Peptidoglycans in cutting fluids-a good indicator of bacterial contamination?

objective. The aim of this study was to estimate the content of peptidoglycans in cutting fluids (CFs) and to assess the possibility of using them as a marker of bacterial contamination in this type of occupational environment. materials and methods. A total of 11 samples of CFs were collected: 8 were taken from the working machine systems and 3 were unused CF samples. The peptidoglycans were determinated with the kinetic version of the Silkworm Larvae Plasma (SLP) test. results. The average concentration of bacteria was 5.58×10 5 CFU/mL, and peptidoglycans – 28.2 ng/mL. The variability for peptidoglycans concentration was less pronounced than that for bacteria (GSD 6 and 13.3, respectively). Taking into consideration the National Research and Safety Institute (INRS –[i] Institut National de Recherche et de Sécurité[/i]) limit value the concentrations of bacteria and peptidoglycans, as well as the usage of the fluids, the analysis showed that peptidoglycans reflect the differences between the studied factors much more accurately than bacteria. The correlation analysis, however, showed that the levels of peptidoglycans in the examined CFs strongly correlated with the concentrations of viable bacteria (R 2 = 0.50, p<0.05). conclusions. The study confirmed that the CFs may contain immunologically active substances of bacterial origin even though they did not show any bacterial growth. Moreover, it showed that the concentrations of peptidoglycans in CFs precisely reflect the exposure to bacteria, and as a structural component of the cell wall can be treated as their marker

Occupational exposure to airborne microorganisms, endotoxins and beta-glucans in poultry houses at different stages of the production cycle

The aim of the presented study was to assess the exposure of poultry workers to airborne microorganisms, endotoxins and β-glucans during different stages of the chicken production cycle in 3 commercially-operated poultry houses. Personal and stationary sampling was carried out to assess exposure to both viable and total microbial aerosols. The stationary measurements of PM10 were performed to establish the level of endotoxins and β-glucans. The concentrations of bacterial and fungal aerosols ranged from 2.5×102 CFU/m3 – 2.9×106 CFU/m3, and from 1.8×102 CFU/m3 – 1.8×105 CFU/m3, respectively. The number of culturable microorganisms was significantly lower than their total counts, constituting from 0.0004% – 6.4% of the total microbial flora. The level of PM10 in poultry facilities did not exceed 4.5 mg/m3. After the flock entered the clean house, the level of endotoxins and β-glucans increased from below detection limit to 8,364 ng/m3 and from 0.8 ng/m3 to 6,886 ng/m3, respectively. The presented study shows that professional activities in poultry farms are associated with constant exposure to bioaerosol, which may pose a health hazard to workers. It was found that workers’ exposure to airborne microorganisms increased with consecutive stages of the chicken production cycle

AIRBORNE TRANSPORT OF BACTERIAL SPORES AND FUNGAL CONIDIA ON NATURAL AND MAN-MADE FIBERS

Bacteria and fungi together with the structures and substances they produce may exert a harmful influence upon exposed individuals leading to numerous adverse health outcomes. As far as a transport of microbial agents on dust particles is relatively widely studied, a role of fibers as their carrier is not well recognized. Natural and man-made fibers’ structure and arrangement supporting such transport were described based on samples derived from both occupational and nonoccupational environments. The ability of fibers to convey microbial propagules loaded with different number of elementary charges in both dry and humid air was studied in newly built aerosolization chamber. The results showed that from 1g of fibers in natural state is possible to isolate up to 9×105 culturable microbes, including pathogens. Tested fibers (especially natural ones) were able to transport in the air up to 100 bacterial spores or fungal conidia per 1 fiber

Evaluation of the Survivability of Microorganisms Deposited on Filtering Respiratory Protective Devices under Varying Conditions of Humidity

Bioaerosols are common biological factors in work environments, which require routine use of filtering respiratory protective devices (FRPDs). Currently, no studies link humidity changes in the filter materials of such devices, during use, with microorganism survivability. Our aim was to determine the microclimate inside FRPDs, by simulating breathing, and to evaluate microorganism survivability under varying humidity conditions. Breathing was simulated using commercial filtering facepiece respirators in a model system. Polypropylene melt-blown nonwoven fabrics with moisture contents of 40%, 80%, and 200%, were used for assessment of microorganisms survivability. A modified AATCC 100-2004 method was used to measure the survivability of ATCC and NCAIM microorganisms: Escherichia coli, Staphylococcus aureus, Bacillus subtilis, Candida albicans and Aspergillus niger. During simulation relative humidity under the facepiece increased after 7 min of usage to 84%–92% and temperature increased to 29–30 °C. S. aureus survived the best on filter materials with 40%–200% moisture content. A decrease in survivability was observed for E. coli and C. albicans when mass humidity decreased. We found that B. subtilis and A. niger proliferated for 48–72 h of incubation and then died regardless of the moisture content. In conclusion, our tests showed that the survivability of microorganisms on filter materials depends on the amount of accumulated moisture and microorganism type

Impact of Mycotoxins Secreted by Aspergillus Molds on the Inflammatory Response of Human Corneal Epithelial Cells

Exposure to molds and mycotoxins not only contributes to the onset of respiratory disease, it also affects the ocular surface. Very few published studies concern the evaluation of the effect of mycotoxin exposure on ocular cells. The present study investigates the effects of aflatoxin B1 (AFB1) and gliotoxin, two mycotoxins secreted by Aspergillus molds, on the biological activity of the human corneal epithelial (HCE) cells. After 24, 48, and 72 h of exposure, cellular viability and inflammatory response were assessed. Both endpoint cell viability colorimetric assays and continuous cell impedance measurements, providing noninvasive real-time assessment of the effect on cells, were performed. Cytokine gene expression and interleukin-8 release were quantified. Gliotoxin appeared more cytotoxic than AFB1 but, at the same time, led to a lower increase of the inflammatory response reflecting its immunosuppressive properties. Real-time cell impedance measurement showed a distinct profile of cytotoxicity for both mycotoxins. HCE cells appeared to be a well-suited in vitro model to study ocular surface reactivity following biological contaminant exposure. Low, but persistent inflammation, caused by environmental factors, such as fungal toxins, leads to irritation and sensitization, and could be responsible for allergic manifestations which, in turn, could lead to mucosal hyper-reactivity

Microbiological Contamination at Workplaces in a Combined Heat and Power (CHP) Station Processing Plant Biomass

The aim of the study was to evaluate the microbial contamination at a plant biomass processing thermal power station (CHP). We found 2.42 × 103 CFU/m3 of bacteria and 1.37 × 104 CFU/m3 of fungi in the air; 2.30 × 107 CFU/g of bacteria and 4.46 × 105 CFU/g of fungi in the biomass; and 1.61 × 102 CFU/cm2 bacteria and 2.39 × 101 CFU/cm2 fungi in filtering facepiece respirators (FFRs). Using culture methods, we found 8 genera of mesophilic bacteria and 7 of fungi in the air; 10 genera each of bacteria and fungi in the biomass; and 2 and 5, respectively, on the FFRs. Metagenomic analysis (Illumina MiSeq) revealed the presence of 46 bacterial and 5 fungal genera on the FFRs, including potential pathogens Candida tropicalis, Escherichia coli, Prevotella sp., Aspergillus sp., Penicillium sp.). The ability of microorganisms to create a biofilm on the FFRs was confirmed using scanning electron microscopy (SEM). We also identified secondary metabolites in the biomass and FFRs, including fumigaclavines, quinocitrinines, sterigmatocistin, and 3-nitropropionic acid, which may be toxic to humans. Due to the presence of potential pathogens and mycotoxins, the level of microbiological contamination at workplaces in CHPs should be monitored