Kirby Institute for Infection and Immunity in Society, UNSW Medicine, UNSW Sydney, Kensington, NSW 2052, Australia.
NSW Health Pathology, Prince of Wales Hospital, Randwick, NSW 2052, Australia.
Viruses. 2020 Oct 23;12(11):1208. doi: 10.3390/v12111208.
Critical to facilitating SARS-CoV-2 point-of-care (POC) testing is assurance that viruses present in specimens are inactivated onsite prior to processing. Here, we conducted experiments to determine the virucidal activity of commercially available Viral Transport Mediums (VTMs) to inactivate SARS-CoV-2. Independent testing methods for viral inactivation testing were applied, including a previously described World Health Organization (WHO) protocol, in addition to a buffer exchange method where the virus is physically separated from the VTM post exposure. The latter method enables sensitive detection of viral viability at higher viral titre when incubated with VTM. We demonstrate that VTM formulations, Primestore Molecular Transport Medium (MTM) and COPAN eNAT™ completely inactivate high-titre SARS-CoV-2 virus (>1 × 10 copies/mL) and are compatible with POC processing. Furthermore, full viral inactivation was rapidly achieved in as little as 2 min of VTM exposure. We conclude that adding certain VTM formulations as a first step post specimen collection will render SARS-CoV-2 non-infectious for transport, or for further in-field POC molecular testing using rapid turnaround GeneXpert platforms or equivalent.
确保在处理标本之前现场灭活存在于标本中的病毒,这对于促进 SARS-CoV-2 即时检测(POC)至关重要。在这里,我们进行了实验以确定市售病毒运输介质(VTM)对 SARS-CoV-2 的病毒灭活活性。应用了独立的病毒灭活测试方法,包括先前描述的世界卫生组织(WHO)方案,以及缓冲液交换方法,其中在暴露后将病毒从 VTM 中物理分离。后一种方法可在与 VTM 孵育时以更高的病毒滴度灵敏地检测病毒活力。我们证明,VTM 配方,即 Primestore 分子运输介质(MTM)和 COPAN eNAT™ 可完全灭活高滴度 SARS-CoV-2 病毒(>1×10 拷贝/mL),并且与 POC 处理兼容。此外,仅需 2 分钟的 VTM 暴露即可快速实现完全病毒灭活。我们得出结论,在标本采集后添加某些 VTM 配方作为第一步,将使 SARS-CoV-2 在运输过程中不具传染性,或者在现场使用快速周转的 GeneXpert 平台或等效平台进行进一步的即时 POCT 分子检测时不具传染性。