Evidence map›Paper›PMID 25127127›Full record

ArticlePloS one2014

Reduction of hydrogen peroxide accumulation and toxicity by a catalase from Mycoplasma iowae.

Rachel E Pritchard, Alexandre J Prassinos, John D Osborne, Ziv Raviv, Mitchell F Balish

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. iScience · 2026
    Article
  2. Assessment of Catalase Inhibition Under e-Beam Irradiation.International journal of molecular sciences · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Global Proteomics RevealedFrontiers in cellular and infection microbiology · 2017
    Article
  13. Article
  14. Review
  15. 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

5 authors at 3 institutions in 1 country.

Rachel E PritchardDepartment of Microbiology, Miami University, Oxford, Ohio, United States of America.
Alexandre J PrassinosDepartment of Microbiology, Miami University, Oxford, Ohio, United States of America.
John D OsborneCenter for Clinical and Translational Science, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Ziv RavivDepartment of Veterinary Preventative Medicine, The Ohio State University, Columbus, Ohio, United States of America.
Mitchell F BalishDepartment of Microbiology, Miami University, Oxford, Ohio, United States of America.
Miami University · USThe Ohio State University · USUniversity of Alabama at Birmingham · US

Funding

Mycoplasma penetrans tip structure and functionR15AI073994 · NIAID · MIAMI UNIVERSITY OXFORD · PI BALISH, MITCHELL F · 2008 to 2014
$841k
NIAID NIH HHS R15 AI073994
6 · The paper itself

Abstract

Mycoplasma iowae is a well-established avian pathogen that can infect and damage many sites throughout the body. One potential mediator of cellular damage by mycoplasmas is the production of H2O2 via a glycerol catabolic pathway whose genes are widespread amongst many mycoplasma species. Previous sequencing of M. iowae serovar I strain 695 revealed the presence of not only genes for H2O2 production through glycerol catabolism but also the first documented mycoplasma gene for catalase, which degrades H2O2. To test the activity of M. iowae catalase in degrading H2O2, we studied catalase activity and H2O2 accumulation by both M. iowae serovar K strain DK-CPA, whose genome we sequenced, and strains of the H2O2-producing species Mycoplasma gallisepticum engineered to produce M. iowae catalase by transformation with the M. iowae putative catalase gene, katE. H2O2-mediated virulence by M. iowae serovar K and catalase-producing M. gallisepticum transformants were also analyzed using a Caenorhabditis elegans toxicity assay, which has never previously been used in conjunction with mycoplasmas. We found that M. iowae katE encodes an active catalase that, when expressed in M. gallisepticum, reduces both the amount of H2O2 produced and the amount of damage to C. elegans in the presence of glycerol. Therefore, the correlation between the presence of glycerol catabolism genes and the use of H2O2 as a virulence factor by mycoplasmas might not be absolute.

Indexed as

AnimalsBacterial ProteinsCaenorhabditis elegansCatalaseHydrogen PeroxideMolecular Sequence DataMycoplasma iowaePhylogenyBacterial ProteinsCatalaseHydrogen Peroxide

Identifiers

PMID25127127
PMCPMC4134286
OpenAlexW2073230599

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.