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Antigen capture enzyme-linked immunosorbent assay for specific detection of reston Ebola virus nucleoprotein

  • Tetsuro Ikegami
  • , Masahiro Niikura
  • , Masayuki Saijo
  • , Mary E. Miranda
  • , Alan B. Calaor
  • , Marvin Hernandez
  • , Luz P. Acosta
  • , Daria L. Manalo
  • , Ichiro Kurane
  • , Yasuhiro Yoshikawa
  • , Shigeru Morikawa

Research output: Contribution to journalArticlepeer-review

Abstract

Antigen capture enzyme-linked immunosorbent assay (ELISA) is one of the most useful methods to detect Ebola virus rapidly. We previously developed an antigen capture ELISA using a monoclonal antibody (MAb), 3-3D, which reacted not only to the nucleoprotein (NP) of Zaire Ebola virus (EBO-Z) but also to the NPs of Sudan (EBO-S) and Reston Ebola (EBO-R) viruses. In this study, we developed antigen capture ELISAs using two novel MAbs, Res2-6C8 and Res2-1D8, specific to the NP of EBO-R. Res2-6C8 and Res2-1D8 recognized epitopes consisting of 4 and 8 amino acid residues, respectively, near the C-terminal region of the EBO-R NP. The antigen capture ELISAs using these two MAbs detected the EBO-R NP in the tissues from EBO-R-infected cynomolgus macaques. The antigen capture ELISAs using Res2-6C8 and Res2-1D8 are useful for the rapid detection of the NP in EBO-R-infected cynomolgus macaques.

Original languageEnglish (US)
Pages (from-to)552-557
Number of pages6
JournalClinical and Diagnostic Laboratory Immunology
Volume10
Issue number4
DOIs
StatePublished - Jul 2003
Externally publishedYes

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Clinical Biochemistry
  • Microbiology (medical)

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