Evidence map›Paper›PMID 22184416›Full record

ArticleInfection and immunity2012

Alkyl hydroperoxide reductase is required for Helicobacter cinaedi intestinal colonization and survival under oxidative stress in BALB/c and BALB/c interleukin-10-/- mice.

Nisanart Charoenlap, Zeli Shen, Megan E McBee, Suresh Muthupalani, Gerald N Wogan, James G Fox, David B Schauer

Abstract read
In one paragraph

Article in Infection and immunity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Frontiers in microbiology · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Frontiers in microbiology · 2022
    Article
  8. Relevance of peroxiredoxins in pathogenic microorganisms.Applied microbiology and biotechnology · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Multidrug Efflux Systems in Helicobacter cinaedi.Antibiotics (Basel, Switzerland) · 2012
    Review
  18. 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 1 institution in 1 country.

Nisanart CharoenlapDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Zeli Shen
Megan E McBee
Suresh Muthupalani
Gerald N Wogan
James G Fox
David B Schauer
Massachusetts Institute of Technology · US

Funding

TOXICOLOGY CORE UNITP30ES002109 · NIEHS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI YAFFE, MICHAEL B · 1985 to 2020
$25.6M
Reaction and Diffusion of NO in Biological SystemsP01CA026731 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI ESSIGMANN, JOHN M · 1985 to 2018
$25.4M
HELIOBACTER INDUCED HEPATITIS AND TUMORIGENESISR01CA067529 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI FOX, JAMES G · 1995 to 2009
$3.2M
H. hepaticus: the pathogenesis of IBDR01DK052413 · NIDDK · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SCHAUER, DAVID B · 1998 to 2007
$2.1M
Diagnosis and Pathobiology of Emerging Enterohepatic Helicobacter spp. in MiceR01RR032307 · NCRR · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI FOX, JAMES G · 2011 to 2011
$438k
NCI NIH HHS P01 CA026731NCI NIH HHS P01CA26731NCI NIH HHS R01 CA067529NCI NIH HHS R01CA067529NCRR NIH HHS R01 RR032307NCRR NIH HHS R01RR032307NIDDK NIH HHS R01 DK052413NIDDK NIH HHS R01DK052413NIEHS NIH HHS P30 ES002109NIEHS NIH HHS P30ES002109
6 · The paper itself

Abstract

Helicobacter cinaedi, a common human intestinal bacterium, has been implicated in various enteric and systemic diseases in normal and immunocompromised patients. Protection against oxidative stress is a crucial component of bacterium-host interactions. Alkyl hydroperoxide reductase C (AhpC) is an enzyme responsible for detoxification of peroxides and is important in protection from peroxide-induced stress. H. cinaedi possesses a single ahpC, which was investigated with respect to its role in bacterial survival during oxidative stress. The H. cinaedi ahpC mutant had diminished resistance to organic hydroperoxide toxicity but increased hydrogen peroxide resistance compared with the wild-type (WT) strain. The mutant also exhibited an oxygen-sensitive phenotype and was more susceptible to killing by macrophages than the WT strain. In vivo experiments in BALB/c and BALB/c interleukin-10 (IL-10)(-/-) mice revealed that the cecal colonizing ability of the ahpC mutant was significantly reduced. The mutant also had diminished ability to induce bacterium-specific immune responses in vivo, as shown by immunoglobulin (IgG2a and IgG1) serum levels. Collectively, these data suggest that H. cinaedi ahpC not only contributes to protecting the organism against oxidative stress but also alters its pathogenic properties in vivo.

Indexed as

Microbial ViabilityOxidative StressStress, PhysiologicalAnimalsBacterial LoadBacterial ProteinsCecumFemaleGene DeletionHelicobacterHelicobacter InfectionsHost-Pathogen InteractionsHydrogen PeroxideInterleukin-10MacrophagesMaleahpC protein, Helicobacter pyloriBacterial ProteinsHydrogen PeroxideIL10 protein, humanIL10 protein, mouseInterleukin-10OxygenPeroxidasesPeroxiredoxinsVirulence Factors

Identifiers

PMID22184416
PMCPMC3294669
OpenAlexW2013584776

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.