quantification of Ogawa LPS in multivalent V. cholerae vaccines.

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참고문헌

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