Evidence map›Paper›PMID 23274667›Full record

ArticleAntimicrobial agents and chemotherapy2013

Mutational and transcriptomic changes involved in the development of macrolide resistance in Campylobacter jejuni.

Haihong Hao, Zonghui Yuan, Zhangqi Shen, Jing Han, Orhan Sahin, Peng Liu, Qijing Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.8field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Molecular Basis of Macrolide Resistance inBioMed research international · 2018
    Article
  11. Article
  12. Review
  13. Article
  14. Frontiers in microbiology · 2017
    Article
  15. Article
  16. Frontiers in microbiology · 2017
    Article
  17. Article
  18. Review
  19. Article
  20. Article
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 2 institutions in 2 countries.

Haihong HaoNational Reference Laboratory of Veterinary Drug Residues (HZAU)/MOA Key Laboratory for Detection of Veterinary Drug Residues in Foods, Huazhong Agricultural University, Wuhan, People's Republic of China.
Zonghui Yuan
Zhangqi Shen
Jing Han
Orhan Sahin
Peng Liu
Qijing Zhang
Iowa State University · USHuazhong Agricultural University · CN

Funding

Mechanisms of Antibiotic Efflux in CampylobacterR01DK063008 · NIDDK · IOWA STATE UNIVERSITY · PI ZHANG, QIJING · 2003 to 2011
$2.1M
NIDDK NIH HHS R01 DK063008NIDDK NIH HHS R01DK063008
6 · The paper itself

Abstract

Macrolide antibiotics are important for clinical treatment of infections caused by Campylobacter jejuni. Development of resistance to this class of antibiotics in Campylobacter is a complex process, and the dynamic molecular changes involved in this process remain poorly defined. Multiple lineages of macrolide-resistant mutants were selected by stepwise exposure of C. jejuni to escalating doses of erythromycin or tylosin. Mutations in target genes were determined by DNA sequencing, and the dynamic changes in the expression of antibiotic efflux transporters and the transcriptome of C. jejuni were examined by real-time reverse transcription-PCR, immunoblotting, and DNA microarray analysis. Multiple types of mutations in ribosomal proteins L4 and L22 occurred early during stepwise selection. On the contrary, the mutations in the 23S rRNA gene, mediating high resistance to macrolides, were observed only in the late-stage mutants. Upregulation of antibiotic efflux genes was observed in the intermediately resistant mutants, and the magnitude of upregulation declined with the occurrence of mutations in the 23S rRNA gene. DNA microarray analysis revealed the differential expression of 265 genes, most of which occurred in the intermediate mutant, including the upregulation of genes encoding ribosomal proteins and the downregulation of genes involved in energy metabolism and motility. These results indicate (i) that mutations in L4 and L22 along with temporal overexpression of antibiotic efflux genes precede and may facilitate the development of high-level macrolide resistance and (ii) that the development of macrolide resistance affects the pathways important for physiology and metabolism in C. jejuni, providing an explanation for the reduced fitness of macrolide-resistant Campylobacter.

Indexed as

TranscriptomeAnti-Bacterial AgentsATP-Binding Cassette, Sub-Family C ProteinsCampylobacter jejuniDrug Resistance, Multiple, BacterialErythromycinGene Expression ProfilingGene Expression Regulation, BacterialGenes, rRNAMacrolidesMicrobial Sensitivity TestsMutationOligonucleotide Array Sequence AnalysisRibosomal ProteinsRNA, Ribosomal, 23STylosinAnti-Bacterial AgentsATP-Binding Cassette, Sub-Family C ProteinsErythromycinMacrolidesRibosomal ProteinsRNA, Ribosomal, 23STylosin

Identifiers

PMID23274667
PMCPMC3591901
OpenAlexW1995420529

What OpenQuestion holds

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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.