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用于严重急性呼吸综合征冠状病毒 2 室内环境监测的生物气溶胶采样器评估。

Evaluation of a bioaerosol sampler for indoor environmental surveillance of Severe Acute Respiratory Syndrome Coronavirus 2.

机构信息

Biology and the Built Environment Center, University of Oregon, Eugene, OR, United States of America.

Energy Studies in Buildings Laboratory, University of Oregon, Eugene, OR, United States of America.

出版信息

PLoS One. 2021 Nov 15;16(11):e0257689. doi: 10.1371/journal.pone.0257689. eCollection 2021.

DOI:10.1371/journal.pone.0257689
PMID:34780482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8592464/
Abstract

The worldwide spread of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has ubiquitously impacted many aspects of life. As vaccines continue to be manufactured and administered, limiting the spread of SARS-CoV-2 will rely more heavily on the early identification of contagious individuals occupying reopened and increasingly populated indoor environments. In this study, we investigated the utility of an impaction-based bioaerosol sampling system with multiple nucleic acid collection media. Heat-inactivated SARS-CoV-2 was utilized to perform bench-scale, short-range aerosol, and room-scale aerosol experiments. Through bench-scale experiments, AerosolSense Capture Media (ACM) and nylon flocked swabs were identified as the highest utility media. In room-scale aerosol experiments, consistent detection of aerosol SARS-CoV-2 was achieved at an estimated aerosol concentration equal to or greater than 0.089 genome copies per liter of room air (gc/L) when air was sampled for eight hours or more at less than one air change per hour (ACH). Shorter sampling periods (75 minutes) yielded consistent detection at ~31.8 gc/L of room air and intermittent detection down to ~0.318 gc/L at (at both 1 and 6 ACH). These results support further exploration in real-world testing scenarios and suggest the utility of indoor aerosol surveillance as an effective risk mitigation strategy in occupied buildings.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)在全球范围内的传播广泛影响了生活的方方面面。随着疫苗的不断生产和接种,限制 SARS-CoV-2 的传播将更加依赖于早期识别在重新开放和人口日益增多的室内环境中具有传染性的个体。在这项研究中,我们研究了一种基于撞击的生物气溶胶采样系统与多种核酸收集介质的实用性。使用热失活的 SARS-CoV-2 进行了台架规模、短程气溶胶和房间规模气溶胶实验。通过台架实验,确定了气溶胶感测捕获介质(ACM)和尼龙植绒拭子是最高效的介质。在房间规模的气溶胶实验中,当在小于每小时 1 次空气交换(ACH)的条件下采样 8 小时或更长时间时,空气中 SARS-CoV-2 的气溶胶浓度估计等于或大于每升房间空气 0.089 基因组拷贝(gc/L)时,可一致检测到气溶胶 SARS-CoV-2。较短的采样时间(75 分钟)可在约 31.8 gc/L 的室内空气中实现一致检测,在 1 和 6 ACH 下可间歇性检测到低至约 0.318 gc/L。这些结果支持在真实测试场景中的进一步探索,并表明室内气溶胶监测作为在占用建筑物中进行有效风险缓解的策略具有实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/87ea6722ee8b/pone.0257689.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/0261a4e70fd5/pone.0257689.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/4a25e6d9d0fa/pone.0257689.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/1cdcfbf6b631/pone.0257689.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/4962de515a3d/pone.0257689.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/87ea6722ee8b/pone.0257689.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/0261a4e70fd5/pone.0257689.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/4a25e6d9d0fa/pone.0257689.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/1cdcfbf6b631/pone.0257689.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/4962de515a3d/pone.0257689.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52d/8592464/87ea6722ee8b/pone.0257689.g005.jpg

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