Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 155 (2009), 3100-3109; DOI  10.1099/mic.0.026997-0
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
mic.0.026997-0v1
155/9/3100    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
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 arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Google Scholar
Right arrow Articles by Tiralongo, J.
Right arrow Articles by Kiefel, M. J.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tiralongo, J.
Right arrow Articles by Kiefel, M. J.
Agricola
Right arrow Articles by Tiralongo, J.
Right arrow Articles by Kiefel, M. J.
Microbiology 155 (2009), 3100-3109; DOI  10.1099/mic.0.026997-0
© 2009 Society for General Microbiology

Inhibition of Aspergillus fumigatus conidia binding to extracellular matrix proteins by sialic acids: a pH effect?

Joe Tiralongo1, Therese Wohlschlager1, Evelin Tiralongo2 and Milton J. Kiefel1

1 Institute for Glycomics, Gold Coast Campus, Griffith University, QLD 4222, Australia
2 School of Pharmacy, Gold Coast Campus, Griffith University, QLD 4222, Australia

Infection by Aspergillus fumigatus, which causes the life-threatening disease invasive aspergillosis, begins with the inhalation of conidia that adhere to and germinate in the lung. Previous studies have shown that A. fumigatus conidia express high levels of the negatively charged 9-carbon sugar sialic acid, and that sialic acid appears to mediate the binding of A. fumigatus conidia to basal lamina proteins. However, despite the ability of sialic acid to inhibit adherence of A. fumigatus conidia, the exact mechanism by which this binding occurs remains unresolved. Utilizing various free sialic acids and other carbohydrates, sialic acid derivatives, sialoglycoconjugates, glycoproteins, {alpha}-keto acid related compounds and amino acids we have found that the binding of A. fumigatus conidia to type IV collagen and fibrinogen was inhibited by (i) glycoproteins (in a sialic acid-independent manner), and (ii) free sialic acids, glucuronic acid and {alpha}-keto acid related compounds. However, inhibition by the latter was found to be the result of a shift in pH from neutral (pH 7.4) to acidic (less than pH 4.6) induced by the relatively high concentrations of free sialic acids, glucuronic acid and {alpha}-keto acid related compounds used in the binding assays. This suggests that previous reports describing inhibition of A. fumigatus conidia binding by free sialic acid may actually be due to a pH shift similar to that shown here. As previously reported, we found that A. fumigatus conidia express only N-acetylneuraminic acid, the most common sialic acid found in nature. However, A. fumigatus appears to do so by an alternative mechanism to that seen in other organisms. We report here that A. fumigatus (i) does not incorporate sialic acid obtained from the environment, (ii) does not synthesize and incorporate sialic acid from exogenous N-acetylmannosamine, and (iii) lacks homologues of known sialic acid biosynthesizing enzymes.

Correspondence
Joe Tiralongo
j.tiralongo{at}griffith.edu.au


Abbreviations: DMB, 1,2-diamino-4,5-methylenedioxybenzene; ECM, extracellular matrix; KDN, 2-keto-3-deoxy-D-glycero-D-galactonononic acid; ManNAc, N-acetylmannosamine; Neu5Ac, N-acetylneuraminic acid; Neu5Ac2en, 2-deoxy-2,3-didehydro-N-acetylneuraminic acid; Neu5,9Ac2, 5-N-acetyl-9-O-acetylneuraminic acid; Neu5,7Ac2, 5-N-acetyl-7-O-acetylneuraminic acid; Sia, sialic acid(s)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2009 Society for General Microbiology.