Rapid Detection and Quantitation of Fungal Spores from Dust Samples Using Real-Time PCR
Public Domain
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2005/03/01
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Description:Recent advances in real-time PCR have permitted accurate, rapid and quantitative identification of microorganisms in pure cultures regardless of viability or culturability. In this study, a simple sample processing method was investigated for rapid identification and quantitation of fungal spores from dust samples using real-time PCR. The proposed method was evaluated for susceptibility to interference from environmental dust samples. The extent of inhibition was calculated using real-time PCR reactions containing Aspergillus fumigatus spores specific primers and probe and various amounts of dust. No interference (p < 0.05) was detected from 0.2 mg of four real-world dust samples. However, dusts weighing > 0.2 mg compromised the assay. The overall results suggest the potential usefulness of our method for monitoring indoor microbial aerosols containing dusts weighing < / = 0.2 mg using real-time PCR. [Description provided by NIOSH]
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ISBN:9780970991515
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Pages in Document:366-374
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NIOSHTIC Number:nn:20030922
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Citation:Bioaerosols, fungi, bacteria, mycotoxins and human health: patho-physiology, clinical effects, exposure assessment, prevention and control in indoor environments and work. Johanning E, ed., Albany, NY: Fungal Research Group Foundation, Inc., 2005 Mar; :366-374
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Email:jkeswani@cdc.gov
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Federal Fiscal Year:2005
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Peer Reviewed:False
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Source Full Name:Bioaerosols, fungi, bacteria, mycotoxins and human health: patho-physiology, clinical effects, exposure assessment, prevention and control in indoor environments and work
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Main Document Checksum:urn:sha-512:766e0c8d51683233392e99c417e5ed4185369d34223cf3acf23716d5c80f783094b603b74d6c26634acd4343d4abf6e8f7c3bfac9a9c6ec99c3fdf3b746f8cb3
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