Evidence map›Paper›PMID 25001605›Full record

ArticleInfection and immunity2014

Effect of nonheme iron-containing ferritin Dpr in the stress response and virulence of pneumococci.

Chun-Zhen Hua, Angela Howard, Richard Malley, Ying-Jie Lu

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. The oxidative stress response ofFrontiers in microbiology · 2023
    Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Stress Physiology of Lactic Acid Bacteria.Microbiology and molecular biology reviews : MMBR · 2016
    Review
  11. Review
  12. Article
  13. 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 1 institution in 2 countries.

Chun-Zhen HuaDivision of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA Division of Infectious Disease, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Angela HowardDivision of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Richard MalleyDivision of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Ying-Jie LuDivision of Infectious Diseases, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA yingjie.lu@childrens.harvard.edu.
Harvard University · US

Funding

Enhancing neonatal immunity to Streptococcus pneumoniaeR01AI100114 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI MALLEY, RICHARD · 2012 to 2016
$2.1M
Identification of protective pneumococcal antigens from a surface protein libraryR21AI103480 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI LU, YINGJIE · 2013 to 2014
$413k
NIAID NIH HHS R01 AI100114NIAID NIH HHS R21 AI103480NIAID NIH HHS R21-AI103480
6 · The paper itself

Abstract

Streptococcus pneumoniae (pneumococcus) produces hydrogen peroxide as a by-product of metabolism and provides a competitive advantage against cocolonizing bacteria. As pneumococci do not produce catalase or an inducible regulator of hydrogen peroxide, the mechanism of resistance to hydrogen peroxide is unclear. A gene responsible for resistance to hydrogen peroxide and iron in other streptococci is that encoding nonheme iron-containing ferritin, dpr, but previous attempts to study this gene in pneumococcus by generating a dpr mutant were unsuccessful. In the current study, we found that dpr is in an operon with the downstream genes dhfr and clpX. We generated a dpr deletion mutant which displayed normal early-log-phase and mid-log-phase growth in bacteriologic medium but survived less well at stationary phase; the addition of catalase partially rescued the growth defect. We showed that the dpr mutant is significantly more sensitive to pH, heat, iron concentration, and oxidative stress due to hydrogen peroxide. Using a mouse model of colonization, we also showed that the dpr mutant displays a reduced ability to colonize and is more rapidly cleared from the nasopharynx. Our results thus suggest that Dpr is important for pneumococcal resistance to stress and for nasopharyngeal colonization.

Indexed as

AnimalsBacterial ProteinsFerritinsHot TemperatureHydrogen-Ion ConcentrationHydrogen PeroxideIronMacrophagesMiceMutationOperonOxidative StressPneumococcal InfectionsStreptococcus pneumoniaeStress, PhysiologicalVirulenceBacterial ProteinsFerritinsHydrogen PeroxideIron

Identifiers

PMID25001605
PMCPMC4187797
OpenAlexW2096102391

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.