Both leukotoxin and poly- N-acetylglucosamine surface polysaccharide protect Aggregatibacter actinomycetemcomitans cells from macrophage killing

Two virulence factors produced by the periodontopathogen Aggregatibacter actinomycetemcomitans are leukotoxin, a secreted lipoprotein that kills human polymorphonuclear leukocytes and macrophages, and poly- N-acetylglucosamine (PGA), a surface polysaccharide that mediates intercellular adhesion, bio...

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Published inMicrobial pathogenesis Vol. 45; no. 3; pp. 173 - 180
Main Authors Venketaraman, Vishwanath, Lin, Albert K., Le, Amy, Kachlany, Scott C., Connell, Nancy D., Kaplan, Jeffrey B.
Format Journal Article
LanguageEnglish
Published Oxford Elsevier India Pvt Ltd 01.09.2008
Elsevier
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Summary:Two virulence factors produced by the periodontopathogen Aggregatibacter actinomycetemcomitans are leukotoxin, a secreted lipoprotein that kills human polymorphonuclear leukocytes and macrophages, and poly- N-acetylglucosamine (PGA), a surface polysaccharide that mediates intercellular adhesion, biofilm formation and detergent resistance. In this study we examined the roles of leukotoxin and PGA in protecting A. actinomycetemcomitans cells from killing by the human macrophage cell line THP-1. Monolayers of THP-1 cells were infected with single-cell suspensions of a wild-type A. actinomycetemcomitans strain, or of isogenic leukotoxin or PGA mutant strains. After 48 h, viable bacteria were enumerated by dilution plating, macrophage morphology was evaluated microscopically, and macrophage viability was measured by a Trypan blue dye exclusion assay. The number of A. actinomycetemcomitans CFUs increased approximately twofold in wells infected with the wild-type strain, but decreased by approximately 70–90% in wells infected with the leukotoxin and PGA mutant strains. Infection with the wild-type or leukotoxin mutant strain caused a significant decrease in THP-1 cell viability, whereas infection with the PGA mutant strain did not result in any detectable changes in THP-1 viability. Pre-treatment of wild-type A. actinomycetemcomitans cells with the PGA-hydrolyzing enzyme dispersin B rendered them sensitive to killing by THP-1 cells. We concluded that both leukotoxin and PGA are necessary for evasion of macrophage killing by A. actinomycetemcomitans.
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Present address: Department of Basic Medical Sciences, Western University of Health Sciences, 309 E Second Street, Pomona, CA 91766-1854, USA.
Present address: Schering-Plough Research Institute, K-15 C-202, Mail Stop 2600, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA.
ISSN:0882-4010
1096-1208
DOI:10.1016/j.micpath.2008.05.007