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Zinc Sequestration by the Neutrophil Protein Calprotectin Enhances Salmonella Growth in the Inflamed Gut

2012; Cell Press; Volume: 11; Issue: 3 Linguagem: Inglês

10.1016/j.chom.2012.01.017

1934-6069

Janet Z. Liu, Stefan Jellbauer, Adam J. Poe, Vivian Ton, Michele Pesciaroli, Thomas E. Kehl‐Fie, Nicole Restrepo, Martin Hosking, Robert A. Edwards, Andrea Battistoni, Paolo Pasquali, Thomas E. Lane, Walter Chazin, Thomas Vogl, Johannes Roth, Eric P. Skaar, Manuela Raffatellu,

Vitamin C and Antioxidants Research

Neutrophils are innate immune cells that counter pathogens by many mechanisms, including release of antimicrobial proteins such as calprotectin to inhibit bacterial growth. Calprotectin sequesters essential micronutrient metals such as zinc, thereby limiting their availability to microbes, a process termed nutritional immunity. We find that while calprotectin is induced by neutrophils during infection with the gut pathogen Salmonella Typhimurium, calprotectin-mediated metal sequestration does not inhibit S. Typhimurium proliferation. Remarkably, S. Typhimurium overcomes calprotectin-mediated zinc chelation by expressing a high affinity zinc transporter (ZnuABC). A S. Typhimurium znuA mutant impaired for growth in the inflamed gut was rescued in the absence of calprotectin. ZnuABC was also required to promote the growth of S. Typhimurium over that of competing commensal bacteria. Thus, our findings indicate that Salmonella thrives in the inflamed gut by overcoming the zinc sequestration of calprotectin and highlight the importance of zinc acquisition in bacterial intestinal colonization.