IAI FigSearch
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mullick, A.
Right arrow Articles by Gros, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mullick, A.
Right arrow Articles by Gros, P.

 Previous Article  |  Next Article 

Infection and Immunity, August 2006, p. 4439-4451, Vol. 74, No. 8
0019-9567/06/$08.00+0     doi:10.1128/IAI.00159-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Cardiac Failure in C5-Deficient A/J Mice after Candida albicans Infection{dagger}

Alaka Mullick,1* Zully Leon,1 Gundula Min-Oo,2 Joanne Berghout,2 Rita Lo,1 Eugene Daniels,3 and Philippe Gros2

Biotechnology Research Institute, 6100 Royalmount Avenue, Montréal, Québec, Canada H4P 2R2,1 Biochemistry Department, McGill University, 3655 Promenade Sir William Osler, Montréal, Québec, Canada H3G 1Y6,2 Anatomy Department, McGill University, 3640 University Street, Montréal, Québec, Canada H3A 2B23

Received 30 January 2006/ Returned for modification 11 March 2006/ Accepted 10 May 2006

The effect of a deficiency in the C5 component of complement on the pathophyisology of infection with the fungal pathogen Candida albicans was studied by using the A/J inbred mouse strain and the BcA17 congenic mouse strain. Acute infection caused by intravenous injection of C. albicans blastospores is associated with rapid fungal replication in the heart, brain, and, in particular, kidneys of C5-deficient mice. Histological studies and analysis of markers for tissue damage indicated that the heart is the organ that is most affected and that it ultimately fails in C5-deficient mice. In A/J and BcA17 mice, tissue damage is associated with (i) cellular infiltration in the heart, which is not seen in the kidney despite the higher fungal load in the latter organ, and (ii) a very strong inflammatory response, including elevated levels of many cytokines and chemokines. This results in cardiomyopathy, which is associated with elevated levels of creatine kinase and cardiac troponin I in the circulation. Damage to the cardiac muscle is associated with metabolic changes, including hypoglycemia, decreased lipid utilization resulting in elevated levels of cardiac triglycerides, and unproductive glucose utilization linked to a dramatic increase in the level of pyruvate dehydrogenase kinase 4 (Pdk4), a negative regulator of the pyruvate dehydrogenase complex.


* Corresponding author. Mailing address: Biotechnology Research Institute, National Research Council, 6100 Royalmount Avenue, Montréal, Québec, Canada H4P 2R2. Phone: (514) 496-6281. Fax: (514) 496-5143. E-mail: alaka.mullick{at}cnrc-nrc.gc.ca.

{dagger} National Research Council publication no. 47757.

Editor: A. Casadevall


Infection and Immunity, August 2006, p. 4439-4451, Vol. 74, No. 8
0019-9567/06/$08.00+0     doi:10.1128/IAI.00159-06
Copyright © 2006, 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 © 2006 by the American Society for Microbiology. All rights reserved.