Related Experiment Video
Updated: Jul 5, 2026

Determination of Microbial Biomass in Soil using Digital Droplet PCR (ddPCR)
Published on: April 24, 2026
Quantitative PCR analysis of fungi and bacteria in building materials and comparison to culture-based analysis
Veli-Matti Pietarinen1, Helena Rintala, Anne Hyvärinen
1National Public Health Institute, Environmental Health Department, P.O. Box 95, Kuopio, 70701, Finland.
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.
Insights
Quantitative PCR (qPCR) offers a more sensitive method for detecting microbial contamination in building materials than traditional culture methods. This advanced technique revealed higher microbial prevalence and concentrations, especially in wooden materials.
Area of Science:
- Environmental Science
- Microbiology
- Building Science
Background:
- Prolonged moisture in buildings promotes microbial growth, releasing airborne contaminants linked to adverse health effects.
- Traditional culture methods have limitations in accurately assessing microbial contamination in building materials.
Purpose of the Study:
- To compare the efficacy of quantitative PCR (qPCR) against culture-based methods for detecting fungi and bacteria in building materials.
- To identify prevalent microbial groups and assess their distribution across various building material types.
Main Methods:
- Analysis of 184 building material samples using both qPCR and standard culture techniques.
- Detection of nine fungal groups and one bacterial genus (Streptomyces) via qPCR.
- Cultivation of fungi and mesophilic actinomycetes using routine methods.
Main Results:
- qPCR detected higher prevalence and concentrations of fungi and Streptomyces compared to culture methods.
- The bacterial genus Streptomyces and the fungal group Penicillium/Aspergillus/Paecilomyces were most common across all materials.
- Wooden materials exhibited the highest microbial prevalence, concentrations, and species diversity.
Conclusions:
- qPCR provides a more comprehensive assessment of microbial contamination in building materials than culture methods.
- Discrepancies between methods highlight qPCR's superior sensitivity, particularly for certain microbial groups.
- Understanding microbial contamination is crucial for indoor air quality and occupant health.
Related Concept Videos
Real Time RT-PCR
The real-time quantification of the number of amplified products is...
Methods to Assess Microbial Populations

