商用消毒剂Virkon®S和Microchem Plus对脊髓灰质炎病毒的功效

Q1 Social Sciences
Leesa Bruggink, David Bagnara, Yi Nong, Matthew Kaye, Linda Hobday, Jade McKenzie, Ann Cornish, Bruce Thorley, Chuan Kok Lim
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引用次数: 0

摘要

世卫组织遏制脊髓灰质炎病毒全球行动计划第4版(GAPIV)描述了在脊髓灰质炎病毒基础设施(pef)中遏制脊髓灰质炎病毒材料的必要条件。通过成功地通过全球根除脊髓灰质炎认证委员会的认证程序,符合《全球根除脊髓灰质炎疫苗计划》的要求,才能获得PEF地位。GAPIV指南涵盖了许多主题,包括废物管理、去污、消毒和灭菌。GAPIV的这一要素要求pef用支持数据证明净化方法的内部验证。方法本研究中用于脊髓灰质炎病毒去污染化学产品验证的方法基于欧洲标准EN14476中概述的流程,并由世卫组织GAPIV指南推荐。在这项研究中,使用终点稀释法评估了消毒剂5% Microchem Plus和1% Virkon®S在有和没有高有机负荷的溶液中对高滴度脊髓灰质炎病毒的功效。以脊髓灰质炎病毒Sabin 1株为对照病毒,0.1 ml中CCID50滴度为8.33 log10(50%细胞培养感染剂量)。结果Microchem Plus处理后脊髓灰质炎病毒滴度为5.5 (CCID50滴度降低2.8),仅部分失活。相比之下,在具有和不具有高有机负荷的溶液中,脊髓灰质炎病毒在经过Virkon®S处理后,CCID50滴度降低了4 log10(分别降低≥6.8和≥5.8)。Virkon®S处理结果在终点稀释试验的检测极限,表明完全失活,或接近完全失活,可以用该试验证明。病毒培养结果通过检测肠道病毒RNA的分子试验得到证实。结论microchem Plus仅能部分灭活脊髓灰质炎病毒,不能作为唯一的去污剂。相比之下,Virkon®S在有和没有高有机负荷的溶液中对高滴度的脊髓灰质炎病毒都表现良好,两者的滴度都降低了4 log10,使Virkon®S成为脊髓灰质炎病毒的合适消毒剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of commercial disinfectants Virkon®S and Microchem Plus against poliovirus

Introduction

The WHO Global Action Plan for Poliovirus Containment, 4th edition (GAPIV) describes the necessary conditions for the containment of poliovirus material in poliovirus-essential facilities (PEFs). PEF status is achieved by successfully undergoing the process of certification by the Global Commission for the Certification of the Eradication of Poliomyelitis in compliance with GAPIV requirements. The GAPIV guidelines cover many topics, including waste management, decontamination, disinfection and sterilization. This element of GAPIV requires PEFs to demonstrate in-house validation of decontamination methods with supporting data.

Methods

The method used for validation of chemical products for poliovirus decontamination in this study was based on processes outlined in European Standard EN14476, as recommended by the WHO GAPIV guidelines. In this study, the disinfectants 5 % Microchem Plus and 1 % Virkon®S were evaluated for efficacy against high titre poliovirus in solutions with and without high organic load using an endpoint dilution assay. A poliovirus Sabin 1 strain was used as the reference virus with the titre 8.33 log10 CCID50 (50 % cell culture infectious dose) in 0.1 ml.

Results

The poliovirus titre after Microchem Plus treatment was calculated as 5.5 (representing a 2.8 CCID50 titre reduction), indicating only partial inactivation. In contrast, poliovirus in solutions with and without high organic load achieved >4 log10 CCID50 titre reduction (≥6.8 and ≥5.8 reduction respectively), after Virkon®S treatment. The Virkon®S treatment results were at the limit of detection of the endpoint dilution assay, indicating complete inactivation, or as near complete that can be demonstrated with the assay. The virus culture results were confirmed by a molecular assay for the detection of enterovirus RNA.

Conclusion

Microchem Plus only partially inactivated poliovirus and cannot be relied upon as the sole decontaminant. In contrast, Virkon®S performed well for both high titre poliovirus in solutions with and without high organic load, achieving >4 log10 titre reduction for both, making Virkon®S a suitable disinfectant for poliovirus.
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来源期刊
Journal of Biosafety and Biosecurity
Journal of Biosafety and Biosecurity Social Sciences-Linguistics and Language
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