Department of Medicine, Section of Pulmonary/Critical Care & Allergy/Immunology, Louisiana State University Health Sciences Center , New Orleans, Louisiana.
Department of Medicine, Division of Pulmonary Sciences & Critical Care, University of Colorado-Anschutz Medical Campus , Aurora, Colorado.
Am J Physiol Lung Cell Mol Physiol. 2018 Jan 1;314(1):L107-L117. doi: 10.1152/ajplung.00277.2017. Epub 2017 Aug 31.
Individuals with alcohol use disorders (AUDs) are at an increased risk of pneumonia and acute respiratory distress syndrome. Data of the lung microbiome in the setting of AUDs are lacking. The objective of this study was to determine the microbial biogeography of the upper and lower respiratory tract in individuals with AUDs compared with non-AUD subjects. Gargle, protected bronchial brush, and bronchoalveolar lavage specimens were collected during research bronchoscopies. Bacterial 16S gene sequencing and phylogenetic analysis was performed, and the alterations to the respiratory tract microbiota and changes in microbial biogeography were determined. The microbial structure of the upper and lower respiratory tract was significantly altered in subjects with AUDs compared with controls. Subjects with AUD have greater microbial diversity [ P < 0.0001, effect size = 16 ± 1.7 observed taxa] and changes in microbial species relative abundances. Furthermore, microbial communities in the upper and lower respiratory tract displayed greater similarity in subjects with AUDs. Alcohol use is associated with an altered composition of the respiratory tract microbiota. Subjects with AUDs demonstrate convergence of the microbial phylogeny and taxonomic communities between distinct biogeographical sites within the respiratory tract. These results support a mechanistic pathway potentially explaining the increased incidence of pneumonia and lung diseases in patients with AUDs.
患有酒精使用障碍(AUD)的个体患肺炎和急性呼吸窘迫综合征的风险增加。关于 AUD 患者肺部微生物组的数据尚缺乏。本研究的目的是确定 AUD 患者与非 AUD 受试者相比,上呼吸道和下呼吸道的微生物区系。在研究性支气管镜检查期间采集漱口液、保护支气管刷和支气管肺泡灌洗液标本。进行细菌 16S 基因测序和系统发育分析,并确定呼吸道微生物群的改变和微生物区系的变化。与对照组相比,AUD 患者的上呼吸道和下呼吸道的微生物结构明显改变。与对照组相比,AUD 患者的微生物多样性更高[P < 0.0001,效应量= 16 ± 1.7 个观察到的分类群],微生物物种相对丰度也发生了变化。此外,AUD 患者的上呼吸道和下呼吸道微生物群落之间的相似性更大。酒精使用与呼吸道微生物群落的组成改变有关。AUD 患者在呼吸道不同生境部位之间显示出微生物系统发育和分类群落的收敛。这些结果支持了一种潜在的机制途径,可能解释了 AUD 患者肺炎和肺部疾病发病率增加的原因。