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建筑环境中微生物组监测的新方法:冷凝捕获的可行性分析。

A new approach of microbiome monitoring in the built environment: feasibility analysis of condensation capture.

机构信息

Biosciences Division, Argonne National Laboratory, Lemont, IL, USA.

Department of Biological Sciences, University of Illinois at Chicago, 845 W. Taylor St, Chicago, IL, 60607, USA.

出版信息

Microbiome. 2023 Jun 8;11(1):129. doi: 10.1186/s40168-023-01555-5.

Abstract

BACKGROUND

Humans emit approximately 30 million microbial cells per hour into their immediate vicinity. However, sampling of aerosolized microbial taxa (aerobiome) remains largely uncharacterized due to the complexity and limitations of sampling techniques, which are highly susceptible to low biomass and rapid sample degradation. Recently, there has been an interest in developing technology that collects naturally occurring water from the atmosphere, even within the built environment. Here, we analyze the feasibility of indoor aerosol condensation collection as a method to capture and analyze the aerobiome.

METHODS

Aerosols were collected via condensation or active impingement in a laboratory setting over the course of 8 h. Microbial DNA was extracted from collected samples and sequenced (16S rRNA) to analyze microbial diversity and community composition. Dimensional reduction and multivariate statistics were employed to identify significant (p < 0.05) differences in relative abundances of specific microbial taxa observed between the two sampling platforms.

RESULTS

Aerosol condensation capture is highly efficient with a yield greater than 95% when compared to expected values. Compared to air impingement, aerosol condensation showed no significant difference (ANOVA, p > 0.05) in microbial diversity. Among identified taxa, Streptophyta and Pseudomonadales comprised approximately 70% of the microbial community composition.

CONCLUSION

The results suggest that condensation of atmospheric humidity is a suitable method for the capture of airborne microbial taxa reflected by microbial community similarity between devices. Future investigation of aerosol condensation may provide insight into the efficacy and viability of this new tool to investigate airborne microorganisms.

IMPORTANCE

On average, humans shed approximately 30 million microbial cells each hour into their immediate environment making humans the primary contributor to shaping the microbiome found within the built environment. In addition, recent events have highlighted the importance of understanding how microorganisms within the built environment are aerosolized and dispersed, but more importantly, the lack in development of technology that is capable of actively sampling the ever-changing aerosolized microbiome, i.e., aerobiome. This research highlights the capability of sampling the aerobiome by taking advantage of naturally occurring atmospheric humidity. Our novel approach reproduces the biological content in the atmosphere and can provide insight into the environmental microbiology of indoor spaces. Video Abstract.

摘要

背景

人类每小时向其周围环境排放约 3000 万个微生物细胞。然而,由于采样技术的复杂性和局限性,气溶胶化微生物类群(气生菌群)的采样仍在很大程度上没有得到描述,这些局限性使得采样技术非常容易受到低生物量和快速样本降解的影响。最近,人们对开发从大气中收集自然存在水的技术产生了兴趣,即使在建筑环境中也是如此。在这里,我们分析了室内气溶胶冷凝收集作为一种捕获和分析气生菌群的方法的可行性。

方法

在实验室环境中,通过冷凝或主动撞击在 8 小时的过程中收集气溶胶。从收集的样本中提取微生物 DNA 并进行测序(16S rRNA),以分析微生物多样性和群落组成。采用降维和多元统计方法来识别两种采样平台之间观察到的特定微生物类群相对丰度的显著差异(p<0.05)。

结果

气溶胶冷凝收集的效率非常高,与预期值相比,产率大于 95%。与空气撞击相比,气溶胶冷凝在微生物多样性方面没有显著差异(ANOVA,p>0.05)。在所鉴定的类群中,石松类和假单胞菌目约占微生物群落组成的 70%。

结论

结果表明,大气湿度的冷凝是一种适合捕获反映设备间微生物群落相似性的气生微生物类群的方法。对气溶胶冷凝的进一步研究可能会深入了解这一新工具在研究空气传播微生物方面的效果和可行性。

重要性

平均而言,人类每小时向其周围环境排放约 3000 万个微生物细胞,这使得人类成为塑造建筑环境中发现的微生物组的主要贡献者。此外,最近的事件强调了了解建筑环境中微生物如何气溶胶化和分散的重要性,但更重要的是,缺乏能够主动采样不断变化的气溶胶化微生物组(即气生菌群)的技术的发展。本研究强调了利用自然存在的大气湿度来采样气生菌群的能力。我们的新方法再现了大气中的生物内容,并能深入了解室内空间的环境微生物学。视频摘要。

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