Mechanistic model of Rothia mucilaginosa adaptation toward persistence in the CF lung, based on a genome reconstructed from metagenomic data.
Mechanistic model of Rothia mucilaginosa adaptation toward persistence in the CF lung, based on a genome reconstructed from metagenomic data.
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基于从元基因组数据重建的基因组,Rothia粘膜粘膜对CF肺部持久性的适应性模型。
DOI:
10.1371/journal.pone.0064285
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发表时间:
2013
期刊:
影响因子:
3.7
通讯作者:
Rohwer F
中科院分区:
文献类型:
--
作者:
Lim YW;Schmieder R;Haynes M;Furlan M;Matthews TD;Whiteson K;Poole SJ;Hayes CS;Low DA;Maughan H;Edwards R;Conrad D;Rohwer F
The impaired mucociliary clearance in individuals with Cystic Fibrosis (CF) enables opportunistic pathogens to colonize CF lungs. Here we show that Rothia mucilaginosa is a common CF opportunist that was present in 83% of our patient cohort, almost as prevalent as Pseudomonas aeruginosa (89%). Sequencing of lung microbial metagenomes identified unique R. mucilaginosa strains in each patient, presumably due to evolution within the lung. The de novo assembly of a near-complete R. mucilaginosa (CF1E) genome illuminated a number of potential physiological adaptations to the CF lung, including antibiotic resistance, utilization of extracellular lactate, and modification of the type I restriction-modification system. Metabolic characteristics predicted from the metagenomes suggested R. mucilaginosa have adapted to live within the microaerophilic surface of the mucus layer in CF lungs. The results also highlight the remarkable evolutionary and ecological similarities of many CF pathogens; further examination of these similarities has the potential to guide patient care and treatment.
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