Real-time PCR for detection of the Aspergillus genus
被引:17
作者:
Goebes, Marian D.
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机构:
Stanford Univ, Terman Engn Ctr B13, Dept Civil & Environm Engn, Stanford, CA 94305 USAStanford Univ, Terman Engn Ctr B13, Dept Civil & Environm Engn, Stanford, CA 94305 USA
Goebes, Marian D.
[1
]
Hildemann, Lynn M.
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机构:Stanford Univ, Terman Engn Ctr B13, Dept Civil & Environm Engn, Stanford, CA 94305 USA
Hildemann, Lynn M.
Kujundzic, Elmira
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机构:Stanford Univ, Terman Engn Ctr B13, Dept Civil & Environm Engn, Stanford, CA 94305 USA
Kujundzic, Elmira
Hernandez, Mark
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机构:Stanford Univ, Terman Engn Ctr B13, Dept Civil & Environm Engn, Stanford, CA 94305 USA
Hernandez, Mark
机构:
[1] Stanford Univ, Terman Engn Ctr B13, Dept Civil & Environm Engn, Stanford, CA 94305 USA
[2] Univ Colorado, Dept Civil & Architectural Engn, Boulder, CO 80309 USA
来源:
JOURNAL OF ENVIRONMENTAL MONITORING
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2007年
/
9卷
/
06期
关键词:
D O I:
10.1039/b618937g
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Aspergillus is a genus of mold that has strong indoor sources, including several species capable of acting as opportunistic pathogens. Previous studies suggest that Aspergillus could serve as an indicator for abnormal mold growth or moisture, making it an important genus for environmental monitoring. Here, a quantitative polymerase chain reaction (qPCR, or real-time PCR) assay is presented for Aspergillus. The assay shows good specificity for the genus, detecting all Aspergillus species tested, although a few non-Aspergillus species are also amplified. Sensitivity testing demonstrates that DNA representing one conidium can be detected. A validation study compared qPCR results against direct microscopy counts using A. fumigatus conidia aerosolized into a laboratory chamber. The assay was then used to quantify Aspergillus in indoor air samples, demonstrating its utility for environmental monitoring. Analysis of a small number of clinical sputum samples showed complete agreement with culturing results.