Lee Amy Huei-Yi, Flibotte Stephane, Sinha Sunita, Paiero Adrianna, Ehrlich Rachel L, Balashov Sergey, Ehrlich Garth D, Zlosnik James E A, Mell Joshua Chang, Nislow Corey
Department of Microbiology and Immunology.
Department of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada.
Genome Res. 2017 Apr;27(4):650-662. doi: 10.1101/gr.213363.116. Epub 2017 Mar 21.
Chronic bacterial infections of the lung are the leading cause of morbidity and mortality in cystic fibrosis patients. Tracking bacterial evolution during chronic infections can provide insights into how host selection pressures-including immune responses and therapeutic interventions-shape bacterial genomes. We carried out genomic and phenotypic analyses of 215 serially collected isolates from 16 cystic fibrosis patients, spanning a period of 2-20 yr and a broad range of epidemic lineages. Systematic phenotypic tests identified longitudinal bacterial series that manifested progressive changes in liquid media growth, motility, biofilm formation, and acute insect virulence, but not in mucoidy. The results suggest that distinct lineages follow distinct evolutionary trajectories during lung infection. Pan-genome analysis identified 10,110 homologous gene clusters present only in a subset of strains, including genes restricted to different molecular types. Our phylogenetic analysis based on 2148 orthologous gene clusters from all isolates is consistent with patient-specific clades. This suggests that initial colonization of patients was likely by individual strains, followed by subsequent diversification. Evidence of clonal lineages shared by some patients was observed, suggesting inter-patient transmission. We observed recurrent gene losses in multiple independent longitudinal series, including complete loss of Chromosome III and deletions on other chromosomes. Recurrently observed loss-of-function mutations were associated with decreases in motility and biofilm formation. Together, our study provides the first comprehensive genome-phenome analyses of infection in cystic fibrosis lungs and serves as a valuable resource for understanding the genomic and phenotypic underpinnings of bacterial evolution.
肺部慢性细菌感染是囊性纤维化患者发病和死亡的主要原因。追踪慢性感染期间的细菌进化可以深入了解宿主选择压力(包括免疫反应和治疗干预)如何塑造细菌基因组。我们对来自16名囊性纤维化患者的215株连续收集的分离株进行了基因组和表型分析,时间跨度为2至20年,涵盖了广泛的流行谱系。系统的表型测试确定了纵向细菌系列,这些系列在液体培养基生长、运动性、生物膜形成和急性昆虫毒力方面表现出渐进性变化,但在黏液样性方面没有变化。结果表明,不同的谱系在肺部感染期间遵循不同的进化轨迹。泛基因组分析确定了仅在一部分菌株中存在的10110个同源基因簇,包括限于不同分子类型的基因。我们基于所有分离株的2148个直系同源基因簇的系统发育分析与患者特异性进化枝一致。这表明患者最初可能是由单个菌株定植,随后发生多样化。观察到一些患者共享克隆谱系的证据,表明存在患者间传播。我们在多个独立的纵向系列中观察到反复出现的基因丢失,包括第三条染色体的完全丢失和其他染色体上的缺失。反复观察到的功能丧失突变与运动性和生物膜形成的降低有关。总之,我们的研究首次对囊性纤维化肺部感染进行了全面的基因组-表型分析,为理解细菌进化的基因组和表型基础提供了宝贵资源。