A non-specific effect of orally administered Escherichia coli.

Roman Gardlik
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引用次数: 1

Abstract

A number of genetically modified bacteria able to deliver a therapeutic gene into target cells has already been tested. Apart from the expected effects of bacterial therapy, the therapeutic bacterial strain also mediates a non-specific effect independent of the gene to be delivered. In this regard, we have recently shown that oral administration of the bacterial strain Escherichia coli XL1-Blue via gastric gavage to rats leads to a non-specific decrease in expression of vascular endothelial growth factor (VEGF) in intestinal wall without corresponding changes in other parameters. We tried to adopt a model of intestinal ischemia and to treat the subsequent hypoxic condition using a strain carrying the effector plasmid encoding hypoxia-inducible factor 1 alpha (HIF-1alpha), as well as the helper plasmid encoding invasion and listeriolysin O. However, the model was ineffective, as obvious from macroscopic and molecular observations. We hypothesize that a competitive behavior of the administered strain in the intestinal microbiota leads to a decrease in activity of HIF-1alpha and reduction in expression of VEGF. Also, a functional disease model would be necessary for the invasion-expressing therapeutic strain to be effective. A different approach using bacterial protein delivery would possibly circumvent these bactofection-related problems.

口服大肠杆菌的非特异性作用。
一些能够将治疗性基因传递到靶细胞的转基因细菌已经经过测试。除了预期的细菌治疗效果外,治疗菌株还介导一种独立于要传递的基因的非特异性效果。在这方面,我们最近的研究表明,大鼠胃灌胃给药大肠杆菌XL1-Blue菌株可导致肠壁血管内皮生长因子(VEGF)表达的非特异性降低,而其他参数没有相应的变化。我们试图建立肠道缺血模型,并利用携带编码缺氧诱导因子1 α (hif - 1α)的效应质粒和编码侵袭性和李斯特菌溶素o的辅助质粒的菌株来治疗随后的缺氧状况。然而,从宏观和分子观察来看,该模型是无效的。我们假设给药菌株在肠道微生物群中的竞争行为导致hif -1 α活性降低和VEGF表达降低。此外,为了使表达侵袭的治疗菌株有效,一个功能性疾病模型是必要的。另一种使用细菌蛋白递送的方法可能会避免这些与细菌感染有关的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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