Probiotic Escherichia coli Nissle 1917 inhibits bacterial persisters that survive fluoroquinolone treatment
Aims Bacterial persisters are rare phenotypic variants in clonal bacterial cultures that can endure antimicrobial therapy and potentially contribute to infection relapse. Here, we investigate the potential of leveraging microbial interactions to disrupt persisters as they resuscitate during the post...
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Published in | Journal of applied microbiology Vol. 132; no. 6; pp. 4020 - 4032 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
Oxford University Press
01.06.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Aims
Bacterial persisters are rare phenotypic variants in clonal bacterial cultures that can endure antimicrobial therapy and potentially contribute to infection relapse. Here, we investigate the potential of leveraging microbial interactions to disrupt persisters as they resuscitate during the post‐antibiotic treatment recovery period.
Methods and Results
We treated stationary‐phase E. coli MG1655 with a DNA‐damaging fluoroquinolone and co‐cultured the cells with probiotic E. coli Nissle following antibiotic removal. We found that E. coli Nissle reduced the survival of fluoroquinolone persisters and their progeny by over three orders of magnitude within 24 h. Using a bespoke H‐diffusion cell apparatus that we developed, we showed that E. coli Nissle antagonized the fluoroquinolone‐treated cells in a contact‐dependent manner. We further demonstrated that the fluoroquinolone‐treated cells can still activate the SOS response as they recover from antibiotic treatment in the presence of E. coli Nissle and that the persisters depend on TolC‐associated efflux systems to defend themselves against the action of E. coli Nissle.
Conclusion
Our results demonstrate that probiotic bacteria, such as E. coli Nissle, have the potential to inhibit persisters as they resuscitate following antibiotic treatment.
Significance and Impact of the Study
Bacterial persisters are thought to underlie chronic infections and they can lead to an increase in antibiotic‐resistant mutants in their progenies. Our data suggest that we can leverage the knowledge we gain on the interactions between microbial strains/species that interfere with persister resuscitation, such as those involving probiotic E. coli Nissle and E. coli MG1655 (a K‐12 strain), to bolster the activity of our existing antibiotics. |
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Bibliography: | This work was supported by funding from the University of Connecticut start‐up fund and the National Institutes of Health (NIH; DP2GM146456‐01). P.J.H. is supported by the NIH Skeletal, Craniofacial and Oral Biology Training Grant, grant number T90DE021989‐11. H.E.E. was supported by the UConn Summer Undergraduate Research Fund. The funders had no role in the design of our experiments or preparation of this manuscript. Funding Information ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Present address Hanna E. Englander, Cutaneous Microbiome & Inflammation Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland, USA |
ISSN: | 1364-5072 1365-2672 |
DOI: | 10.1111/jam.15541 |