Abstract

The commonly believed mechanism of colistin against Gram-negative bacteria is to cause cell membrane lysis, whereas the mechanism of colistin against Gram-positive bacteria is extremely fragmented. In this study, we found that colistin treatment on Bacillus subtilis WB800, Paenibacillus polymyxa C12 and Paenibacillus polymyxa ATCC842 enhances not only the activities of α-ketoglutaric dehydrogenase and malate dehydrogenase in tricarboxylic acid (TCA) cycle, but also the relative expression levels of their encoding genes. Additionally, the oxaloacetate concentration also increases. Interestingly, the analysis of the relative expression of genes specific for respiratory chain showed that colistin treatment stimulates the respiratory chain in Gram-positive bacteria. Accordingly, the NAD+/NADH ratio increases and the oxidative level is then boosted up. As a result, the intensive oxidative damages are induced in Gram-positive bacteria and cells are killed. Notably, both rotenone and oligomycin, respectively, inhibiting NADH dehydrogenase and phosphorylation on respiratory chain can downgrade oxidative stress formation, thus alleviating the colistin-induced killing of Gram-positive cells. Besides, thiourea-based scavenging for reactive oxygen species also rescues the colistin-subjected cells. These data collectively demonstrate that colistin stimulates both TCA cycle and respiratory chain in Gram-positive bacteria, leading to the enhancement of NADH metabolism and resulting in the generation of oxidative damages in Gram-positive cells. Our studies provide a better understanding of antibacterial mechanism of colistin against Gram-positive bacteria, which is important for knowledge on bacterial resistance to colistin happening via the inhibition of respiratory chain and manipulation of its production.

Highlights

  • As a kind of alkaline polypeptide antibiotic produced by Paenibacillus polymyxa, polymyxin E, called colistin, is increasingly used as one of the last-line therapeutic options for treatment on infections from multidrug-resistant Gram-negative bacteria [1,2,3]

  • Oxidative Stress Caused by Colistin in Gram-Positive Bacteria

  • Minimal inhibitory concentration (MIC) of colistin against three Gram-positive bacteria was measured by disk diffusion assay

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Summary

Introduction

As a kind of alkaline polypeptide antibiotic produced by Paenibacillus polymyxa, polymyxin E, called colistin, is increasingly used as one of the last-line therapeutic options for treatment on infections from multidrug-resistant Gram-negative bacteria [1,2,3]. The commonly believed mechanism of its action on the Gram-negatives is to cause cell membrane lysis [4]. Colistin can electrostatically interact with negatively charged lipopolysaccharide (LPS) and replace divalent cations on the outer membrane (OM) [5,6]. It will penetrate OM via a self-promoted uptake mechanism and will result in the leakage of the inner membrane (IM), leading to cell death [7]. The proposed mechanism claimed that the positively charged residues on colistin may target the negatively charged

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