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本文引用的文献

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Detection of Merkel cell polyomavirus on environmental surfaces.检测环境表面的 Merkel 细胞多瘤病毒。
J Med Virol. 2011 Aug;83(8):1435-9. doi: 10.1002/jmv.22110. Epub 2011 May 26.
2
Detection of adeno- and lentiviral (HIV1) contaminations on laboratory surfaces as a tool for the surveillance of biosafety standards.检测实验室表面的腺病毒和慢病毒(HIV1)污染,作为监测生物安全标准的工具。
J Appl Microbiol. 2011 Jul;111(1):70-82. doi: 10.1111/j.1365-2672.2011.05042.x. Epub 2011 May 20.
3
Environmental survey to assess viral contamination of air and surfaces in hospital settings.环境调查评估医院环境中空气和表面的病毒污染情况。
J Hosp Infect. 2011 Mar;77(3):242-7. doi: 10.1016/j.jhin.2010.10.010. Epub 2011 Jan 31.
4
Norovirus in the hospital setting: virus introduction and spread within the hospital environment.医院环境中的诺如病毒:病毒在医院环境中的引入和传播。
J Hosp Infect. 2011 Feb;77(2):106-12. doi: 10.1016/j.jhin.2010.09.035. Epub 2010 Dec 16.
5
A 2009 varicella outbreak in a Connecticut residential facility for adults with intellectual disability.2009 年康涅狄格州一家专为智障成年人设立的住宿机构发生的水痘暴发疫情。
J Infect Dis. 2010 Nov 15;202(10):1486-91. doi: 10.1086/656773. Epub 2010 Oct 7.
6
Virus shedding and environmental deposition of novel A (H1N1) pandemic influenza virus: interim findings.新型甲型(H1N1)流感病毒的病毒脱落和环境沉积:中期研究结果。
Health Technol Assess. 2010 Oct;14(46):237-354. doi: 10.3310/hta14460-04.
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Tracking environmental norovirus contamination in a pediatric primary immunodeficiency unit.追踪小儿原发性免疫缺陷病房中的环境诺如病毒污染情况。
J Clin Microbiol. 2010 Jul;48(7):2552-6. doi: 10.1128/JCM.00066-10. Epub 2010 May 5.
8
The growth of H. pertussis on media without blood.百日咳杆菌在无血液培养基上的生长
Br J Exp Pathol. 1947 Aug;28(4):295-307.
9
Food-borne norovirus-outbreak at a military base, Germany, 2009.2009 年德国某军事基地发生的食源性诺如病毒暴发。
BMC Infect Dis. 2010 Feb 17;10:30. doi: 10.1186/1471-2334-10-30.
10
Respiratory viral RNA on toys in pediatric office waiting rooms.儿科候诊室玩具上的呼吸道病毒 RNA。
Pediatr Infect Dis J. 2010 Feb;29(2):102-4. doi: 10.1097/inf.0b013e3181b6e482.

比较从污染物表面采集样本以回收病毒的方法。

Comparison of surface sampling methods for virus recovery from fomites.

机构信息

Department of Civil and Environmental Engineering, Environmental and Water Studies, Stanford University, Stanford, CA 94305-4020, USA.

出版信息

Appl Environ Microbiol. 2011 Oct;77(19):6918-25. doi: 10.1128/AEM.05709-11. Epub 2011 Aug 5.

DOI:10.1128/AEM.05709-11
PMID:21821742
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3187074/
Abstract

The role of fomites in infectious disease transmission relative to other exposure routes is difficult to discern due, in part, to the lack of information on the level and distribution of virus contamination on surfaces. Comparisons of studies intending to fill this gap are difficult because multiple different sampling methods are employed and authors rarely report their method's lower limit of detection. In the present study, we compare a subset of sampling methods identified from a literature review to demonstrate that sampling method significantly influences study outcomes. We then compare a subset of methods identified from the review to determine the most efficient methods for recovering virus from surfaces in a laboratory trial using MS2 bacteriophage as a model virus. Recoveries of infective MS2 and MS2 RNA are determined using both a plaque assay and quantitative reverse transcription-PCR, respectively. We conclude that the method that most effectively recovers virus from nonporous fomites uses polyester-tipped swabs prewetted in either one-quarter-strength Ringer's solution or saline solution. This method recovers a median fraction for infective MS2 of 0.40 and for MS2 RNA of 0.07. Use of the proposed method for virus recovery in future fomite sampling studies would provide opportunities to compare findings across multiple studies.

摘要

由于缺乏有关表面病毒污染程度和分布的信息,很难确定污染物在传染病传播中的作用相对于其他暴露途径的作用。由于采用了多种不同的采样方法,而且作者很少报告其方法的检测下限,因此,旨在填补这一空白的研究之间的比较很困难。在本研究中,我们比较了文献综述中确定的一组采样方法,以证明采样方法对研究结果有重大影响。然后,我们从综述中确定了一组方法,以确定使用 MS2 噬菌体作为模型病毒在实验室试验中从表面回收病毒的最有效方法。使用噬菌斑测定法和定量逆转录-PCR 分别测定感染性 MS2 和 MS2 RNA 的回收率。我们得出的结论是,从非多孔污染物中最有效地回收病毒的方法是使用预先润湿在 1/4 强度林格氏溶液或盐溶液中的聚酯拭子。该方法对感染性 MS2 的回收率中位数为 0.40,对 MS2 RNA 的回收率中位数为 0.07。在未来的污染物采样研究中使用建议的方法进行病毒回收,将为跨多项研究比较发现提供机会。