Recovery and Quantification of Norovirus in Air Samples from Experimentally Produced Aerosols

IF 4.1 2区 农林科学 Q2 ENVIRONMENTAL SCIENCES Food and Environmental Virology Pub Date : 2024-03-21 DOI:10.1007/s12560-024-09590-7
Kitwadee Rupprom, Yuwanda Thongpanich, Woravat Sukkham, Fuangfa Utrarachkij, Leera Kittigul
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Abstract

Norovirus is the leading cause of acute gastroenteritis in humans across all age groups worldwide. Norovirus-infected patients can produce aerosolized droplets which play a role in gastroenteritis transmission. The study aimed to assess bioaerosol sampling in combination with a virus concentrating procedure to facilitate molecular detection of norovirus genogroup (G) II from experimentally contaminated aerosols. Using a nebulizer within an experimental chamber, aerosols of norovirus GII were generated at known concentrations. Air samples were then collected in both 5 mL and 20 mL water using the SKC BioSampler at a flow rate of 12.5 L/min, 15 min. Subsequently, the virus in collected water was concentrated using speedVac centrifugation and quantified by RT-qPCR. The optimal distances between the nebulizer and the SKC BioSampler yielded high recoveries of the virus for both 5 and 20 mL collections. Following nebulization, norovirus GII RNA was detectable up to 120 min in 5 mL and up to 240 min in 20 mL collection. The concentrations of norovirus GII RNA recovered from air samples in the aerosol chamber ranged from 102 to 105 genome copies/mL, with average recoveries of 25 ± 12% for 5 mL and 22 ± 19% for 20 mL collections. These findings provide quantitative data on norovirus GII in aerosols and introduce a novel virus concentrating method for aerosol collection in water, thus enhancing surveillance of this virus.

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从实验产生的气溶胶中回收空气样本中的诺罗病毒并进行定量。
诺如病毒是导致全球各年龄组人类急性肠胃炎的主要原因。诺如病毒感染者会产生气溶胶飞沫,在肠胃炎传播过程中起到一定作用。该研究旨在评估生物气溶胶采样与病毒浓缩程序的结合,以促进从实验污染的气溶胶中分子检测诺如病毒基因群(G)II。在实验箱内使用雾化器产生已知浓度的诺如病毒 GII 气溶胶。然后使用 SKC BioSampler 以 12.5 升/分钟的流速在 15 分钟内收集 5 毫升和 20 毫升水中的空气样本。随后,使用 speedVac 离心浓缩收集水中的病毒,并通过 RT-qPCR 进行定量。雾化器和 SKC 生物取样器之间的最佳距离使 5 毫升和 20 毫升采集水的病毒回收率都很高。雾化后,诺如病毒 GII RNA 在 5 mL 采集的 120 分钟内和 20 mL 采集的 240 分钟内均可检测到。从气溶胶室的空气样本中回收的诺如病毒 GII RNA 浓度为 102 至 105 基因组拷贝/毫升,5 毫升样本的平均回收率为 25 ± 12%,20 毫升样本的平均回收率为 22 ± 19%。这些研究结果提供了气溶胶中诺如病毒 GII 的定量数据,并介绍了一种新型的水中气溶胶收集病毒浓缩方法,从而加强了对这种病毒的监测。
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来源期刊
Food and Environmental Virology
Food and Environmental Virology ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.50
自引率
2.90%
发文量
35
审稿时长
1 months
期刊介绍: Food and Environmental Virology publishes original articles, notes and review articles on any aspect relating to the transmission of pathogenic viruses via the environment (water, air, soil etc.) and foods. This includes epidemiological studies, identification of novel or emerging pathogens, methods of analysis or characterisation, studies on survival and elimination, and development of procedural controls for industrial processes, e.g. HACCP plans. The journal will cover all aspects of this important area, and encompass studies on any human, animal, and plant pathogenic virus which is capable of transmission via the environment or food.
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