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Published on: July 7, 2020
Dissecting the Molecular Mechanism of Colistin Resistance in mcr-1 Bacteria
Jianguo Li1,2, Roger Beuerman2,3, Chandra S Verma1,4,5
1Bioinformatics Institute, A*STAR, 30 Biopolis street, Matrix, Singapore 138671.
Abstract:
Colistin or polymyxin B is the last resort antibiotic to treat infections of multidrug-resistant Gram-negative bacteria by disrupting their outer membranes. The recent emergence of Gram-negative bacteria that demonstrate colistin resistance, particularly plasmid-mediated mobile colistin resistance (mcr), poses a big challenge to the treatment of multidrug resistance infections. Using molecular dynamics simulations, we explore the mechanism of colistin resistance in a model lipid A bilayer mimicking the Gram-negative mcr-1 bacterial outer membrane. The simulation results reveal that the outer membrane of normal Gram-negative bacteria is stabilized by salt bridges between positively charged divalent ions and negatively charged phosphate groups of the membranes. In the presence of positively charged polymyxin B, these salt bridges are disrupted, and calcium is released into the aqueous phase, resulting in membrane disruption. In contrast, the lipid A in the outer membrane of mcr-1 bacteria has a novel modification, this being a covalently attached phosphoethanolamine group. This group enables the formation of a large number of hydrogen bonds between the amine and phosphate groups, resulting in an electrostatic net on the membrane. This extensive noncovalent electrostatic cross-linking between the lipid molecules collectively enhances the membrane stability and results in resistance to the action of cationic peptides such as polymyxin B. The simulation results shed new atomistic insights for understanding the mechanistic basis of colistin resistance and provide clues for the design of new membrane disruptors and permeabilizers to treat mcr-1 infections.
Insights
Mobile colistin resistance (mcr) in Gram-negative bacteria challenges antibiotic treatments. Molecular dynamics simulations reveal mcr-1 bacteria resist colistin by forming a stable membrane through novel lipid A modifications, blocking antibiotic action.
Area of Science:
- Microbiology and Molecular Biology
- Biophysics and Computational Chemistry
Background:
- Colistin and polymyxin B are last-resort antibiotics against multidrug-resistant Gram-negative bacteria.
- Emergence of plasmid-mediated mobile colistin resistance (mcr) genes poses a significant threat to public health.
- Understanding the molecular mechanisms of mcr is crucial for developing new therapeutic strategies.
Purpose of the Study:
- To elucidate the atomistic mechanism of colistin resistance conferred by mcr-1.
- To investigate how modifications in lipid A affect bacterial outer membrane stability.
- To provide insights for designing novel agents to overcome mcr-mediated resistance.
Main Methods:
- Molecular dynamics (MD) simulations of model lipid A bilayers.
- Mimicking both normal and mcr-1 modified Gram-negative bacterial outer membranes.
- Analysis of electrostatic interactions, salt bridges, and hydrogen bonding within the membrane.
Main Results:
- Normal membranes are stabilized by salt bridges disrupted by polymyxin B, leading to membrane damage.
- mcr-1 associated lipid A exhibits a novel phosphoethanolamine modification.
- This modification creates extensive hydrogen bonding and electrostatic cross-linking, enhancing membrane stability and conferring resistance to polymyxin B.
Conclusions:
- The phosphoethanolamine modification in mcr-1 bacteria significantly increases outer membrane stability.
- This enhanced stability acts as a barrier against cationic antimicrobial peptides like colistin and polymyxin B.
- Findings offer atomistic insights into colistin resistance and guide the development of new drugs targeting mcr-1 infections.
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