Antiviral activity of povidone-iodine gargle and mouthwash solution against Enterovirus A71, Coxsackieviruses A16, A10 and A6.

W X Ang, S H Tan, K T Wong, D Perera, U R Kuppusamy, K C Ong
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Abstract

Hand, Foot and Mouth Disease (HFMD), a highly contagious viral disease common among infants and young children, is primarily caused by Enterovirus A71 (EV-A71) and Coxsackievirus A16 (CVA16). Nonetheless, emerging enteroviruses, such as CV-A10 and CV-A6, have also caused widespread outbreaks globally, in part due to the absence of effective antiviral therapies, and the high personto-person transmission rate. Person-to-person transmission is usually through fecal-oral or oral-oral routes, and sometimes via droplets. As the oral cavity is a primary site for early virus infection and replication, controlling oral viral shedding can mitigate the risk of transmission through this route. Povidone-iodine (PVP-I), a widely used antiseptic, has shown broad-spectrum antimicrobial properties but antiviral studies against HFMD-causing enteroviruses are limited, especially for CV-A10 and CVA6. Our study demonstrated that a 1% PVP-I solution (final concentration of 0.5%) exhibited virucidal activity against EV-A71, CV-A16, CV-A10, and CV-A6. All seven EV-A71 isolates and five CV-A16 isolates showed a significant virus titer reduction after a 1-minute incubation, while five CV-A10 isolates and two CV-A6 isolates required a 5-minute incubation to achieve this. The virucidal activity was confirmed through the EN14476:2013+A2:2019 virucidal quantitative suspension test, wherein all four viruses were completely inactivated after a 30-minute incubation with PVP-I at 37°C under both clean and dirty conditions. Western blot analysis suggested that PVP-I could affect the VP1 structural proteins of EV-A71. Our results suggest that PVP-I could serve as a potential virucidal agent to reduce the risk of person-to-person transmission of HFMD.

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聚维酮碘漱口水和漱口液对肠病毒 A71、柯萨奇病毒 A16、A10 和 A6 的抗病毒活性。
手足口病(HFMD)是一种常见于婴幼儿的高传染性病毒性疾病,主要由肠道病毒 A71(EV-A71)和柯萨奇病毒 A16(CVA16)引起。然而,新出现的肠道病毒,如 CV-A10 和 CV-A6,也在全球范围内引起了广泛的爆发,部分原因是缺乏有效的抗病毒疗法,以及人际传播率高。人与人之间的传播通常通过粪-口或口-口途径,有时也通过飞沫传播。由于口腔是早期病毒感染和复制的主要部位,控制口腔病毒脱落可降低通过这一途径传播的风险。聚维酮碘 (PVP-I) 是一种广泛使用的消毒剂,具有广谱抗菌特性,但针对手足口病致病肠道病毒的抗病毒研究却很有限,尤其是针对 CV-A10 和 CVA6 的研究。我们的研究表明,1% PVP-I 溶液(最终浓度为 0.5%)对 EV-A71、CV-A16、CV-A10 和 CV-A6 具有杀病毒活性。所有 7 个 EV-A71 分离物和 5 个 CV-A16 分离物在 1 分钟培养后病毒滴度都显著降低,而 5 个 CV-A10 分离物和 2 个 CV-A6 分离物则需要 5 分钟培养才能达到这一效果。杀病毒活性通过 EN14476:2013+A2:2019 杀病毒定量悬浮液测试得到了证实,在清洁和不清洁条件下,PVP-I 在 37°C 孵育 30 分钟后,所有四种病毒都被完全灭活。Western 印迹分析表明,PVP-I 可影响 EV-A71 的 VP1 结构蛋白。我们的研究结果表明,PVP-I 可以作为一种潜在的杀病毒剂,降低手足口病的人际传播风险。
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