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Portable automatic bioaerosol sampling system for rapid on-site detection of targeted airborne microorganisms

室内生物气溶胶 生物气溶胶 微生物 多路复用 环境科学 生物战 生化工程 工艺工程 计算机科学 纳米技术 工程类 生物 化学 毒理 材料科学 生态学 生物信息学 遗传学 气溶胶 有机化学 细菌
作者
Evgeny V. Usachev,Anna V. Pankova,Elina A. Rafailova,Oleg V. Pyankov,Igor E. Agranovski
出处
期刊:Journal of Environmental Monitoring [Royal Society of Chemistry]
卷期号:14 (10): 2739-2739 被引量:18
标识
DOI:10.1039/c2em30317e
摘要

Bioaerosols could cause various severe human and animal diseases and their opportune and qualitative precise detection and control is becoming a significant scientific and technological topic for consideration. Over the last few decades bioaerosol detection has become an important bio-defense related issue. Many types of portable and stationary bioaerosol samplers have been developed and, in some cases, integrated into automated detection systems utilizing various microbiological techniques for analysis of collected microbes. This paper describes a personal sampler used in conjunction with a portable real-time PCR technique. It was found that a single fluorescent dye could be successfully used in multiplex format for qualitative detection of numerous targeted bioaerosols in one PCR tube making the suggested technology a reliable "first alert" device. This approach has been specifically developed and successfully verified for rapid detection of targeted microorganisms by portable PCR devices, which is especially important under field conditions, where the number of microorganisms of interest usually exceeds the number of available PCR reaction tubes. The approach allows detecting targeted microorganisms and triggering some corresponding sanitary and quarantine procedures to localize possible spread of dangerous infections. Following detailed analysis of the sample under controlled laboratory conditions could be used to exactly identify which particular microorganism out of a targeted group has been rapidly detected in the field. It was also found that the personal sampler has a collection efficiency higher than 90% even for small-sized viruses (>20 nm) and stable performance over extended operating periods. In addition, it was found that for microorganisms used in this project (bacteriophages MS2 and T4) elimination of nucleic acids isolation and purification steps during sample preparation does not lead to the system sensitivity reduction, which is extremely important for development of miniature bioaerosol monitoring instrumentation in the future.
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