Enzyme-Linked Immunosorbent Assay for Detection of Filovirus Species-Specific Antibodies

Author:

Nakayama Eri1234,Yokoyama Ayaka1234,Miyamoto Hiroko1234,Igarashi Manabu1234,Kishida Noriko1234,Matsuno Keita1234,Marzi Andrea1234,Feldmann Heinz1234,Ito Kimihito1234,Saijo Masayuki1234,Takada Ayato1234

Affiliation:

1. Department of Global Epidemiology, Hokkaido University Research Center for Zoonosis Control, Sapporo, Hokkaido, Japan

2. Laboratory of Influenza Virus Surveillance, Center for Influenza Virus Research, National Institute of Infectious Diseases, Tokyo, Japan

3. Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rocky Mountain Laboratories, Hamilton, Montana

4. Department of Virology 1, National Institute of Infectious Diseases, Tokyo, Japan

Abstract

ABSTRACT Several enzyme-linked immunosorbent assays (ELISAs) for the detection of filovirus-specific antibodies have been developed. However, diagnostic methods to distinguish antibodies specific to the respective species of filoviruses, which provide the basis for serological classification, are not readily available. We established an ELISA using His-tagged secreted forms of the transmembrane glycoproteins (GPs) of five different Ebola virus (EBOV) species and one Marburg virus (MARV) strain as antigens for the detection of filovirus species-specific antibodies. The GP-based ELISA was evaluated by testing antisera collected from mice immunized with virus-like particles as well as from humans and nonhuman primates infected with EBOV or MARV. In our ELISA, little cross-reactivity of IgG antibodies was observed in most of the mouse antisera. Although sera and plasma from some patients and monkeys showed notable cross-reactivity with the GPs from multiple filovirus species, the highest reactions of IgG were uniformly detected against the GP antigen homologous to the virus species that infected individuals. We further confirmed that MARV-specific IgM antibodies were specifically detected in specimens collected from patients during the acute phase of infection. These results demonstrate the usefulness of our ELISA for diagnostics as well as ecological and serosurvey studies.

Publisher

American Society for Microbiology

Subject

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

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