IAI FigSearch
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
IAI.00612-08v1
76/10/4713    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Google Scholar
Right arrow Articles by Gomes-Pereira, S.
Right arrow Articles by Gomes, M. S.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gomes-Pereira, S.
Right arrow Articles by Gomes, M. S.

 Previous Article  |  Next Article 

Infection and Immunity, October 2008, p. 4713-4719, Vol. 76, No. 10
0019-9567/08/$08.00+0     doi:10.1128/IAI.00612-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Increased Susceptibility to Mycobacterium avium in Hemochromatosis Protein HFE-Deficient Mice{triangledown}

Sandra Gomes-Pereira,1,4 Pedro Nuno Rodrigues,2,3 Rui Appelberg,1,3 and Maria Salomé Gomes1,3*

Laboratory of Microbiology and Immunology of Infection,1 Iron Genes and the Immune System, IBMC—Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal,2 ICBAS—Instituto de Ciências Biomédicas de Abel Salazar, Universidade do Porto, Porto, Portugal,3 Escola Superior de Tecnologia da Saúde do Porto, Instituto Politécnico do Porto, Porto, Portugal4

Received 20 May 2008/ Returned for modification 20 June 2008/ Accepted 2 August 2008

Mycobacterium avium is an opportunistic infectious agent in immunocompromised patients, living inside macrophage phagosomes. As for other mycobacterial species, iron availability is a critical factor for M. avium survival and multiplication. Indeed, an association between host secondary iron overload and increased susceptibility to these mycobacteria is generally acknowledged. However, studies on the impact of primary iron overload on M. avium infection have not been performed. In this work, we used animal models of primary iron overload that mimic the human disease hereditary hemochromatosis. This pathology is characterized by increased serum transferrin saturation with iron deposition in parenchymal cells, mainly in the liver, and is most often associated with mutations in the gene encoding the molecule HFE. In this paper, we demonstrate that mice of two genetically determined primary iron overload phenotypes, Hfe–/– and β2m–/–, show an increased susceptibility to experimental infection with M. avium and that during infection these animals accumulate iron inside granuloma macrophages. β2m–/– mice were found to be more susceptible than Hfe–/– mice, but depleting Hfe–/– mice of CD8+ cells had no effect on resistance to infection. Overall, our results suggest that serum iron, rather than total liver iron, levels have a considerable impact on susceptibility to M. avium infection.


* Corresponding author. Mailing address: Laboratory of Microbiology and Immunology of Infection, IBMC—Instituto de Biologia Molecular e Celular, Rua do Campo Alegre 823, 4150-180 Porto, Portugal. Phone: 351 226074900. Fax: 351 226099157. E-mail: sgomes{at}ibmc.up.pt

{triangledown} Published ahead of print on 11 August 2008.

Editor: A. J. Bäumler


Infection and Immunity, October 2008, p. 4713-4719, Vol. 76, No. 10
0019-9567/08/$08.00+0     doi:10.1128/IAI.00612-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. J. Virol. Eukaryot. Cell
Microbiol. Mol. Biol. Rev. Clin. Vaccine Immunol. All ASM Journals

Copyright © 2008 by the American Society for Microbiology. All rights reserved.