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Comparison of Zika virus inactivation methods for reagent production and disinfection methods

Supporting Files Public Domain
File Language:
English


Details

  • Alternative Title:
    J Virol Methods
  • Personal Author:
  • Description:
    Zika virus (ZIKV) infection remains a public health concern necessitating demand for long-term virus production for diagnostic assays and R&D activities. Inactivated virus constitutes an important component of the Trioplex rRT-PCR assay and serological IgM assay (MAC-ELISA). The aim of our study is to establish standard methods of ZIKV inactivation while maintaining antigenicity and RNA integrity. We tested viral supernatants by four different inactivation methods: 1. Heat inactivation at 56 °C and 60 °C; 2. Gamma-Irradiation; 3. Chemical inactivation by Beta-propiolactone (BPL) and 4. Fast-acting commercial disinfecting agents. Effectivity was measured by cytopathic effect (CPE) and plaque assay. RNA stability and antigenicity were measured by RT-PCR and MAC-ELISA, respectively. Results: Heat inactivation: Low titer samples, incubated at 56 °C for 2 h, showed neither CPE or plaques compared to high titer supernatants that required 2.5 h. Inactivation occurred at 60 °C for 60 min with all virus titers. Gamma irradiation: Samples irradiated at ≥3 Mrad for low virus concentrations and ≥5Mrad for high virus titer completely inactivated virus. Chemical Inactivation: Neither CPE nor plaques were observed with ≥0.045 % BPL inactivation of ZIKV. Disinfectant: Treatment of viral supernatants with Micro-Chem Plus™, inactivated virus in 2 min, whereas, Ethanol (70 %) and STERIS Coverage® Spray TB inactivated the virus in 5 min.
  • Source:
    J Virol Methods. 287:114004
  • Document Type:
  • Volume:
    287
  • Collection(s):
  • Main Document Checksum:
    urn:sha-512:296ff57eba185be7ade89e300ad7d93cb8264397b7c417005a9a82ede63c6e45cdda410d3b1d471df34371990bf607f9a67f6a8a237478071a064fdde419a933
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    Filetype[PDF - 597.08 KB ]
File Language:
English
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