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关于JUUL™电子烟烟雾和气溶胶成分如何影响人支气管上皮细胞感染新型冠状病毒的新见解

New Insights into How JUUL™ Electronic Cigarette Aerosols and Aerosol Constituents Affect SARS-CoV-2 Infection of Human Bronchial Epithelial Cells.

作者信息

Phandthong Rattapol, Wong Man, Song Ann, Martinez Teresa, Talbot Prue

机构信息

Department of Molecular, Cell and System Biology, University of California, Riverside, CA 92521, USA.

出版信息

bioRxiv. 2022 Aug 24:2022.08.23.505031. doi: 10.1101/2022.08.23.505031.

Abstract

BACKGROUND

The relationship between the use of tobacco products and SARS-CoV-2 infection is poorly understood and controversial. Most studies have been done with tobacco cigarettes, while few have examined the effect of electronic cigarettes (ECs) on SARS-CoV-2 infection. We tested the hypothesis that EC fluids and aerosols with high concentrations of nicotine promote SARS-COV-2 infection by increasing viral entry into human respiratory epithelial cells.

METHODS

Responses of BEAS-2B cells to authentic JUUL™ aerosols or their individual constituents (propylene glycol (PG)/vegetable glycerin (VG) and nicotine) were compared using three exposure platforms: submerged culture, air-liquid-interface (ALI) exposure in a cloud chamber, and ALI exposure in a Cultex® system, which produces authentic heated EC aerosols. SARS-CoV-2 infection machinery was assessed using immunohistochemistry and Western blotting. Specifically, the levels of the SARS-CoV-2 receptor ACE2 (angiotensin converting enzyme 2) and a spike modifying enzyme, TMPRSS2 (transmembrane serine protease 2), were evaluated. Following each exposure, lentivirus pseudoparticles with spike protein and a green-fluorescent reporter were used to test viral penetration and the susceptibility of BEAS-2B cells to infection.

RESULTS

Nicotine, EC fluids, and authentic JUUL™ aerosols increased both ACE2 levels and TMPRSS2 activity, which in turn increased viral particle entry into cells. While most data were in good agreement across the three exposure platforms, cells were more responsive to treatments when exposed at the ALI in the Cultex system, even though the exposures were brief and intermittent. In the Cultex system, PG/VG, PG/VG/nicotine, and JUUL™ aerosols significantly increased infection above clean air controls. However, both the PG/VG and JUUL™ treatments were significantly lower than nicotine/PG/VG. PG/VG increased infection only in the Cultex® system, which produces heated aerosol.

CONCLUSION

Our data are consistent with the conclusion that authentic JUUL™ aerosols or their individual constituents (nicotine or PG/VG) increase SARS-CoV-2 infection. The strong effect produced by nicotine was modulated in authentic JUUL aerosols, demonstrating the importance of studying mixtures and aerosols from actual EC products. These data support the idea that vaping increases the likelihood of contracting COVID-19.

摘要

背景

烟草制品的使用与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染之间的关系尚不清楚且存在争议。大多数研究针对的是香烟,而很少有研究考察电子烟对SARS-CoV-2感染的影响。我们检验了这样一个假设,即高浓度尼古丁的电子烟液和烟雾通过增加病毒进入人呼吸道上皮细胞的能力来促进SARS-CoV-2感染。

方法

使用三种暴露平台比较了BEAS-2B细胞对正品JUUL™烟雾或其单个成分(丙二醇(PG)/蔬菜甘油(VG)和尼古丁)的反应:浸没培养、在云雾室中的气液界面(ALI)暴露以及在Cultex®系统中的ALI暴露,该系统可产生正品加热电子烟烟雾。使用免疫组织化学和蛋白质印迹法评估SARS-CoV-2感染机制。具体而言,评估了SARS-CoV-2受体血管紧张素转换酶2(ACE2)和一种刺突修饰酶跨膜丝氨酸蛋白酶2(TMPRSS2)的水平。每次暴露后,使用带有刺突蛋白和绿色荧光报告基因的慢病毒假颗粒来测试病毒穿透情况以及BEAS-2B细胞对感染的易感性。

结果

尼古丁、电子烟液和正品JUUL™烟雾均增加了ACE2水平和TMPRSS2活性,进而增加了病毒颗粒进入细胞的能力。虽然在这三种暴露平台上的大多数数据吻合度良好,但在Cultex系统中进行ALI暴露时,细胞对处理的反应更明显,尽管暴露时间短暂且不连续。在Cultex系统中,PG/VG、PG/VG/尼古丁和JUUL™烟雾显著增加了感染率,高于清洁空气对照组。然而,PG/VG和JUUL™处理组均显著低于尼古丁/PG/VG组。PG/VG仅在产生加热烟雾的Cultex®系统中增加了感染率。

结论

我们的数据与以下结论一致,即正品JUUL™烟雾或其单个成分(尼古丁或PG/VG)会增加SARS-CoV-2感染。尼古丁产生的强烈作用在正品JUUL烟雾中受到调节,这表明研究实际电子烟产品的混合物和烟雾的重要性。这些数据支持了吸电子烟会增加感染2019冠状病毒病可能性的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ae/9435402/06930a17492f/nihpp-2022.08.23.505031v1-f0001.jpg

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