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Acquisition of Expression of the Pseudomonas aeruginosa ExoU Cytotoxin Leads to Increased Bacterial Virulence in a Murine Model of Acute Pneumonia and Systemic Spread

机译:铜绿假单胞菌ExoU细胞毒素表达的获取导致急性肺炎和系统性传播的小鼠模型中细菌毒性增加。

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摘要

Pseudomonas aeruginosa is the nosocomial bacterial pathogen most commonly isolated from the respiratory tract. Animal models of this infection are extremely valuable for studies of virulence and immunity. We thus evaluated the utility of a simple model of acute pneumonia for analyzing P. aeruginosa virulence by characterizing the course of bacterial infection in BALB/c mice following application of bacteria to the nares of anesthetized animals. Bacterial aspiration into the lungs was rapid, and 67 to 100% of the inoculum could be recovered within minutes from the lungs, with 0.1 to 1% of the inoculum found intracellularly shortly after infection. At later time points up to 10% of the bacteria were intracellular, as revealed by gentamicin exclusion assays on single-cell suspensions of infected lungs. Expression of exoenzyme U (ExoU) by P. aeruginosa is associated with a cytotoxic effect on epithelial cells in vitro and virulence in animal models. Insertional mutations in the exoU gene confer a noncytotoxic phenotype on mutant strains and decrease virulence for animals. We used the model of acute pneumonia to determine whether introduction of the exoU gene into noncytotoxic strains of P. aeruginosa lacking this gene affected virulence. Seven phenotypically noncytotoxic P. aeruginosa strains were transformed with pUCP19exoUspcU which carries the exoU gene and its associated chaperone. Three of these strains became cytotoxic to cultured epithelial cells in vitro. These strains all secreted ExoU, as confirmed by detection of the ExoU protein with specific antisera. The 50% lethal dose of exoU-expressing strains was significantly lower for all three P. aeruginosa isolates carrying plasmid pUCP19exoUspcU than for the isogenic exoU-negative strains. mRNA specific for ExoU was readily detected in the lungs of animals infected with the transformed P. aeruginosa strains. Introduction of the exoU gene confers a cytotoxic phenotype on some, but not all, otherwise-noncytotoxic P. aeruginosa strains and, for recombinant strains that could express ExoU, there was markedly increased virulence in a murine model of acute pneumonia and systemic spread.
机译:铜绿假单胞菌是最常见于呼吸道的医院细菌病原体。这种感染的动物模型对于毒力和免疫力研究非常有价值。因此,我们通过将细菌应用于麻醉动物的鼻孔以表征BALB / c小鼠中细菌感染的过程,从而评估了一种简单的急性肺炎模型用于分析铜绿假单胞菌毒力的效用。细菌迅速吸入肺中,在几分钟内可从肺中回收67-100%的接种物,感染后不久在细胞内发现0.1-1%的接种物。在随后的时间点,多达10%的细菌在细胞内,如庆大霉素排除法对受感染肺的单细胞悬液显示的那样。铜绿假单胞菌表达外酶U(ExoU)与体外对上皮细胞的细胞毒性作用以及动物模型中的毒力有关。 exoU基因中的插入突变赋予突变株非细胞毒性表型,并降低了动物的毒力。我们使用急性肺炎模型来确定将exoU基因引入缺乏该基因的铜绿假单胞菌的非细胞毒性菌株是否会影响毒力。用携带exoU基因及其相关伴侣蛋白的pUCP19exoUspcU转化了7种在表型上无细胞毒性的铜绿假单胞菌菌株。这些菌株中的三个对体外培养的上皮细胞具有细胞毒性。如通过用特异性抗血清检测ExoU蛋白所证实的,这些菌株全部分泌ExoU。对于表达质粒pUCP19exoUspcU的所有三种铜绿假单胞菌分离株,表达exoU菌株的50%致死剂量均显着低于同基因的exoU阴性菌株。在被转化的铜绿假单胞菌菌株感染的动物的肺中很容易检测到ExoU特异的mRNA。 exoU基因的引入赋予一些但不是全部非细胞毒性铜绿假单胞菌菌株细胞毒性表型,对于可表达ExoU的重组菌株,急性肺炎和全身性传播的鼠模型中的毒力显着增加。

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