Inhibition of Streptococcus mutans biofilms with bacterial-derived outer membrane vesicles

Abstract Background Biofilms are microbial communities surrounded by a self-produced extracellular matrix which protects them from environmental stress. Bacteria within biofilms are 10- to 1000-fold more resistant to antibiotics, making it challenging but imperative to develop new therapeutics that...

Full description

Bibliographic Details
Main Authors: Yihui Wang, Joseph P. Hoffmann, Sarah M. Baker, Kerstin Höner zu Bentrup, William C. Wimley, Joseph A. Fuselier, Jacob P. Bitoun, Lisa A. Morici
Format: Article
Language:English
Published: BMC 2021-08-01
Series:BMC Microbiology
Subjects:
Online Access:https://doi.org/10.1186/s12866-021-02296-x
id doaj-a404412068b94913a0083574a378a3b7
record_format Article
spelling doaj-a404412068b94913a0083574a378a3b72021-08-29T11:10:02ZengBMCBMC Microbiology1471-21802021-08-0121111210.1186/s12866-021-02296-xInhibition of Streptococcus mutans biofilms with bacterial-derived outer membrane vesiclesYihui Wang0Joseph P. Hoffmann1Sarah M. Baker2Kerstin Höner zu Bentrup3William C. Wimley4Joseph A. Fuselier5Jacob P. Bitoun6Lisa A. Morici7Department of Microbiology and Immunology, Tulane University School of MedicineDepartment of Microbiology and Immunology, Tulane University School of MedicineDepartment of Microbiology and Immunology, Tulane University School of MedicineDepartment of Microbiology and Immunology, Tulane University School of MedicineDepartment of Biochemistry and Molecular Biology, Tulane University School of MedicineDepartment of Medicine, Tulane University School of MedicineDepartment of Microbiology and Immunology, Tulane University School of MedicineDepartment of Microbiology and Immunology, Tulane University School of MedicineAbstract Background Biofilms are microbial communities surrounded by a self-produced extracellular matrix which protects them from environmental stress. Bacteria within biofilms are 10- to 1000-fold more resistant to antibiotics, making it challenging but imperative to develop new therapeutics that can disperse biofilms and eradicate infection. Gram-negative bacteria produce outer membrane vesicles (OMV) that play critical roles in communication, genetic exchange, cargo delivery, and pathogenesis. We have previously shown that OMVs derived from Burkholderia thailandensis inhibit the growth of drug-sensitive and drug-resistant bacteria and fungi. Results Here, we examine the antibiofilm activity of Burkholderia thailandensis OMVs against the oral biofilm-forming pathogen Streptococcus mutans. We demonstrate that OMV treatment reduces biofilm biomass, biofilm integrity, and bacterial cell viability. Both heat-labile and heat-stable components, including 4-hydroxy-3-methyl-2-(2-non-enyl)-quinoline and long-chain rhamnolipid, contribute to the antibiofilm activity of OMVs. When OMVs are co-administered with gentamicin, the efficacy of the antibiotic against S. mutans biofilms is enhanced. Conclusion These studies indicate that bacterial-derived OMVs are highly effective biological nanoparticles that can inhibit and potentially eradicate biofilms.https://doi.org/10.1186/s12866-021-02296-xBiofilmNanoparticleBacteriaBurkholderia
collection DOAJ
language English
format Article
sources DOAJ
author Yihui Wang
Joseph P. Hoffmann
Sarah M. Baker
Kerstin Höner zu Bentrup
William C. Wimley
Joseph A. Fuselier
Jacob P. Bitoun
Lisa A. Morici
spellingShingle Yihui Wang
Joseph P. Hoffmann
Sarah M. Baker
Kerstin Höner zu Bentrup
William C. Wimley
Joseph A. Fuselier
Jacob P. Bitoun
Lisa A. Morici
Inhibition of Streptococcus mutans biofilms with bacterial-derived outer membrane vesicles
BMC Microbiology
Biofilm
Nanoparticle
Bacteria
Burkholderia
author_facet Yihui Wang
Joseph P. Hoffmann
Sarah M. Baker
Kerstin Höner zu Bentrup
William C. Wimley
Joseph A. Fuselier
Jacob P. Bitoun
Lisa A. Morici
author_sort Yihui Wang
title Inhibition of Streptococcus mutans biofilms with bacterial-derived outer membrane vesicles
title_short Inhibition of Streptococcus mutans biofilms with bacterial-derived outer membrane vesicles
title_full Inhibition of Streptococcus mutans biofilms with bacterial-derived outer membrane vesicles
title_fullStr Inhibition of Streptococcus mutans biofilms with bacterial-derived outer membrane vesicles
title_full_unstemmed Inhibition of Streptococcus mutans biofilms with bacterial-derived outer membrane vesicles
title_sort inhibition of streptococcus mutans biofilms with bacterial-derived outer membrane vesicles
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2021-08-01
description Abstract Background Biofilms are microbial communities surrounded by a self-produced extracellular matrix which protects them from environmental stress. Bacteria within biofilms are 10- to 1000-fold more resistant to antibiotics, making it challenging but imperative to develop new therapeutics that can disperse biofilms and eradicate infection. Gram-negative bacteria produce outer membrane vesicles (OMV) that play critical roles in communication, genetic exchange, cargo delivery, and pathogenesis. We have previously shown that OMVs derived from Burkholderia thailandensis inhibit the growth of drug-sensitive and drug-resistant bacteria and fungi. Results Here, we examine the antibiofilm activity of Burkholderia thailandensis OMVs against the oral biofilm-forming pathogen Streptococcus mutans. We demonstrate that OMV treatment reduces biofilm biomass, biofilm integrity, and bacterial cell viability. Both heat-labile and heat-stable components, including 4-hydroxy-3-methyl-2-(2-non-enyl)-quinoline and long-chain rhamnolipid, contribute to the antibiofilm activity of OMVs. When OMVs are co-administered with gentamicin, the efficacy of the antibiotic against S. mutans biofilms is enhanced. Conclusion These studies indicate that bacterial-derived OMVs are highly effective biological nanoparticles that can inhibit and potentially eradicate biofilms.
topic Biofilm
Nanoparticle
Bacteria
Burkholderia
url https://doi.org/10.1186/s12866-021-02296-x
work_keys_str_mv AT yihuiwang inhibitionofstreptococcusmutansbiofilmswithbacterialderivedoutermembranevesicles
AT josephphoffmann inhibitionofstreptococcusmutansbiofilmswithbacterialderivedoutermembranevesicles
AT sarahmbaker inhibitionofstreptococcusmutansbiofilmswithbacterialderivedoutermembranevesicles
AT kerstinhonerzubentrup inhibitionofstreptococcusmutansbiofilmswithbacterialderivedoutermembranevesicles
AT williamcwimley inhibitionofstreptococcusmutansbiofilmswithbacterialderivedoutermembranevesicles
AT josephafuselier inhibitionofstreptococcusmutansbiofilmswithbacterialderivedoutermembranevesicles
AT jacobpbitoun inhibitionofstreptococcusmutansbiofilmswithbacterialderivedoutermembranevesicles
AT lisaamorici inhibitionofstreptococcusmutansbiofilmswithbacterialderivedoutermembranevesicles
_version_ 1721187079568752640