Evidence map›Paper›PMID 37348862›Full record

ArticleBioinformatics (Oxford, England)2023

Plasmid permissiveness of wastewater microbiomes can be predicted from 16S rRNA sequences by machine learning.

Danesh Moradigaravand, Liguan Li, Arnaud Dechesne, Joseph Nesme, Roberto de la Cruz, Huda Ahmad, Manuel Banzhaf, Søren J Sørensen, Barth F Smets, Jan-Ulrich Kreft

Open access · goldAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 5 institutions in 4 countries.

Danesh MoradigaravandLaboratory of Infectious Disease Epidemiology, KAUST Smart-Health Initiative and Biological and Environmental Science and Engineering (BESE) Division, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.ORCID 0000-0001-6652-5617
Liguan LiDepartment of Environmental Engineering, Technical University of Denmark, 2800 Kgs Lyngby, Denmark.ORCID 0000-0003-4349-0532
Arnaud DechesneDepartment of Environmental Engineering, Technical University of Denmark, 2800 Kgs Lyngby, Denmark.ORCID 0000-0002-6638-2158
Joseph NesmeDepartment of Biology, University of Copenhagen, 2100 Copenhagen, Denmark.ORCID 0000-0003-1929-5040
Roberto de la CruzCenter for Computational Biology, University of Birmingham, Birmingham, B15 2TT, United Kingdom.ORCID 0000-0001-5669-4302
Huda AhmadLaboratory of Infectious Disease Epidemiology, KAUST Smart-Health Initiative and Biological and Environmental Science and Engineering (BESE) Division, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.
Manuel BanzhafInstitute of Microbiology and Infection, University of Birmingham, Birmingham, B15 2TT, United Kingdom.ORCID 0000-0002-4682-1037
Søren J SørensenDepartment of Biology, University of Copenhagen, 2100 Copenhagen, Denmark.ORCID 0000-0001-6227-9906
Barth F SmetsDepartment of Environmental Engineering, Technical University of Denmark, 2800 Kgs Lyngby, Denmark.ORCID 0000-0003-4119-6292
Jan-Ulrich KreftCenter for Computational Biology, University of Birmingham, Birmingham, B15 2TT, United Kingdom.ORCID 0000-0002-2351-224X
University of Birmingham · GBKing Abdullah University of Science and Technology · SATechnical University of Denmark · DKUniversity of Copenhagen · DKChinese University of Hong Kong · HK

Funding

Medical Research Council MR/P028195/1
6 · The paper itself

Abstract

motivationWastewater treatment plants (WWTPs) harbor a dense and diverse microbial community. They constantly receive antimicrobial residues and resistant strains, and therefore provide conditions for horizontal gene transfer (HGT) of antimicrobial resistance (AMR) determinants. This facilitates the transmission of clinically important genes between, e.g. enteric and environmental bacteria, and vice versa. Despite the clinical importance, tools for predicting HGT remain underdeveloped.

resultsIn this study, we examined to which extent water cycle microbial community composition, as inferred by partial 16S rRNA gene sequences, can predict plasmid permissiveness, i.e. the ability of cells to receive a plasmid through conjugation, based on data from standardized filter mating assays using fluorescent bio-reporter plasmids. We leveraged a range of machine learning models for predicting the permissiveness for each taxon in the community, representing the range of hosts a plasmid is able to transfer to, for three broad host-range resistance IncP plasmids (pKJK5, pB10, and RP4). Our results indicate that the predicted permissiveness from the best performing model (random forest) showed a moderate-to-strong average correlation of 0.49 for pB10 [95% confidence interval (CI): 0.44-0.55], 0.43 for pKJK5 (0.95% CI: 0.41-0.49), and 0.53 for RP4 (0.95% CI: 0.48-0.57) with the experimental permissiveness in the unseen test dataset. Predictive phylogenetic signals occurred despite the broad host-range nature of these plasmids. Our results provide a framework that contributes to the assessment of the risk of AMR pollution in wastewater systems. AVAILABILITY AND IMPLEMENTATION: The predictive tool is available as an application at https://github.com/DaneshMoradigaravand/PlasmidPerm.

Indexed as

MicrobiotaWastewaterGene Transfer, HorizontalPermissivenessPhylogenyPlasmidsRNA, Ribosomal, 16SRNA, Ribosomal, 16SWastewater

Identifiers

PMID37348862
PMCPMC10318386
OpenAlexW4381610822

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.