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Title: Restructuring of Enterococcus faecalis biofilm architecture in response to antibiotic-induced stress

Journal Article · · npj Biofilms and Microbiomes
 [1];  [1]; ORCiD logo [2];  [1]
  1. Univ. of Minnesota, Minneapolis, MN (United States). Dept. of Microbiology and Immunology
  2. Univ. of Minnesota, Minneapolis, MN (United States). Dept. of Microbiology and Immunology. Dept. of Lab Medicine and Pathology

Bacterial biofilms are intrinsically resistant to antimicrobial treatment, which contributes to microbial persistence in clinical infections. Enterococcus faecalis is an opportunistic pathogen that readily forms biofilms and is the most prevalent enterococcal species identified in healthcare-associated infections. Since intrinsic resistance to multiple antibiotics is common for enterococci, and antibiotic resistance is elevated in biofilm populations, it is imperative to understand the mechanisms involved. Previously, we identified two glycosyltransferase genes whose disruption resulted in impaired nascent biofilm formation in the presence of antibiotic concentrations subinhibitory for parent growth and biofilm formation. The glycosyltransferases are involved in synthesis of the cell-wall-associated rhamnopolysaccharide Epa. Here we examined the effect of epa mutations on the temporal development of E. faecalis biofilms, and on the effects of antibiotics on pre-formed biofilms using scanning electron microscopy. We show that ΔepaOX mutant cells arrange into complex multidimensional biofilms independent of antibiotic exposure, while parent cells form biofilms that are monolayers in the absence of antibiotics. Remarkably, upon exposure to antibiotics parent biofilm cells restructure into complex three-dimensional biofilms resembling those of the ΔepaOX mutant without antibiotics. All biofilms exhibiting complex cellular architectures were less structurally stable than monolayer biofilms, with the biofilm cells exhibiting increased detachment. Our results indicate that E. faecalis biofilms restructure in response to cellular stress whether induced by antibiotics in the case of parent cells, or by deficiencies in Epa composition for the ΔepaOX strain. The data demonstrate a link between cellular architecture and antibiotic resistance of E. faecalis biofilms.

Research Organization:
Univ. of Minnesota, Minneapolis, MN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES); National Inst. of Health (NIH) (United States); National Science Foundation (NSF)
Grant/Contract Number:
FG02-93ER20097; AI58134; AI122742; T90 DE0227232; DMR-1229263
OSTI ID:
1425576
Journal Information:
npj Biofilms and Microbiomes, Vol. 3; ISSN 2055-5008
Publisher:
Springer NatureCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 44 works
Citation information provided by
Web of Science

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Fitness Restoration of a Genetically Tractable Enterococcus faecalis V583 Derivative To Study Decoration-Related Phenotypes of the Enterococcal Polysaccharide Antigen journal July 2019
Exopolysaccharide-mediated surface penetration as new virulence trait in Enterococcus faecalis journal January 2019
PolyGlcNAc-containing exopolymers enable surface penetration by non-motile Enterococcus faecalis journal February 2019
Exploiting biofilm phenotypes for functional characterization of hypothetical genes in Enterococcus faecalis journal September 2019
Biofilm Formation Drives Transfer of the Conjugative Element ICE Bs1 in Bacillus subtilis journal September 2018
Decoration of the enterococcal polysaccharide antigen EPA is essential for virulence, cell surface charge and interaction with effectors of the innate immune system journal May 2019
PolyGlcNAc-containing exopolymers enable surface penetration by non-motile Enterococcus faecalis text January 2019
Isolation of a novel phage and targeting biofilms of drug-resistant oral enterococci journal January 2020