Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kgs. Lyngby, Denmark
Department of Clinical Microbiology, Rigshospitalet, Copenhagen, Denmark.
mBio. 2018 Apr 10;9(2):e00269-18. doi: 10.1128/mBio.00269-18.
Evolution by natural selection under complex and dynamic environmental conditions occurs through intricate and often counterintuitive trajectories affecting many genes and metabolic solutions. To study short- and long-term evolution of bacteria , we used the natural model system of cystic fibrosis (CF) infection. In this work, we investigated how and through which trajectories evolution of occurs when migrating from the environment to the airways of CF patients, and specifically, we determined reduction of growth rate and metabolic specialization as signatures of adaptive evolution. We show that central metabolic pathways of three distinct lineages coevolving within the same environment become restructured at the cost of versatility during long-term colonization. Cell physiology changes from naive to adapted phenotypes resulted in (i) alteration of growth potential that particularly converged to a slow-growth phenotype, (ii) alteration of nutritional requirements due to auxotrophy, (iii) tailored preference for carbon source assimilation from CF sputum, (iv) reduced arginine and pyruvate fermentation processes, and (v) increased oxygen requirements. Interestingly, although convergence was evidenced at the phenotypic level of metabolic specialization, comparative genomics disclosed diverse mutational patterns underlying the different evolutionary trajectories. Therefore, distinct combinations of genetic and regulatory changes converge to common metabolic adaptive trajectories leading to within-host metabolic specialization. This study gives new insight into bacterial metabolic evolution during long-term colonization of a new environmental niche. Only a few examples of real-time evolutionary investigations in environments outside the laboratory are described in the scientific literature. Remembering that biological evolution, as it has progressed in nature, has not taken place in test tubes, it is not surprising that conclusions from our investigations of bacterial evolution in the CF model system are different from what has been concluded from laboratory experiments. The analysis presented here of the metabolic and regulatory driving forces leading to successful adaptation to a new environment provides an important insight into the role of metabolism and its regulatory mechanisms for successful adaptation of microorganisms in dynamic and complex environments. Understanding the trajectories of adaptation, as well as the mechanisms behind slow growth and rewiring of regulatory and metabolic networks, is a key element to understand the adaptive robustness and evolvability of bacteria in the process of increasing their fitness when conquering new territories.
自然选择在复杂和动态的环境条件下进行,通过影响许多基因和代谢解决方案的复杂且常常违反直觉的轨迹来实现。为了研究细菌的短期和长期进化,我们使用了囊性纤维化 (CF) 感染的自然模型系统。在这项工作中,我们研究了当从环境迁移到 CF 患者的气道时,进化是如何以及通过哪些轨迹发生的,特别是,我们确定了生长速率降低和代谢特化作为适应性进化的特征。我们表明,在同一个环境中共同进化的三个不同 谱系的中心代谢途径在长期定植过程中以牺牲多功能性为代价进行了重构。从幼稚表型到适应表型的细胞生理变化导致 (i) 生长潜力的改变,特别是趋同到缓慢生长表型,(ii) 由于营养缺陷导致营养需求的改变,(iii) 对 CF 痰中碳源同化的定制偏好,(iv) 减少精氨酸和丙酮酸发酵过程,以及 (v) 增加氧气需求。有趣的是,尽管在代谢特化的表型水平上证明了趋同,但比较基因组学揭示了不同进化轨迹背后的不同突变模式。因此,不同的遗传和调控变化组合趋同于常见的代谢适应性轨迹,导致宿主内代谢特化。这项研究深入了解了细菌在新环境小生境中长期定植过程中的代谢进化。在科学文献中仅描述了少数在实验室外进行实时进化研究的实例。记住,正如自然界中发生的那样,生物进化并没有在试管中进行,因此,我们对 CF 模型系统中细菌进化的研究结论与从实验室实验中得出的结论不同,这并不奇怪。本文对导致成功适应新环境的代谢和调控驱动力的分析为理解微生物在动态和复杂环境中成功适应的代谢及其调控机制的作用提供了重要的见解。了解适应的轨迹,以及导致生长缓慢和重新布线调控和代谢网络的机制,是理解细菌在征服新领地时增加适应性和可进化性的关键因素。