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铜绿假单胞菌对囊性纤维化患者气道的遗传适应性。

Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients.

作者信息

Smith Eric E, Buckley Danielle G, Wu Zaining, Saenphimmachak Channakhone, Hoffman Lucas R, D'Argenio David A, Miller Samuel I, Ramsey Bonnie W, Speert David P, Moskowitz Samuel M, Burns Jane L, Kaul Rajinder, Olson Maynard V

机构信息

Genome Center, Program in Molecular and Cellular Biology, University of Washington, Seattle, WA 98195, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 May 30;103(22):8487-92. doi: 10.1073/pnas.0602138103. Epub 2006 May 10.

Abstract

In many human infections, hosts and pathogens coexist for years or decades. Important examples include HIV, herpes viruses, tuberculosis, leprosy, and malaria. With the exception of intensively studied viral infections such as HIV/AIDs, little is known about the extent to which the clonal expansion that occurs during long-term infection by pathogens involves important genetic adaptations. We report here a detailed, whole-genome analysis of one such infection, that of a cystic fibrosis (CF) patient by the opportunistic bacterial pathogen Pseudomonas aeruginosa. The bacteria underwent numerous genetic adaptations during 8 years of infection, as evidenced by a positive-selection signal across the genome and an overwhelming signal in specific genes, several of which are mutated during the course of most CF infections. Of particular interest is our finding that virulence factors that are required for the initiation of acute infections are often selected against during chronic infections. It is apparent that the genotypes of the P. aeruginosa strains present in advanced CF infections differ systematically from those of "wild-type" P. aeruginosa and that these differences may offer new opportunities for treatment of this chronic disease.

摘要

在许多人类感染中,宿主和病原体共存数年或数十年。重要的例子包括艾滋病毒、疱疹病毒、结核病、麻风病和疟疾。除了像艾滋病毒/艾滋病这样经过深入研究的病毒感染外,对于病原体长期感染期间发生的克隆扩增在多大程度上涉及重要的基因适应性,人们知之甚少。我们在此报告对一种此类感染的详细全基因组分析,即一名囊性纤维化(CF)患者被机会性细菌病原体铜绿假单胞菌感染的情况。在8年的感染过程中,细菌经历了众多基因适应性变化,全基因组的正选择信号以及特定基因中的压倒性信号证明了这一点,其中一些基因在大多数CF感染过程中发生了突变。我们特别感兴趣的发现是,急性感染起始所需的毒力因子在慢性感染期间常常被淘汰。很明显,晚期CF感染中存在的铜绿假单胞菌菌株的基因型与“野生型”铜绿假单胞菌的基因型有系统性差异,而且这些差异可能为治疗这种慢性疾病提供新的机会。

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