Duan Kangmin, Dammel Carol, Stein Jeffrey, Rabin Harvey, Surette Michael G
Department of Microbiology and Infectious Diseases, University of Calgary, Calgary, AB, Canada T2N 4N1.
Mol Microbiol. 2003 Dec;50(5):1477-91. doi: 10.1046/j.1365-2958.2003.03803.x.
The change in gene expression patterns in response to host environments is a prerequisite for bacterial infection. Bacterial diseases often occur as an outcome of the complex interactions between pathogens and the host. The indigenous, usually non-pathogenic microflora is a ubiquitous constituent of the host. In order to understand the interactions between pathogens and the resident microflora and how they affect the gene expression patterns of the pathogens and contribute to bacterial diseases, the interactions between pathogenic Pseudomonas aeruginosa and avirulent oropharyngeal flora (OF) strains isolated from sputum samples of cystic fibrosis (CF) patients were investigated. Animal experiments using a rat lung infection model indicate that the presence of OF bacteria enhanced lung damage caused by P. aeruginosa. Genome-wide transcriptional analysis with a lux reporter-based promoter library demonstrated that approximately 4% of genes in the genome responded to the presence of OF strains using an in vitro system. Characterization of a subset of the regulated genes indicates that they fall into seven functional classes, and large portions of the upregulated genes are genes important for P. aeruginosa pathogenesis. Autoinducer-2 (AI-2)-mediated quorum sensing, a proposed interspecies signalling system, accounted for some, but not all, of the gene regulation. A substantial amount of AI-2 was detected directly in sputum samples from CF patients and in cultures of most non-pseudomonad bacteria isolated from the sputa. Transcriptional profiling of a set of defined P. aeruginosa virulence factor promoters revealed that OF and exogenous AI-2 could upregulate overlapping subsets of these genes. These results suggest important contributions of the host microflora to P. aeruginosa infection by modulating gene expression via interspecies communications.
响应宿主环境而发生的基因表达模式变化是细菌感染的先决条件。细菌性疾病往往是病原体与宿主之间复杂相互作用的结果。本土的、通常无致病性的微生物群是宿主中普遍存在的组成部分。为了了解病原体与常驻微生物群之间的相互作用,以及它们如何影响病原体的基因表达模式并导致细菌性疾病,我们研究了致病性铜绿假单胞菌与从囊性纤维化(CF)患者痰液样本中分离出的无毒口咽菌群(OF)菌株之间的相互作用。使用大鼠肺部感染模型进行的动物实验表明,OF细菌的存在加剧了铜绿假单胞菌引起的肺部损伤。使用基于lux报告基因的启动子文库进行的全基因组转录分析表明,在体外系统中,基因组中约4%的基因对OF菌株的存在有反应。对一组受调控基因的表征表明,它们可分为七个功能类别,并且大部分上调基因是对铜绿假单胞菌致病性很重要的基因。自诱导物-2(AI-2)介导的群体感应,一种推测的种间信号系统,解释了部分而非全部的基因调控。在CF患者的痰液样本以及从痰液中分离出的大多数非假单胞菌细菌培养物中直接检测到了大量的AI-2。对一组确定的铜绿假单胞菌毒力因子启动子的转录谱分析表明,OF和外源性AI-2可以上调这些基因的重叠子集。这些结果表明,宿主微生物群通过种间通讯调节基因表达,对铜绿假单胞菌感染有重要影响。