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Microbial indoor air quality and respiratory symptoms of children were studied in 24 schools with visible moisture and mold problems, and in eight non-damaged schools. School buildings of concrete/brick and wooden construction were included. The indoor environment investigations included technical building inspections for visible moisture signs and microbial sampling using six-stage impactor for viable airborne microbes. Children's health information was collected by questionnaires. The effect of moisture damage on concentrations of fungi was clearly seen in buildings of concrete/brick construction, but not in wooden school buildings. Occurrence of Cladosporium, Aspergillus versicolor, Stachybotrys, and actinobacteria showed some indicator value for moisture damage. Presence of moisture damage in school buildings was a significant risk factor for respiratory symptoms in schoolchildren. Association between moisture damage and respiratory symptoms of children was significant for buildings of concrete/brick construction but not for wooden school buildings. The highest symptom prevalence was found during spring seasons, after a long exposure period in damaged schools. The results emphasize the importance of the building frame as a determinant of exposure and symptoms.

In this study, we evaluated the use of RT-qPCR assays targeting rRNA gene sequences for the detection of fecal bacteria in water samples. We challenged the RT-qPCR assays against RNA extracted from sewage effluent (n = 14), surface water (n = 30), and treated source water (n = 15) samples. Additionally, we applied the same assays using DNA as the qPCR template. The targeted fecal bacteria were present in most of the samples tested, although in several cases, the detection frequency increased when RNA was used as the template. For example, the majority of samples that tested positive for E. coli and Campylobacter spp. in surface waters, and for human-specific Bacteroidales, E. coli, and Enterococcus spp. in treated source waters were only detected when rRNA was used as the original template. The difference in detection frequency using rRNA or rDNA (rRNA gene) was sample- and assay-dependent, suggesting that the abundance of active and nonactive populations differed between samples. Statistical analyses for each population exhibiting multiple quantifiable results showed that the rRNA copy numbers were significantly higher than the rDNA counterparts (p < 0.05). Moreover, the detection frequency of rRNA-based assays were in better agreement with the culture-based results of E. coli, intestinal enterococci, and thermotolerant Campylobacter spp. in surface waters than that of rDNA-based assays, suggesting that rRNA signals were associated to active bacterial populations. Our data show that using rRNA-based approaches significantly increases detection sensitivity for common fecal bacteria in environmental waters. These findings have important implications for microbial water quality monitoring and public health risk assessments.

No abstract

Microbes are present everywhere in outdoor air. However, the general characterization of outdoor air mycobiota and bacterial flora is incomplete. In this study, seasonal variations in outdoor air microbial concentrations and differences between a landfill, urban and rural sites were compared. Samples were collected monthly for a period of one year. Airborne dust samples were collected onto polyvinyl chloride filters. Filter samples were analyzed for ergosterol, and 14 species or assay groups of fungi and for the bacterial genus Streptomyces by using quantitative PCR. Viable bacteria and fungi were collected with a cascade impactor twice each month from the three sampling sites. The concentrations in the different sampling sites varied depending on the species. The concentrations of Penicillium and Aspergillus species were significantly higher in the waste center compared with the other sites, while the concentration of Cladosporium spp. was highest in the rural area. The highest concentrations of Streptomyces and Cladosporium species were observed in warmer weather periods. Similar observations were made for ergosterol. Group and species seasonal variation was less distinct for Penicillium and Aspergillus. According to the present results, both season and environment are determinants of microbial communities in outdoor air.