Shimasaki Noriko, Okaue Akira, Kikuno Ritsuko, Shinohara Katsuaki
National Institute of Infectious Diseases.
Kitasato Research Center for Environmental Science.
Biocontrol Sci. 2018;23(2):61-69. doi: 10.4265/bio.23.61.
Exact evaluation of the performance of surgical masks and biohazard protective clothing materials against pathogens is important because it can provide helpful information that healthcare workers can use to select suitable materials to reduce infection risk. Currently, to evaluate the protective performance of nonwoven fabrics used in surgical masks against viral aerosols, a non-standardized test method using phi-X174 phage aerosols is widely performed because actual respiratory viruses pose an infection risk during testing and the phage is a safe virus to humans. This method of using a phage is simply modified from a standard method for evaluation of filter performance against bacterial aerosols using Staphylococcus aureus, which is larger than virus particles. However, it is necessary to perform such evaluations based on the size of the actual pathogen particles. Thus, we developed a new method that can be performed safely using inactivated viral particles and can quantitate the influenza virus in aerosols by antigen-capture ELISA (Shimasaki et al., 2016a) . In this study, we used three different microbial aerosols of phi-X174 phage, influenza virus, and S. aureus and tested the filter efficiency by capturing microbial aerosols for two medical nonwoven fabrics. We compared the filter efficiency against each airborne microbe to analyze the dependency of filter efficiency on the microbial particle size. Our results showed that against the three types of spherical microbe particles, the filter efficiencies against influenza virus particles were the lowest and those against phi-X174 phages were the highest for both types of nonwoven fabrics. The experimental results mostly corresponded with theoretical calculations. We conclude that the filter efficiency test using the phi-X174 phage aerosol may overestimate the protective performance of nonwoven fabrics with filter structure compared to that against real pathogens such as the influenza virus.
准确评估手术口罩和生物危害防护服材料对病原体的防护性能非常重要,因为它可以提供有用信息,医护人员可据此选择合适的材料以降低感染风险。目前,为评估手术口罩中使用的无纺布对病毒气溶胶的防护性能,一种使用φ-X174噬菌体气溶胶的非标准化测试方法被广泛采用,这是因为实际的呼吸道病毒在测试过程中存在感染风险,而噬菌体对人类是一种安全的病毒。这种使用噬菌体的方法只是对使用比病毒颗粒更大的金黄色葡萄球菌评估过滤器对细菌气溶胶性能的标准方法进行了简单修改。然而,有必要根据实际病原体颗粒的大小进行此类评估。因此,我们开发了一种新方法,该方法可以使用灭活病毒颗粒安全地进行,并可通过抗原捕获酶联免疫吸附测定法定量气溶胶中的流感病毒(岛崎等人,2016年a)。在本研究中,我们使用了φ-X174噬菌体、流感病毒和金黄色葡萄球菌三种不同的微生物气溶胶,并对两种医用无纺布捕获微生物气溶胶的过滤效率进行了测试。我们比较了对每种空气传播微生物的过滤效率,以分析过滤效率对微生物颗粒大小的依赖性。我们的结果表明,对于两种无纺布,针对三种球形微生物颗粒,对流感病毒颗粒的过滤效率最低,对φ-X174噬菌体的过滤效率最高。实验结果大多与理论计算相符。我们得出结论,与针对流感病毒等实际病原体相比,使用φ-X174噬菌体气溶胶的过滤效率测试可能高估了具有过滤结构的无纺布的防护性能。