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Development and Validation of Three Automated High-Throughput Molecular Tests to Detect Monkeypox Virus Infections.

Authors :
Anderson, Mark
Hodges, Austin
Luk, Ka-Cheung
Olivo, Ana
Forberg, Kenn
Meyer, Todd V
Strobel, Carolyn
Kim, Mark
Toolsie, Dan
Moore, Nicholas M
Goldstein, Yitzchak
Rodgers, Mary
Lucic, Danijela
Cloherty, Gavin
Source :
Journal of Infectious Diseases; 2024 Supplement, Vol. 229, pS137-S143, 7p
Publication Year :
2024

Abstract

Background The 2022 outbreak of the clade IIb monkeypox virus and subsequent global spread lead to an urgent need for the development of high-throughput, sensitive, and reproducible diagnostic tests. Methods We developed 3 assays to detect monkeypox virus, 2 (MPXV+ and MPXV) for m2000 RealTime and 1 (MPXV) for Alinity m platforms. Dual targets in E9L and B6R (MPXV+) and J2L and B7R (MPXV) increased mutation resistance. In silico prediction indicates MPXV+ cross-reactivity with orthopox viruses and specific monkeypox virus detection with MPXV. Results m2000 RealTime MPXV+ and MPXV assay sensitivity was determined to be 3.2 plaque-forming units/mL using a reference virus culture diluted into universal transport medium (UTM). Alinity m MPXV lower limit of detection was 200 copies/mL using monkeypox virus plasmids in pooled UTM matrix. m2000 RealTime MPXV+ and MPXV assays were validated with lesion swabs in UTM and 1:1 saliva to UTM mixtures. Commercially available and remnant clinical lesion specimens in UTM were tested with RealTime MPXV+, RealTime MPXV and Alinity m MPXV assays and demonstrated high agreement to known mpox (MPX)-positive specimens. Conclusions RealTime MPXV+, RealTime MPXV, and Alinity MPXV are high throughput and sensitive assays used for the detection of monkeypox virus. These assays maybe useful during MPX outbreaks. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221899
Volume :
229
Database :
Complementary Index
Journal :
Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
176300912
Full Text :
https://doi.org/10.1093/infdis/jiad406