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Development of an Immunochromatography Assay to Detect Marburg Virus and Ravn Virus
Katendi Changula1, Masahiro Kajihara2, Shino Muramatsu3
1Department of Paraclinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka 10101, Zambia.
Abstract:
The recent outbreaks of Marburg virus disease (MVD) in Guinea, Ghana, Equatorial Guinea, and Tanzania, none of which had reported previous outbreaks, imply increasing risks of spillover of the causative viruses, Marburg virus (MARV) and Ravn virus (RAVV), from their natural host animals. These outbreaks have emphasized the need for the development of rapid diagnostic tests for this disease. Using monoclonal antibodies specific to the viral nucleoprotein, we developed an immunochromatography (IC) assay for the rapid diagnosis of MVD. The IC assay was found to be capable of detecting approximately 102-4 50% tissue culture infectious dose (TCID50)/test of MARV and RAVV in the infected culture supernatants. We further confirmed that the IC assay could detect the MARV and RAVV antigens in the serum samples from experimentally infected nonhuman primates. These results indicate that the IC assay to detect MARV can be a useful tool for the rapid point-of-care diagnosis of MVD.
Insights
Recent Marburg virus disease (MVD) outbreaks highlight the need for rapid diagnostics. A new immunochromatography assay using monoclonal antibodies can quickly detect Marburg virus (MARV) and Ravn virus (RAVV) antigens.
Area of Science:
- Virology
- Immunology
- Diagnostic Development
Background:
- Recent Marburg virus disease (MVD) outbreaks in previously unaffected regions suggest increased spillover risk from natural hosts.
- The causative agents, Marburg virus (MARV) and Ravn virus (RAVV), pose significant public health threats.
- Effective control of MVD outbreaks necessitates the development of rapid and reliable diagnostic tools.
Purpose of the Study:
- To develop and evaluate an immunochromatography (IC) assay for the rapid diagnosis of Marburg virus disease (MVD).
- To assess the sensitivity and specificity of the developed IC assay for detecting MARV and RAVV.
Main Methods:
- Development of an immunochromatography (IC) assay utilizing monoclonal antibodies targeting the MARV/RAVV nucleoprotein.
- Testing the IC assay's ability to detect MARV and RAVV in infected culture supernatants.
- Validation of the IC assay using serum samples from experimentally infected nonhuman primates.
Main Results:
- The developed IC assay demonstrated the capability to detect approximately 10^2-4 TCID50/test of MARV and RAVV in culture supernatants.
- MARV and RAVV antigens were successfully detected in serum samples from nonhuman primates experimentally infected with the viruses.
- The assay showed promising sensitivity for detecting viral antigens.
Conclusions:
- The developed immunochromatography assay is a valuable tool for the rapid point-of-care diagnosis of Marburg virus disease (MVD).
- This rapid diagnostic capability can aid in timely clinical management and outbreak containment efforts.
- Further validation in clinical settings is warranted to confirm its utility in real-world MVD surveillance.
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