Institute for Infectious Diseases, University of Bern, Bern, Switzerland.
Institute of Virology and Immunology, 3147 Mittelhäusern, Switzerland.
Microb Genom. 2020 Dec;6(12). doi: 10.1099/mgen.0.000485. Epub 2020 Dec 9.
Environmental factors, such as cigarette smoking or lung infections, may influence chronic obstructive pulmonary disease (COPD) progression by modifying the respiratory tract microbiome. However, whether the disease itself induces or maintains dysbiosis remains undefined. In this longitudinal study, we investigated the oropharyngeal microbiota composition and disease progression of mice (in cages of 5-10 mice per cage) before, during and up to 3 months after chronic cigarette smoke exposure or exposure to room air for 6 months. Cigarette smoke exposure induced pulmonary emphysema measurable at the end of exposure for 6 months, as well as 3 months following smoke exposure cessation. Using both classical culture methods and 16S rRNA sequencing, we observed that cigarette smoke exposure altered the relative composition of the oropharyngeal microbiota and reduced its diversity ( <0.001). More than 60 taxa were substantially reduced after 6 months of smoke exposure ( <0.001) However, oropharyngeal microbiota disordering was reversed 3 months after smoke exposure cessation and no significant difference was observed compared to age-matched control mice. The effects of lung infection with on established smoke-induced emphysema and on the oropharyngeal microbiota were also evaluated. Inoculation with induced lung damage and altered the microbiota composition for a longer time compared to control groups infected but not previously exposed to smoke (=0.01). Our data demonstrate effects of cigarette smoke and pneumococcus infection leading to altered microbiota and emphysema development. The reversal of the disordering of the microbiota composition, but not lung damage, following smoke exposure cessation and after clearance of infection suggest that changes in lung structure are not sufficient to sustain a disordered microbiota in mice. Whether changes in the airway microbiota contribute to inducing emphysema requires further investigation.
环境因素,如吸烟或肺部感染,可能通过改变呼吸道微生物组来影响慢性阻塞性肺疾病(COPD)的进展。然而,疾病本身是否诱导或维持了菌群失调仍未定义。在这项纵向研究中,我们在慢性吸烟暴露之前、期间和暴露结束后长达 3 个月时,研究了小鼠(每笼 5-10 只)的口咽微生物组组成和疾病进展。吸烟暴露在 6 个月的暴露结束时诱导了可测量的肺气肿,并在吸烟暴露停止后 3 个月也诱导了肺气肿。使用经典培养方法和 16S rRNA 测序,我们观察到吸烟暴露改变了口咽微生物组的相对组成并降低了其多样性(<0.001)。在 6 个月的吸烟暴露后,超过 60 个分类群的数量显著减少(<0.001)。然而,吸烟暴露停止 3 个月后,口咽微生物组紊乱得到逆转,与年龄匹配的对照小鼠相比无显著差异。还评估了肺炎链球菌感染对已建立的吸烟诱导的肺气肿和口咽微生物组的影响。与对照组相比,感染但未先前暴露于烟雾的小鼠 (=0.01)的肺部损伤和微生物组组成的改变时间更长。我们的数据表明,香烟烟雾和肺炎球菌感染的影响导致了微生物组的改变和肺气肿的发展。吸烟暴露停止后和感染清除后,微生物组组成紊乱的逆转,但肺部损伤没有逆转,这表明肺部结构的变化不足以维持小鼠的微生物组紊乱。气道微生物组的变化是否有助于诱导肺气肿,需要进一步研究。