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吸烟者气道表面液体通过铁-乳铁蛋白失衡促进细菌生长和生物膜形成。

Airway surface liquid from smokers promotes bacterial growth and biofilm formation via iron-lactoferrin imbalance.

机构信息

Department of Internal Medicine, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, 6312 Pappajohn Biomedical Discovery Building. Newton Road, Iowa City, IA, 52242, USA.

Department of Chemistry, College of Liberal Arts & Sciences, University of Iowa, Iowa City, IA, USA.

出版信息

Respir Res. 2018 Mar 10;19(1):42. doi: 10.1186/s12931-018-0743-x.

Abstract

BACKGROUND

Smoking is a leading cause of respiratory infections worldwide. Tobacco particulate matter disrupts iron homeostasis in the lungs and increases the iron content in the airways of smokers. The airway epithelia secrete lactoferrin to quench iron required for bacteria to proliferate and cause lung infections. We hypothesized that smokers would have increased bacterial growth and biofilm formation via iron lactoferrin imbalance.

METHODS

We collected bronchoalveolar lavage (BAL) samples from non-smokers and smokers. We challenged these samples using a standard inoculum of Staphylococcus aureus and Pseudomonas aeruginosa and quantified bacterial growth and biofilm formation. We measured both iron and lactoferrin in the samples. We investigated the effect of supplementing non-smoker BAL with cigarette smoke extract (CSE) or ferric chloride and the effect of supplementing smoker BAL with lactoferrin on bacterial growth and biofilm formation.

RESULTS

BAL from smokers had increased bacterial growth and biofilm formation compared to non-smokers after both S. aureus and P. aeruginosa challenge. In addition, we found that samples from smokers had a higher iron to lactoferrin ratio. Supplementing the BAL of non-smokers with cigarette smoke extract and ferric chloride increased bacterial growth. Conversely, supplementing the BAL of smokers with lactoferrin had a concentration-dependent decrease in bacterial growth and biofilm formation.

CONCLUSION

Cigarette smoking produces factors which increase bacterial growth and biofilm formation in the BAL. We propose that smoking disrupts the iron-to-lactoferrin in the airways. This finding offers a new avenue for potential therapeutic interventions to prevent respiratory infections in smokers.

摘要

背景

吸烟是全球范围内导致呼吸道感染的主要原因。烟草颗粒物质会破坏肺部的铁稳态,并增加吸烟者气道中的铁含量。气道上皮细胞分泌乳铁蛋白以抑制细菌增殖和引起肺部感染所需的铁。我们假设吸烟者会因铁乳铁蛋白失衡而导致细菌生长和生物膜形成增加。

方法

我们从非吸烟者和吸烟者中收集支气管肺泡灌洗液 (BAL) 样本。我们使用金黄色葡萄球菌和铜绿假单胞菌的标准接种物挑战这些样本,并量化细菌生长和生物膜形成。我们测量了样本中的铁和乳铁蛋白。我们研究了向非吸烟者 BAL 中补充香烟烟雾提取物 (CSE) 或氯化铁以及向吸烟者 BAL 中补充乳铁蛋白对细菌生长和生物膜形成的影响。

结果

与非吸烟者相比,金黄色葡萄球菌和铜绿假单胞菌挑战后,吸烟者的 BAL 中细菌生长和生物膜形成增加。此外,我们发现吸烟者的样本中铁与乳铁蛋白的比例更高。向非吸烟者的 BAL 中补充香烟烟雾提取物和氯化铁会增加细菌生长。相反,向吸烟者的 BAL 中补充乳铁蛋白会导致细菌生长和生物膜形成呈浓度依赖性下降。

结论

吸烟会产生增加 BAL 中细菌生长和生物膜形成的因素。我们提出吸烟会破坏气道中的铁乳铁蛋白。这一发现为预防吸烟者呼吸道感染的潜在治疗干预提供了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c9f/5845328/78f3bb3fbaee/12931_2018_743_Fig1_HTML.jpg

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