Servicio de Microbiología, Hospital Universitario Ramón y Cajal, and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain.
Red Española de Investigación en Patología Infecciosa (REIPI), Madrid, Spain.
mBio. 2017 Sep 26;8(5):e00959-17. doi: 10.1128/mBio.00959-17.
Cystic fibrosis (CF) lung microbiota composition has recently been redefined by the application of next-generation sequencing (NGS) tools, identifying, among others, previously undescribed anaerobic and uncultivable bacteria. In the present study, we monitored the fluctuations of this ecosystem in 15 CF patients during a 1-year follow-up period, describing for the first time, as far as we know, the presence of predator bacteria in the CF lung microbiome. In addition, a new computational model was developed to ascertain the hypothetical ecological repercussions of a prey-predator interaction in CF lung microbial communities. Fifteen adult CF patients, stratified according to their pulmonary function into mild ( = 5), moderate ( = 9), and severe ( = 1) disease, were recruited at the CF unit of the Ramón y Cajal University Hospital (Madrid, Spain). Each patient contributed three or four induced sputum samples during a 1-year follow-up period. Lung microbiota composition was determined by both cultivation and NGS techniques and was compared with the patients' clinical variables. Results revealed a particular microbiota composition for each patient that was maintained during the study period, although some fluctuations were detected without any clinical correlation. For the first time, and predator bacteria were shown in CF lung microbiota and reduced-genome bacterial parasites of the phylum were also consistently detected. The newly designed computational model allows us to hypothesize that inoculation of predators into the pulmonary microbiome might contribute to the control of chronic colonization by CF pathogens in early colonization stages. The application of NGS to sequential samples of CF patients demonstrated the complexity of the organisms present in the lung (156 species) and the constancy of basic individual colonization patterns, although some differences between samples from the same patient were observed, probably related to sampling bias. and predator bacteria were found for the first time by NGS as part of the CF lung microbiota, although their ecological significance needs to be clarified. The newly designed computational model allows us to hypothesize that inoculation of predators into the lung microbiome can eradicate CF pathogens in early stages of the process. Our data strongly suggest that lower respiratory microbiome fluctuations are not necessarily related to the patient's clinical status.
囊性纤维化 (CF) 肺部微生物群落组成最近通过下一代测序 (NGS) 工具得到了重新定义,确定了以前未描述的厌氧和不可培养细菌。在本研究中,我们在 1 年的随访期间监测了 15 名 CF 患者的这个生态系统的波动,首次描述了 CF 肺部微生物组中捕食菌的存在。此外,还开发了一种新的计算模型,以确定 CF 肺部微生物群落中捕食者-猎物相互作用的假设生态影响。15 名成年 CF 患者根据肺功能分为轻度 ( = 5)、中度 ( = 9) 和重度 ( = 1) 疾病,在西班牙马德里 Ramón y Cajal 大学医院的 CF 病房招募。每位患者在 1 年的随访期间贡献了 3 或 4 个诱导痰样本。通过培养和 NGS 技术确定肺部微生物群落组成,并与患者的临床变量进行比较。结果显示,每个患者都有特定的微生物群落组成,在研究期间保持不变,尽管没有任何临床相关性的检测到一些波动。首次在 CF 肺部微生物组中显示出 和 捕食菌,并且还一致检测到了门的减少基因组细菌寄生虫。新设计的计算模型使我们能够假设将捕食者接种到肺部微生物组中可能有助于在早期定植阶段控制 CF 病原体的慢性定植。将 NGS 应用于 CF 患者的连续样本中,证明了存在于肺部的生物体的复杂性 (156 种),并且基本个体定植模式的恒定性,尽管观察到来自同一患者的样本之间存在一些差异,可能与采样偏差有关。首次通过 NGS 在 CF 肺部微生物组中发现 和 捕食菌,尽管它们的生态意义需要进一步澄清。新设计的计算模型使我们能够假设将捕食者接种到肺部微生物组中可以在该过程的早期阶段消灭 CF 病原体。我们的数据强烈表明,下呼吸道微生物组的波动不一定与患者的临床状况有关。