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含奥拉宁手部消毒剂对诺如病毒的抗病毒活性。

Antiviral Activity of Olanexidine-Containing Hand Rub against Human Noroviruses.

机构信息

Department of Molecular Virology and Microbiology, Baylor College of Medicinegrid.39382.33 (BCM), Houston, Texas, USA.

Naruto Research Institute, Research and Development Center, Otsuka Pharmaceutical Factory, Inc., Naruto, Tokushima, Japan.

出版信息

mBio. 2022 Apr 26;13(2):e0284821. doi: 10.1128/mbio.02848-21. Epub 2022 Mar 17.

Abstract

Human norovirus (HuNoV) is the leading cause of epidemic and sporadic acute gastroenteritis worldwide. HuNoV transmission occurs predominantly by direct person-to-person contact, and its health burden is associated with poor hand hygiene and a lack of effective antiseptics and disinfectants. Specific therapies and methods to prevent and control HuNoV spread previously were difficult to evaluate because of the lack of a cell culture system to propagate infectious virus. This barrier has been overcome with the successful cultivation of HuNoV in nontransformed human intestinal enteroids (HIEs). Here, we report using the HIE cultivation system to evaluate the virucidal efficacy of an olanexidine gluconate-based hand rub (OLG-HR) and 70% ethanol (EtOH) against HuNoVs. OLG-HR exhibited fast-acting virucidal activity against a spectrum of HuNoVs including GII.4 Sydney[P31], GII.4 Den Haag[P4], GII.4 New Orleans[P4], GII.3[P21], GII.17[P13], and GI.1[P1] strains. Exposure of HuNoV to OLG-HR for 30 to 60 s resulted in complete loss of the ability of virus to bind to the cells and reduced binding to glycans in porcine gastric mucin. By contrast, the virucidal efficiency of EtOH on virus infectivity was strain specific. Dynamic light scattering (DLS) and electron microscopy of virus-like particles (VLPs) show that OLG-HR treatment causes partial disassembly and possibly conformational changes in VP1, interfering with histo-blood group antigen (HBGA) binding and infectivity, whereas EtOH treatment causes particle disassembly and clumping of the disassembled products, leading to loss of infectivity while retaining HBGA binding. The highly effective inactivation of HuNoV infectivity by OLG-HR suggests that this compound could reduce HuNoV transmission. Human noroviruses (HuNoVs) are highly contagious and cause nonbacterial acute gastroenteritis in all age groups worldwide. Since the introduction of rotavirus vaccines, HuNoVs have become the leading cause of diarrheal illness in children. These viruses are very stable in the environment and resistant to common disinfectants. This study evaluated the virucidal efficacy of a new disinfectant, olanexidine-based hand rub (OLG-HR), against HuNoV strains in an human intestinal stem cell-derived enteroid (HIE) cultivation system. Exposure of multiple HuNoV strains to OLG-HR for 30 to 60 s resulted in complete loss of infectivity and binding to HBGAs, possibly due to partial disassembly and conformational changes in the major virus capsid (VP1). By comparison, the virucidal efficiency of EtOH was strain specific, leading to loss of infectivity while retaining HBGA binding. These findings show the utility of the HIE cultivation system to test the effectiveness of disinfectants and report a highly effective product.

摘要

人类诺如病毒(HuNoV)是全球范围内导致流行和散发急性胃肠炎的主要原因。HuNoV 主要通过直接的人与人接触传播,其健康负担与手部卫生不良以及缺乏有效消毒剂和防腐剂有关。由于缺乏可繁殖感染性病毒的细胞培养系统,以前针对 HuNoV 传播的特定疗法和方法难以评估。通过成功在未转化的人肠类器官(HIE)中培养 HuNoV,这一障碍已经得到克服。在这里,我们报告了使用 HIE 培养系统来评估基于奥拉昔啶葡萄糖酸盐的手部消毒剂(OLG-HR)和 70%乙醇(EtOH)对 HuNoVs 的杀病毒功效。OLG-HR 对包括 GII.4 Sydney[P31]、GII.4 Den Haag[P4]、GII.4 New Orleans[P4]、GII.3[P21]、GII.17[P13]和 GI.1[P1]株在内的多种 HuNoVs 表现出快速的杀病毒活性。HuNoV 暴露于 OLG-HR 30 至 60 秒会导致病毒完全丧失与细胞结合的能力,并降低与猪胃粘蛋白中聚糖的结合。相比之下,EtOH 对病毒感染性的杀病毒效率具有菌株特异性。病毒样颗粒(VLPs)的动态光散射(DLS)和电子显微镜显示,OLG-HR 处理会导致 VP1 的部分解体和可能的构象变化,从而干扰组织血型抗原(HBGA)结合和感染力,而 EtOH 处理会导致颗粒解体和解体产物的聚集,从而在保留 HBGA 结合的同时丧失感染力。OLG-HR 对 HuNoV 感染性的高效灭活表明,该化合物可减少 HuNoV 的传播。人类诺如病毒(HuNoVs)具有高度传染性,可在全球所有年龄段引起非细菌性急性胃肠炎。自轮状病毒疫苗问世以来,HuNoVs 已成为儿童腹泻病的主要病因。这些病毒在环境中非常稳定,并且对普通消毒剂具有抗性。本研究评估了一种新消毒剂,基于奥拉昔啶的手部消毒剂(OLG-HR),在人类肠道干细胞衍生的类器官(HIE)培养系统中对 HuNoV 株的杀病毒功效。将多种 HuNoV 株暴露于 OLG-HR 30 至 60 秒会导致完全丧失感染性和与 HBGA 的结合,这可能是由于主要病毒衣壳(VP1)的部分解体和构象变化所致。相比之下,EtOH 的杀病毒效率具有菌株特异性,导致在保留 HBGA 结合的同时丧失感染力。这些发现显示了 HIE 培养系统在测试消毒剂有效性方面的实用性,并报告了一种非常有效的产品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a75/9040745/0bfc8008ccb5/mbio.02848-21-f001.jpg

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