Evidence map›Paper›PMID 28127804›Full record

ArticleMolecular microbiology2017

Perturbation of manganese metabolism disrupts cell division in Streptococcus pneumoniae.

Julia E Martin, John P Lisher, Malcolm E Winkler, David P Giedroc

Abstract read
In one paragraph

Article in Molecular microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
–field-weighted citation impact
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

49 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. The global proteome ofFrontiers in cellular and infection microbiology · 2025
    Article
  5. Review
  6. Article
  7. Calcium RescuesMicroorganisms · 2024
    Article
  8. Article
  9. Review
  10. The five homologous CiaR-controlled Ccn sRNAs ofbioRxiv : the preprint server for biology · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Zinc acquisition and its contribution toFrontiers in cellular and infection microbiology · 2023
    Article
  18. Review
  19. Article
  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.

Julia E MartinDepartment of Chemistry, Indiana University, Bloomington, IN, 47405-7102, USA.
John P LisherDepartment of Chemistry, Indiana University, Bloomington, IN, 47405-7102, USA.
Malcolm E WinklerDepartment of Biology, Indiana University, Bloomington, IN, 47405, USA.ORCID 0000-0002-1482-2588
David P GiedrocDepartment of Chemistry, Indiana University, Bloomington, IN, 47405-7102, USA.ORCID 0000-0002-2342-1620

Funding

Transition Metal Homeostasis and Reactive Sulfur Species in Bacterial PathogensR35GM118157 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI DAVID P. GIEDROC · 2016 to 2026
$5.9M
ZINC COORDINATION AND REGULATION OF ZINC METALLOPROTEINSR01GM042569 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI GIEDROC, DAVID P. · 1996 to 2015
$4.9M
Dynamics of bacterial peptidoglycan synthesisR01GM113172 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI BRUN, YVES V, VANNIEUWENHZE, MICHAEL S · 2015 to 2018
$3.5M
Mechanisms of Chemokine Killing and Resistance of Streptococcus pneumoniaeR01GM114315 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI WINKLER, MALCOLM E. · 2015 to 2018
$1.1M
NIGMS NIH HHS R01 GM042569NIGMS NIH HHS R01 GM113172NIGMS NIH HHS R01 GM114315NIGMS NIH HHS R35 GM118157
6 · The paper itself

Abstract

Manganese (Mn) is an essential micronutrient and required cofactor in bacteria. Despite its importance, excess Mn can impair bacterial growth, the mechanism of which remains largely unexplored. Here, we show that proper Mn homeostasis is critical for cellular growth of the major human respiratory pathogen Streptococcus pneumoniae. Perturbations in Mn homeostasis genes, psaBCA, encoding the Mn importer, and mntE, encoding the Mn exporter, lead to Mn sensitivity during aerobiosis. Mn-stressed cells accumulate iron and copper, in addition to Mn. Impaired growth is a direct result of Mn toxicity and does not result from iron-mediated Fenton chemistry, since cells remain sensitive to Mn during anaerobiosis or when hydrogen peroxide biogenesis is significantly reduced. Mn-stressed cells are significantly elongated, whereas Mn-limitation imposed by zinc addition leads to cell shortening. We show that Mn accumulation promotes aberrant dephosphorylation of cell division proteins via hyperactivation of the Mn-dependent protein phosphatase PhpP, a key enzyme involved in the regulation of cell division. We discuss a mechanism by which cellular Mn:Zn ratios dictate PhpP specific activity thereby regulating pneumococcal cell division. We propose that Mn-metalloenzymes are particularly susceptible to hyperactivation or mismetallation, suggesting the need for exquisite cellular control of Mn-dependent metabolic processes.

Indexed as

Adhesins, BacterialAerobiosisATP-Binding Cassette TransportersBacterial ProteinsCell DivisionCopperGene Expression Regulation, BacterialHomeostasisIon TransportIronManganeseOxidative StressStreptococcus pneumoniaeVirulenceZincAdhesins, BacterialATP-Binding Cassette TransportersBacterial ProteinsCopperIronManganesepsaB protein, StreptococcusZinc

Identifiers

PMID28127804
PMCPMC5380469

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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.