Evidence map›Paper›PMID 38918467›Full record

ArticleNature microbiology2024

Spatial mapping of mobile genetic elements and their bacterial hosts in complex microbiomes.

Benjamin Grodner, Hao Shi, Owen Farchione, Albert C Vill, Ioannis Ntekas, Peter J Diebold, David T Wu, Chia-Yu Chen, David M Kim, Warren R Zipfel and 2 more

Abstract read
In one paragraph

Article in Nature microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

  1. Review
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  15. Article
  16. Microbiome Single Cell Atlases Generated with a Commercial Instrument.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Benjamin GrodnerMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Hao ShiMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Owen FarchioneMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Albert C VillMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Ioannis NtekasMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Peter J DieboldMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
David T WuDivision of Periodontology, Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, MA, USA.ORCID http://orcid.org/0000-0002-9752-5377
Chia-Yu ChenDivision of Periodontology, Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, MA, USA.
David M KimDivision of Periodontology, Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, MA, USA.
Warren R ZipfelMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0003-2640-329X
Ilana L BritoMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0002-2250-3480
Iwijn De VlaminckMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA. vlaminck@cornell.edu.ORCID http://orcid.org/0000-0001-6085-7311

Funding

Precision monitoring of kidney transplants via single-cell and single-molecule sequencingDP2AI138242 · NIAID · CORNELL UNIVERSITY · PI DE VLAMINCK, IWIJN · 2017 to 2017
$2.3M
Spatially Resolved Metagenomics to Explore Tumor-Microbiome Interactions in Human Colorectal CancerR33CA235302 · NCI · CORNELL UNIVERSITY · PI BRITO, ILANA LAUREN, DE VLAMINCK, IWIJN · 2019 to 2021
$1.1M
Broad wavelength range Zeiss 780 NLO/confocal system for the Cornell Imaging CoreS10OD018516 · OD · CORNELL UNIVERSITY · PI ZIPFEL, WARREN R · 2014 to 2014
$834k
NCI NIH HHS R33 CA235302NIAID NIH HHS DP2 AI138242NIH HHS S10 OD018516U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1DP2AI138242U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1R33CA235302U.S. Department of Health & Human Services | National Institutes of Health (NIH) S10OD018516
6 · The paper itself

Abstract

The exchange of mobile genetic elements (MGEs) facilitates the spread of functional traits including antimicrobial resistance within bacterial communities. Tools to spatially map MGEs and identify their bacterial hosts in complex microbial communities are currently lacking, limiting our understanding of this process. Here we combined single-molecule DNA fluorescence in situ hybridization (FISH) with multiplexed ribosomal RNA-FISH to enable simultaneous visualization of both MGEs and bacterial taxa. We spatially mapped bacteriophage and antimicrobial resistance (AMR) plasmids and identified their host taxa in human oral biofilms. This revealed distinct clusters of AMR plasmids and prophage, coinciding with densely packed regions of host bacteria. Our data suggest spatial heterogeneity in bacterial taxa results in heterogeneous MGE distribution within the community, with MGE clusters resulting from horizontal gene transfer hotspots or expansion of MGE-carrying strains. Our approach can help advance the study of AMR and phage ecology in biofilms.

Indexed as

BacteriaBacteriophagesBiofilmsGene Transfer, HorizontalIn Situ Hybridization, FluorescenceInterspersed Repetitive SequencesMicrobiotaPlasmidsProphagesDrug Resistance, BacterialHumansMouth

Identifiers

PMID38918467
PMCPMC11371653

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.