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High-Resolution Longitudinal Dynamics of the Cystic Fibrosis Sputum Microbiome and Metabolome through Antibiotic Therapy

机译:通过抗生素疗法囊性纤维化痰微生物微生物和代谢物的高分辨率纵向动态

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Microbial diversity in the cystic fibrosis (CF) lung decreases over decades as pathogenic bacteria such as Pseudomonas aeruginosa take over. The dynamics of the CF microbiome and metabolome over shorter time frames, however, remain poorly studied. Here, we analyze paired microbiome and metabolome data from 594 sputum samples collected over 401?days from six adult CF subjects (subject mean?=?179?days) through periods of clinical stability and 11 CF pulmonary exacerbations (CFPE). While microbiome profiles were personalized (permutational multivariate analysis of variance [PERMANOVA] r 2 ?=?0.79, P ? P ?=?0.002). This included periods where the microbiomes of different subjects became highly similar (UniFrac distance, n ?=?14?days) during the development of a CFPE (LME P ?=?0.0045 and P ?=?0.029, respectively). Collectively, comparing samples across disease states showed there was a reduction of these two measures during antibiotic treatment (LME P ?=?0.0096 and P ?=?0.014, respectively), but the stability data and CFPE data were not significantly different from each other. Metabolome alpha-diversity was higher during CFPE than during stability (LME P ?=?0.0085), but no consistent metabolite signatures of CFPE across subjects were identified. Virulence-associated metabolites from P. aeruginosa were temporally dynamic but were not associated with any disease state. One subject died during the collection period, enabling a detailed look at changes in the 194?days prior to death. This subject had over 90% Pseudomonas in the microbiome at the beginning of sampling, and that level gradually increased to over 99% prior to death. This study revealed that the CF microbiome and metabolome of some subjects are dynamic through time. Future work is needed to understand what drives these temporal dynamics and if reduction of anaerobes correlate to clinical response to CFPE therapy. IMPORTANCE Subjects with cystic fibrosis battle polymicrobial lung infections throughout their lifetime. Although antibiotic therapy is a principal treatment for CF lung disease, we have little understanding of how antibiotics affect the CF lung microbiome and metabolome and how much the community changes on daily timescales. By analyzing 594 longitudinal CF sputum samples from six adult subjects, we show that the sputum microbiome and metabolome are dynamic. Significant changes occur during times of stability and also through pulmonary exacerbations (CFPEs). Microbiome alpha-diversity increased as a CFPE developed and then decreased during treatment in a manner corresponding to the reduction in the log ratio of anaerobic bacteria to classic pathogens. Levels of metabolites from the pathogen P. aeruginosa were also highly variable through time and were negatively associated with anaerobes. The microbial dynamics observed in this study may have a significant impact on the outcome of antibiotic therapy for CFPEs and overall subject health.
机译:囊性纤维化(CF)肺部的微生物多样性几十年来作为致病菌细菌,例如假单胞菌铜绿假单胞菌。然而,CF微生物组和代谢物在较短的时间框架上的动态仍然很差。在这里,我们分析来自在401次以上的594个痰样品中分析成对的微生物组和代谢物数据,从六个成年CF受试者(受试者意味着?= 179./2天),通过临床稳定性和11cf肺癌(CFPE)。虽然微生物组简档是个性化的(偏转多元分析的差异[alplenova] r 2?=?0.79,p?p?= 0.002)。在开发CFPE期间(LME P?= 0.0045和P≤0.029分别)在不同受试者的微生物体变得高度相似(Unifrac距离,N?= 14天)的周期。共同地,比较疾病状态的样品显示在抗生素治疗期间减少了这两种措施(LME P?= 0.0096和P?= 0.014),但稳定性数据和CFPE数据彼此没有显着差异。 CFPE期间,代谢物α-多样性比稳定性在稳定性期间更高(LME P?= 0.0085),但鉴定了跨对象的CFPE一致的代谢物签名。来自P.铜绿假单胞菌的毒力相关的代谢物在时间上动态但与任何疾病状态无关。一个主题在收集期间死亡,使得在死亡前的194天的时间详细了解变化。在取样开始时,该受试者在微生物组中有超过90%的假单胞菌,并且在死亡之前,这种水平逐渐增加到超过99%。该研究表明,一些受试者的CF微生物组和代谢物是动态的通过时间。需要未来的工作来了解驱动这些时间动态的驱动器,以及厌氧的减少与对CFPE治疗的临床反应相关。患有囊性纤维化的重要性受试者在整个寿命期间患有囊性纤维化的肺部感染。虽然抗生素治疗是CF肺病的主要治疗方法,但我们几乎没有了解抗生素如何影响CF肺部微生物组和代谢物,以及社区每日时间的变化程度。通过从六个成年受试者分析594个纵向CF痰样品,我们表明痰微生物组和代谢物是动态的。在稳定性和肺癌(CFPE)期间发生重大变化。微生物组α-多样性随着CFPE开发的,然后在治疗期间减少,以对应于厌氧细菌对经典病原体的日志比的降低的方式减少。来自病原体P.铜绿假单胞菌的代谢物水平也通过时间的高度变化,与厌氧相关。本研究中观察到的微生物动态可能对CFP和整体主题健康的抗生素治疗结果产生重大影响。
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