Evidence map›Paper›PMID 22919613›Full record

ArticleFrontiers in cellular and infection microbiology2012

A fluoroquinolone resistance associated mutation in gyrA Affects DNA supercoiling in Campylobacter jejuni.

Jing Han, Yang Wang, Orhan Sahin, Zhangqi Shen, Baoqing Guo, Jianzhong Shen, Qijing Zhang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
6.7field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 73 citations in OpenAlex.

  1. Trial
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  13. Antimicrobial resistance patterns and genes ofOpen veterinary journal · 2024
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  15. First Report ofInternational journal of molecular sciences · 2023
    Article
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  19. SVR-flaA typing of erythromycin- and ciprofloxacin-resistant Campylobacter jejuni strains isolated from poultry slaughterhouses in southern Brazil.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2023
    Article
  20. Genomic Characterization of Antibiotic-ResistantAntibiotics (Basel, Switzerland) · 2023
    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.

Jing HanDepartment of Veterinary Microbiology and Preventive Medicine, Iowa State University Ames, IA, USA.
Yang Wang
Orhan Sahin
Zhangqi Shen
Baoqing Guo
Jianzhong Shen
Qijing Zhang
Iowa State University · USChina 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

The prevalence of fluoroquinolone (FQ)-resistant Campylobacter has become a concern for public health. To facilitate the control of FQ-resistant (FQ(R)) Campylobacter, it is necessary to understand the impact of FQ(R) on the fitness of Campylobacter in its natural hosts as understanding fitness will help to determine and predict the persistence of FQ(R)Campylobacter. Previously it was shown that acquisition of resistance to FQ antimicrobials enhanced the in vivo fitness of FQ(R)Campylobacter. In this study, we confirmed the role of the Thr-86-Ile mutation in GyrA in modulating Campylobacter fitness by reverting the mutation to the wild-type (WT) allele, which resulted in the loss of the fitness advantage. Additionally, we determined if the resistance-conferring GyrA mutations alter the enzymatic function of the DNA gyrase. Recombinant WT gyrase and mutant gyrases with three different types of mutations (Thr-86-Ile, Thr-86-Lys, and Asp-90-Asn), which are associated with FQ(R) in Campylobacter, were generated in E. coli and compared for their supercoiling activities using an in vitro assay. The mutant gyrase with the Thr-86-Ile change showed a greatly reduced supercoiling activity compared with the WT gyrase, while other mutant gyrases did not show an altered supercoiling. Furthermore, we measured DNA supercoiling within Campylobacter cells using a reporter plasmid. Consistent with the results from the in vitro supercoiling assay, the FQ(R) mutant carrying the Thr-86-Ile change in GyrA showed much less DNA supercoiling than the WT strain and the mutant strains carrying other mutations. Together, these results indicate that the Thr-86-Ile mutation, which is predominant in clinical FQ(R)Campylobacter, modulates DNA supercoiling homeostasis in FQ(R)Campylobacter.

Indexed as

Drug Resistance, BacterialAmino Acid SubstitutionAnimalsAnti-Bacterial AgentsCampylobacter jejuniDNA, BacterialDNA GyraseDNA, SuperhelicalFluoroquinolonesHumansMutagenesis, Site-DirectedMutation, MissenseAnti-Bacterial AgentsDNA, BacterialDNA GyraseDNA, SuperhelicalFluoroquinolonesCampylobacterDNA supercoilingfitnessfluoroquinolone resistanceGyrA mutation

Identifiers

PMID22919613
PMCPMC3417464
OpenAlexW2147688143

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.