Evidence map›Paper›PMID 39110759›Full record

ArticlePloS one2024

Role of the polyamine transporter PotABCD during biofilm formation by Streptococcus pneumoniae.

Brenda Vieira, Jessica B Alcantara, Giulia Destro, Maria E S Guerra, Sheila Oliveira, Carolina A Lima, Giovanna B Longato, Anders P Hakansson, Luciana C Leite, Michelle Darrieux and 1 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

11 authors.

Brenda VieiraLaboratório de Biologia Molecular de Microrganismos, Universidade São Francisco, Bragança Paulista, Brazil.ORCID 0000-0002-1505-973X
Jessica B AlcantaraLaboratório de Biologia Molecular de Microrganismos, Universidade São Francisco, Bragança Paulista, Brazil.
Giulia DestroLaboratório de Biologia Molecular de Microrganismos, Universidade São Francisco, Bragança Paulista, Brazil.
Maria E S GuerraLaboratório de Biologia Molecular de Microrganismos, Universidade São Francisco, Bragança Paulista, Brazil.
Sheila OliveiraLaboratório de Biologia Molecular de Microrganismos, Universidade São Francisco, Bragança Paulista, Brazil.ORCID 0000-0001-9259-4659
Carolina A LimaLaboratório de Farmacologia Molecular e Compostos Bioativos, Universidade São Francisco, Bragança Paulista, Brazil.
Giovanna B LongatoLaboratório de Farmacologia Molecular e Compostos Bioativos, Universidade São Francisco, Bragança Paulista, Brazil.
Anders P HakanssonDivision of Experimental Infection Medicine, Department of Translational Medicine, Lund University, Lund, Sweden.ORCID 0000-0002-2834-6009
Luciana C LeiteLaboratório de Desenvolvimento de Vacinas, Instituto Butantan, São Paulo, Brazil.
Michelle DarrieuxLaboratório de Biologia Molecular de Microrganismos, Universidade São Francisco, Bragança Paulista, Brazil.
Thiago R ConversoLaboratório de Biologia Molecular de Microrganismos, Universidade São Francisco, Bragança Paulista, Brazil.ORCID 0000-0001-5631-4541

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Streptococcus pneumoniae is a bacterium of great global importance, responsible for more than one million deaths per year. This bacterium is commonly acquired in the first years of life and colonizes the upper respiratory tract asymptomatically by forming biofilms that persist for extended times in the nasopharynx. However, under conditions that alter the bacterial environment, such as viral infections, pneumococci can escape from the biofilm and invade other niches, causing local and systemic disease of varying severity. The polyamine transporter PotABCD is required for optimal survival of the organism in the host. Immunization of mice with recombinant PotD can reduce subsequent bacterial colonization. PotD has also been suggested to be involved in pneumococcal biofilm development. Therefore, in this study we aimed to elucidate the role of PotABCD and polyamines in pneumococcal biofilm formation. First, the formation of biofilms was evaluated in the presence of exogenous polyamines-the substrate transported by PotABCD-added to culture medium. Next, a potABCD-negative strain was used to determine biofilm formation in different model systems using diverse levels of complexity from abiotic surface to cell substrate to in vivo animal models and was compared with its wild-type strain. The results showed that adding more polyamines to the medium stimulated biofilm formation, suggesting a direct correlation between polyamines and biofilm formation. Also, deletion of potABCD operon impaired biofilm formation in all models tested. Interestingly, more differences between wild-type and mutant strains were observed in the more complex model, which emphasizes the significance of employing more physiological models in studying biofilm formation.

Indexed as

BiofilmsStreptococcus pneumoniaeAnimalsBacterial ProteinsMembrane Transport ProteinsMiceOperonPneumococcal InfectionsPolyaminesBacterial ProteinsMembrane Transport ProteinsPolyamines

Identifiers

PMID39110759
PMCPMC11305561

What OpenQuestion holds

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Registered trials

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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.