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使用实时聚合酶链反应分析受潮损坏且有过敏患者居住的室内真菌污染情况。

Indoor fungal contamination of moisture-damaged and allergic patient housing analysed using real-time PCR.

作者信息

Bellanger A-P, Reboux G, Roussel S, Grenouillet F, Didier-Scherer E, Dalphin J-C, Millon L

机构信息

Laboratoire de Parasitologie-Mycologie, Centre Hospitalier Universitaire, Besançon, France.

出版信息

Lett Appl Microbiol. 2009 Aug;49(2):260-6. doi: 10.1111/j.1472-765X.2009.02653.x. Epub 2009 May 27.

DOI:10.1111/j.1472-765X.2009.02653.x
PMID:19486284
Abstract

AIMS

The aim of our study was to compare, using real-time (Rt) PCR, quantitative levels of five fungal species in three kinds of dwellings.

METHODS AND RESULTS

Three groups of homes were recruited: moisture-damaged homes (MDH, n = 30), allergic patient homes (APH, n = 25) and paired control homes (CH, n = 55). Five moulds with allergenic compounds or mycotoxin production characteristics (Cladosporium sphaerospermum, Penicillium chrysogenum, Aspergillus versicolor, Alternaria alternata and Stachybotrys chartarum) were quantified using Rt-PCR. Cycle threshold results were expressed in spore equivalent per volume or surface unit using a direct calculation based on a spore standard curve. MDH presented significantly higher amounts of DNA from C. sphaerospermum in both air and surface samples than CH (P < 0.001). APH presented slightly elevated amounts of DNA from A. versicolor in both air and surface samples, compared to CH (P < 0.05).

CONCLUSION

Rt-PCR quantification of targeted fungal species is a rapid, reliable tool that could be included in a global indoor mould evaluation.

SIGNIFICANCE AND IMPACT OF THE STUDY

Quantification of C. sphaerospermum using Rt-PCR can help to better target social service intervention in MDH. Quantification of A. versicolor DNA could be informative for characterization of APH.

摘要

目的

我们研究的目的是使用实时(Rt)PCR比较三种住宅中五种真菌的定量水平。

方法与结果

招募了三组房屋:受潮损坏房屋(MDH,n = 30)、过敏患者房屋(APH,n = 25)和配对对照房屋(CH,n = 55)。使用Rt-PCR对五种具有致敏化合物或产霉菌毒素特性的霉菌(球形枝孢菌、产黄青霉、杂色曲霉、链格孢菌和黑葡萄穗霉)进行定量。循环阈值结果以每体积或表面单位的孢子当量表示,通过基于孢子标准曲线的直接计算得出。MDH的空气和表面样本中球形枝孢菌的DNA含量均显著高于CH(P < 0.001)。与CH相比,APH的空气和表面样本中杂色曲霉的DNA含量略有升高(P < 0.05)。

结论

对目标真菌物种进行Rt-PCR定量是一种快速、可靠的工具,可纳入全球室内霉菌评估。

研究的意义和影响

使用Rt-PCR对球形枝孢菌进行定量有助于更好地确定MDH中的社会服务干预目标。对杂色曲霉DNA进行定量可能有助于对APH进行特征描述。

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