Evidence map›Paper›PMID 33244063›Full record

ArticleScientific reports2020

Integron gene cassettes harboring novel variants of D-alanine-D-alanine ligase confer high-level resistance to D-cycloserine.

Md Ajijur Rahman, Frank Kaiser, Shirin Jamshidi, Marta Freitas Monteiro, Khondaker Miraz Rahman, Peter Mullany, Adam P Roberts

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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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

7 authors at 3 institutions in 3 countries.

Md Ajijur RahmanDepartment of Microbial Diseases, University College London, 256 Gray's Inn Road, London, WC1X 8LD, UK.
Frank KaiserDepartment of Microbial Diseases, University College London, 256 Gray's Inn Road, London, WC1X 8LD, UK.
Shirin JamshidiSchool of Cancer and Pharmaceutical Science, King's College London, London, SE1 9NH, UK.
Marta Freitas MonteiroDepartment of Microbial Diseases, University College London, 256 Gray's Inn Road, London, WC1X 8LD, UK.
Khondaker Miraz RahmanSchool of Cancer and Pharmaceutical Science, King's College London, London, SE1 9NH, UK.
Peter MullanyDepartment of Microbial Diseases, University College London, 256 Gray's Inn Road, London, WC1X 8LD, UK.
Adam P RobertsDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA, UK. Adam.Roberts@lstmed.ac.uk.
University College London · GBKing's College London · GBLiverpool School of Tropical Medicine · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibiotic resistance poses an increasing threat to global health. To tackle this problem, the identification of principal reservoirs of antibiotic resistance genes (ARGs) plus an understanding of drivers for their evolutionary selection are important. During a PCR-based screen of ARGs associated with integrons in saliva-derived metagenomic DNA of healthy human volunteers, two novel variants of genes encoding a D-alanine-D-alanine ligase (ddl6 and ddl7) located within gene cassettes in the first position of a reverse integron were identified. Treponema denticola was identified as the likely host of the ddl cassettes. Both ddl6 and ddl7 conferred high level resistance to D-cycloserine when expressed in Escherichia coli with ddl7 conferring four-fold higher resistance to D-cycloserine compared to ddl6. A SNP was found to be responsible for this difference in resistance phenotype between the two ddl variants. Molecular dynamics simulations were used to explain the mechanism of this phenotypic change at the atomic scale. A hypothesis for the evolutionary selection of ddl containing integron gene cassettes is proposed, based on molecular docking of plant metabolites within the ATP and D-cycloserine binding pockets of Ddl.

Indexed as

Anti-Bacterial AgentsCycloserineDrug Resistance, BacterialEscherichia coliHumansIntegronsMolecular Docking SimulationPeptide SynthasesTreponema denticolaAnti-Bacterial AgentsCycloserineD-alanylalanine synthetasePeptide Synthases

Identifiers

PMID33244063
PMCPMC7691350
OpenAlexW3106776774

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.