Department of Pulmonary Medicine, Miguel Servet University Hospital, CIBERES, Instituto de Investigación Sanitaria (ISS) Aragón, Zaragoza, Spain.
Department of Pulmonary Medicine, Miguel Servet University Hospital, CIBERES, Instituto de Investigación Sanitaria (ISS) Aragón, Zaragoza, Spain.
Arch Bronconeumol. 2021 Nov;57(11):681-689. doi: 10.1016/j.arbr.2020.05.017.
Dysbiosis in lung cancer has been underexplored. The aim of this study was to define the bacterial and fungal microbiota of the bronchi in central lung cancer and to compare it with that of the oral and intestinal compartments.
Twenty-five patients with central lung cancer and sixteen controls without antimicrobial intake during the previous month were recruited. Bacterial and fungal distribution was determined by massive sequencing of bronchial biopsies and saliva and faecal samples. Complex computational analysis was performed to define the core lung microbiota.
Affected and contralateral bronchi of patients have almost identical microbiota dominated by Streptococcus, whereas Pseudomonas was the dominant genera in controls. Oral and pulmonary ecosystems were significantly more similar in patients, probably due to microaspirations. Streptococcal abundance in the bronchi differentiated patients from controls according to a ROC curve analysis (90.9% sensitivity, 83.3% specificity, AUC=0.897). The saliva of patients characteristically showed a greater abundance of Streptococcus, Rothia, Gemella and Lactobacillus. The mycobiome of controls (Candida) was significantly different from that of patients (Malassezia). Cancer patients' bronchial mycobiome was similar to their saliva, but different from their contralateral bronchi.
The central lung cancer microbiome shows high levels of Streptococcus, and differs significantly in its composition from that of control subjects. Changes are not restricted to tumour tissue, and seem to be the consequence of microaspirations from the oral cavity. These findings could be useful in the screening and even diagnosis of this disease.
肺癌中的微生态失调尚未得到充分研究。本研究旨在确定中心型肺癌支气管内的细菌和真菌微生物群,并将其与口腔和肠道部位进行比较。
招募了 25 名患有中心型肺癌的患者和 16 名无抗菌药物摄入的对照者。通过对支气管活检、唾液和粪便样本进行大规模测序来确定细菌和真菌的分布。进行了复杂的计算分析以定义核心肺微生物群。
患者的患病和对照侧支气管具有几乎相同的微生物群,主要由链球菌主导,而铜绿假单胞菌是对照者的优势属。由于微吸入,口腔和肺部生态系统在患者中更为相似。根据 ROC 曲线分析,支气管中链球菌的丰度可将患者与对照者区分开(90.9%的敏感性,83.3%的特异性,AUC=0.897)。患者的唾液中特征性地表现出链球菌、罗特氏菌、金氏菌和乳杆菌丰度较高。对照者的真菌组(假丝酵母属)与患者的真菌组(马拉色菌属)明显不同。癌症患者的支气管真菌组与唾液相似,但与对侧支气管不同。
中心型肺癌微生物组显示高水平的链球菌,其组成与对照者有显著差异。变化不仅局限于肿瘤组织,似乎是口腔微吸入的结果。这些发现可能有助于该疾病的筛查甚至诊断。