A Method For Numerical Characterization Of Indoor Climates By A Biosensor Using A Xerophilic Fungus

A “fungal index” is proposed as a new climate parameter for the characterization of the indoor environment. The index quantifies the environmental conditions in relation to the ability of fungi to grow by means of the response of a xerophilic fungus Eurotium herbariorum. The growth response of this fungus was found to be climate-dependent. The indoor environment in a residential building in Japan (1991-1992) was quantitatively assessed by this approach. In the assessment, the variation in microclimate, which differs greatly within and between rooms, could be demonstrated.     

The relationship between measured moisture conditions and fungal concentrations in water-damaged building materials

We determined the moisture levels, relative humidity (RH) or moisture content (MC) of materials, and concentrations of culturable fungi, actinomycetes and total spores as well as a composition of fungal flora in 122 building material samples collected from 18 moisture problem buildings. The purpose of this work was to clarify if the is any correlation between the moisture parameters and microbial levels or generic composition depending on the type of materials and the time passed after a water damage. The results showed an agreement between the concentrations of total spores and culturable fungi for the wood, wood-based and gypsum board samples (r > 0.47). The concentrations of total spores and/or culturable fungi correlated with RH of materials particularly among the wood and insulation materials (r > 0.79), but not usually with MC (r < 0.45). For the samples collected from ongoing damage, there was a correlation between RH of materials and the concentrations of total spores and culturable fungi (r > 0.51), while such a relationship could not be observed for the samples taken from dry damage. A wide range of fungal species were found in the samples from ongoing damage, whereas Penicillia and in some cases yeasts dominated the fungal flora in the dry samples. This study indicates that fungal contamination can be evaluated on the basis of moisture measurements of constructions in ongoing damage, but the measurements are not solely adequate for estimation of possible microbial growth in dry damage.     

Determination of fungal spore release from wet building materials

The release and transport of fungal spores from water-damaged building materials is a key factor for understanding the exposure to particles of fungal origin as a possible cause of adverse health effects associated to growth of fungi indoors. In this study, the release of spores from nine species of typical indoor fungi has been measured under controlled conditions. The fungi were cultivated for a period of 4-6 weeks on sterilized wet wallpapered gypsum boards at a relative humidity (RH) of approximately 97%. A specially designed small chamber (P-FLEC) was placed on the gypsum board. The release of fungal spores was induced by well-defined jets of air impacting from rotating nozzles. The spores and other particles released from the surface were transported by the air flowing from the chamber through a top outlet to a particle counter and sizer. For two of the fungi (Penicillium chrysogenum and Trichoderma harzianum), the number of spores produced on the gypsum board and subsequently released was quantified. Also the relationship between air velocities from 0.3 to 3 m/s over the surface and spore release has been measured. The method was found to give very reproducible results for each fungal isolate, whereas the spore release is very different for different fungi under identical conditions. Also, the relationship between air velocity and spore release depends on the fungus. For some fungi a significant number of particles smaller than the spore size were released. The method applied in the study may also be useful for field studies and for generation of spores for exposure studies.     

Airborne viable, non-viable, and allergenic fungi in a rural agricultural area of India: a 2-year study at five outdoor sampling stations

The information on airborne allergenic fungal flora in rural agricultural areas is largely lacking. Adequate information is not available to the bioaerosol researchers regarding the choice of single versus multiple sampling stations for the monitoring of both viable and non-viable airborne fungi. There is no long-term study estimating the ratios of viable and non-viable fungi in the air and earlier studies did not focus on the fractions of airborne allergenic fungi with respect to the total airborne fungal load. To fill these knowledge gaps, volumetric paired assessments of airborne viable and non-viable fungi were performed in five outdoor sampling stations during two consecutive years in a rural agricultural area of India. Samples were collected at 10-day intervals by the Burkard Personal Slide Sampler and the Andersen Two-Stage Viable Sampler. The data on the concentrations of total and individual fungal types from five stations and 2 different years were analyzed and compared by statistical methods. The allergenicity of the prevalent airborne viable fungi was estimated by the skin-prick tests of >100 rural allergy patients using the antigenic fungal extracts from isolates collected with the Andersen sampler. The ranges of total fungal spore concentration were 82-2365 spores per cubic meter of air (spores/m3) in the first sampling year and 156-2022 spores/m3 in the second sampling year. The concentration ranges of viable fungi were 72-1796 colony-forming units per cubic meter of air (CFU/m3) in the first sampling year and 155-1256 CFU/m3 in the second sampling year. No statistically significant difference was observed between the total spore data of the 2 years, however, the data between five stations showed a significant difference (P<0.0001). No statistically significant difference existed between stations and years with respect to the concentration of viable fungi. When the data of individual allergenic fungal concentrations were compared between stations and years, no statistically significant difference was observed in all cases except for Aspergillus japonicus and Rhizopus nigricans, which showed significant difference in case of stations and years, respectively. The ratios between the total fungal spores collected by the Burkard sampler and the viable fungi collected by the Andersen sampler from all sampling stations ranged between 0.29 and 7.61. The antigenic extracts of eight prevalent viable airborne fungi (A. flavus, A. japonicus, A. fumigatus, Alternaria alternata, Cladosporium cladosporioides, Curvularia pallescens, Fusarium roseum, and R. nigricans) demonstrated >60% positive reactions in the skin prick test. These selected allergenic fungi collectively represented 31.7-63.2% of the total airborne viable fungi in different stations. The study concluded that: (i) a rich fungal airspora existed in the rural study area, (ii) to achieve representative information on the total airborne fungal spores of an area, the monitoring in multiple sampling stations is preferable over a single sampling station; for viable fungi, however, one station can be considered, (iii) the percentage of airborne fungal viability is higher in rural agricultural areas, and (iv) approximately 52% of the viable airborne fungi in the rural study area were allergenic.     

Microbiological Events After a Fire in a High-rise Building

Water used to control a fire on an upper floor in a highrise office building wetted furnishings and construction materials on lower floors and resulted in the amplification of microorganisms especially mesophilic and thermotolerant fungi. Concentrations of fungi in indoor air including Aspergillus, Penicillium and Paecilomyces approached or exceeded 10⁴ colony forming units per cubic meter (cfu/m³). Airborne endotoxin levels increased about 1 order of magnitude over background levels. Sampling for fungi using both culture plate impactors and spore traps showed that spores were migrating from water damaged to undamaged areas in the office complex. Elevator shafts traversing water damaged floors likely provided the major dispersion pathway of spores into occupied areas. Construction materials such as plaster ceilings that had been wetted during the fire but were free of visual fungal contamination were found to be strong fungal reservoirs after the building had thoroughly dried. Management of microbial contaminants after a fire in a highrise building is an important public health concern and therefore an essential aspect of building restoration.     

Use of (1-3)-beta-d-glucan concentrations in dust as a surrogate method for estimating specific fungal exposures

Indoor exposure to fungi has been associated with respiratory symptoms,often attributed to their cell wall component, (1-3)-beta-D-glucan. Performing(1-3)-beta-D-glucan analysis is less time consuming and labor intensive than cultivation or microscopic counting of fungal spores. This has prompted many to use(1-3)-beta-D-glucan as a surrogate for fungal exposure. The aim of this study was to examine which indoor fungal species are major contributors to the (1-3)-beta-D-glucan concentration in field dust samples. We used the quantitative polymerase chain reaction (QPCR) method to analyze 36 indoor fungal species in 297 indoor dust samples. These samples were also simultaneously analyzed for (1-3)-beta-D-glucan concentration using the endpoint chromogenic Limulus Amebocyte lysate assay. Linear regression analysis, followed by factor analysis and structural equation modeling, were utilized in order to identify fungal species that mostly contribute to the (1-3)-beta-D-glucan concentration in field dust samples. The study revealed that Cladosporium and Aspergillus genera, as well as Epicoccum nigrum, Penicillium brevicompactum and Wallemia sebi were the most important contributors to the (1-3)-beta-D-glucan content of these home dust samples. The species that contributed most to the (1-3)-beta-D-glucan concentration were also the most prevalent in indoor environments. However, Alternaria alternata, a common fungal species in indoor dust, did not seem to be a significant source of (1-3)-beta-D-glucan. PRACTICAL IMPLICATIONS: This study revealed that the (1-3)-beta-D-glucan content of different fungal species varies widely. (1-3)-beta-D-glucan inhouse dust from the Greater Cincinnati area may be a good marker for some fungal species of the Cladosporium and Aspergillus genera. In contrast, Alternaria alternata did not contribute much to the (1-3)-beta-D-glucan load. Therefore, (1-3)-beta-D-glucan concentration in field samples as a surrogate for total fungal exposure should be used with caution.     

Levels of microbial agents in floor dust during remediation of a water-damaged office building

We examined the effects of remediation on loads of culturable fungi in floor dust collected from a large water-damaged office building during four cross-sectional surveys (2002, 2004, 2005, and 2007, respectively). We created a binary remediation variable for each year for each sampled workstation using information on remediation associated with water damage obtained from building management and used generalized linear mixed-effects models. We found significantly lower levels of culturable total and hydrophilic fungi at remediated workstations than at non-remediated workstations in 2004 and 2005 after completion of major remediation. The remediation effect, however, disappeared in 2007. The fraction of hydrophilic to total fungal concentrations was lowest in 2004, increased in 2005, and was highest in 2007. Our results indicate that the 2003 remediation lowered dust indices of dampness temporarily, but remediation was incomplete, consistent with a building assessment report of water infiltration. This study demonstrates the utility of longitudinal evaluation of microbial indices during remediation of water damage in this building, in which elimination of sources of moisture was not fully addressed. Our findings indicate that the fraction of hydrophilic fungi derived from concentrations of fungal species may be a useful index for assessing the long-term effectiveness of remediation. PRACTICAL IMPLICATIONS: This study demonstrates the utility of longitudinal evaluation of microbial indices during remediation of water damage in this building, in which elimination of sources of moisture was incomplete. Our findings indicate that the fraction of hydrophilic fungi derived from concentrations of fungal species may be a useful index for assessing the long-term effectiveness of remediation.     

Biodeterioration of sandstone under the influence of different humidity levels in laboratory conditions

Excessive moisture in building materials supports microbial growth. It has been referred that relative humidity more than 55% promotes the microbial growth. To test the effect of different relative humidity tropical chamber test was set up at 52%, 76%, 85% and 96% RH and maximum diversity of fungi was found at 85% and 96% RH. Two fungi Aspergillus sydowi and Aspergillus flavipes were present throughout the course of study from moderate to highly abundant form. It was observed that Fusarium moniliforme, Cephalosporium acremonium, Papulospora sp. proliferated at higher relative humidity (i.e. at 85% and 96.6% RH) and Fusarium roseum, Fusarium oxysporum only at 96% RH level. The relative humidity level lower than 62%, i.e. at 52% level exhibited no fungal growth on sandstone surface during two-year observations. During the study pattern it was noticed that diversity decreased gradually and dominance of particular species increased with the time factor. Analysis of sandstone after fungal colonization by X-ray diffraction and SEM showed the formation of newly formed biomineral.     

Fungal spore transport through a building structure

The study carried out laboratory measurements with a full-scale timber frame structure to determine penetration of inert particles with size distribution from 0.6 to 4 microm and spores of Penicillium and Cladosporium through the structure. Pressure difference over and air leakage through the structure were varied. Measurements at moderate pressure differences resulted in the penetration factors within the range of 0.05-0.2 for inert particles, and indicated also the penetration of fungal spores through the structure. The measurements showed that the penetration was highly dependent on pressure difference over the structure but not on holes in surface boards of the structure. The results show that surface contacts between the frames and mineral wool may have a significant effect on penetration. The penetration was approximately constant within particle size rage of 0.6-2.5 microm, but particles with diameter of 4.0 microm did not penetrate through the structure at all even at a higher-pressure difference of 20 Pa, except in the case of direct flow-path through the structure. Results have important consequences for practical design showing that penetration of fungal spores through the building envelope is difficult to prevent by sealing. The only effective way to prevent penetration seems to be balancing or pressurizing the building. In cold climates, moisture condensation risk should be taken into account if pressure is higher indoors than outdoors. Determined penetration factors were highly dependent on the pressure difference. Mechanical exhaust ventilation needs a special consideration as de-pressurizing the building may cause health risk if there is hazardous contamination in the building envelope exists.     

Microbiology on Indoor Air `99– What is New and Interesting? An Overview of Selected Papers Presented in Edinburgh,August, 1999

A multidisciplinary approach to microbiological implications of indoor air is fruitful for research as well as management of health and building problems. The Finnish and the Danish mold programs are examples of such productive collaborative studies. Dust samples taken from classrooms in schools where occupants complain of building-related symptoms (BRS) demonstrated an inflammatory potential in vitro, measured as a release of cytokine interleukin (IL)-8. An increase of the metabolite NO and liberation of tumor necrosis factor (TNF)-alpha and other cytokines during exposure were obtained in vivo, was presented based on these programs and on epidemiological studies on residential fungal contamination and health conducted in Canada and The Netherlands. New methods for assessing fungal exposure are PCA analysis for the toxigenic mold Stachybotrys chartarum and EPS-Asp/Pen for detecting of Aspergillus and Penicillium in dust. Based on a limited data set it is shown that emission rates of fungal spores are inversely proportional to relative humidity (RH), directly related to flow rate and to surface loading. Poor maintenance, risk constructions and risk materials are described in several studies as the main causes of water damage in buildings.     

Fungi ingestion as an important factor influencing heavy metal intake in roe deer: evidence from faeces

In nature, animals have to cope with the fluctuating bioavailable metal pool in their habitat, which results in a seasonal variability of heavy metal levels in the animal body. Indeed, a pronounced summer-autumnal peak of heavy metals in roe deer (Capreolus capreolus L.) kidney was recently found in Slovenia. Considering the well-known hyperaccumulative ability of fungi, their ingestion was hypothesised to be one of the main reasons for the peak. Although fungi as a group are known to be a seasonally important food source for roe deer, data on their composition in the nutrition of the species have been lacking. To ascertain the importance of fungi ingestion on heavy metal intake in roe deer, we simultaneously studied fungal spores (by microscopic determination) and heavy metal levels (by inductively coupled plasma mass spectrometry and atomic absorption spectrometry) in roe deer faeces, collected in the period July-November 2001 at Veliki Vrh, the Salek Valley, Slovenia. Irrespective of species, fungal spores were present in 89% of faeces; the following genera were found to be consumed by roe deer: Lycoperdon, Calvatia, Hypholoma, Coprinus, Russula, Elaphomyces, Xerocomus, Enteloma, Amanita, Cortinarius, Agaricus, Inocybe, Boletus, Macrolepiota, Suillus and Pluteus. While the importance of fungi ingestion on the seasonal variability of other metals is less clear, it doubtless influences Hg intake in roe deer, which is confirmed by: (a) the high frequency of fungi in roe deer nutrition; (b) their hyperaccumulative ability; (c) the temporal distribution of Hg in roe deer faeces; (d) differences among three classes of faeces established on the basis of the frequency of spores present; (e) the correlation between the number of fungal genera present and Hg levels in faeces. Therefore, the influence of fungi ingestion has to be taken into consideration in assessing the hazard due to the accumulation of mercury along the food-chain.     

Fungal spore source strength tester: laboratory evaluation of a new concept

The airborne fungal spore concentration measured with air samplers during specific time intervals does not always adequately represent the maximum spore concentration levels, because of the sporadic nature of spore release. Hence, a reliable method is needed to directly assess the indoor fungal sources with respect to their spore aerosolization potential. In this study, the newly developed fungal spore source strength tester (FSSST), which aerosolizes spores from growth surfaces and samples the airborne fungi into a bioaerosol sampler, was evaluated in the laboratory. The FSSST's operational flow rates of 30 and 12.5 l/min were tested. The fungal spores released from moldy surfaces were measured with an optical particle counter. Simultaneously, the spores were collected by a bioaerosol sampler: either with a 37-mm filter cassette or with the BioSampler. Three material types, ceiling tile, gypsum board and plastic sheet coated with agar, were tested after they were inoculated with the fungus Aspergillus versicolor. In addition, gypsum board naturally contaminated with various fungi (obtained from a mold-problem home) was tested in the laboratory using the FSSST. In all three laboratory-inoculated materials, the release rate of A. versicolor was found to be higher when the FSSST operated at 30 l/min than at 12.5 l/min. Nevertheless, even at 12.5 l/min the number of spores aerosolized from the source during 10 min was found sufficient to reflect the highest level of release that may occur in indoor environments. At 12.5 l/min, the release rate of A. versicolor during the first 10-min period was (23.9 +/- 17.7)x10(4) cm(-2) for ceiling tile, (1.3 +/- 0.3)x10(4) cm(-2) for gypsum board and (0.13 +/- 0.08)x10(4) cm(-2) for agar surface (based on the samples collected with the BioSampler). The spore release rate was higher during the first 10 min than during the second 10 min of the FSSST application. It was observed that the particles aerosolized from the A. versicolor culture included spore aggregates and single spores, as well as mycelial fragments. Overall, 0.6 +/- 0.3% of spores detected on 1 cm2 of ceiling tile inoculated with A. versicolor were aerosolized during the 10-min source testing. The respective number was 9.2 +/- 1.0% for the laboratory-inoculated gypsum board, 0.002 +/- 0.001% for the laboratory-inoculated plastic covered with agar and 1.8 +/- 0.2% for naturally contaminated gypsum board. Our data suggest that the FSSST provides very favorable conditions for the spore aerosolization and thus can be used in the field to assess the maximum potential spore release from a fungal source.     

Quantitative profiling of built environment bacterial and fungal communities reveals dynamic material dependent growth patterns and microbial interactions

Indoor microbial communities vary in composition and diversity depending on material type, moisture levels, and occupancy. In this study, we integrated bacterial cell counting, fungal biomass estimation, and fluorescence-assisted cell sorting (FACS) with amplicon sequencing of bacterial (16S rRNA) and fungal (ITS) communities to investigate the influence of wetting on medium density fiberboard (MDF) and gypsum wallboard. Surface samples were collected longitudinally from wetted materials maintained at high relative humidity (~95%). Bacterial and fungal growth patterns were strongly time-dependent and material-specific. Fungal growth phenotypes differed between materials: spores dominated MDF surfaces while fungi transitioned from spores to hyphae on gypsum. FACS confirmed that most of the bacterial cells were intact (viable) on both materials over the course of the study. Integrated cell count and biomass data (quantitative profiling) revealed that small changes in relative abundance often resulted from large changes in absolute abundance, while negative correlations in relative abundances were explained by rapid growth of only one group of bacteria or fungi. Comparisons of bacterial-bacterial and fungal-bacterial networks suggested a top-down control of fungi on bacterial growth, possibly via antibiotic production. In conclusion, quantitative profiling provides novel insights into microbial growth dynamics on building materials with potential implications for human health.     

Effect of relative humidity on the aerosolization and total inflammatory potential of fungal particles from dust‐inoculated gypsum boards

The aim of this study was to investigate the effect of relative humidity (RH) on the aerosolization and total inflammatory potential (TIP) of microbial particles released from gypsum boards inoculated with dust samples from homes. After microbial colonization, the gypsum boards were incubated at either high or low RH. The aerosolized particles (0.54–19.8 μm), culturable fungi, β‐glucan and the TIP of the aerosolized particles were quantified. Despite the colonization of several fungal groups, Penicillium dominated the aerosolized fraction. Higher emission rates of particles and culturable fungi were found from low RH compared with high RH in both the inhalable and particulate matter <1 μm (PM₁) fractions, and the TIP was accordingly higher. However, for the aerosolized fractions, the TIP or concentration β‐glucan relative to the number of fungi or particles present was higher from high RH compared with low RH. Despite the low number of culturable fungi in PM₁, this fraction showed a high TIP, and the concentration of β‐glucan correlated strongly with the TIP of this fraction. The individual particles of the aerosolized PM₁ fraction were more inflammatory than the larger particles of the inhalable fraction, and β‐glucan may be an important contributor to the inflammatory potential of the aerosolized particles.     

Airborne fungal volatile organic compounds in rural and urban dwellings: detection of mould contamination in 94 homes determined by visual inspection and airborne fungal volatile organic compounds method

Moulds can both degrade the materials and structures they colonise and contribute to the appearance of symptoms and diseases in the inhabitants of contaminated dwellings. Only few data have compared the levels of contamination in urban and rural environments and the results are not consistent. The aim of this study was to use a fungal contamination index, based on the detection of specific Microbial Volatile Organic Compounds (MVOC), to determine the exposure to moulds of individuals living in urban and rural dwellings. For this purpose, 94 dwellings (47 in an urban setting in Clermont-Ferrand and 47 in rural areas of the Auvergne region, France) were studied.By demonstrating marked disparities between the proportion of visible contamination (19%) and that of active, visible and/or hidden contamination (59%) and the fact that almost all visible contamination was identified by MVOC, we were able to show that use of the index seemed relevant to confirm the actual presence of fungal contamination in a dwelling. Furthermore, it was possible to demonstrate a relationship between moulds and the presence of water on surfaces (condensation, infiltrations, water damage, etc.). A higher proportion of positive fungal contamination index in rural homes was observed compared to the proportion in urban ones (68% versus 49%; p < 0.05).     

Assessment of airborne bacteria and fungi in food courts

A study was undertaken to determine the effect of variations in temperature, relative humidity, occupancy density and location (indoor/outdoor) on the concentrations of viable airborne bacterial and fungal spores at an air-conditioned and a non air-conditioned food stall in Singapore. Typically, bioaerosols consisted of 50.5% bacteria and 49.5% fungi in the indoor environment. In contrast, for the outdoor environment, bacteria on an average only accounted for 20.6% of culturable airborne microorganisms whereas fungal concentrations were 79.4%. Results on bioaerosol size distributions revealed that 67% of indoor bacteria and 68% of outdoor bacteria, 85% of indoor fungi and 68% of outdoor fungi were associated with fine mode particulates (<3.3 μm). Occupant density was the key factor that affected indoor airborne bacteria concentrations while concentrations of outdoor airborne bacteria depended strongly on ambient temperature. Indoor fungal concentration was positively correlated to relative humidity whereas outdoor fungal concentration was positively correlated to relative humidity and negatively correlated to temperature. The study also compared the biological air quality between a non air-conditioned food stall (Stall A) and an air-conditioned food stall (Stall B). The dining area of the former had lower bacterial concentrations as compared to the latter, while fungal spore’s concentrations showed a reverse trend. The dominant airborne bacteria genera were Staphylococcus, Pseudomonas, Alcaligens, and Corynebacterium whereas Penicillium, Aspergillus and Cladosporium were the most common fungal genera and groups in both food stalls.     

Evaluation of a procedure to isolate culturable microorganisms from carpet dust

Details of a method to isolate culturable bacteria and fungi from carpet dust were evaluated to isolate the greatest numbers of these agents. Four broad groups were evaluated: mesophilic and thermophilic bacteria and moderately hydrophilic and xerophilic fungi. Features studied included: 1) mixing time; 2) addition of glass beads; 3) length of time dust settled before suspensions were plated; 4) relative concentrations of microorganisms in the fibrous and fine dust fractions; and 5) storage temperature and period. The findings are preliminary because of the small number of samples, but a votexing time of at least 2 min with glass beads gave the best results in terms of the highest estimate of the concentration of culturable bacteria or fungi. Microorganisms were retrievable-from the upper portion of a suspending liquid for at least 30 min with little detectable change in concentration. Both bacteria and fungi were more abundant in the fine than the fibrous dust fraction. No significant losses were observed for samples stored up to 25 days at 5 degrees C or 25 degrees C. This procedure optimized measurement of total concentration, but may not identify the range of genera and species in dust if microorganisms present in small numbers and as single units are underrepresented relative to those in clusters and aggregates.     

Culturable and Total Fungi in Dust Accumulated in Air Ducts in Single-Family Houses

Abstract Fungal spore content in dust accumulated in air ducts was investigated in 24 mechanically ventilated single-family houses of which 15 had also a central air heating system. Dust was collected from the ducts simultaneously with cleaning of the ventilation systems. Besides spore concentrations and flora of culturable fungi, total fungal spore concentrations were determined in dust samples by the aqueous two-phase technique and spore counting with epifluorescence microscopy. Culturable spore concentrations in the dust varied from 10⁴ to 10⁷ CFU/g and total spore concentrations from 107 to 108 spores/g. Total spore concentrations in the duct dust were significantly higher in the air heated houses than in the other mechanically ventilated houses. The difference resulted mainly from a higher proportion of recirculation air and a higher age of the air heated houses. Cladosporium, Penicillium, Aspergillus and yeasts consisted of >90% of fungal flora in the dust. Although total spore concentrations were at the same level both in the exhaust and in the supply ducts in both types of house, culturable fungal spore concentrations were slightly higher in the exhaust ducts than in the supply ducts. The proportion of culturable spores was <5% of total spores in dust accumulated in the ducts.     

Air sampling results in relation to extent of fungal colonization of building materials in some water-damaged buildings

We studied the extent and nature of fungal colonization of building materials in 58 naturally ventilated apartments that had suffered various kinds of water damage in relation to air sampling done before the physical inspections. The results of air samples from each apartment were compared by rank order of species with pooled data from outdoor air. Approximately 90% of the apartments that had significant amounts of fungi in wall cavities were identified by air sampling. There was no difference in the average fungal colony forming unit values per m3 between the 15 apartments with the most fungal contamination and the 15 with the least. In contrast, the prevalence of samples with fungal species significantly different than the pooled outdoor air between the more contaminated versus the less contaminated apartments was approximately 10-fold. We provide information on methods to document fungal contamination in buildings.     

Association between indoor mold and asthma among children in Buffalo, New York

Asthma is a leading chronic disease among children and places a significant burden on public health. Exposure to indoor mold has been associated with asthma symptoms. However, many mold assessments have relied on visual or other identification of damp conditions and mold presence, thus have not examined associations with specific fungal genera. The objective of this case-control study was to examine the relationship between airborne mold concentrations and asthma status among children and to identify the contribution from specific mold genera in air. Participants completed a questionnaire of home environmental conditions and underwent indoor air sampling in the home, from which viable and total-count fungal spores were quantified. The most prevalent fungi in the homes were the allergenic molds Cladosporium (98% and 87% of homes from viable and total count samples, respectively) and Penicillium (91% and 73%). There were no significant differences in mean fungal concentrations between the homes of cases and controls, although the observed rate of exposure to several molds was higher among the cases. Among children who lacked a family history of asthma, cases had significantly higher exposures to viable Aspergillus. Measured humidity levels in the home corresponded with some self-reported indicators of mold and dampness. PRACTICAL IMPLICATIONS: The results of this study support existing literature that indoor fungal exposures play a role in current asthma status and that some qualitative assessments of mold exposure correspond to fungi present in indoor air.