Accession Number : AD1009282


Title :   Validation of the Filovirus Plaque Assay for Use in Preclinical Studies


Descriptive Note : Journal Article


Corporate Author : USAMRIID Frederick United States


Personal Author(s) : Shurtleff, Amy C ; Bloomfield,Holly A ; Mort,Shannon ; Orr,Steven A ; Audet,Brian ; Whitaker,Thomas ; Richards,Michelle J ; Bavari,Sina


Full Text : http://www.dtic.mil/dtic/tr/fulltext/u2/1009282.pdf


Report Date : 02 Sep 2016


Pagination or Media Count : 24


Abstract : A plaque assay for quantitating filoviruses in virus stocks, prepared viral challenge inocula and samples from research animals has recently been fully characterized and standardized for use across multiple institutions performing BSL-4 studies. After standardization studies were completed, Good Laboratory Practices (GLP)-compliant plaque assay method validation studies to demonstrate suitability for reliable and reproducible measurement of Marburg Virus Angola (MARV) variant and Ebola virus Kikwit (EBOV) variant commenced at USAMRIID. Validation parameters tested included accuracy, precision, linearity, robustness, stability of the virus stocks and system suitability. The MARV and EBOV assays were confirmed to be accurate to 0.5 log10 PFU/mL. Repeatability precision, intermediate precision, and reproducibility precision were sufficient to return viral titers with a CV of 30 , deemed acceptable variation for a cell-based bioassay. Intraclass correlation statistical techniques for evaluation of the assays precision when the same plaques were quantitated by 2 analysts returned values passing acceptance criteria, indicating high agreement between analysts. The assay was shown to be accurate and specific when run on NHP serum and plasma samples diluted in plaque assay medium, with negligible matrix effects. Virus stocks demonstrated stability for freeze-thaw cycles typical of normal usage during assay retests. The results demonstrated that the EBOV and MARV plaque assays are accurate, precise and robust for filovirus titration in samples associated with the performance of GLP animal model studies.


Descriptors :   Viruses , zoonotic diseases , CLINICAL TRIALS , validation


Distribution Statement : APPROVED FOR PUBLIC RELEASE