1. Uropathogenic Escherichia coli employs both evasion and resistance to subvert innate immune-mediated zinc toxicity for dissemination
- Author
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Ronan Kapetanovic, Jayde A. Gawthorne, Minh-Duy Phan, Kate M. Peters, Nicholas D. Condon, Claudia J. Stocks, Nguyen Thi Khanh Nhu, Alastair G. McEwan, Maud E. S. Achard, Alvin W. Lo, Matthew J. Sweet, and Mark A. Schembri
- Subjects
Urology ,Clone (cell biology) ,chemistry.chemical_element ,macrophage ,Zinc ,urologic and male genital diseases ,medicine.disease_cause ,Microbiology ,03 medical and health sciences ,antimicrobial responses ,medicine ,Humans ,Uropathogenic Escherichia coli ,Macrophage ,Escherichia coli ,Pathogen ,Escherichia coli Infections ,030304 developmental biology ,0303 health sciences ,Multidisciplinary ,Innate immune system ,biology ,business.industry ,030306 microbiology ,Biological Sciences ,Evasion (ethics) ,biology.organism_classification ,female genital diseases and pregnancy complications ,Immunity, Innate ,3. Good health ,PNAS Plus ,chemistry ,TraDIS ,Zinc toxicity ,UPEC ,business ,Bacteria - Abstract
Significance Uropathogenic Escherichia coli (UPEC) is responsible for most urinary tract infections and is also a frequent cause of sepsis, thus necessitating an understanding of UPEC-mediated subversion of innate immunity. The role of zinc in the innate immune response against UPEC infection, and whether this pathogen counters this response, has not been examined. Here we demonstrate, both in vitro and in vivo, that UPEC both evades and resists innate immune-mediated zinc toxicity to persist and disseminate within the host. Moreover, we have defined the set of UPEC genes conferring zinc resistance and have developed highly selective E. coli reporter systems to track zinc toxicity. These innovative approaches substantially enhance our understanding of immune-mediated metal ion toxicity and bacterial pathogenesis., Toll-like receptor (TLR)-inducible zinc toxicity is a recently described macrophage antimicrobial response used against bacterial pathogens. Here we investigated deployment of this pathway against uropathogenic Escherichia coli (UPEC), the major cause of urinary tract infections. Primary human macrophages subjected EC958, a representative strain of the globally disseminated multidrug-resistant UPEC ST131 clone, to zinc stress. We therefore used transposon-directed insertion site sequencing to identify the complete set of UPEC genes conferring protection against zinc toxicity. Surprisingly, zinc-susceptible EC958 mutants were not compromised for intramacrophage survival, whereas corresponding mutants in the nonpathogenic E. coli K-12 strain MG1655 displayed significantly reduced intracellular bacterial loads within human macrophages. To investigate whether the intramacrophage zinc stress response of EC958 reflected the response of only a subpopulation of bacteria, we generated and validated reporter systems as highly specific sensors of zinc stress. Using these tools we show that, in contrast to MG1655, the majority of intramacrophage EC958 evades the zinc toxicity response, enabling survival within these cells. In addition, EC958 has a higher tolerance to zinc than MG1655, with this likely being important for survival of the minor subset of UPEC cells exposed to innate immune-mediated zinc stress. Indeed, analysis of zinc stress reporter strains and zinc-sensitive mutants in an intraperitoneal challenge model in mice revealed that EC958 employs both evasion and resistance against zinc toxicity, enabling its dissemination to the liver and spleen. We thus demonstrate that a pathogen of global significance uses multiple mechanisms to effectively subvert innate immune-mediated zinc poisoning for systemic spread.
- Published
- 2019
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