Extracellular Polymeric Substance Protects Some Cells in an <i>Escherichia coli</i> Biofilm from the Biomechanical Consequences of Treatment with Magainin 2

Bacterial biofilms have long been recognized as a source of persistent infections and industrial contamination with their intransigence generally attributed to their protective layer of extracellular polymeric substances (EPS). EPS, consisting of secreted nucleic acids, proteins, and polysaccharides...

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Main Authors: Helen M. Greer, Kanesha Overton, Megan A. Ferguson, Eileen M. Spain, Louise E. O. Darling, Megan E. Núñez, Catherine B. Volle
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/9/5/976
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spelling doaj-81403204bbe44478bfead00889c9487f2021-04-30T23:04:37ZengMDPI AGMicroorganisms2076-26072021-04-01997697610.3390/microorganisms9050976Extracellular Polymeric Substance Protects Some Cells in an <i>Escherichia coli</i> Biofilm from the Biomechanical Consequences of Treatment with Magainin 2Helen M. Greer0Kanesha Overton1Megan A. Ferguson2Eileen M. Spain3Louise E. O. Darling4Megan E. Núñez5Catherine B. Volle6Department of Biology, Cottey College, Nevada, MO 64772, USADepartment of Biology, Cottey College, Nevada, MO 64772, USADepartment of Chemistry, State University of New York, New Paltz, NY 12561, USADepartment of Chemistry, Occidental College, Los Angeles, CA 90041, USADepartment of Biological Sciences and Program in Biochemistry, Wellesley College, Wellesley, MA 02481, USADepartment of Chemistry and Program in Biochemistry, Wellesley College, Wellesley, MA 02481, USADepartments of Biology and Chemistry, Cornell College, Mount Vernon, IA 52314, USABacterial biofilms have long been recognized as a source of persistent infections and industrial contamination with their intransigence generally attributed to their protective layer of extracellular polymeric substances (EPS). EPS, consisting of secreted nucleic acids, proteins, and polysaccharides, make it difficult to fully eliminate biofilms by conventional chemical or physical means. Since most bacteria are capable of forming biofilms, understanding how biofilms respond to new antibiotic compounds and components of the immune system has important ramifications. Antimicrobial peptides (AMPs) are both potential novel antibiotic compounds and part of the immune response in many different organisms. Here, we use atomic force microscopy to investigate the biomechanical changes that occur in individual cells when a biofilm is exposed to the AMP magainin 2 (MAG2), which acts by permeabilizing bacterial membranes. While MAG2 is able to prevent biofilm initiation, cells in an established biofilm can withstand exposure to high concentrations of MAG2. Treated cells in the biofilm are classified into two distinct populations after treatment: one population of cells is indistinguishable from untreated cells, maintaining cellular turgor pressure and a smooth outer surface, and the second population of cells are softer than untreated cells and have a rough outer surface after treatment. Notably, the latter population is similar to planktonic cells treated with MAG2. The EPS likely reduces the local MAG2 concentration around the stiffer cells since once the EPS was enzymatically removed, all cells became softer and had rough outer surfaces. Thus, while MAG2 appears to have the same mechanism of action in biofilm cells as in planktonic ones, MAG2 cannot eradicate a biofilm unless coupled with the removal of the EPS.https://www.mdpi.com/2076-2607/9/5/976biofilmmagainin 2atomic force microscopycell stiffnesssurface roughness
collection DOAJ
language English
format Article
sources DOAJ
author Helen M. Greer
Kanesha Overton
Megan A. Ferguson
Eileen M. Spain
Louise E. O. Darling
Megan E. Núñez
Catherine B. Volle
spellingShingle Helen M. Greer
Kanesha Overton
Megan A. Ferguson
Eileen M. Spain
Louise E. O. Darling
Megan E. Núñez
Catherine B. Volle
Extracellular Polymeric Substance Protects Some Cells in an <i>Escherichia coli</i> Biofilm from the Biomechanical Consequences of Treatment with Magainin 2
Microorganisms
biofilm
magainin 2
atomic force microscopy
cell stiffness
surface roughness
author_facet Helen M. Greer
Kanesha Overton
Megan A. Ferguson
Eileen M. Spain
Louise E. O. Darling
Megan E. Núñez
Catherine B. Volle
author_sort Helen M. Greer
title Extracellular Polymeric Substance Protects Some Cells in an <i>Escherichia coli</i> Biofilm from the Biomechanical Consequences of Treatment with Magainin 2
title_short Extracellular Polymeric Substance Protects Some Cells in an <i>Escherichia coli</i> Biofilm from the Biomechanical Consequences of Treatment with Magainin 2
title_full Extracellular Polymeric Substance Protects Some Cells in an <i>Escherichia coli</i> Biofilm from the Biomechanical Consequences of Treatment with Magainin 2
title_fullStr Extracellular Polymeric Substance Protects Some Cells in an <i>Escherichia coli</i> Biofilm from the Biomechanical Consequences of Treatment with Magainin 2
title_full_unstemmed Extracellular Polymeric Substance Protects Some Cells in an <i>Escherichia coli</i> Biofilm from the Biomechanical Consequences of Treatment with Magainin 2
title_sort extracellular polymeric substance protects some cells in an <i>escherichia coli</i> biofilm from the biomechanical consequences of treatment with magainin 2
publisher MDPI AG
series Microorganisms
issn 2076-2607
publishDate 2021-04-01
description Bacterial biofilms have long been recognized as a source of persistent infections and industrial contamination with their intransigence generally attributed to their protective layer of extracellular polymeric substances (EPS). EPS, consisting of secreted nucleic acids, proteins, and polysaccharides, make it difficult to fully eliminate biofilms by conventional chemical or physical means. Since most bacteria are capable of forming biofilms, understanding how biofilms respond to new antibiotic compounds and components of the immune system has important ramifications. Antimicrobial peptides (AMPs) are both potential novel antibiotic compounds and part of the immune response in many different organisms. Here, we use atomic force microscopy to investigate the biomechanical changes that occur in individual cells when a biofilm is exposed to the AMP magainin 2 (MAG2), which acts by permeabilizing bacterial membranes. While MAG2 is able to prevent biofilm initiation, cells in an established biofilm can withstand exposure to high concentrations of MAG2. Treated cells in the biofilm are classified into two distinct populations after treatment: one population of cells is indistinguishable from untreated cells, maintaining cellular turgor pressure and a smooth outer surface, and the second population of cells are softer than untreated cells and have a rough outer surface after treatment. Notably, the latter population is similar to planktonic cells treated with MAG2. The EPS likely reduces the local MAG2 concentration around the stiffer cells since once the EPS was enzymatically removed, all cells became softer and had rough outer surfaces. Thus, while MAG2 appears to have the same mechanism of action in biofilm cells as in planktonic ones, MAG2 cannot eradicate a biofilm unless coupled with the removal of the EPS.
topic biofilm
magainin 2
atomic force microscopy
cell stiffness
surface roughness
url https://www.mdpi.com/2076-2607/9/5/976
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