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首页> 外文期刊>BMC Microbiology >Prevention of siderophore- mediated gut-derived sepsis due to P. aeruginosa can be achieved without iron provision by maintaining local phosphate abundance: role of pH
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Prevention of siderophore- mediated gut-derived sepsis due to P. aeruginosa can be achieved without iron provision by maintaining local phosphate abundance: role of pH

机译:通过保持局部磷酸盐的丰度,可以在不补充铁的情况下预防铜绿假单胞菌铁载体介导的肠道败血症的发生:pH的作用

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Background During extreme physiological stress, the intestinal tract can be transformed into a harsh environment characterized by regio- spatial alterations in oxygen, pH, and phosphate concentration. When the human intestine is exposed to extreme medical interventions, the normal flora becomes replaced by pathogenic species whose virulence can be triggered by various physico-chemical cues leading to lethal sepsis. We previously demonstrated that phosphate depletion develops in the mouse intestine following surgical injury and triggers intestinal P. aeruginosa to express a lethal phenotype that can be prevented by oral phosphate ([Pi]) supplementation. Results In this study we examined the role of pH in the protective effect of [Pi] supplementation as it has been shown to be increased in the distal gut following surgical injury. Surgically injured mice drinking 25 mM [Pi] at pH 7.5 and intestinally inoculated with P. aeruginosa had increased mortality compared to mice drinking 25 mM [Pi] at pH 6.0 (p C. elegans. Transcriptional analysis of P. aeruginosa demonstrated enhanced expression of various genes involved in media alkalization at pH 6.0 and a global increase in the expression of all iron-related genes at pH 7.5. Maintaining the pH at 6.0 via phosphate supplementation led to significant attenuation of iron-related genes as demonstrated by microarray and confirmed by QRT-PCR analyses. Conclusion Taken together, these data demonstrate that increase in pH in distal intestine of physiologically stressed host colonized by P. aeruginosa can lead to the expression of siderophore-related virulence in bacteria that can be prevented without providing iron by maintaining local phosphate abundance at pH 6.0. This finding is particularly important as provision of exogenous iron has been shown to have untoward effects when administered to critically ill and septic patients. Given that phosphate, pH, and iron are near universal cues that dictate the virulence status of a broad range of microorganisms relevant to serious gut origin infection and sepsis in critically ill patients, the maintenance of phosphate and pH at appropriate physiologic levels to prevent virulence activation in a site specific manner can be considered as a novel anti-infective therapy in at risk patients.
机译:背景技术在极端的生理压力下,肠道可能会转变为恶劣的环境,其特征在于氧,pH和磷酸盐浓度的区域性变化。当人的肠道受到极端医学干预时,正常菌群将被致病菌种所替代,致病菌的毒力可能由导致致命性败血症的各种物理化学线索触发。我们先前证明,外科手术损伤后在小鼠肠中发生磷酸盐消耗,并触发肠道铜绿假单胞菌表达一种致命的表型,可以通过口服磷酸盐(Pi)补充来预防。结果在这项研究中,我们检查了pH在补充Pi的保护作用中的作用,因为已经显示pH在手术损伤后在远端肠中增加。与在pH值为6.0时喝25 mM Pi的小鼠相比,在pH 7.5时喝25 mM Pi并经肠道接种的受手术损伤的小鼠死亡率增加(线虫)。各种基因参与了pH 6.0的介质碱化和所有与铁相关的基因在pH 7.5的表达的整体增加,通过磷酸盐补充将pH维持在6.0会导致铁相关基因的显着衰减,这已通过微阵列证实并证实结论综上所述,这些数据表明铜绿假单胞菌定植的具有生理压力的宿主的远端肠道pH升高可导致细菌中铁载体相关毒力的表达,如果不通过维持局部铁含量来防止铁的表达pH 6.0时磷酸盐的丰度这一发现特别重要,因为已证明提供外源铁会产生不利影响当用于重症和败血病患者时。鉴于磷酸盐,pH和铁接近普遍的线索,它们决定了与重症患者严重肠源性感染和败血症相关的各种微生物的毒力状态,因此将磷酸盐和pH维持在适当的生理水平以防止毒力激活以特定部位的方式进行治疗可以被认为是高危患者的新型抗感染治疗方法。

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