Literature DB >> 32157424

Mechanisms of bactericidal action and resistance of polymyxins for Gram-positive bacteria.

Jianhua Yin1, Qiu Meng1, Dan Cheng1, Jianv Fu1, Qixia Luo2, Yanqiu Liu1, Zhiliang Yu3.   

Abstract

Polymyxins are cationic antimicrobial peptides used as the last-line therapy to treat multidrug-resistant Gram-negative bacterial infections. The bactericidal activity of polymyxins against Gram-negative bacteria relies on the electrostatic interaction between the positively charged polymyxins and the negatively charged lipid A of lipopolysaccharide (LPS). Given that Gram-positive bacteria lack an LPS-containing outer membrane, it is generally acknowledged that polymyxins are less active against Gram-positive bacteria. However, Gram-positive bacteria produce negatively charged teichoic acids, which may act as the target of polymyxins. More and more studies suggest that polymyxins have potential as a treatment for Gram-positive bacterial infection. This mini-review discusses recent advances in the mechanism of the antibacterial activity and resistance of polymyxins in Gram-positive bacteria.Key Points• Teichoic acids play a key role in the action of polymyxins on Gram-positive bacteria.• Polymyxin kills Gram-positive bacteria by disrupting cell surface and oxidative damage.• Modification of teichoic acids and phospholipids contributes to polymyxin resistance in Gram-positive bacteria.• Polymyxins have potential as a treatment for Gram-positive bacterial infection.

Entities:  

Keywords:  Gram-positive bacteria; Mode of action; Polymyxin resistance; Polymyxins

Mesh:

Substances:

Year:  2020        PMID: 32157424     DOI: 10.1007/s00253-020-10525-y

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  77 in total

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5.  Resistance phenotypes mediated by aminoacyl-phosphatidylglycerol synthases.

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8.  Staphylococcus aureus strains lacking D-alanine modifications of teichoic acids are highly susceptible to human neutrophil killing and are virulence attenuated in mice.

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Authors:  Ambrose L Cheung; Arnold S Bayer; Michael R Yeaman; Yan Q Xiong; Alan J Waring; Guido Memmi; Niles Donegan; Siyang Chaili; Soo-Jin Yang
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Review 2.  Causes of polymyxin treatment failure and new derivatives to fill the gap.

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Review 3.  Topical Antibiofilm Agents With Potential Utility in the Treatment of Chronic Rhinosinusitis: A Narrative Review.

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Review 6.  Polymyxins, the last-resort antibiotics: Mode of action, resistance emergence, and potential solutions.

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7.  Colistin-degrading proteases confer collective resistance to microbial communities during polymicrobial infections.

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