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. 2012 Mar;56(3):1157-61.
doi: 10.1128/AAC.05151-11. Epub 2011 Dec 12.

Antibacterial activity of sphingoid bases and fatty acids against Gram-positive and Gram-negative bacteria

Affiliations

Antibacterial activity of sphingoid bases and fatty acids against Gram-positive and Gram-negative bacteria

Carol L Fischer et al. Antimicrob Agents Chemother. 2012 Mar.

Abstract

There is growing evidence that the role of lipids in innate immunity is more important than previously realized. How lipids interact with bacteria to achieve a level of protection, however, is still poorly understood. To begin to address the mechanisms of antibacterial activity, we determined MICs and minimum bactericidal concentrations (MBCs) of lipids common to the skin and oral cavity--the sphingoid bases D-sphingosine, phytosphingosine, and dihydrosphingosine and the fatty acids sapienic acid and lauric acid--against four Gram-negative bacteria and seven Gram-positive bacteria. Exact Kruskal-Wallis tests of these values showed differences among lipid treatments (P < 0.0001) for each bacterial species except Serratia marcescens and Pseudomonas aeruginosa. D-sphingosine (MBC range, 0.3 to 19.6 μg/ml), dihydrosphingosine (MBC range, 0.6 to 39.1 μg/ml), and phytosphingosine (MBC range, 3.3 to 62.5 μg/ml) were active against all bacteria except S. marcescens and P. aeruginosa (MBC > 500 μg/ml). Sapienic acid (MBC range, 31.3 to 375.0 μg/ml) was active against Streptococcus sanguinis, Streptococcus mitis, and Fusobacterium nucleatum but not active against Escherichia coli, Staphylococcus aureus, S. marcescens, P. aeruginosa, Corynebacterium bovis, Corynebacterium striatum, and Corynebacterium jeikeium (MBC > 500 μg/ml). Lauric acid (MBC range, 6.8 to 375.0 μg/ml) was active against all bacteria except E. coli, S. marcescens, and P. aeruginosa (MBC > 500 μg/ml). Complete killing was achieved as early as 0.5 h for some lipids but took as long as 24 h for others. Hence, sphingoid bases and fatty acids have different antibacterial activities and may have potential for prophylactic or therapeutic intervention in infection.

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Figures

Fig 1
Fig 1
Kinetic killing of select bacteria with lipid treatments at 10 times the MIC. Where no bacteria were recovered, +1 was added to the zero values before log transformation of the data. A geometric mean of n = 3 is shown for each data point. The error bars show standard errors of the mean (SEM). (A) F. nucleatum with d-sphingosine, phytosphingosine, and lauric acid. (B) S. sanguinis with d-sphingosine, phytosphingosine, and sapienic acid. Additional kill kinetics are shown in Fig. S1C to F in the supplemental material.

References

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