Institute for Infectious Diseases, University of Bern, , Bern, Switzerland.
Thorax. 2013 Dec;68(12):1150-6. doi: 10.1136/thoraxjnl-2012-202917. Epub 2013 Aug 14.
Molecular methods based on phylogenetic differences in the 16S rRNA gene are able to characterise the microbiota of the respiratory tract in health and disease.
Our goals were (1) to characterise bacterial communities in lower and upper airways of patients with interstitial lung disease (ILD) and (2) to compare the results with the microbiota of patients with Pneumocystis pneumonia (PCP) and normal controls.
We examined the upper and lower respiratory tract of 18 patients with ILD of whom 5, 6, and 7 had idiopathic interstitial pneumonia (IIP), non-IIP and sarcoidosis, respectively. In addition, six immune-compromised patients with PCP and nine healthy subjects were included as controls. Exclusion criteria were recent bacterial/viral respiratory tract infection, HIV-positivity and subjects receiving antibiotic therapy. Bronchoalveolar lavage fluid and oropharyngeal swabs were simultaneously collected, and microbiota was characterised by ultra-deep 16S rRNA gene sequencing.
The microbiota in lower airways of the majority of patients (30; 90%) primarily consisted of Prevotellaceae, Streptococcaceae and Acidaminococcaceae. α and β diversity measurements revealed no significant differences in airway microbiota composition between the five different groups of patients. Comparison of bacterial populations in upper and lower respiratory tract showed significant topographical discontinuities for 7 (23%) individuals.
IIP, non-IIP and sarcoidosis are not associated with disordered airway microbiota and a pathogenic role of commensals in the disease process is therefore unlikely. Nevertheless, molecular analysis of the topographical microbiota continuity along the respiratory tract may provide additional information to assist management of individual patients.
基于 16S rRNA 基因的系统发育差异的分子方法能够描述健康和疾病状态下呼吸道的微生物群落。
我们的目标是(1)描述特发性间质性肺病(ILD)患者下呼吸道和上呼吸道的细菌群落,(2)将结果与卡氏肺孢子菌肺炎(PCP)患者和正常对照者的微生物群进行比较。
我们检查了 18 名ILD 患者的上呼吸道和下呼吸道,其中 5、6 和 7 名患者分别患有特发性间质性肺炎(IIP)、非 IIP 和结节病。此外,还纳入了 6 名免疫功能低下的 PCP 患者和 9 名健康受试者作为对照。排除标准为近期细菌/病毒呼吸道感染、HIV 阳性和接受抗生素治疗的患者。同时采集支气管肺泡灌洗液和口咽拭子,通过超深度 16S rRNA 基因测序来描述微生物群。
大多数患者(30;90%)下呼吸道的微生物群主要由普雷沃氏菌科、链球菌科和氨基酸球菌科组成。α 和β多样性测量结果表明,五个不同患者组的气道微生物群组成无显著差异。上呼吸道和下呼吸道细菌种群的比较显示,7 名患者(23%)存在明显的地域连续性差异。
IIP、非 IIP 和结节病与气道微生物群紊乱无关,因此共生菌在疾病过程中发挥致病作用的可能性不大。然而,对呼吸道沿线地域微生物群连续性的分子分析可能会提供额外的信息,以帮助管理个别患者。