| Literature DB >> 27466385 |
Maiken Worsøe Rosenstierne1, Helen Karlberg2, Karoline Bragstad3, Gunnel Lindegren2, Malin Lundahl Stoltz2, Cristiano Salata4, Anne-Marte Bakken Kran5, Susanne Gjeruldsen Dudman3, Ali Mirazimi6, Anders Fomsgaard7.
Abstract
Rapid bedside inactivation of Ebola virus would be a solution for the safety of medical and technical staff, risk containment, sample transport, and high-throughput or rapid diagnostic testing during an outbreak. We show that the commercially available Magna Pure lysis/binding buffer used for nucleic acid extraction inactivates Ebola virus. A rapid bedside inactivation method for nucleic acid tests is obtained by simply adding Magna Pure lysis/binding buffer directly into vacuum blood collection EDTA tubes using a thin needle and syringe prior to sampling. The ready-to-use inactivation vacuum tubes are stable for more than 4 months, and Ebola virus RNA is preserved in the Magna Pure lysis/binding buffer for at least 5 weeks independent of the storage temperature. We also show that Ebola virus RNA can be manually extracted from Magna Pure lysis/binding buffer-inactivated samples using the QIAamp viral RNA minikit. We present an easy and convenient method for bedside inactivation using available blood collection vacuum tubes and reagents. We propose to use this simple method for fast, safe, and easy bedside inactivation of Ebola virus for safe transport and routine nucleic acid detection.Entities:
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Year: 2016 PMID: 27466385 PMCID: PMC5035422 DOI: 10.1128/JCM.00346-16
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948