Polyamines can increase resistance of Neisseria gonorrhoeae to mediators of the innate human host defense.
Goytia. Maira M; Shafer. William M WM
Key Findings
- Polyamines increase Neisseria gonorrhoeae resistance to cationic antimicrobial peptides such as LL-37 and polymyxin B.
- s positive charge, and does not rely on bacterial polyamine transporters.",
Practical Outcomes
- For biohackers considering LL-37 supplementation or using polyamine-rich supplements, this research suggests that high polyamine levels might blunt LL-37's antimicrobial action against certain pathogens. Monitoring or moderating polyamine intake could be important when aiming to support innate immunity with LL-37. However, the findings are specific to gonorrhea and do not directly translate to broader health protocols.
Summary
The study shows that naturally occurring polyamines (like spermine and spermidine) can make the gonorrhea bacteria more resistant to the body's natural antimicrobial peptide LL-37 and to other similar peptides, but they don't affect resistance to regular antibiotics. This effect depends on how much polyamine is present and can be reversed.
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.
Study Information
pubmed
2010
2010-05-03T00:00:00.000Z
10.1128/iai.01301-09