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突变菌的艰难生存:在囊性纤维化肺部的持续存在与进化之间如何存活

The Challenging Life of Mutators: How Survives between Persistence and Evolution in Cystic Fibrosis Lung.

作者信息

Rossitto Martina, Fox Valeria, Vrenna Gianluca, Tuccio Guarna Assanti Vanessa, Essa Nour, Lepanto Maria Stefania, Raimondi Serena, Agosta Marilena, Cortazzo Venere, Fini Vanessa, Granaglia Annarita, Montemitro Enza, Cutrera Renato, Perno Carlo Federico, Bernaschi Paola

机构信息

Multimodal Laboratory Medicine, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.

Microbiology and Diagnostic Immunology Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.

出版信息

Microorganisms. 2024 Oct 11;12(10):2051. doi: 10.3390/microorganisms12102051.

Abstract

Cystic fibrosis (CF) is a life-threatening genetic disease characterised by chronic lung infections sustained by opportunistic pathogens such as During the chronic long-lasting lung infections, adapts to the host environment. Hypermutability, mainly due to defects in the DNA repair system, resulting in an increased spontaneous mutation rate, represents a way to boost the rapid adaptation frequently encountered in CF isolates. We selected 609 isolates from 51 patients with CF chronically colonised by to study, by full-length genome sequencing, the longitudinal evolution of the bacterium. We recovered at least one hypermutable (mutator) isolate in 57% of patients. By combining genomic information and phenotypic analyses, we followed the evolutionary pathways of the mutator strains, identifying their contribution to multi-drug resistance and the emergence of new sub-lineages. By implementing patient clinical data, we observed that mutators preferentially follow a specific evolutionary trajectory in patients with a negative clinical outcome and that maintenance antibiotic polytherapy, based on alternating molecules, apparently reduces the occurrence of hypermutability. Finally, we draw attention to the possibility that modulator-induced changes in the pulmonary environment may be associated with the onset of hypermutability.

摘要

囊性纤维化(CF)是一种危及生命的遗传疾病,其特征是由铜绿假单胞菌等机会性病原体引发的慢性肺部感染。在慢性长期肺部感染过程中,铜绿假单胞菌会适应宿主环境。高突变性主要源于DNA修复系统缺陷,导致自发突变率增加,这是囊性纤维化分离株中常见的促进快速适应的一种方式。我们从51例被铜绿假单胞菌长期定植的囊性纤维化患者中选取了609株分离株,通过全基因组测序研究该细菌的纵向进化。我们在57%的患者中至少分离出一株高突变(突变体)菌株。通过整合基因组信息和表型分析,我们追踪了突变体菌株的进化途径,确定了它们对多药耐药性的影响以及新亚系的出现。通过纳入患者临床数据,我们观察到,在临床结局为阴性的患者中,突变体优先遵循特定的进化轨迹,并且基于交替使用不同分子的维持性抗生素联合治疗似乎可降低高突变性的发生。最后,我们提请注意这样一种可能性,即调节因子引起的肺部环境变化可能与高突变性的发生有关。

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