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. 2022 Mar;13(1):9-16.
doi: 10.1016/j.shaw.2021.09.002. Epub 2021 Sep 29.

Bioaerosol Exposure and in vitro Activation of Toll-like Receptors in a Norwegian Waste Sorting Plant

Affiliations

Bioaerosol Exposure and in vitro Activation of Toll-like Receptors in a Norwegian Waste Sorting Plant

Elke Eriksen et al. Saf Health Work. 2022 Mar.

Abstract

Background: The global shift toward greener societies demands new technologies and work operations in the waste-management sector. However, progressive industrial methods do not necessarily consider workers' health. This study characterized workers' exposure to bioaerosols and investigated the bioaerosols' potential to engage the immune system in vitro.

Methods: Full shift personal aerosol sampling was conducted over three consecutive days. Dust load was analyzed by gravimetry, fungal and actinobacterial spores were analyzed by scanning electron microscopy, and endotoxin by limulus amebocyte lysate (LAL) assay. In vitro exposure of HEK cells to airborne dust samples was used to investigate the potential of inducing an inflammatory reaction.

Results: The total dust exposure level exceeded the recommended occupational exposure limit (OEL) of 5.0 mg/m3 in 3 out of 15 samples. The inhalable endotoxin level exceeded the recommended exposure level by a 7-fold, whereas the fungal spore level exceeded the recommended exposure level by an 11-fold. Actinobacterial spores were identified in 8 out of 14 samples. In vitro experiments revealed significant TLR2 activation in 9 out of 14 samples vs. significant TLR4 activation in all samples.

Conclusion: The present study showed that the dust samples contained potentially health-impairing endotoxin, fungi, and actinobacterial levels. Furthermore, the sampled dust contained microbial components capable of inducing TLR activation and thus have the potential to evoke an inflammatory response in exposed individuals.

Keywords: Bacteria; Dust; Fungi; Occupational exposure; Toll-Like Receptors; Waste Management.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Fig. 1
Fig. 1
Time per work operation. Monday: sample 1–5, Tuesday: sample 6–10, Wednesday: sample 11–15.
Fig. 2
Fig. 2
Comparison of bacterial and fungal DNA copies m−3 after ddPCR. Sample #3 was not available for DNA extraction.
Fig. 3
Fig. 3
Comparison of SEAP activity in HEK cells. HEK null: gray, TLR2: orange, TLR4: blue. Error-bars indicate standard deviation. Asterisk indicates significance levels: ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001.

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