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High-throughput mapping of the phage resistance landscape in E. coli

View ORCID ProfileVivek K. Mutalik, Benjamin A. Adler, Harneet S. Rishi, Denish Piya, Crystal Zhong, View ORCID ProfileBritt Koskella, Richard Calendar, Pavel Novichkov, View ORCID ProfileMorgan N. Price, View ORCID ProfileAdam M. Deutschbauer, View ORCID ProfileAdam P. Arkin
doi: https://doi.org/10.1101/2020.02.15.951020
Vivek K. Mutalik
1Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA
2Innovative Genomics Institute, Berkeley, CA, 94704, USA
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  • ORCID record for Vivek K. Mutalik
  • For correspondence: vkmutalik@lbl.gov aparkin@lbl.gov
Benjamin A. Adler
2Innovative Genomics Institute, Berkeley, CA, 94704, USA
3Department of Bioengineering, University of California - Berkeley, Berkeley, CA, 94720, USA
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Harneet S. Rishi
4Biophysics Graduate Group, University of California - Berkeley, Berkeley, CA, 94720, USA
5Designated Emphasis Program in Computational and Genomic Biology, University of California - Berkeley, Berkeley, CA, 94720, USA
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Denish Piya
2Innovative Genomics Institute, Berkeley, CA, 94704, USA
3Department of Bioengineering, University of California - Berkeley, Berkeley, CA, 94720, USA
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Crystal Zhong
1Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA
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Britt Koskella
6Department of Integrative Biology, University of California - Berkeley, Berkeley, CA, 94720, USA
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Richard Calendar
7Department of Molecular and Cell Biology, University of California - Berkeley, Berkeley, CA, 94720, USA
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Pavel Novichkov
1Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA
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Morgan N. Price
1Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA
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Adam M. Deutschbauer
1Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA
2Innovative Genomics Institute, Berkeley, CA, 94704, USA
8Department of Plant and Microbial Biology, University of California - Berkeley, Berkeley, CA, 94720, USA
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Adam P. Arkin
1Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA
2Innovative Genomics Institute, Berkeley, CA, 94704, USA
3Department of Bioengineering, University of California - Berkeley, Berkeley, CA, 94720, USA
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  • For correspondence: vkmutalik@lbl.gov aparkin@lbl.gov
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Abstract

Bacteriophages (phages) are critical players in the dynamics and function of microbial communities and drive processes as diverse as global biogeochemical cycles and human health. Phages tend to be predators finely tuned to attack specific hosts, even down to the strain level, which in turn defend themselves using an array of mechanisms. However, to date, efforts to rapidly and comprehensively identify bacterial host factors important in phage infection and resistance have yet to be fully realized. Here, we globally map the host genetic determinants involved in resistance to 14 phylogenetically diverse double-stranded DNA phages using two model Escherichia coli strains (K-12 and BL21) with known sequence divergence to demonstrate strain-specific differences. Using genome-wide loss-of-function and gain-of-function genetic technologies, we are able to confirm previously described phage receptors as well as uncover a number of previously unknown host factors that confer resistance to one or more of these phages. We uncover differences in resistance factors that strongly align with the susceptibility of K-12 and BL21 to specific phage. We also identify both phage specific mechanisms, such as the unexpected role of cyclic-di-GMP in host sensitivity to phage N4, and more generic defenses, such as the overproduction of colanic acid capsular polysaccharide that defends against a wide array of phages. Our results indicate that host responses to phages can occur via diverse cellular mechanisms. Our systematic and high-throughput genetic workflow to characterize phage-host interaction determinants can be extended to diverse bacteria to generate datasets that allow predictive models of how phage-mediated selection will shape bacterial phenotype and evolution. The results of this study and future efforts to map the phage resistance landscape will lead to new insights into the coevolution of hosts and their phage, which can ultimately be used to design better phage therapeutic treatments and tools for precision microbiome engineering.

Footnotes

  • https://doi.org/10.6084/m9.figshare.11859216.v1

  • https://doi.org/10.6084/m9.figshare.11413128

  • https://doi.org/10.6084/m9.figshare.11838879.v2

Copyright 
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-ND 4.0 International license.
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Posted February 16, 2020.
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High-throughput mapping of the phage resistance landscape in E. coli
Vivek K. Mutalik, Benjamin A. Adler, Harneet S. Rishi, Denish Piya, Crystal Zhong, Britt Koskella, Richard Calendar, Pavel Novichkov, Morgan N. Price, Adam M. Deutschbauer, Adam P. Arkin
bioRxiv 2020.02.15.951020; doi: https://doi.org/10.1101/2020.02.15.951020
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High-throughput mapping of the phage resistance landscape in E. coli
Vivek K. Mutalik, Benjamin A. Adler, Harneet S. Rishi, Denish Piya, Crystal Zhong, Britt Koskella, Richard Calendar, Pavel Novichkov, Morgan N. Price, Adam M. Deutschbauer, Adam P. Arkin
bioRxiv 2020.02.15.951020; doi: https://doi.org/10.1101/2020.02.15.951020

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