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Salmonella employs multiple mechanisms to subvert the TLR-inducible zinc-mediated antimicrobial response of human macrophages.
Kapetanovic, Ronan; Bokil, Nilesh J; Achard, Maud E S; Ong, Cheryl-Lynn Y; Peters, Kate M; Stocks, Claudia J; Phan, Minh-Duy; Monteleone, Mercedes; Schroder, Kate; Irvine, Katharine M; Saunders, Bernadette M; Walker, Mark J; Stacey, Katryn J; McEwan, Alastair G; Schembri, Mark A; Sweet, Matthew J.
Afiliação
  • Kapetanovic R; Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Australia; IMB Centre for Inflammation and Disease Research, The University of Queensland, Brisbane, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Bokil NJ; Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Australia; IMB Centre for Inflammation and Disease Research, The University of Queensland, Brisbane, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Achard ME; School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Ong CL; School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Peters KM; School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Stocks CJ; Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Australia; IMB Centre for Inflammation and Disease Research, The University of Queensland, Brisbane, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Phan MD; School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Monteleone M; Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Australia; IMB Centre for Inflammation and Disease Research, The University of Queensland, Brisbane, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Schroder K; Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Australia; IMB Centre for Inflammation and Disease Research, The University of Queensland, Brisbane, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Irvine KM; IMB Centre for Inflammation and Disease Research, The University of Queensland, Brisbane, Australia; School of Medicine, The University of Queensland, Woolloongabba, Australia; and.
  • Saunders BM; School of Life Sciences, University of Technology, Sydney, Australia.
  • Walker MJ; School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Stacey KJ; School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • McEwan AG; School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Schembri MA; School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia;
  • Sweet MJ; Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Australia; IMB Centre for Inflammation and Disease Research, The University of Queensland, Brisbane, Australia; Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia; m.sweet
FASEB J ; 30(5): 1901-12, 2016 05.
Article em En | MEDLINE | ID: mdl-26839376
ABSTRACT
We aimed to characterize antimicrobial zinc trafficking within macrophages and to determine whether the professional intramacrophage pathogen Salmonella enterica serovar Typhimurium (S Typhimurium) subverts this pathway. Using both Escherichia coli and S Typhimurium, we show that TLR signaling promotes the accumulation of vesicular zinc within primary human macrophages. Vesicular zinc is delivered to E. coli to promote microbial clearance, whereas S. Typhimurium evades this response via Salmonella pathogenicity island (SPI)-1. Even in the absence of SPI-1 and the zinc exporter ZntA, S Typhimurium resists the innate immune zinc stress response, implying the existence of additional host subversion mechanisms. We also demonstrate the combinatorial antimicrobial effects of zinc and copper, a pathway that S. Typhimurium again evades. Our use of complementary tools and approaches, including confocal microscopy, direct assessment of intramacrophage bacterial zinc stress responses, specific E. coli and S Typhimurium mutants, and inductively coupled plasma mass spectroscopy, has enabled carefully controlled characterization of this novel innate immune antimicrobial pathway. In summary, our study provides new insights at the cellular level into the well-documented effects of zinc in promoting host defense against infectious disease, as well as the complex host subversion strategies employed by S Typhimurium to combat this pathway.-Kapetanovic, R., Bokil, N. J., Achard, M. E. S., Ong, C.-L. Y., Peters, K. M., Stocks, C. J., Phan, M.-D., Monteleone, M., Schroder, K., Irvine, K. M., Saunders, B. M., Walker, M. J., Stacey, K. J., McEwan, A. G., Schembri, M. A., Sweet, M. J. Salmonella employs multiple mechanisms to subvert the TLR-inducible zinc-mediated antimicrobial response of human macrophages.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Salmonella / Salmonella typhimurium / Zinco / Receptores Toll-Like / Macrófagos Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Salmonella / Salmonella typhimurium / Zinco / Receptores Toll-Like / Macrófagos Idioma: En Ano de publicação: 2016 Tipo de documento: Article