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Title: Bacillus licheniformis in geogenic dust induces inflammation in respiratory epithelium

Journal Article · · Environmental Research
 [1];  [1]; ;  [1];  [2];  [3]
  1. Wesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, University of Western Australia, Perth, WA (Australia)
  2. School of Medicine, University of Tasmania, Hobart, Tasmania (Australia)
  3. Telethon Kids Institute, University of Western Australia, Perth, Western Australia (Australia)

Highlights: • Earth-derived geogenic dust exposure can lead to infections in the human airway. • Spore-forming Bacillus licheniformis is present in rural geogenic PM{sub 10.} • Heat-treating geogenic dust removes its stimulatory effects on airway epithelium. • High airway IL-6 and IL-8 levels are induced by live Bacillus licheniformis. • Bacillus licheniformis may exacerbate infections associated with dust exposure. Exposure to environmental geogenic (or earth-derived) dust can lead to more frequent and severe infections in the human airway. Particulate matter < 10 µm (PM{sub 10}) is the component of air pollution that is commonly associated with the exacerbation of respiratory diseases. We have previously demonstrated that mice exposed to geogenic dust PM{sub 10} experienced an exacerbation of inflammatory responses to influenza A virus. Whether geogenic dust PM{sub 10} also exacerbates respiratory bacterial infection is not yet known, nor are the components of the dust that drive these responses. We treated airway bronchial epithelial cells (NuLi-1) with UV-irradiated geogenic dust PM{sub 10} from six remote Western Australian towns. High levels of IL-6 and IL-8 production were observed, as well as persistent microbial growth. 16 S rRNA sequencing of the growth identified the microbe as Bacillus licheniformis, a spore-forming, environmentally abundant bacterium. We next investigated the interaction of B. licheniformis with respiratory epithelium in vitro to determine whether this exacerbated infection with a bacterial respiratory pathogen (non-typeable Haemophilus influenzae, NTHi). Heat treatment (100 °C) of all PM{sub 10} samples eliminated B. licheniformis contamination and reduced epithelial inflammatory responses, suggesting that heat-labile and/or microbial factors were involved in the host response to geogenic dust PM{sub 10}. We then exposed NuLi-1 epithelium to increasing doses of the isolated Bacillus licheniformis (multiplicity of infection of 10:1, 1:1 or 0.1:1 bacteria: cells) for 1, 3, and 24 h. B. licheniformis and NTHi infection (association and invasion) was assessed using a standard gentamicin survival assay, and epithelial release of IL-6 and IL-8 was measured using a bead based immunoassay. B. licheniformis was cytotoxic to NuLi-1 cells at 24 h. At 3 h post-challenge, B. licheniformis elicited high IL-6 and IL-8 inflammatory responses from NuLi-1 cells compared with cells treated with heat-treated geogenic dust PM{sub 10} (p < 0.0001). Whilst treatment of cells with B. licheniformis increased inflammation, this did not make the cells more susceptible to NTHi infection. This study highlights that geogenic dust PM{sub 10} can harbour viable bacterial spores that induce inflammation in respiratory epithelium. The impact on respiratory health from inhalation of bacterial spores in PM{sub 10} in arid environments may be underestimated. Further investigation into the contribution of B. licheniformis and the wider dust microbiome to respiratory infection is warranted.

OSTI ID:
23095646
Journal Information:
Environmental Research, Vol. 164; Other Information: Copyright (c) 2018 Elsevier Inc. All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0013-9351
Country of Publication:
United States
Language:
English