3D printers are increasingly run at home. Nanoparticle emissions from those printers have been reported, which raises the question whether adverse health effects from ultrafine particles (UFP) can be elicited by 3D printers. We exposed 26 healthy adults in a single-blinded, randomized, cross-over design to emissions of a desktop 3D printer using fused deposition modeling (FDM) for 1 hour (high UFP-emitting acrylonitrile butadiene styrene [ABS] vs low-emitting polylactic acid [PLA]). Before and after exposures, cytokines (IL-1β, IL-6, TNF-α, INF-γ) and ECP in nasal secretions, exhaled nitric oxide (FeNO), urinary 8-isoprostaglandin F (8-iso PGF ), and self-reported symptoms were assessed. The exposures had no significant differential effect on 8-iso PGF and nasal biomarkers. However, there was a difference (P < .05) in the time course of FeNO, with higher levels after ABS exposure. Moreover, indisposition and odor nuisance were increased for ABS exposure. These data suggest that 1 hour of exposure to 3D printer emissions had no acute effect on inflammatory markers in nasal secretions and urine. The slight relative increase in FeNO after ABS printing compared to PLA might be due to eosinophilic inflammation from inhaled UFP particles. This possibility should be investigated in further studies using additional biomarkers and longer observation periods.

cMany bacteria form surface-attached communities known as biofilms. Due to the extreme resistance of these bacterial biofilms to antibiotics and mechanical stresses, biofilms are of growing interest not only in microbiology but also in medicine and industry. Previous studies have determined the extracellular polymeric substances present in the matrix of biofilms formed by Bacillus subtilis NCIB 3610. However, studies on the physical properties of biofilms formed by this strain are just emerging. In particular, quantitative data on the contributions of biofilm matrix biopolymers to these physical properties are lacking. Here, we quantitatively investigated three physical properties of B. subtilis NCIB 3610 biofilms: the surface roughness and stiffness and the bulk viscoelasticity of these biofilms. We show how specific biomolecules constituting the biofilm matrix formed by this strain contribute to those biofilm properties. In particular, we demonstrate that the surface roughness and surface elasticity of 1-day-old NCIB 3610 biofilms are strongly affected by the surface layer protein BslA. For a second strain, B. subtilis B-1, which forms biofilms containing mainly ␥-polyglutamate, we found significantly different physical biofilm properties that are also differently affected by the commonly used antibacterial agent ethanol. We show that B-1 biofilms are protected from ethanol-induced changes in the biofilm's stiffness and that this protective effect can be transferred to NCIB 3610 biofilms by the sole addition of ␥-polyglutamate to growing NCIB 3610 biofilms. Together, our results demonstrate the importance of specific biofilm matrix components for the distinct physical properties of B. subtilis biofilms. Bacteria embed themselves with secreted biopolymers (1-3), building a community that is referred to as a biofilm. Such biofilms can be formed by a variety of Gram-positive as well as Gram-negative bacteria (4). The composition of the biofilm matrix is dependent on the biofilm-forming bacterium and environmental conditions such as shear forces experienced, temperature, and nutrient availability (5); the matrix can consist of different extracellular polymeric substances (EPSs), such as polysaccharides, proteins, lipids, and nucleic acids (6). Biofilms can grow on various surfaces (7-9). While Bacillus subtilis biofilms are formed on solid nutrient surfaces or at liquid-air interfaces (10, 11), other bacteria can produce biofilms on surfaces under water-saturated conditions (in liquid) (12). Due to their high mechanical stability (13,14) and their resistance to antibiotic or chemical treatment (15-18), such biofilms present significant problems in both industry and health care (19)(20)(21)(22). Although the compositions of many biofilm matrices are known, the biomolecular reason for the outstanding resistance of bacterial biofilms is not well understood. Only a few studies have investigated the influence of specific matrix components on the mechanical properties of biofilms (23, 24). The majority of recent studies...

We report here the draft genome sequence of the Bacillus subtilis strain B-1, a strain known to form biofilms. The biofilm matrix mainly consists of the biopolymer γ-polyglutamate (γ-PGA). The sequence of the genome of this strain allows the study of specific genes involved in biofilm formation.