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Author Notes:

Corresponding author. Mailing address: Department of Microbiology and Immunology, Emory University School of Medicine, VAMC Room 5A181, 1670 Clairmont Rd., Decatur, GA 30033. Phone: (404) 728-7688. Fax: (404) 329-2210. E-mail: wshafer@emory.edu

We are sincerely thankful to Eun-Hee Lee-Delon and Yaramah Zalucki for helpful discussions, to Sanjay Ram for valuable advice regarding complement activity and for reading the paper before submission, to David Stephens for providing NHS, to Lane Pucko for help in manuscript preparation, and to Yih-Ling Tzeng for providing the DNA used to construct the FA19 misR-misS mutant.

We are grateful to E.-H. Lee-Delon for constructing this strain.

Editor: J. N. Weiser

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Research Funding:

This work was partially supported by National Institutes of Health grants AI-062755-05 (W.M.S.) and AI-031496-20 (P. F. Sparling, University of North Carolina) and by a VA Merit Review grant to W.M.S. W.M.S. is the recipient of a Senior Research Career Scientist Award from the VA Medical Research Service.

Polyamines Can Increase Resistance of Neisseria gonorrhoeae to Mediators of the Innate Human Host Defense

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Journal Title:

Infection and Immunity

Volume:

Volume 78, Number 7

Publisher:

, Pages 3187-3195

Type of Work:

Article | Final Publisher PDF

Abstract:

Polyamines are biogenic polycationic molecules involved in key cellular functions. Extracellular polyamines found in bodily fluids or laboratory media can be imported by bacteria or bind to negatively charged bacterial surface structures, where they can impair binding of antimicrobials. We hypothesized that the presence of polyamines in fluids that bathe urogenital mucosal surfaces could alter the susceptibility of the sexually transmitted strict human pathogen Neisseria gonorrhoeae to mediators of the innate host defense. Herein we report that polyamines can significantly increase gonococcal resistance to two structurally diverse cationic antimicrobial peptides (polymyxin B and LL-37) but not to antibiotics that exert activity in the cytosol or periplasm (e.g., ciprofloxacin, spectinomycin, or penicillin). The capacity of polyamines to increase gonococcal resistance to cationic antimicrobial peptides was dose dependent, correlated with the degree of cationicity, independent of a polyamine transport system involving the polyamine permeases PotH and PotI, and was reversible. In addition, we found that polyamines increase gonococcal resistance to complement-mediated killing by normal human serum. We propose that polyamines in genital mucosal fluids may enhance gonococcal survival during infection by reducing bacterial susceptibility to host-derived antimicrobials that function in innate host defense.

Copyright information:

© 2010, American Society for Microbiology

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