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DOI 10.1021/acsinfecdis.3c00423

Медицинская библиотека · ACS infectious diseases · 2023

A Flexible, Quantitative Plasmonic-Fluor Lateral Flow Assay for the Rapid Detection of Orthoebolavirus zairense and Orthoebolavirus sudanense.

Qavi Abraham J, Jiang Qisheng, Aman M Javad, Vu Hong, Zetlin Larry, Dye John M, Froude Jeffrey W, Leung Daisy W, Holtsberg Frederick, Crick Scott L, Amarasinghe Gaya K

СтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

Filoviruses comprise a family of single-stranded, negative-sense RNA viruses with a significant impact on human health. Given the risk for disease outbreaks, as highlighted by the recent outbreaks across Africa, there is an unmet need for flexible diagnostic technologies that can be deployed in resource-limited settings. Herein, we highlight the use of plasmonic-fluor lateral flow assays (PF-LFA) for the rapid, quantitative detection of an Ebolavirus-secreted glycoprotein, a marker for infection. Plasmonic fluors are a class of ultrabright reporter molecules that combine engineered nanorods with conventional fluorophores, resulting in improved analytical sensitivity. We have developed a PF-LFA for Orthoebolavirus zairense (EBOV) and Orthoebolavirus sudanense (SUDV) that provides estimated limits of detection as low as 0.446 and 0.641 ng/mL, respectively. Furthermore, our assay highlights a high degree of specificity between the two viral species while also maintaining a turnaround time as short as 30 min. To highlight the utility of our PF-LFA, we demonstrate the detection of EBOV infection in non-human primates. Our PF-LFA represents an enormous step forward in the development of a robust, field-deployable assay for filoviruses.

Для цитирования: Qavi Abraham J, Jiang Qisheng, Aman M Javad, Vu Hong, Zetlin Larry, Dye John M, Froude Jeffrey W, Leung Daisy W, Holtsberg Frederick, Crick Scott L, Amarasinghe Gaya K. A Flexible, Quantitative Plasmonic-Fluor Lateral Flow Assay for the Rapid Detection of Orthoebolavirus zairense and Orthoebolavirus sudanense.. ACS infectious diseases. 2023. DOI: 10.1021/acsinfecdis.3c00423.

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