Evidence map›Paper›PMID 17631628›Full record

ArticleJournal of bacteriology2007

SpxB is a suicide gene of Streptococcus pneumoniae and confers a selective advantage in an in vivo competitive colonization model.

Gili Regev-Yochay, Krzysztof Trzcinski, Claudette M Thompson, Marc Lipsitch, Richard Malley

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

74 citing papers in PubMed, 102 citations in OpenAlex.

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  16. The oxidative stress response ofFrontiers in microbiology · 2023
    Review
  17. Article
  18. Article
  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Gili Regev-YochayDepartment of Epidemiology and Department of Immunology and Infectious Diseases, Harvard School of Public Health, 677 Huntington Ave., Boston, MA 02115, USA. gregev@hsph.harvard.edu
Krzysztof Trzcinski
Claudette M Thompson
Marc Lipsitch
Richard Malley
Harvard University · USBoston Children's Hospital · US

Funding

VACCINATION AND THE EVOLUTIONARY DYNAMICS OF PNEUMOCOCCIR01AI048935 · NIAID · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI LIPSITCH, MARC · 2001 to 2016
$8.8M
Mechanisms of Immunity to Pneumococcal ColonizationR01AI066013 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI MALLEY, RICHARD · 2007 to 2011
$2.1M
Pneumococcal immunization through a novel mechanismR01AI067737 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI MALLEY, RICHARD · 2006 to 2010
$2.0M
NIAID NIH HHS 2R01AI48935NIAID NIH HHS R01 AI048935NIAID NIH HHS R01 AI066013NIAID NIH HHS R01AI066013NIAID NIH HHS R01 AI067737NIAID NIH HHS R01AI067737
6 · The paper itself

Abstract

The human bacterial pathogen Streptococcus pneumoniae dies spontaneously upon reaching stationary phase. The extent of S. pneumoniae death at stationary phase is unusual in bacteria and has been conventionally attributed to autolysis by the LytA amidase. In this study, we show that spontaneous pneumococcal death is due to hydrogen peroxide (H(2)O(2)), not LytA, and that the gene responsible for H(2)O(2) production (spxB) also confers a survival advantage in colonization. Survival of S. pneumoniae in stationary phase was significantly prolonged by eliminating H(2)O(2) in any of three ways: chemically by supplementing the media with catalase, metabolically by growing the bacteria under anaerobic conditions, or genetically by constructing DeltaspxB mutants that do not produce H(2)O(2). Likewise, addition of H(2)O(2) to exponentially growing S. pneumoniae resulted in a death rate similar to that of cells in stationary phase. While DeltalytA mutants did not lyse at stationary phase, they died at a rate similar to that of the wild-type strain. Furthermore, we show that the death process induced by H(2)O(2) has features of apoptosis, as evidenced by increased annexin V staining, decreased DNA content, and appearance as assessed by transmission electron microscopy. Finally, in an in vivo rat model of competitive colonization, the presence of spxB conferred a selective advantage over the DeltaspxB mutant, suggesting an explanation for the persistence of this gene. We conclude that a suicide gene of pneumococcus is spxB, which induces an apoptosis-like death in pneumococci and confers a selective advantage in nasopharyngeal cocolonization.

Indexed as

AnimalsAnimals, NewbornApoptosisBacterial ProteinsHumansHydrogen PeroxideMicroscopy, Electron, TransmissionMutationNasopharynxPneumococcal InfectionsPyruvate OxidaseRatsRats, Sprague-DawleyStreptococcus pneumoniaeBacterial ProteinsHydrogen PeroxidePyruvate Oxidase

Identifiers

PMID17631628
PMCPMC2045178
OpenAlexW2149824175

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.