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Spatial Mapping of Mobile Genetic Elements and their Cognate Hosts in Complex Microbiomes

View ORCID ProfileBenjamin Grodner, View ORCID ProfileHao Shi, Owen Farchione, View ORCID ProfileAlbert C. Vill, View ORCID ProfileIoannis Ntekas, View ORCID ProfilePeter J. Diebold, View ORCID ProfileWarren R. Zipfel, View ORCID ProfileIlana L. Brito, View ORCID ProfileIwijn De Vlaminck
doi: https://doi.org/10.1101/2023.06.09.544291
Benjamin Grodner
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA
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Hao Shi
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA
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Owen Farchione
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA
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Albert C. Vill
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA
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  • ORCID record for Albert C. Vill
Ioannis Ntekas
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA
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  • ORCID record for Ioannis Ntekas
Peter J. Diebold
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA
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Warren R. Zipfel
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA
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Ilana L. Brito
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA
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  • ORCID record for Ilana L. Brito
Iwijn De Vlaminck
1Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA
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  • ORCID record for Iwijn De Vlaminck
  • For correspondence: vlaminck@cornell.edu
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ABSTRACT

The frequent exchange of mobile genetic elements (MGEs) between bacteria accelerates the spread of functional traits, including antimicrobial resistance, within the human microbiome. Yet, progress in understanding these intricate processes has been hindered by the lack of tools to map the spatial spread of MGEs in complex microbial communities, and to associate MGEs to their bacterial hosts. To overcome this challenge, we present an imaging approach that pairs single molecule DNA Fluorescence In Situ Hybridization (FISH) with multiplexed ribosomal RNA FISH, thereby enabling the simultaneous visualization of both MGEs and host bacterial taxa. We used this methodology to spatially map bacteriophage and antimicrobial resistance (AMR) plasmids in human oral biofilms, and we studied the heterogeneity in their spatial distributions and demonstrated the ability to identify their host taxa. Our data revealed distinct clusters of both AMR plasmids and prophage, coinciding with densely packed regions of host bacteria in the biofilm. These results suggest the existence of specialized niches that maintain MGEs within the community, possibly acting as local hotspots for horizontal gene transfer. The methods introduced here can help advance the study of MGE ecology and address pressing questions regarding antimicrobial resistance and phage therapy.

Competing Interest Statement

H.S. is a co-founder at Kanvas Biosciences. I.D.V. is a member of the Scientific Advisory Board of Karius Inc., and GenDX and co-founder of Kanvas Biosciences. H.S. and I.D.V. are listed as inventors on patents related to multiplexed imaging methods.

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-NC-ND 4.0 International license.
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Posted June 09, 2023.
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Spatial Mapping of Mobile Genetic Elements and their Cognate Hosts in Complex Microbiomes
Benjamin Grodner, Hao Shi, Owen Farchione, Albert C. Vill, Ioannis Ntekas, Peter J. Diebold, Warren R. Zipfel, Ilana L. Brito, Iwijn De Vlaminck
bioRxiv 2023.06.09.544291; doi: https://doi.org/10.1101/2023.06.09.544291
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Spatial Mapping of Mobile Genetic Elements and their Cognate Hosts in Complex Microbiomes
Benjamin Grodner, Hao Shi, Owen Farchione, Albert C. Vill, Ioannis Ntekas, Peter J. Diebold, Warren R. Zipfel, Ilana L. Brito, Iwijn De Vlaminck
bioRxiv 2023.06.09.544291; doi: https://doi.org/10.1101/2023.06.09.544291

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