Evidence map›Paper›PMID 34282723›Full record

ArticleeLife2021

Linking plasmid-based beta-lactamases to their bacterial hosts using single-cell fusion PCR.

Peter J Diebold, Felicia N New, Michael Hovan, Michael J Satlin, Ilana L Brito

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Digital PCR linkage analysis resolvesMicrobiology spectrum · 2026
    Article
  2. Mapping 25 years of research on gut microbiota and antibiotic resistance: bibliometric insights and future directions.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Review
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  5. Microbiome Single Cell Atlases Generated with a Commercial Instrument.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

5 authors at 2 institutions in 1 country.

Peter J DieboldMeinig School of Biomedical Engineering, Cornell University, Ithaca, United States.ORCID 0000-0002-9189-9941
Felicia N NewMeinig School of Biomedical Engineering, Cornell University, Ithaca, United States.
Michael HovanRobert Wood Johnson Medical School, New Brunswick, United States.
Michael J SatlinWeill Cornell Medicine, Cornell University, New York, United States.
Ilana L BritoMeinig School of Biomedical Engineering, Cornell University, Ithaca, United States.ORCID 0000-0002-2250-3480
Cornell University · USJohnson University · US

Funding

Systems-Level Perspectives of Horizontal Gene Transfer Within the Human MicrobiomeDP2HL141007 · NHLBI · CORNELL UNIVERSITY · PI BRITO, ILANA LAUREN · 2017 to 2020
$2.6M
Rapid Identification of Neutropenic Patients at High Risk of CRE BacteremiaK23AI114994 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI SATLIN, MICHAEL JOSEPH · 2015 to 2019
$925k
NHLBI NIH HHS DP2 HL141007NIAID NIH HHS K23 AI114994
6 · The paper itself

Abstract

The horizonal transfer of plasmid-encoded genes allows bacteria to adapt to constantly shifting environmental pressures, bestowing functional advantages to their bacterial hosts such as antibiotic resistance, metal resistance, virulence factors, and polysaccharide utilization. However, common molecular methods such as short- and long-read sequencing of microbiomes cannot associate extrachromosomal plasmids with the genome of the host bacterium. Alternative methods to link plasmids to host bacteria are either laborious, expensive, or prone to contamination. Here we present the One-step Isolation and Lysis PCR (OIL-PCR) method, which molecularly links plasmid-encoded genes with the bacterial 16S rRNA gene via fusion PCR performed within an emulsion. After validating this method, we apply it to identify the bacterial hosts of three clinically relevant beta-lactamases within the gut microbiomes of neutropenic patients, as they are particularly vulnerable multidrug-resistant infections. We successfully detect the known association of a multi-drug resistant plasmid with

Indexed as

AnimalsAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesCell FusionChickensDrug Resistance, Multiple, BacterialEubacterialesFecesGene Transfer, HorizontalHumansKlebsiella pneumoniaeMicrobiotaPlasmidsPolymerase Chain ReactionRNA, Ribosomal, 16SAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesRNA, Ribosomal, 16Santibiotic resistance genesfusion PCRgeneticsgenomicshorizontal gene transferhumanhuman microbiomeinfectious diseasemicrobiologyplasmid

Identifiers

PMID34282723
PMCPMC8294855
OpenAlexW3184356459

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.