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  Population dynamics of cross-protection against β-lactam antibiotics in droplet microreactors

Zhao, X., Ruelens, P., Farr, A. D., de Visser, J. A. G. M., & Baraban, L. (2023). Population dynamics of cross-protection against β-lactam antibiotics in droplet microreactors. Frontiers in Microbiology, 14: 1294790. doi:10.3389/fmicb.2023.1294790.

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 Creators:
Zhao, Xinne, Author
Ruelens, Philip, Author
Farr, Andrew D.1, Author           
de Visser, J. Arjan G. M., Author
Baraban, Larysa, Author
Affiliations:
1Department Microbial Population Biology, Max Planck Institute for Evolutionary Biology, Max Planck Society, ou_2421699              

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 Abstract: Introduction: Bacterial strains that are resistant to antibiotics may protect not only themselves, but also sensitive bacteria nearby if resistance involves antibiotic degradation. Such cross-protection poses a challenge to effective antibiotic therapy by enhancing the long-term survival of bacterial infections, however, the current understanding is limited.

Methods: In this study, we utilize an automated nanoliter droplet analyzer to study the interactions between Escherichia coli strains expressing a β-lactamase (resistant) and those not expressing it (sensitive) when exposed to the β-lactam antibiotic cefotaxime (CTX), with the aim to define criteria contributing to cross-protection.

Results: We observed a cross-protection window of CTX concentrations for the sensitive strain, extending up to approximately 100 times its minimal inhibitory concentration (MIC). Through both microscopy and enzyme activity analyses, we demonstrate that bacterial filaments, triggered by antibiotic stress, contribute to cross-protection.

Discussion: The antibiotic concentration window for cross-protection depends on the difference in β-lactamase activity between co-cultured strains: larger differences shift the ‘cross-protection window’ toward higher CTX concentrations. Our findings highlight the dependence of opportunities for cross-protection on the relative resistance levels of the strains involved and suggest a possible specific role for filamentation.

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Language(s): eng - English
 Dates: 2023-09-152023-12-062023-12-212023-12
 Publication Status: Issued
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.3389/fmicb.2023.1294790
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Title: Frontiers in Microbiology
  Abbreviation : Front. Microbiol.
Source Genre: Journal
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Publ. Info: Lausanne : Frontiers Media
Pages: - Volume / Issue: 14 Sequence Number: 1294790 Start / End Page: - Identifier: ISSN: 1664-302X
CoNE: https://pure.mpg.de/cone/journals/resource/1664-302X