Development of a specific MPXV antigen detection immunodiagnostic assay
Human monkeypox (mpox) has recently become a global public health emergency; however, assays that detect mpox infection are not widely available, largely due to cross-reactivity within the Orthopoxvirus genus. Immunoassay development was largely confined to researchers who focus on biothreats and en...
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Published in: | Frontiers in microbiology Vol. 14; p. 1243523 |
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Main Authors: | , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Frontiers Media S.A
07-09-2023
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Subjects: | |
Online Access: | Get full text |
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Summary: | Human monkeypox (mpox) has recently become a global public health emergency; however, assays that detect mpox infection are not widely available, largely due to cross-reactivity within the
Orthopoxvirus
genus. Immunoassay development was largely confined to researchers who focus on biothreats and endemic areas (Central and West Africa) until the 2022 outbreak. As was noted in the COVID-19 pandemic, antigen detection assays, integrated with molecular assays, are necessary to help curb the spread of disease. Antigen-detecting immunoassays offer the advantage of providing results ranging from within min to h and in lateral flow formats; they can be deployed for point-of-care, home, or field use. This study reports the development of an mpox-specific antigen detection immunoassay developed on a multiplexed, magnetic-bead-based platform utilizing reagents from all research sectors (commercial, academic, and governmental). Two semi-quantitative assays were developed in parallel and standardized with infectious mpox virus (MPXV) cell culture fluid and MPXV-positive non-human primate (NHP) sera samples. These assays could detect viral antigens in serum, were highly specific toward MPXV as compared to other infectious orthopoxviruses (vaccinia virus, cowpox virus, and camelpox virus), and exhibited a correlation with quantitative PCR results from an NHP study. Access to a toolbox of assays for mpox detection will be key for identifying cases and ensuring proper treatment, as MPXV is currently a global traveler. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Stuart Dowall, UK Health Security Agency (UKHSA), United Kingdom; Sreelekshmy Mohandas, Indian Council of Medical Research (ICMR), India Keersten M. Ricks orcid.org/0000-0002-2854-9308 ORCID: Ian Davis orcid.org/0000-0002-1566-4972 Christopher P. Stefan orcid.org/0000-0003-4891-447X Eric M. Mucker orcid.org/0000-0002-4656-5379 Jay W. Hooper orcid.org/0000-0002-4475-0415 Edited by: E. Diane Williamson, Defence Science and Technology Laboratory, United Kingdom |
ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2023.1243523 |