Abstract

Sphingolipids are important structural membrane components and, together with cholesterol, are often organized in lipid rafts, where they act as signaling molecules in many cellular functions. They play crucial roles in regulating pathobiological processes, such as cancer, inflammation, and infectious diseases. The bioactive metabolites ceramide, sphingosine-1-phosphate, and sphingosine have been shown to be involved in the pathogenesis of several microbes. In contrast to ceramide, which often promotes bacterial and viral infections (for instance, by mediating adhesion and internalization), sphingosine, which is released from ceramide by the activity of ceramidases, kills many bacterial, viral, and fungal pathogens. In particular, sphingosine is an important natural component of the defense against bacterial pathogens in the respiratory tract. Pathologically reduced sphingosine levels in cystic fibrosis airway epithelial cells are normalized by inhalation of sphingosine, and coating plastic implants with sphingosine prevents bacterial infections. Pretreatment of cells with exogenous sphingosine also prevents the viral spike protein of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) from interacting with host cell receptors and inhibits the propagation of herpes simplex virus type 1 (HSV-1) in macrophages. Recent examinations reveal that the bactericidal effect of sphingosine might be due to bacterial membrane permeabilization and the subsequent death of the bacteria.

Highlights

  • This review focuses on sphingosine and its role in infectious diseases, and briefly discusses ceramide—a bioactive sphingolipid—and its derivative, sphingosine-1-phosphate

  • In 2017, our group showed that the high susceptibility of cystic fibrosis patients and mice to P. aeruginosa, S. aureus, and Acinetobacter baumanii was related to β1-integrin accumulation due to the increased ceramide level on the luminal membrane upper-airway epithelial cells in these hosts [22]

  • The results revealed that the accumulation of ceramide in cystic fibrosis cells trapped β1-integrins in the luminal membrane of CF bronchial, tracheal, and nasal epithelial cells

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Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Sphingosine (Sph) constitutes a class of natural products containing a long aliphatic chain with a polar 2-amino-1,3-diol terminus (2-amino-4-trans-octadecene-1,3-diol) It occurs in the cell membranes of all animals and many plants and plays an important role in various complex biological processes, such as cell growth, differentiation, autophagic processes and development [14,15]. Sphingosine has been connected with a variety of cellular processes, such as the induction of cell cycle arrest and apoptosis by modulating protein kinases and other signaling pathways [14]. It has roles in regulating the actin cytoskeleton and endocytosis, and has been shown to inhibit phosphokinase C (PKC) [17]. Inhaled nebulized sphingosine has been shown to be effective in both preventing and treating pneumonia in multiple CF mouse models without producing severe toxic side effects [21,22,23,24]

Sphingosine and Bacteria
Staphylococcus aureus
Pseudomonas aeruginosa
Neisseria gonorrhoeae
Sphingosine and Viruses
Model how sphingosine prevents
Sphingosine and Fungi
Conclusions
Findings
Methods
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