Evidence map›Paper›PMID 30375423›Full record

ArticleScientific reports2018

Transcriptome analysis of extended-spectrum β-lactamase-producing Escherichia coli and methicillin-resistant Staphylococcus aureus exposed to cefotaxime.

P R Brochmann, A Hesketh, B Jana, G H Brodersen, L Guardabassi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 52% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

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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 2 countries.

P R BrochmannUniversity of Copenhagen, Faculty of Health and Medical Sciences, Department of Veterinary and Animal Sciences, Frederiksberg, Denmark.
A HeskethUniversity of Cambridge, Department of Biochemistry and Cambridge Systems Biology Centre, Cambridge, United Kingdom. a.hesketh@brighton.ac.uk.
B JanaUniversity of Copenhagen, Faculty of Health and Medical Sciences, Department of Veterinary and Animal Sciences, Frederiksberg, Denmark.
G H BrodersenUniversity of Copenhagen, Faculty of Health and Medical Sciences, Department of Veterinary and Animal Sciences, Frederiksberg, Denmark.
L GuardabassiUniversity of Copenhagen, Faculty of Health and Medical Sciences, Department of Veterinary and Animal Sciences, Frederiksberg, Denmark. lg@sund.ku.dk.
University of Copenhagen · DKUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies on bacterial response to antibiotics mainly focused on susceptible strains. Here we characterized the transcriptional responses of distinct cephalosporin-resistant bacteria of public health relevance to cefotaxime (CTX), a cephalosporin widely used in clinical practice. Adaptation to therapeutic concentrations of CTX (30 µg/ml) was investigated by RNA sequencing in mid-exponential phase cultures of a methicillin-resistant Staphylococcus aureus (MRSA) and two genetically diverse E. coli producing CTX-M-15 or CMY-2 β-lactamase following genome sequencing and annotation for each strain. MRSA showed the most notable adaptive changes in the transcriptome after exposure to CTX, mainly associated with cell envelope functions. This reprogramming coincided with a transient reduction in cell growth, which also occurred in the CMY-2-producing E. coli but not in the CTX-M-15-producing strain. Re-establishment of growth in the CMY-2 producer proceeded without any notable adaptive transcriptional response, while limited reprogramming of gene transcription was observed in the CTX-M-15 producer. Our data show that the transcriptional response of CTX-resistant bacteria to CTX depends on the bacterial species, level of resistance and resistance determinant involved. Gene products induced in the presence of CTX may play an essential role for bacterial survival during therapy and merit further investigation as possible targets for potentiating CTX.

Indexed as

beta-Lactamasesbeta-LactamsCefotaximeEscherichia coliGene Expression ProfilingHumansMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsTranscriptomebeta-Lactamasesbeta-LactamsCefotaxime

Identifiers

PMID30375423
PMCPMC6207760
OpenAlexW2898299242

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.