Determinants of house dust,endotoxin, and β‐(1→3)‐D‐glucan in homes of Danish children

Little is known about the geographic variation and determinants of bacterial endotoxin and β ‐(1,3)‐d ‐glucan in Danish house dust. In a population of 317 children, we: (i) described loads and concentrations of floor dust, endotoxin, and β‐(1→3)‐d ‐glucan and (ii) their correlations and (iii) assessed their determinants; (iv) Finally, we compared our findings with previous European studies. Bedroom floor dust was analyzed for endotoxin content by the kinetic limulus amoebocyte lysate assay and for β‐(1→3)‐d ‐glucan by the inhibition enzyme immunoassay. The parents answered questions regarding potential determinants. We found: geometric means (geometric standard deviations) 186 mg/m² (4.3) for dust; 5.46 × 10³EU/m² (8.0) and 31.1 × 10³EU/g (2.6) for endotoxin; and 142 μg/m² (14.3) and 0.71 × 10³ μg/g (7.3) for β‐(1→3)‐d ‐glucan. High correlations (r > 0.75) were found between floor dust and endotoxin and β‐(1→3)‐d ‐glucan loads, while endotoxin and β‐(1→3)‐d ‐glucan concentrations were moderately correlated (r = 0.36–0.41) with the dust load. Having a carpet was positively associated with dust load and with endotoxin and β‐(1→3)‐d ‐glucan concentrations. Pet keeping, dwelling type, and dwelling location were determinants of endotoxin concentrations. No other determinants were associated with β‐(1→3)‐d ‐glucan concentrations. Compared with other European studies, we found lower β‐(1→3)‐d ‐glucan loads and concentrations but higher endotoxin loads and concentrations suggesting a geographically determined different composition of Danish floor dust compared with other European regions.     

Endotoxin and β(1→3)-Glucan in House Dust and the Relation with Home Characteristics: A Pilot Study in 25 German Houses

Abstract Residential microbial exposure has been suggested to be involved in the development of asthma. This paper describes bacterial endotoxin and mold β(1→3)-glucan levels in house dust and the relationship to selected home characteristics. Dust was sampled from mattresses and living room and bedroom floors of 25 houses in Germany. Endotoxin and β(1→3)-glucan levels ranged from 200-48,600 EU/g dust (100-32,900 EU/m² sampled surface) and 182-3,507 μg/g (157-3,652 μg/m²), respectively. Bio-contaminant levels were highest on living room floors and lowest in mattresses. Dust, endotoxin and β(1→3)-glucan levels were 2–3 times higher on living room floors of centrally heated houses built after 1970 compared to older individually heated houses. This was not found for mattresses and bedroom floors. No associations between biocontaminant levels and other selected home characteristics (temperature, relative humidity, damp spots and insulation of windows) were found. β(1→3)-glucan levels were associated with total culturable fungi (per m²) in house dust, as well as with the fungal genus Alternaria (per g dust and per m²). In conclusion endotoxin and β(1→3)-glucan were readily detectable in house dust and significantly associated with heating system and/or age of the home.     

Endotoxin,extracellular polysaccharides,and β(1‐3)‐glucan concentrations in dust and their determinants in four European birth cohorts: results from the HITEA project

Early‐life exposure to microbial agents may play a protective role in asthma and allergies development. Geographical differences in the prevalence of these diseases exist, but the differences in early‐life indoor microbial agent levels and their determinants have been hardly studied. We aimed to describe the early‐life levels of endotoxin, extracellular polysaccharides (EPS), and β(1‐3)‐glucans in living room dust of four geographically spread European birth cohorts (LISA in Germany, PIAMA in the Netherlands, INMA in Spain, and LUKAS2 in Finland) and to assess their determinants. A total of 1572 dust samples from living rooms of participants were analyzed for endotoxin, Penicillium/Aspergillus EPS, and β(1‐3)‐glucans. Information on potential determinants was obtained through questionnaires. Concentrations of endotoxin, EPS, and β(1‐3)‐glucans were different across cohorts. Concentrations of endotoxin and EPS were respectively lower and higher in INMA than in other cohorts, while glucans were higher in LUKAS2. Season of sampling, dog ownership, dampness, and the number of people living at home were significantly associated with concentrations of at least one microbial agent, with heterogeneity of effect estimates of the determinants across cohorts. In conclusion, both early‐life microbial exposure levels and exposure determinants differ across cohorts derived from diverse European countries.