Evidence map›Paper›PMID 35301310›Full record

ArticleNature communications2022

Strain-level characterization of broad host range mobile genetic elements transferring antibiotic resistance from the human microbiome.

Samuel C Forster, Junyan Liu, Nitin Kumar, Emily L Gulliver, Jodee A Gould, Alejandra Escobar-Zepeda, Tapoka Mkandawire, Lindsay J Pike, Yan Shao, Mark D Stares and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
10.9field-weighted citation impact, top 1% of its field
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

77 citing papers in PubMed, 162 citations in OpenAlex.

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  19. PeerJ · 2026
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17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 2 countries.

Samuel C Forster *Host-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK. sam.forster@hudson.org.au.ORCID http://orcid.org/0000-0003-4144-2537
Junyan Liu *Host-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
Nitin KumarHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.ORCID http://orcid.org/0000-0002-2140-4923
Emily L GulliverCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Clayton, Vic, 3168, Australia.ORCID http://orcid.org/0000-0002-1820-6619
Jodee A GouldCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Clayton, Vic, 3168, Australia.
Alejandra Escobar-ZepedaHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
Tapoka MkandawireHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.ORCID http://orcid.org/0000-0002-3751-0114
Lindsay J PikeHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
Yan ShaoHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
Mark D StaresHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
Hilary P BrowneHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.ORCID http://orcid.org/0000-0002-1305-2470
B Anne NevilleHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK.
Trevor D LawleyHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, CB10 1SA, UK. tl2@sanger.ac.uk.ORCID http://orcid.org/0000-0002-4805-621X
Wellcome Sanger Institute · GBHudson Institute of Medical Research · AU

Funding

Wellcome TrustWellcome Trust 206194
6 · The paper itself

Abstract

Mobile genetic elements (MGEs) carrying antibiotic resistance genes (ARGs) disseminate ARGs when they mobilise into new bacterial hosts. The nature of such horizontal gene transfer (HGT) events between human gut commensals and pathogens remain poorly characterised. Here, we compare 1354 cultured commensal strains (540 species) to 45,403 pathogen strains (12 species) and find 64,188 MGE-mediated ARG transfer events between the two groups using established methods. Among the 5931 MGEs, we find 15 broad host range elements predicted to have crossed different bacterial phyla while also occurring in animal and environmental microbiomes. We experimentally demonstrate that predicted broad host range MGEs can mobilise from commensals Dorea longicatena and Hungatella hathewayi to pathogen Klebsiella oxytoca, crossing phyla simultaneously. Our work establishes the MGE-mediated ARG dissemination network between human gut commensals and pathogens and highlights broad host range MGEs as targets for future ARG dissemination management.

Indexed as

Host SpecificityMicrobiotaAnimalsAnti-Bacterial AgentsBacteriaDrug Resistance, MicrobialGenes, BacterialHumansInterspersed Repetitive SequencesAnti-Bacterial Agents

Identifiers

PMID35301310
PMCPMC8931123
OpenAlexW4220795136

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.