Department of Molecular, Cell and Systems Biology, University of California, Riverside, California, United States.
Am J Physiol Lung Cell Mol Physiol. 2024 Feb 1;326(2):L175-L189. doi: 10.1152/ajplung.00300.2022. Epub 2023 Dec 26.
Data on the relationship between electronic cigarettes (ECs) and SARS-CoV-2 infection are limited and contradictory. Our objectives were to investigate the impact of EC aerosols on SARS-CoV-2 infection of human bronchial epithelial cells and identify the causative chemical(s). Fully differentiated human bronchial epithelial tissues (hBETs) were exposed at the air-liquid interface (ALI) to aerosols produced from JUUL "Virginia Tobacco" and BLU ECs, as well as nicotine, propylene glycol (PG), vegetable glycerin (VG), and benzoic acid, and infection was then evaluated with SARS-CoV-2 pseudoparticles. Pseudoparticle infection of hBETs increased with aerosols produced from PG/VG, PG/VG plus nicotine, or BLU ECs; however, JUUL EC aerosols did not increase infection compared with controls. Increased infection in PG/VG alone was due to enhanced endocytosis, whereas increased infection in PG/VG plus nicotine or in BLU ECs was caused by nicotine-induced elevation of the aerosol's pH, which correlated with increased transmembrane protease, serine 2 (TMPRSS2) activity. Notably, benzoic acid in JUUL aerosols mitigated the enhanced infection caused by PG/VG or nicotine, offering protection that lasted for at least 48 h after exposure. In conclusion, the study demonstrates that EC aerosols can impact susceptibility to SARS-CoV-2 infection depending on their specific ingredients. PG/VG alone or PG/VG plus nicotine enhanced infection through different mechanisms, whereas benzoic acid in JUUL aerosols mitigated the increased infection caused by certain ingredients. These findings highlight the complex relationship between ECs and SARS-CoV-2 susceptibility, emphasizing the importance of considering the specific aerosol ingredients when evaluating the potential effects of ECs on infection risk. Data on the relationship between electronic cigarettes (ECs) and SARS-CoV-2 infection are limited and contradictory. We investigated the impact of EC aerosols and their ingredients on SARS-CoV-2 infection of human bronchial epithelial cells. Our data show that specific ingredients in EC aerosols impact the susceptibility to SARS-CoV-2 infection. Propylene glycol (PG)/vegetable glycerin (VG) alone or PG/VG plus nicotine enhanced infection through different mechanisms, whereas benzoic acid in JUUL aerosols mitigated the increased infection caused by these ingredients.
关于电子烟(ECs)与 SARS-CoV-2 感染之间的关系的数据有限且相互矛盾。我们的目的是研究 EC 气溶胶对人支气管上皮细胞 SARS-CoV-2 感染的影响,并确定致病化学物质。完全分化的人支气管上皮组织(hBET)在气液界面(ALI)暴露于 JUUL“弗吉尼亚烟草”和 BLU EC 产生的气溶胶,以及尼古丁、丙二醇(PG)、蔬菜甘油(VG)和苯甲酸,并随后用 SARS-CoV-2 假病毒评估感染情况。hBET 感染假病毒的数量随着 PG/VG、PG/VG 加尼古丁或 BLU EC 产生的气溶胶的增加而增加;然而,与对照相比,JUUL EC 气溶胶并未增加感染。PG/VG 单独增加感染归因于内吞作用增强,而 PG/VG 加尼古丁或 BLU EC 增加感染是由于尼古丁引起的气溶胶 pH 值升高,这与跨膜蛋白酶,丝氨酸 2(TMPRSS2)活性增加有关。值得注意的是,JUUL 气溶胶中的苯甲酸减轻了 PG/VG 或尼古丁引起的增强感染,提供了至少 48 小时的暴露后保护。总之,该研究表明,EC 气溶胶会根据其特定成分影响对 SARS-CoV-2 感染的易感性。PG/VG 单独或 PG/VG 加尼古丁通过不同的机制增强感染,而 JUUL 气溶胶中的苯甲酸减轻了某些成分引起的感染增加。这些发现强调了 EC 与 SARS-CoV-2 易感性之间复杂的关系,强调了在评估 EC 对感染风险的潜在影响时考虑特定气溶胶成分的重要性。