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本文引用的文献

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Experimental methods for studying microbial survival in extraterrestrial environments.研究微生物在外层空间环境中生存的实验方法。
J Microbiol Methods. 2010 Jan;80(1):1-13. doi: 10.1016/j.mimet.2009.10.004. Epub 2009 Oct 23.
2
Aerosolization of fungi, (1-->3)-beta-D glucan, and endotoxin from flood-affected materials collected in New Orleans homes.从新奥尔良家庭收集的受洪水影响材料中真菌、(1→3)-β-D-葡聚糖和内毒素的气溶胶化。
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Use of an ATP assay to determine viable microbial biomass in Fennoscandian Shield groundwater from depths of 3-1000 m.利用ATP检测法测定芬诺斯坎迪亚盾形地3至1000米深处地下水中的活微生物量。
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Detection and quantification of Wallemia sebi in aerosols by real-time PCR, conventional PCR, and cultivation.通过实时PCR、常规PCR和培养法对气溶胶中的西氏瓦勒霉菌进行检测和定量分析。
Appl Environ Microbiol. 2004 Dec;70(12):7295-302. doi: 10.1128/AEM.70.12.7295-7302.2004.
5
Detection of viable fungal spores contaminant on documents and rapid control of the effectiveness of an ethylene oxide disinfection using ATP assay.使用ATP检测法检测文件上的存活真菌孢子污染物并快速控制环氧乙烷消毒的有效性。
Luminescence. 2003 Mar-Apr;18(2):113-21. doi: 10.1002/bio.710.
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ATP as a biomarker of viable microorganisms in clean-room facilities.三磷酸腺苷作为洁净室设施中活微生物的生物标志物。
J Microbiol Methods. 2003 Mar;52(3):367-77. doi: 10.1016/s0167-7012(02)00192-6.
7
Fungal fragments as indoor air biocontaminants.作为室内空气生物污染物的真菌碎片。
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Fungi: toxic killers or unavoidable nuisances?真菌:有毒杀手还是不可避免的麻烦?
Ann Allergy Asthma Immunol. 2001 Dec;87(6 Suppl 3):52-6. doi: 10.1016/s1081-1206(10)62342-3.
9
Methods for integrated air sampling and dna analysis for detection of airborne fungal spores.用于检测空气中真菌孢子的空气采样与DNA分析一体化方法。
Appl Environ Microbiol. 2001 Jun;67(6):2453-9. doi: 10.1128/AEM.67.6.2453-2459.2001.
10
Performance of Air-O-Cell, Burkard, and Button Samplers for total enumeration of airborne spores.用于空气中孢子总数计数的空气冲击式采样器、伯卡德采样器和纽扣式采样器的性能
AIHAJ. 2000 Nov-Dec;61(6):855-64. doi: 10.1080/15298660008984598.

具有超疏水表面的静电采样器对真菌生物气溶胶的采集效率。

Collection efficiencies of an electrostatic sampler with superhydrophobic surface for fungal bioaerosols.

机构信息

Department of Environmental Sciences, Rutgers University, New Brunswick, NJ 08901, USA.

出版信息

Indoor Air. 2011 Apr;21(2):110-20. doi: 10.1111/j.1600-0668.2010.00685.x. Epub 2011 Feb 1.

DOI:10.1111/j.1600-0668.2010.00685.x
PMID:21204982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4027968/
Abstract

UNLABELLED

We recently developed an electrostatic precipitator with superhydrophobic surface (EPSS), which collects particles into a 10- to 40-μl water droplet allowing achievement of very high concentration rates (defined as the ratio of particle concentration in the collection liquid vs. the airborne particle concentration per time unit) when sampling airborne bacteria. Here, we analyzed the performance of this sampler when collecting three commonly found fungal spores--Cladosporium cladosporioides, Penicillium melinii, and Aspergillus versicolor--under different operating conditions. We also adapted adenosine triphosphate (ATP)-based bioluminescence for the analysis of collection efficiency and the concentration rates. The collection efficiency ranged from 10 to 36% at a sampling flow rate of 10 l/min when the airborne fungal spore concentration was approximately 10(5)-10(6) spores/m(3) resulting in concentration rates in the range of 1 × 10(5)-3 × 10(5)/min for a 10-μl droplet. The collection efficiency was inversely proportional to the airborne spore concentration and it increased to above 60% for common ambient spore concentrations, e.g., 10(4)-10(5) spores/m(3). The spore concentrations determined by the ATP-based method were not statistically different from those determined by microscopy and allowed us to analyze spore concentrations that were too low to be reliably detected by microscopy.

PRACTICAL IMPLICATIONS

The new electrostatic precipitator with superhydrophobic surface (EPSS) collects airborne fungal spores into small water droplets (10 and 40 μl) allowing achievement of concentration rates that are higher than those of most currently available bioaerosol samplers. Biosamplers with high concentration rates enable detection of low ambient aerial bioaerosol concentrations in various environments, including indoors air, and would be useful for improved exposure assessment. A successful adaptation of the adenosine triphosphate (ATP)-based bioluminescence assay for the quantification of fungal spores from a specific species enables fast sample analysis in laboratory investigations. This rapid assay could be especially useful when investigating the performance of biological samplers as a function of multiple operational parameters.

摘要

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我们最近开发了一种带有超疏水表面的静电沉淀器(EPSS),当采集空气中的细菌时,它可以将颗粒收集到 10-40μl 的水滴中,从而实现非常高的浓度率(定义为收集液中的颗粒浓度与单位时间内空气中的颗粒浓度之比)。在这里,我们分析了该采样器在不同操作条件下收集三种常见真菌孢子(枝孢菌、青霉和曲霉)时的性能。我们还采用了三磷酸腺苷(ATP)生物发光来分析收集效率和浓度率。当空气中真菌孢子浓度约为 10(5)-10(6)孢子/m(3)时,采样流速为 10l/min,收集效率范围为 10-36%,导致 10-μl 液滴的浓度率在 1×10(5)-3×10(5)/min 范围内。收集效率与空气中的孢子浓度成反比,对于常见的环境孢子浓度(例如 10(4)-10(5)孢子/m(3)),收集效率增加到 60%以上。基于 ATP 的方法确定的孢子浓度与显微镜确定的孢子浓度没有统计学差异,并且允许我们分析显微镜无法可靠检测到的低浓度孢子。

实际意义

新型带有超疏水表面的静电沉淀器(EPSS)将空气中的真菌孢子收集到小水滴(10 和 40μl)中,实现了高于大多数现有生物气溶胶采样器的浓度率。高浓度率的生物采样器可以检测各种环境(包括室内空气)中的低环境空气生物气溶胶浓度,对于改进暴露评估将非常有用。成功地将三磷酸腺苷(ATP)生物发光测定法应用于特定物种真菌孢子的定量分析,使实验室研究中的样品快速分析成为可能。当研究生物采样器作为多个操作参数的函数的性能时,这种快速测定法可能特别有用。