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液体皂和手部消毒剂对手部污染诺如病毒的效果。

Effectiveness of liquid soap and hand sanitizer against Norwalk virus on contaminated hands.

机构信息

Center for Global Safe Water, Hubert Department of Global Health, Rollins School of Public Health, Emory University, 1518 Clifton Road, Atlanta, GA 30322, USA.

出版信息

Appl Environ Microbiol. 2010 Jan;76(2):394-9. doi: 10.1128/AEM.01729-09. Epub 2009 Nov 20.

Abstract

Disinfection is an essential measure for interrupting human norovirus (HuNoV) transmission, but it is difficult to evaluate the efficacy of disinfectants due to the absence of a practicable cell culture system for these viruses. The purpose of this study was to screen sodium hypochlorite and ethanol for efficacy against Norwalk virus (NV) and expand the studies to evaluate the efficacy of antibacterial liquid soap and alcohol-based hand sanitizer for the inactivation of NV on human finger pads. Samples were tested by real-time reverse transcription-quantitative PCR (RT-qPCR) both with and without a prior RNase treatment. In suspension assay, sodium hypochlorite concentrations of >or=160 ppm effectively eliminated RT-qPCR detection signal, while ethanol, regardless of concentration, was relatively ineffective, giving at most a 0.5 log(10) reduction in genomic copies of NV cDNA. Using the American Society for Testing and Materials (ASTM) standard finger pad method and a modification thereof (with rubbing), we observed the greatest reduction in genomic copies of NV cDNA with the antibacterial liquid soap treatment (0.67 to 1.20 log(10) reduction) and water rinse only (0.58 to 1.58 log(10) reduction). The alcohol-based hand sanitizer was relatively ineffective, reducing the genomic copies of NV cDNA by only 0.14 to 0.34 log(10) compared to baseline. Although the concentrations of genomic copies of NV cDNA were consistently lower on finger pad eluates pretreated with RNase compared to those without prior RNase treatment, these differences were not statistically significant. Despite the promise of alcohol-based sanitizers for the control of pathogen transmission, they may be relatively ineffective against the HuNoV, reinforcing the need to develop and evaluate new products against this important group of viruses.

摘要

消毒是阻断人类诺如病毒(HuNoV)传播的重要措施,但由于缺乏可行的细胞培养系统来培养这些病毒,因此很难评估消毒剂的效果。本研究旨在筛选次氯酸钠和乙醇对诺如病毒(NV)的效果,并进一步评估抗菌皂液和酒精基洗手液对 NV 在人手指垫上失活的效果。在有和没有预先进行 RNase 处理的情况下,通过实时逆转录定量 PCR(RT-qPCR)对样本进行测试。在悬浮液测定中,浓度>或=160ppm 的次氯酸钠能有效消除 RT-qPCR 检测信号,而乙醇无论浓度如何,效果均相对较差,只能使 NV cDNA 的基因组拷贝数最多减少 0.5 个对数。使用美国材料试验协会(ASTM)标准手指垫方法及其改进版(带摩擦),我们观察到抗菌皂液处理(0.67 到 1.20 个对数减少)和仅水冲洗(0.58 到 1.58 个对数减少)可使 NV cDNA 的基因组拷贝数减少最多。相比之下,酒精基洗手液的效果相对较差,仅使 NV cDNA 的基因组拷贝数减少 0.14 到 0.34 个对数。尽管用 RNase 预处理手指垫洗脱液后,NV cDNA 的基因组拷贝数始终低于未经 RNase 预处理的洗脱液,但这些差异无统计学意义。尽管酒精基消毒剂在控制病原体传播方面有一定前景,但它们对 HuNoV 的效果可能相对较差,这也进一步强调了开发和评估针对这组重要病毒的新产品的必要性。

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