WebMay 10, 2024 · Hantaan virus (HTNV) and Puumala virus (PUUV) are rodent-borne hantaviruses that are the primary causes of hemorrhagic fever with renal syndrome (HFRS) in Europe and Asia. The development of well characterized animal models of HTNV and PUUV infection is critical for the evaluation and the potential licensure of HFRS … CDC uses an enzyme-linked immunosorbent assay (ELISA) to detect IgM antibodies to SNV and to diagnose acute infections with other hantaviruses. This assay is also available in some state health laboratories. An IgG test is used in conjunction with the IgM-capture test. See more At the time of the 1993 outbreak in the Four Corners area, cross-reactive antibodies to the previously known hantaviruses (e.g., Hantaan, Seoul, Puumala, and … See more Isolation of hantaviruses (see below) from human sources is difficult, and the viruses causing HPS seem to be no exception to this rule. To date, no isolates of SNV-like viruses have been recovered from humans, and … See more IHC testing of formalin-fixed tissues with specific monoclonal and polyclonal antibodies can be used to detect hantavirus antigens … See more
VIRAL PLAQUE ASSAY – Laboratory Exercises in Microbiology
WebMar 2, 2007 · Hantaan virus (HTNV), the prototype virus within the Hantavirus genus, ... For SFSV, concentrations were determined by a plaque assay as described earlier (6, 18). Briefly, virus was treated as described above with the exception that Vero E6 cells, after infection, were covered with an agar overlay (50% modified Eagle medium [2×] [Gibco], … WebFig. 1. Dose-response curve for Hantaan virus. Serial two-fold virus dilutions were assayed in triplicate cultures, and the number of plaques per well of each virus dilution was … body as html powershell
Is it necessary to perform the plaque purification in using Bac-to …
WebThe 76--118 strain of Hantaan virus was titrated in E6 (Vero) cells by the plaque method using agarose overlay medium. Visible plaques, formed 10 days post-infection, were … WebPseudovirus-based neutralization assays (PBNA) were developed by employing vesicular stomatitis virus (VSV) backbone incorporated with HTNV or SEOV glycoproteins (VSVΔG*-HTNVG or VSVΔG*-SEOVG). 56 and 51 single amino acid substitutions of glycoprotein (GP) in HTNV and SEOV were selected and introduced into the reference plasmid. WebAn enzyme-linked focus formation assay (FFA) for Hantaan virus titering that is twice as fast as traditional assays is established and the effects of favipiravir and another … body ashes into tree