Evidence map›Paper›PMID 31103037›Full record

ArticleJournal of neuroinflammation2019

Pneumolysin and the bacterial capsule of Streptococcus pneumoniae cooperatively inhibit taxis and motility of microglia.

Sabrina Hupp, Denis Grandgirard, Timothy J Mitchell, Stephen L Leib, Lucy J Hathaway, Asparouh I Iliev

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

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  11. Assessing Microglial Dynamics by Live Imaging.Frontiers in immunology · 2021
    Review
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

6 authors at 2 institutions in 2 countries.

Sabrina HuppInstitute of Anatomy, University of Bern, Baltzerstrasse 2, 3012, Bern, Switzerland.
Denis GrandgirardInstitute for Infectious Diseases, University of Bern, Friedbühlstrasse 51, 3010, Bern, Switzerland.
Timothy J MitchellInstitute of Microbiology and Infection, College of Medical and Dental Sciences, Biosciences Building, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Stephen L LeibInstitute for Infectious Diseases, University of Bern, Friedbühlstrasse 51, 3010, Bern, Switzerland.
Lucy J HathawayInstitute for Infectious Diseases, University of Bern, Friedbühlstrasse 51, 3010, Bern, Switzerland.
Asparouh I IlievInstitute of Anatomy, University of Bern, Baltzerstrasse 2, 3012, Bern, Switzerland. asparouh.iliev@ana.unibe.ch.ORCID http://orcid.org/0000-0002-1343-2967
University of Bern · CHUniversity of Birmingham · GB

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 160136Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 162583Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 170844
6 · The paper itself

Abstract

backgroundStreptococcus pneumoniae is the cause of a highly lethal form of meningitis in humans. Microglial cells in the brain represent the first line of defense against pathogens, and they participate in the inflammatory response. The cholesterol-dependent cytolysin pneumolysin and the bacterial capsule are key pathogenic factors, known to exacerbate the course of pneumococcal meningitis.

methodsWe utilized live imaging and immunostaining of glial cells in dissociated and acute brain slice cultures to study the effect of pneumococcal factors, including the cholesterol-dependent cytolysin pneumolysin and the pneumococcal capsule, on microglial motility and taxis.

resultsIn brain tissue, primary microglia cells showed an enhanced response towards lysates from bacteria lacking capsules and pneumolysin as they moved rapidly to areas with an abundance of bacterial factors. The presence of bacterial capsules and pneumolysin cumulatively inhibited microglial taxis. In mixed cultures of astrocytes and microglia, the motility of microglia was inhibited by capsular components within minutes after exposure. The reduced motility was partially reversed by mannan, a mannose receptor inhibitor. The effects on microglia were not mediated by astrocytes because pure microglial cells responded to various pneumococcal lysates similarly with distinct cell shape changes as seen in mixed cultures.

conclusionsOur data indicate that microglia possess the capacity for a very agile response towards bacterial pathogens, but key pathogenic factors, such as pneumococcal capsules and pneumolysin, inhibited this response shortly after a bacterial challenge. Furthermore, we demonstrate for the first time that the bacterial capsule affects cellular behaviors such as motility and taxis.

Indexed as

AnimalsBacterial CapsulesBacterial ProteinsCell MovementCells, CulturedChemotaxisCoculture TechniquesMiceMice, Inbred C57BLMicrogliaOrgan Culture TechniquesStreptococcus pneumoniaeStreptolysinsBacterial ProteinsplY protein, Streptococcus pneumoniaeStreptolysinsBacterial capsuleMeningitisMicrogliaPneumolysinStreptococcus pneumoniae

Identifiers

PMID31103037
PMCPMC6525981
OpenAlexW2945804817

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.