Potential Implications of the Lung Microbiota in Patients with Chronic Obstruction Pulmonary Disease and Non-Small Cell Lung Cancer

• Published in: Frontiers in cellular and infection microbiology 2022-07, Vol.12, p.937864-937864
• Main Authors: He, Jia-Qi, Chen, Qin, Wu, Sheng-Jun, Wang, De-Qin, Zhang, Shen-Yingjie, Zhang, Song-Zhao, Chen, Rui-Lin, Wang, Jia-Feng, Wang, Zhen, Yu, Chen-Huan
• Format: Article
• Language: English
• Subjects: Cellular and Infection Microbiology; clinical trial; complication; COPD; lung dysbiosis; NSCLC
• ISSN: 2235-2988; 2235-2988
• DOI: 10.3389/fcimb.2022.937864

Recently, chronic obstructive pulmonary disease (COPD) has been considered as a common risk factor of non-small cell lung cancer (NSCLC). However, very few studies have been conducted on the effects of COPD on the lung microbiota in patients with NSCLC. To identify the lung microbiota in patients with COPD and NSCLC (CN), the microbiome of the induced sputa of 90 patients was analyzed using 16S rDNA sequencing. The results showed no significant differences in the bacterial diversities of induced sputa among patients with COPD, NSCLC, and CN and no intrinsic differences among patients with different pathological types of lung cancer. After surgical operation, the diversities of the induced sputa in patients with CN significantly decreased. More remarkably, both the microbial community phenotypes and the components of the induced sputa in patients with CN obviously differed from those in patients with COPD or NSCLC. The relative abundances of Streptococcus , Veillonella , Moraxella , and Actinomyces significantly decreased, but those of Neisseria and Acinetobacter significantly increased in patients with CN compared with those in patients with COPD or NSCLC alone, resulting in increased Gram-negative microbiota and, therefore, in potential pathogenicity and stress tolerance, as well as in enhancement of microbial glycolipid metabolism, amino acid metabolism, and oxidative stress. Although COPD did not affect the number of pulmonary flora species in patients with NSCLC, these significant alterations in the microbial populations, phenotypes, and functions of induced sputa due to COPD would contribute to inflammation-derived cancer progression in patients with CN.