Impact of metal ion homeostasis of genetically modified Escherichia coli Nissle 1917 and K12 (W3110) strains on colonization properties in the murine intestinal tract

Kupz, Andreas, Fischer, André, Nies, Dietrich H., Grass, Gregor, Göbel, Ulf B., Bereswill, Stefan, and Heimesaat, Markus M. (2013) Impact of metal ion homeostasis of genetically modified Escherichia coli Nissle 1917 and K12 (W3110) strains on colonization properties in the murine intestinal tract. European Journal of Microbiology and Immunology, 3 (3). pp. 229-235.

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Abstract

Metal ions are integral parts of pro- as well as eukaryotic cell homeostasis. Escherichia coli proved a valuable in vitro model organism to elucidate essential mechanisms involved in uptake, storage, and export of metal ions. Given that E. coli Nissle 1917 is able to overcome murine colonization resistance, we generated several E. coli Nissle 1917 mutants with defects in zinc, iron, copper, nickel, manganese homeostasis and performed a comprehensive survey of the impact of metal ion transport and homeostasis for E. coli colonization capacities within the murine intestinal tract. Seven days following peroral infection of conventional mice with E. coli Nissle 1917 strains exhibiting defined defects in zinc or iron uptake, the respective mutant and parental strains could be cultured at comparable, but low levels from the colonic lumen. We next reassociated gnotobiotic mice in which the microbiota responsible for colonization resistance was abrogated by broad-spectrum antibiotics with six different E. coli K12 (W3110) mutants. Seven days following peroral challenge, each mutant and parental strain stably colonized duodenum, ileum, and colon at comparable levels. Taken together, defects in zinc, iron, copper, nickel, and manganese homeostasis do not compromise colonization capacities of E. coli in the murine intestinal tract.

Item ID: 30886
Item Type: Article (Research - C1)
ISSN: 2062-8633
Keywords: metal ion homeostasis and transport, metal ion mutant strains, iron homeostasis, zinc homeostasis, copper homeostasis, periplasmic copper stress, manganese homeostasis, enterobactin, E. coli Nissle 1917, E. coli K12 (W3110), colonization resistance, gnotobiotic mice, bacterial fitness, bacterial colonization capacity
Funders: German Research Foundation (DFG), German Federal Ministry of Education and Research (BMBF)
Projects and Grants: DFG grant SFB633 TP A7, DFG grant GR2061/1-3, DFG grant SFB633 TP B6, BMBF "Lab in a hanky" project TP 1.1, BMBF "Lab in a hanky" project TP 8.2
Date Deposited: 28 Feb 2014 06:40
FoR Codes: 06 BIOLOGICAL SCIENCES > 0605 Microbiology > 060502 Infectious Agents @ 40%
11 MEDICAL AND HEALTH SCIENCES > 1103 Clinical Sciences > 110309 Infectious Diseases @ 40%
06 BIOLOGICAL SCIENCES > 0605 Microbiology > 060503 Microbial Genetics @ 20%
SEO Codes: 97 EXPANDING KNOWLEDGE > 970106 Expanding Knowledge in the Biological Sciences @ 45%
92 HEALTH > 9201 Clinical Health (Organs, Diseases and Abnormal Conditions) > 920109 Infectious Diseases @ 35%
92 HEALTH > 9201 Clinical Health (Organs, Diseases and Abnormal Conditions) > 920105 Digestive System Disorders @ 20%
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