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Effectiveness of Liquid Soap and Hand Sanitizer against Norwalk Virus on Contaminated Hands

机译:洗手液和洗手液对受污染的手上的诺沃克病毒的功效

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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 ≥160 ppm effectively eliminated RT-qPCR detection signal, while ethanol, regardless of concentration, was relatively ineffective, giving at most a 0.5 log10 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 log10 reduction) and water rinse only (0.58 to 1.58 log10 reduction). The alcohol-based hand sanitizer was relatively ineffective, reducing the genomic copies of NV cDNA by only 0.14 to 0.34 log10 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.
机译:消毒是中断人类诺如病毒(HuNoV)传播的必要措施,但是由于缺乏针对这些病毒的可行的细胞培养系统,因此难以评估消毒剂的功效。这项研究的目的是筛选次氯酸钠和乙醇对诺沃克病毒(NV)的功效,并扩大研究范围,以评估抗菌液皂和酒精类洗手液对人类手指垫上的NV灭活的功效。样品通过实时逆转录定量PCR(RT-qPCR)进行测试,无论是否经过RNA酶处理。在悬浮液分析中,浓度≥160ppm的次氯酸钠有效消除了RT-qPCR检测信号,而乙醇(无论浓度如何)相对无效,NV的基因组拷贝最多减少了0.5 log 10 cDNA。使用美国材料试验学会(ASTM)标准的指垫方法及其改进方法(通过摩擦),我们观察到了用抗菌液皂液处理后NV cDNA基因组拷贝的最大减少(0.67至1.20 log 10 减少)和仅用水冲洗(减少0.58至1.58 log 10 )。酒精基洗手液相对无效,与基线相比,NV cDNA的基因组拷贝仅减少了0.14至0.34 log 10 。尽管与未使用RNase的前者相比,用RNase预处理的指垫洗脱液中NV cDNA的基因组拷贝浓度始终较低,但这些差异在统计学上并不显着。尽管有希望使用基于酒精的消毒剂来控制病原体传播,但它们对HuNoV可能相对无效,从而增加了针对这一重要病毒组开发和评估新产品的需求。

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