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Human-associated microbiota suppress invading bacteria even under disruption by antibiotics

View ORCID ProfileAndrew D. Letten, View ORCID ProfileMichael Baumgartner, Katia R. Pfrunder-Cardozo, Jonathan Levine, Alex R. Hall
doi: https://doi.org/10.1101/2020.09.02.279307
Andrew D. Letten
1School of Biological Sciences, University of Queensland, Brisbane, Queensland 4072, Australia
2Institute of Integrative Biology, Department of Environmental Systems Science, ETH Zürich, 8092 Zürich, Switzerland
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  • For correspondence: a.letten@uq.edu.au
Michael Baumgartner
2Institute of Integrative Biology, Department of Environmental Systems Science, ETH Zürich, 8092 Zürich, Switzerland
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Katia R. Pfrunder-Cardozo
2Institute of Integrative Biology, Department of Environmental Systems Science, ETH Zürich, 8092 Zürich, Switzerland
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Jonathan Levine
3Dept of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, 08544-1003 USA
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Alex R. Hall
2Institute of Integrative Biology, Department of Environmental Systems Science, ETH Zürich, 8092 Zürich, Switzerland
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Abstract

In light of their adverse impacts on resident microbial communities, it is widely predicted that broad-spectrum antibiotics can promote the spread of resistance by releasing resistant strains from competition with other strains and species. We investigated the invasion success of a resistant strain of Escherichia coli inoculated into human-associated communities in the presence and absence of the broad and narrow spectrum antibiotics rifampicin and polymyxin B, respectively. We found strong evidence of community-level suppression of the resistant strain in the absence of antibiotics and, despite large changes in community composition and abundance following rifampicin exposure, suppression of the invading resistant strain was maintained in both antibiotic treatments. Instead, the strength of competitive suppression was more strongly associated with the individual donor from which the community was sampled. This suggests microbiome composition strongly influences susceptibility to invasion by antibiotic-resistant strains, but at least some antibiotic-associated disruption can be tolerated before invasion susceptibility increases. A deeper understanding of this association will aid the development of ecologically-aware strategies for managing antibiotic resistance.

Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted September 02, 2020.
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Human-associated microbiota suppress invading bacteria even under disruption by antibiotics
Andrew D. Letten, Michael Baumgartner, Katia R. Pfrunder-Cardozo, Jonathan Levine, Alex R. Hall
bioRxiv 2020.09.02.279307; doi: https://doi.org/10.1101/2020.09.02.279307
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Human-associated microbiota suppress invading bacteria even under disruption by antibiotics
Andrew D. Letten, Michael Baumgartner, Katia R. Pfrunder-Cardozo, Jonathan Levine, Alex R. Hall
bioRxiv 2020.09.02.279307; doi: https://doi.org/10.1101/2020.09.02.279307

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