Does the air condition system in busses spread allergic fungi into driver space?

The aim of this study was to establish whether the air-conditioning system in buses constitutes an additional source of indoor air contamination with fungi, and whether or not the fungi concentration depends on the period from the last disinfection of the system, combined with replacement of the cabin dust particle filter. The air samples to fungi analysis using impact method were taken in 30 buses (20 with an air-conditioning system, ACS; 10 with a ventilation system, VS) in two series: 1 and 22 weeks after cabin filter replacement and disinfection of the air-conditioning system. During one test in each bus were taken two samples: before the air-conditioning or ventilation system switched on and 6 min after operating of these systems. The atmospheric air was the external background (EB). After 1 week of use of the system, the fungi concentrations before starting of the ACS and VS system were 527.8 and 1053.0 cfu/m3, respectively, and after 22 weeks the concentrations were 351.9 and 1069.6 cfu/m3, respectively. While in the sample after 6 min of ACS and VS system operating, the fungi concentration after 1 week of use was 127.6 and 233.7 cfu/m3, respectively, and after 22 weeks it was 113.3 and 324.9 cfu/m3, respectively. Results do not provide strong evidence that air-conditioning system is an additional source of indoor air contamination with fungi. A longer operation of the system promoted increase of fungi concentration in air-conditioned buses only.

The capability of fungi isolated from moldy dwellings to produce toxins.

OBJECTIVES: The main objective was analysis and assessment of toxinogenic capabilities of fungi isolated from moldy surfaces in residential rooms in an urban agglomeration situated far from flooded areas in moderate climate zone. MATERIAL AND METHODS: The assessment of environmental exposure to mycotoxins was carried out in samples collected from moldy surfaces in form of scrapings and airborne dust from 22 moldy dwellings in winter season. In each sample 2 mycotoxins were analyzed: sterigmatocystin and roquefortine C produced by Aspergillus versicolor and Penicillium chrysogenum, respectively. Mycotoxins were analyzed by high-performance liquid chromatography (HPLC) in: scrapings from moldy surfaces, mixture of all species of fungi cultured from scrapings on microbiological medium (malt extract agar), pure cultures of Aspergillus versicolor and Penicillium chrysogenum cultured from scrapings on microbiological medium; mycotoxins in the indoor air dust were also analyzed. RESULTS: The production of sterigmatocystin by individual strains of Aspergillus versicolor cultured on medium was confirmed for 8 of 13 isolated strains ranging 2.1-235.9 µg/g and production of roquefortine C by Penicillium chrysogenum for 4 of 10 strains ranging 12.9-27.6 µg/g. In 11 of 13 samples of the mixture of fungi cultured from scrapings, in which Aspergillus versicolor was found, sterigmatocystin production was at the level of 3.1-1683.2 µg/g, whereas in 3 of 10 samples in which Penicillium chrysogenum occurred, the production of roquefortine C was 0.9-618.9 µg/g. The analysis did not show in any of the tested air dust and scrapings samples the presence of analyzed mycotoxins in the amount exceeding the determination limit. CONCLUSIONS: The capability of synthesis of sterigmatocystin by Aspergillus versicolor and roquefortine C by Penicillium chrysogenum growing in mixtures of fungi from scrapings and pure cultures in laboratory conditions was confirmed. The absence of mycotoxins in scrapings and air dust samples indicates an insignificant inhalatory exposure to mycotoxins among inhabitants in moldy flats of urban agglomeration situated far from flooded territories. Int J Occup Med Environ Health 2016;29(5):823-836.

Visible fungi growth and dampness assessed using a questionnaire versus airborne fungi, (1→3)-ß-D-glucan and fungal spore concentrations in flats.

INTRODUCTION: The study aimed at determination of the usefulness of the subjective assessment of selected signs of fungi growth in flats and microclimate parameters to indicate the actual air contamination with culturable fungi, (1→3)-ß-D-glucans and fungal spores. MATERIAL AND METHODS: This analysis covered 22 flats, the inhabitants of which declared in a questionnaire interview the presence of the developed mycelium on solid surfaces in the flat. Air samples for determination of the culturable fungi, (1→3)-ß-D-glucans and (viable and non-viable) fungal spores concentrations indoor and outdoor the flats during the heating period were collected. During bioaerosol sampling microclimate parameters were measured. Predictive models for concentrations of the tested biological agents with regard to various ways to assess fungal contamination of air in a flat (on the basis of a questionnaire or a questionnaire and microclimate measurements) were built. RESULTS: The arithmetic means of temperature, relative humidity, CO2 concentration and air flow velocity in the flats were respectively: 20.5°C, 53%, 1431.6 ppm and 0 m/s. The geometric mean concentrations of airborne fungi, (1→3)-ß-D-glucans and fungal spores in these premises amounted to 2.9×102 cfu/m3, 1.6 ng/m3 and 5.7×103 spores/m3, respectively. The subjective assessment of fungi growth signs and microclimate characteristics were moderately useful for evaluation of the actual airborne fungi and (1→3)-ß-D-glucan concentrations (maximum percent of explained variance (VE) = 61% and 67%, respectively), and less useful in evaluation of the actual fungal spore concentrations (VE < 29%). In the case of fungi, higher usefulness was indicated of the questionnaire evaluation supported by microclimate measurements (VE = 61.2%), as compared to the evaluation only by means of a questionnaire (VE = 46.9%). CONCLUSIONS: Subjective evaluation of fungi growth signs in flats, separately or combined with microclimate measurements, appeared to be moderately useful for quantitative evaluation of the actual air contamination with fungi and their derivatives, but more extensive studies are needed to strengthen those findings.

Assessment of exposure to fungi in the heavily contaminated work environment (a solid waste sorting plant) based on the ergosterol analysis.

OBJECTIVES: This paper reports on the results of the study aimed at application of ergosterol as an quantitative indicator of fungal bioaerosol present in the indoor air in occupational environment heavily contaminated with organic dust as well as its comparison with the culturable method. MATERIAL AND METHODS: The study was conducted in the indoor solid waste sorting plant. Using Andersen impactor adapted to 1 plate at the flow rate of 30 l/min, indoor air was sampled in the workers' breathing zone. Ergosterol was sampled using gelatinous filter (1000 l of air) and then analyzed by means of the spectrophotometric method. Fungi were sampled on malt extract agar (MEA) medium (3 replications: 2 l, 7.5 l, 15 l of air) and analyzed by means of the culturable method. Based on ergosterol analyzes, concentration of fungi was calculated. Results were given as the range assuming min. as 5.1 pg ergosterol/spore and max as 1.7 pg ergosterol/spore. RESULTS: The average concentrations of ergosterol in a working room (arithmetic mean (AM), standard deviation (SD); minimum-maximum (min.-max)) were, respectively: 2.16, 0.72; 0.85-2.92 µg/m3; fungi calculated based on ergosterol - 424.1×103-1272.4×103, 140.1×103- 420.4×103, 167×103-1716.5×103 CFU/m3, and culturable fungi - 13×103, 9.7×103, 1.9×103-34×103 CFU/m3). It was revealed that concentrations of calculated fungi were even 2 orders of magnitude higher than culturable fungi. CONCLUSIONS: The quantitative assessment of moldiness by means of ergosterol measurement seems to be a reliable indicator for environments heavily contaminated with organic dust, where viable and non-viable fungi are present in high proportions. Based on that result, more restrictive (as compared to a similar assessment carried out by means of the culturable method) hygienic recommendations, especially those related to the use of preventive measures protecting the employees' respiratory tract, should have been undertaken.

Children's residential exposure to selected allergens and microbial indicators: endotoxins and (1→3)-ß-D-glucans.

OBJECTIVES: The study was aimed at assessment of exposure to endotoxins, (1→3)-ß-D-glucans and mite, cockroach, cat, dog allergens present in settled dust in premises of children as agents which may be significantly correlated with the occurrence of allergic symptoms and diseases in children. MATERIALS AND METHODS: The study covered 50 homes of one-or two-year-old children in Poland. Samples of settled dust were taken from the floor and the child's bed. The levels of (1→3)-ß-D-glucans (floor), endotoxins (floor) and allergens of mite, cat, dog and cockroach (floor and bed) were analyzed. RESULTS: Average geometric concentrations (geometric standard deviation) of endotoxins, (1→3)-ß-D-glucans, Der p1, Fel d1, Can f1 and Bla g1 in children homes were on the floor 42 166.0 EU/g (3.2), 20 478.4 ng/g (2.38), 93.9 ng/g (6.58), 119.8 ng/g (13.0), 288.9 ng/g (3.4), 0.72 U/g (4.4) and in their beds (only allergens) 597.8 ng/g (14.2), 54.1 ng/g (4.4), 158.6 ng/g (3.1) 0.6 U/g (2.9), respectively. When the floor was covered with the carpet, higher concentrations of endotoxins, (1→3)-ß-D-glucans and allergens (each type) were found in the settled dust (p < 0.05). The trend was opposite in case of allergens (except dog) analyzed from bed dust and significantly higher concentrations were found in the rooms with smooth floor (p < 0.05). CONCLUSIONS: Among the analyzed factors only the type of floor significantly modified both the level of biological indicators and allergens. The results of this study could be the base for verifying a hypothesis that carpeting may have a protective role against high levels of cockroach, dog and cat allergens.

[Biological contamination in office buildings related to ventilation/air conditioning system]. / Czynniki biologiczne wplywajace na jakosc powietrza w pomieszczeniach biurowych.

BACKGROUND: Indoor air is contaminated with microorganisms coming from both the atmospheric air and sources present in premises. The aim of this study was to analyze the concentrations of biological agents in office buildings, dependending on ventilation/air conditioning system and season. MATERIALS AND METHODS: The study covered office buildings (different in the system of ventila-tion/air conditioning). Air samples for assessing the levels of inhalable dust, endotoxins and (1-->3)-beta-D-glucans, were taken at the selected stationary points of each building during summer and winter. The air was sampled for 6 h, using portable sets consisting of the GilAir 5 pump and the head filled with a filter of fiber glass. The samples for the presence of airborne bacteria and fungi were collected twice during the day using the impaction method. RESULTS: Average concentrations of inhalable dust, bacteria, fungi, endotoxins and (1-->3)-beta-D-glucans in office premises were 0.09 mg/m3, 6.00 x 10(2) cfu/m3, 4.59 x 10(1) cfu/m3, 0.42 ng/m3 and 3.91 ng/m3, respectively. Higher concentrations of the investigated agents were found in summer. In premises with air conditioning concentrations of airborne fungi, (1-->3)-beta-D-glucans and inhalable dust were significantly lower in winter. In summer the trend was reverse except for (1-->3)-beta-D-glucans. CONCLUSIONS: Concentrations of biological agents were affected by the season and the presence of air conditioning. Concentrations of inhalable dust, bacteria, fungi, endotoxins and (1-->3)-beta-D-glucans, observed inside the office buildings, were significantly higher in summer than in winter. The presence of the air conditioning system modified in various ways the levels of biological agents. Its influence was greater on the concentration of fungi and (1-->3)-beta-D-glucans than on that of bacteria and endotoxins.

Fungal aerosol in the process of poultry breeding--quantitative and qualitative analysis.

BACKGROUND: The aim of this study was to assess fungal air contamination in the processes associated with poultry breeding depending on the season. The evaluation was based on the determined concentrations of fungi and qualitative identification of isolated microorganisms. MATERIALS AND METHODS: The study covered 2 hatcheries and 3 hen buildings. The air was sampled in spring, summer and autumn directly onto a filter using air aspirator. For the quantitative analysis of fungi, the medium MEA with chloramphenicol and streptomycin was used. The qualitative identification of fungi was carried out based on macro- and microscopic analysis. RESULTS: The concentrations of total airborne mesophilic fungi in breeding facilities ranged from 1.22 x 10(3) to 5.87 x 10(5) cfu/m3 with the arithmetic mean value 1.60 x 10(5) cfu/m5. In 45% of the taken samples, these levels exceeded the reference value recommended in Poland for occupational environment exposure. The fungi concentration in the air of poultry houses was significantly modified by season (p = 0.04). A higher concentration of fungi occurred in autumn (p = 0.05). The dominant fungal microflora in the air was composed of molds (88%), with the most prevalent genus Acremonium. Yeasts constituted another 10% of bioaerosol and were mainly represented by genus Candida. The fungal aerosol contained two species qualified to the 2 group of risk--Aspergillus fumigatus and Candida tropicalis. CONCLUSIONS: Facilities of poultry farms are contaminated with high concentrations of fungal aerosols, especially in a colder season, often exceeding the recommended limits. Among the fungi, there are also present pathogenic microorganisms that may pose a risk to farm workers' health.

[Exposure to bioaerosols among CAFO workers (swine feeding)]. / Ocena narazenia na bioaerozole pracowników zatrudnionych przy intensywnej hodowli trzody chlewnej.

BACKGROUND: In this paper the exposure assessment to airborne biohazards (organic dust, microorganisms, endotoxins and ((1 --> 3)-beta-D-glucans) as well as to ammonia and hydrogen sulfide among CAFO (swine farms) workers is presented. MATERIALS AND METHODS: Occupational exposure assessment was carried out on 30 swine farms. Personal dosimetry was carried out among 90 swine farm workers to assess the exposure to organic dust, endotoxins and glucans. Concentrations of ammonia and hydrogen sulfide were measured using Draeger pipes. Endotoxins were assayed with the LAL test in a kinetic, chromogenic version and ((1 --> 3)-beta-D-glucans with the Glucatell test in a kinetic version. RESULTS: Concentrations of inhalable dust ranged from 0.16 to 37.2 mg/m3, with AM = 3.65 mg/m3, whereas AM for respirable fraction was 0.39 mg/m3 with the range from zero to 4.28 mg/m3. Mean concentration of culturable bacteria was 4.79 x 10 (5) jtk/m3, and fungi concentration was ten times lower - 1.55 x 10(4) jtk/m3. Exposure to endotoxins with high degree of differentiation ranged from 95 to 147 885 EU/m3 in inhalable and from 5.5 to 18 708 EU/m3 in respirable fractions. Glucan concentrations ranged from 6 to > 5200 ng/m3 in unhalable and from 1 to 800 ng/m3 in respirable fraction. Ammonia concentrations in the workplace air ranged from 1.78 mg/m3 (2.50 ppm) to 30.1 mg/m3 (42.4 ppm). Hydrogen sulfide did not exceed the level of 4.1 mg/m3. CONCLUSION: Work conditions found in CAFOs may induce adverse effects on workers' respiratory system and should be considered as an important harmful agent. The protection of workers respiratory airways should be recommended.

[Waste sorting plants--recognition of exposure to biological agents (moulds)]. / Sortownia odpadów komunalnych--rozpoznanie narazenia na czynniki biologiczne (grzyby strzepkowe).

BACKGROUND: The aim of the study was to recognize exposure to biological agents in the air of waste sorting plants. This publication contains the characteristics of technical solutions in use during sorting of waste and the results of quantitative analysis in terms of the presence of moulds and inhalable dust in the air. MATERIAL AND METHODS: The study was conducted in the summertime inside two waste sorting plants with different production capacity ("big" and "small"). To evaluate inhalable dust in the air, 53 samples were collected using personal samplers on glass fiber filters. To assess mycological contamination of the air, 30 triple samples were directly collected on Petri dishes (Malt Extract Agar medium), using the volumetric impact method in the worker's respiratory zone. Samples were incubated for 5 days at 30 degrees C. Outcomes of the total number of moulds were provided in cfu/m3 (cfu--colony forming units). RESULTS: The mean concentration of inhalable dust, determined in the "big" waste sorting plant, was 2.38 mg/m3 and in the "small" plant 1.12 mg/m3. The quantitative analysis revealed the following values of the total number of moulds present in the air: 1) "big" waste sorting plant, 2.9 x 10(4) cfu/m3 (work premises) and 3.6 x 10(3) jtk/m3 (office premises); 2) "small" waste sorting plant, 7.8 x 10(4) cfu/m3 (work premises) and 2.5 x 10(3) jtk/m3 (office premises). CONCLUSIONS: Mould concentrations determined in the environment of waste sorting plants were high. To protect health of workers in this kind of plants, preventive programs focused on the protection of the skin and respiratory system should be implemented. Offices should be properly isolated from work premises to minimize spreading of inhalable dust.

[Assessment of occupational exposure to fungal aerosols in wastewater treatment plants]. / Ocena zawodowej ekspozycji na aerozole grzybowe w oczyszczalniach scieków.

BACKGROUND: The quantitative assessment and qualitative identification of moulds at workplaces in wastewater treatment plants were the aim of the study. MATERIALS AND METHODS: The study was carried out in four wastewater treatment plants, where 15 stationary points were selected according to mechanical, biological and sewage sludge treatment processes. In addition, background level samples from the city area were also collected. Bioaerosols were sampled with use of a Burkard Aerosol Sampler and directly put on Malt Extract Agar plates. Identification of moulds was based on morphological properties described in the professional literature. RESULTS: The identified concentrations of moulds were low and ranged between 0.11 and 16.75 x 10(2) cfu/m3. The highest mean levels of fungal microflora were found during sewage sludge treatment processes. In total, there were 65 fungal isolates, of which 80% were found in wastewater treatment plants. In bioaerosol samples of the occupational origin, the highest (40%) amount of isolates originated from sewage sludge treatment processes and the lowest (25%) from biological treatment stages. In wastewater treatment plants, moulds of Aspergillus genus predominated and represented nearly 35% of all identified fungi. Comparing to background levels, the content of this genus was almost 4.5 times higher. Pathogenic Aspergillus fumigatus was found at all stages of wastewater treatment and Trichophyton genus at the stage of mechanical treatment. Moreover, there were numerous moulds of Mucor, Penicillium and Alternaria genera. In background samples moulds of Penicillium genus predominated and no pathogenic species were found. CONCLUSIONS: The obtained results reveal that the sewage sludge is the main source of mould emission into the air at workplaces in wastewater treatment plants. On account of the presence of moulds with the evidenced infectious and allergic activity it is suggested that personal protective equipment should be used by employees.

[Occupational exposure to mesophilic microorganisms associated with commercial processing of compost for mushroom production]. / Ocena ekspozycji zawodowej na drobnoustroje mezofilne podczas prac zwiazanych z produkcja podloza do przemyslowej uprawy grzybów.

BACKGROUND: The aim of the study was to assess the occupational exposure to mesophilic microorganisms associated with commercial processing of compost for mushroom production. MATERIALS AND METHODS: The air samples for microbiological analysis were collected directly on Petri dishes with Malt Extract Agar medium using Burkard Air Sampler. The quantitative and qualitative identification of mesophilic bacteria and mesophilic fungi were performed using the standard microbiological procedures. RESULTS: Considerable variation in exposure to bioaerosols within the sectors of compost production were observed. The highest level of mesophilic bacteria in the air (4.17 x 10(4) cfu/m3) was measured during the mixing of raw materials with water and loading of the final compost piles to the pasteurization tunnels (3.54 x 10(4) cfu/m3). The highest concentration of mesophilic fungi was found in the air samples collected during the manual unrolling of straw (1.62 x 10(4) cfu/m3) and dosing of mycelium to the compost (1.15 x 10(4) cfu/m3). Among 33 identified bacteria and fungi species, Pasteurella sp, Proteus mirabilis, Streptomyces sp, Corynebacterium sp and Aspergillusfumigatus create the potential risk for health of exposed workers. CONCLUSIONS: The presence of microorganisms found in the air creats the potential risk for human health, therefore the use of personal equipment, protecting the respiratory tract and skin of exposed workers is strongly recommended.