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Infection and Immunity, March 2000, p. 1271-1275, Vol. 68, No. 3
Medical and Research Service, Veterans
Administration Medical Center, Iowa City, Iowa
52246,1 and Departments of Internal
Medicine2 and
Microbiology,3 The University of Iowa
College of Medicine, Iowa City, Iowa 52242
Received 15 September 1999/Returned for modification 8 November
1999/Accepted 6 December 1999
Chelation of iron to iron-binding proteins is a strategy of host
defense. Some pathogens counter this via the secretion of low-molecular-weight iron-chelating agents (siderophores). Human phagocytes possess a high-capacity mechanism for iron acquisition from
low-molecular-weight iron chelates. Efficient acquisition and
sequestration of iron bound to bacterial siderophores by host phagocytes could provide a secondary mechanism to limit microbial access to iron. In the present work we report that human neutrophils, macrophages, and myeloid cell lines can acquire iron from the two
Pseudomonas aeruginosa siderophores. Analogous to iron
acquisition from other low-molecular-weight chelates, iron acquisition
from the siderophores is ATP independent, induced by multivalent
cationic metals, and unaffected by inhibitors of endocytosis and
pinocytosis. In vivo, this process could serve as an additional
mechanism of host defense to limit iron availability to invading
siderophore-producing microbes.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Iron Acquisition from Pseudomonas
aeruginosa Siderophores by Human Phagocytes: an Additional
Mechanism of Host Defense through Iron Sequestration?
*
Corresponding author. Mailing address: Department of
Medicine, The University of Iowa, 200 Hawkins Dr., SW54 GH, Iowa City, IA 52242. Phone: (319) 356-3674. Fax: (319) 356-4600. E-mail: bradley-britigan{at}uiowa.edu.
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