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Novel monoclonal antibodies broadly reactive to human recombinant sapovirus‐like particles
Authors:Noritoshi Kitamoto  Tomoichiro Oka  Kazuhiko Katayama  Tian‐Cheng Li  Naokazu Takeda  Yoji Kato  Tatsuya Miyoshi  Tomoyuki Tanaka
Institution:1. School of Human Science and Environment, University of Hyogo, Hyogo 670‐0092;2. Department of Virology II, National Institute of Infectious Diseases, Tokyo 208‐0011;3. Food Animal Health Research Program, Ohio Agricultural Research and Development Center, Department of Veterinary Preventive Medicine, Ohio State University, Wooster, 44691, OH, USA;4. Thailand‐Japan Research Collaboration Center on Emerging and Re‐emerging Infections, Nonthaburi 11000, Thailand;5. Sakai City Institute of Public Health, Osaka 590‐0953, Japan.
Abstract:Sapovirus (SaV), a member of the family Caliciviridae, is an important cause of acute epidemic gastroenteritis in humans. Human SaV is genetically and antigenically diverse and can be classified into four genogroups (GI, GII, GIV, and GV) and 16 genotypes (7 GI GI.1–7], 7 GII, GII.1–7], 1 GIV and 1 GV), based on capsid sequence similarities. Monoclonal antibodies (MAbs) are powerful tools for examining viruses and proteins. PAI myeloma cells were fused with spleen cells from mice immunized with a single type of recombinant human SaV virus‐like particles (VLPs) (GI.1, GI.5, GI.6, GII.3, GIV, or GV). Sixty‐five hybrid clones producing MAbs were obtained. Twenty‐four MAbs were characterized by ELISA, according to their cross‐reactivity to each VLP (GI.1, GI.5, GI.6, GII.2, GII.3, GII.4, GII.7, GIV, and GV). The MAbs were classified by this method into: (i) MAbs broadly cross‐reactive to all GI, GII, GIV and GV strains; (ii) those reactive in a genogroup‐specific; and (iii) those reactive in a genotype‐specific manner. Further analysis of three broadly cross‐reactive MAbs with a competitive ELISA demonstrated that at least two different common epitopes are located on the capsid protein of human SaVs in the four genogroups. The MAbs generated and characterized in this study will be useful tools for further study of the antigenic and structural topography of the human SaV virion and for developing new diagnostic assays for human SaV.
Keywords:cross‐reactivity  monoclonal antibody  sapovirus
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