Evidence map›Paper›PMID 21646483›Full record

ArticleAntimicrobial agents and chemotherapy2011

Low fitness cost of the multidrug resistance gene cfr.

Jacqueline M LaMarre, Jeffrey B Locke, Karen J Shaw, Alexander S Mankin

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Ribosome-targeting antibiotics and resistanceRSC medicinal chemistry · 2023
    Review
  3. Occurrence ofAntibiotics (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Article
  6. Emergence ofAntibiotics (Basel, Switzerland) · 2020
    Article
  7. Antimicrobial agents and chemotherapy · 2019
    Article
  8. Device-Associated Meningitis by Linezolid-ResistantJournal of neurosciences in rural practice · 2019
    Article
  9. Linezolid and Rifampicin Combination to CombatFrontiers in microbiology · 2019
    Article
  10. A high incidence and coexistence of multiresistance genes cfr and optrA among linezolid-resistant enterococci isolated from a teaching hospital in Wenzhou, China.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2018
    Article
  11. Article
  12. Article
  13. Targeting Antibiotic Resistance.Angewandte Chemie (International ed. in English) · 2016
    Review
  14. Article
  15. Evolving resistance among Gram-positive pathogens.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2015
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  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

4 authors at 2 institutions in 1 country.

Jacqueline M LaMarreCenter for Pharmaceutical Biotechnology, University of Illinois, 900 S. Ashland Ave., Chicago, IL 60607, USA.
Jeffrey B Locke
Karen J Shaw
Alexander S Mankin
Arcturus Therapeutics (United States) · USUniversity of Illinois Urbana-Champaign · US

Funding

New mechanism of resistance to oxazolidinone antibiotics in Staphylococcus aureusR01AI072445 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MANKIN, ALEXANDER S · 2007 to 2010
$1.6M
NIAID NIH HHS R01 AI072445NIAID NIH HHS R01AI072445
6 · The paper itself

Abstract

The recently described rRNA methyltransferase Cfr that methylates the conserved 23S rRNA residue A2503, located in a functionally critical region of the ribosome, confers resistance to an array of ribosomal antibiotics, including linezolid. A number of reports of linezolid-resistant cfr-positive clinical strains indicate the possible rapid spread of this resistance mechanism. Since the rate of dissemination and the efficiency of maintenance of a resistance gene depend on the fitness cost associated with its acquisition, we investigated the fitness cost of cfr expression in a laboratory Staphylococcus aureus strain. We found that acquisition of the cfr gene does not produce any appreciable reduction in the cell growth rate. Only in a cogrowth competition experiment was some loss of fitness observed because Cfr-expressing cells slowly lose to the cfr-negative control strain. Interestingly, cells expressing wild-type and catalytically inactive Cfr had very similar growth characteristics, indicating that the slight fitness cost associated with cfr acquisition stems from expression of the Cfr polypeptide rather than from the modification of the conserved rRNA residue. In some clinical isolates, cfr is coexpressed with the erm gene, which encodes a methyltransferase targeting another 23S rRNA residue, A2058. Dimethylation of A2058 by Erm notably increases the fitness cost associated with the Cfr-mediated methylation of A2503. The generally low fitness cost of cfr acquisition observed in our experiments with the laboratory S. aureus strain offers a microbiological explanation for the apparent spread of the cfr gene among pathogens.

Indexed as

AcetamidesBacterial ProteinsDrug Resistance, Multiple, BacterialHumansLinezolidMethyltransferasesMicrobial Sensitivity TestsOxazolidinonesRNA, RibosomalRNA, Ribosomal, 23SStaphylococcal InfectionsStaphylococcus aureusAcetamidesBacterial ProteinsCFR protein, Staphylococcus aureusLinezolidMethyltransferasesOxazolidinonesRNA, RibosomalRNA, Ribosomal, 23S

Identifiers

PMID21646483
PMCPMC3147626
OpenAlexW2106212705

What OpenQuestion holds

Textmetadata
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.