Evidence map›Paper›PMID 25512311›Full record

ArticleJournal of bacteriology2015

Bright fluorescent Streptococcus pneumoniae for live-cell imaging of host-pathogen interactions.

Morten Kjos, Rieza Aprianto, Vitor E Fernandes, Peter W Andrew, Jos A G van Strijp, Reindert Nijland, Jan-Willem Veening

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in Journal of bacteriology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

53 citing papers in PubMed, 90 citations in OpenAlex.

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  8. Direct Quantification of Protein-Protein Interactions in Living Bacterial Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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 3 institutions in 2 countries.

Morten KjosMolecular Genetics Group, Groningen Biomolecular Sciences and Biotechnology Institute, Center for Synthetic Biology, University of Groningen, Groningen, The Netherlands.
Rieza ApriantoMolecular Genetics Group, Groningen Biomolecular Sciences and Biotechnology Institute, Center for Synthetic Biology, University of Groningen, Groningen, The Netherlands.
Vitor E FernandesDepartment of Infection, Immunity and Inflammation, University of Leicester, Leicester, United Kingdom.
Peter W AndrewDepartment of Infection, Immunity and Inflammation, University of Leicester, Leicester, United Kingdom.
Jos A G van StrijpDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Reindert NijlandDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Jan-Willem VeeningMolecular Genetics Group, Groningen Biomolecular Sciences and Biotechnology Institute, Center for Synthetic Biology, University of Groningen, Groningen, The Netherlands j.w.veening@rug.nl.
University of Groningen · NLUniversity Medical Center Utrecht · NLUniversity of Leicester · GB

Funding

European Research Council 337399Medical Research Council G0501416
6 · The paper itself

Abstract

Streptococcus pneumoniae is a common nasopharyngeal resident in healthy people but, at the same time, one of the major causes of infectious diseases such as pneumonia, meningitis, and sepsis. The shift from commensal to pathogen and its interaction with host cells are poorly understood. One of the major limitations for research on pneumococcal-host interactions is the lack of suitable tools for live-cell imaging. To address this issue, we developed a generally applicable strategy to create genetically stable, highly fluorescent bacteria. Our strategy relies on fusing superfolder green fluorescent protein (GFP) or a far-red fluorescent protein (RFP) to the abundant histone-like protein HlpA. Due to efficient translation and limited cellular diffusion of these fusions, the cells are 25-fold brighter than those of the currently best available imaging S. pneumoniae strain. These novel bright pneumococcal strains are fully virulent, and the GFP reporter can be used for in situ imaging in mouse tissue. We used our reporter strains to study the effect of the polysaccharide capsule, a major pneumococcal virulence factor, on different stages of infection. By dual-color live-cell imaging experiments, we show that unencapsulated pneumococci adhere significantly better to human lung epithelial cells than encapsulated strains, in line with previous data obtained by classical approaches. We also confirm with live-cell imaging that the capsule protects pneumococci from neutrophil phagocytosis, demonstrating the versatility and usability of our reporters. The described imaging tools will pave the way for live-cell imaging of pneumococcal infection and help further understanding of the mechanisms of pneumococcal pathogenesis.

Indexed as

Host-Pathogen InteractionsAnimalsBacterial ProteinsCell TrackingFemaleFluorescenceGenes, ReporterGreen Fluorescent ProteinsHumansLungMicePneumococcal InfectionsStreptococcus pneumoniaeVirulence FactorsBacterial ProteinsGreen Fluorescent ProteinsVirulence Factors

Identifiers

PMID25512311
PMCPMC4325099
OpenAlexW2167185424

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.