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建筑材料中真菌和细菌的定量PCR分析及其与基于培养的分析方法的比较。

Quantitative PCR analysis of fungi and bacteria in building materials and comparison to culture-based analysis.

作者信息

Pietarinen Veli-Matti, Rintala Helena, Hyvärinen Anne, Lignell Ulla, Kärkkäinen Päivi, Nevalainen Aino

机构信息

National Public Health Institute, Environmental Health Department, P.O. Box 95, Kuopio, 70701, Finland.

出版信息

J Environ Monit. 2008 May;10(5):655-63. doi: 10.1039/b716138g. Epub 2008 Mar 20.

DOI:10.1039/b716138g
PMID:18449403
Abstract

Prolonged moisture on building materials can lead to microbial growth on them. Microbes can emit spores, metabolites and structural parts into the indoor air and thus, cause adverse health effects of people living and working in these buildings. So far, culture methods have been used for assessment of microbial contamination of building materials. In this work, we used quantitative PCR (qPCR) for the detection of selected fungal and bacterial groups in 184 building materials of different types and compared the results with culture-based analysis. Nine either commonly found species, genera or groups of fungi, or those considered as moisture damage indicators, and one bacterial genus, Streptomyces, were determined using qPCR. Fungi and mesophilic actinomycetes were also cultivated using standard media and conditions of the routine analysis. The bacterial genus Streptomyces and the fungal group Penicillium/Aspergillus/Paecilomyces were the most prevalent microbial groups in all building material types, followed by Stachybotrys chartarum and Trichoderma viride/atroviride/koningii. The highest prevalences, concentrations and species diversity was observed on wooden materials. In general, the results of the two methods did not correlate well, since concentrations of fungi and streptomycetes were higher and their occurrence more prevalent when determined by qPCR compared to culture-based results. However, with increasing concentrations, the correlation generally increased. The qPCR assay did not detect Aspergillus versicolor and Acremonium strictum as often as culture.

摘要

建筑材料上的长期潮湿会导致其上微生物滋生。微生物会向室内空气中释放孢子、代谢产物和结构成分,从而对在这些建筑物中生活和工作的人的健康产生不利影响。到目前为止,培养方法一直用于评估建筑材料的微生物污染情况。在这项研究中,我们使用定量聚合酶链反应(qPCR)检测了184种不同类型建筑材料中选定的真菌和细菌类群,并将结果与基于培养的分析结果进行了比较。使用qPCR确定了9种常见的真菌物种、属或类群,或被视为潮湿损害指标的真菌,以及1个细菌属链霉菌。还使用常规分析的标准培养基和条件培养了真菌和嗜温放线菌。链霉菌属细菌和青霉/曲霉/拟青霉真菌类群是所有建筑材料类型中最普遍的微生物类群,其次是炭疽菌和绿色木霉/深绿木霉 /康宁木霉。在木质材料上观察到最高的患病率、浓度和物种多样性。总体而言,两种方法的结果相关性不佳,因为与基于培养的结果相比,通过qPCR测定时真菌和链霉菌的浓度更高,其出现也更普遍。然而,随着浓度的增加,相关性通常会增加。qPCR检测不像培养法那样经常检测到杂色曲霉和局限顶孢霉。

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