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Title: Limited cross-reactivity of mouse monoclonal antibodies against Dengue virus capsid protein among four serotypes
Authors: Megumi Noda
Promsin Masrinoul
Chaweewan Punkum
Chonlatip Pipattanaboon
Pongrama Ramasoota
Chayanee Setthapramote
Tadahiro Sasaki
Mikiko Sasayama
Akifumi Yamashita
Takeshi Kurosu
Kazuyoshi Ikuta
Tamaki Okabayashi
Mahidol University
Tohoku University
Osaka University
Keywords: Medicine
Issue Date: 22-Nov-2012
Citation: Biologics: Targets and Therapy. Vol.6, (2012), 409-416
Abstract: Background: Dengue illness is one of the important mosquito-borne viral diseases in tropical and subtropical regions. Four serotypes of dengue virus (DENV-1, DENV-2, DENV-3, and DENV-4) are classified in the Flavivirus genus of the family Flaviviridae. We prepared monoclonal antibodies against DENV capsid protein from mice immunized with DENV-2 and determined the cross-reactivity with each serotype of DENV and Japanese encephalitis virus. Methods and results: To clarify the relationship between the cross-reactivity of monoclonal antibodies and the diversity of these viruses, we examined the situations of faviviruses by analyses of phylogenetic trees. Among a total of 60 prepared monoclonal antibodies specific for DENV, five monoclonal antibodies stained the nuclei of infected cells and were found to be specific to the capsid protein. Three were specific to DENV-2, while the other two were cross-reactive with DENV-2 and DENV-4. No monoclonal antibodies were cross-reactive with all four serotypes. Phylogenetic analysis of DENV amino acid sequences of the capsid protein revealed that DENV-2 and DENV-4 were clustered in the same branch, while DENV-1 and DENV-3 were clustered in the other branch. However, these classifications of the capsid protein were different from those of the envelope and nonstructural 1 proteins. Phylogenetic distances between the four serotypes of DENV were as different as those of other faviviruses, such as Japanese encephalitis virus and West Nile virus. Large variations in the DENV serotypes were comparable with the differences between species of favivirus. Furthermore, the diversity of favivirus capsid protein was much greater than that of envelope and nonstructural 1 proteins. Conclusion: In this study, we produced specific monoclonal antibodies that can be used to detect DENV-2 capsid protein, but not a cross-reactive one with all serotypes of DENV capsid protein. The high diversity of the DENV capsid protein sequence by phylogenetic analysis supported the low cross-reactivity of monoclonal antibodies against DENV capsid protein. © 2012 Noda et al, publisher and licensee Dove Medical Press Ltd.
ISSN: 11775491
Appears in Collections:Scopus 2011-2015

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