Evidence map›Paper›PMID 26256439›Full record

ArticleScientific reports2015

Streptomyces natalensis programmed cell death and morphological differentiation are dependent on oxidative stress.

Tiago Beites, Paulo Oliveira, Beatriz Rioseras, Sílvia D S Pires, Rute Oliveira, Paula Tamagnini, Pedro Moradas-Ferreira, Ángel Manteca, Marta V Mendes

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  5. Streptomyces coelicolor Vesicles: Many Molecules To Be Delivered.Applied and environmental microbiology · 2022
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  12. The Inhibition of Antibiotic Production inFrontiers in microbiology · 2020
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  13. Review
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  16. Alpha-ketoglutarate protectsBiochemistry and biophysics reports · 2017
    Article
  17. Article
  18. 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

9 authors at 3 institutions in 2 countries.

Tiago Beites1] i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal [2] IBMC-Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Paulo Oliveira1] i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal [2] IBMC-Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Beatriz Rioserasrea de Microbiología, Departamento de Biología Funcional e IUOPA, Facultad de Medicina, Universidad de Oviedo, Oviedo, Spain.
Sílvia D S Pires1] i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal [2] IBMC-Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal [3] ICBAS-Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Porto, Portugal.
Rute Oliveira1] i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal [2] IBMC-Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Paula Tamagnini1] i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal [2] IBMC-Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal [3] Faculdade de Ciências, Departamento de Biologia, Universidade do Porto, Porto, Portugal.
Pedro Moradas-Ferreira1] i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal [2] IBMC-Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal [3] ICBAS-Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Porto, Portugal.
Ángel Mantecarea de Microbiología, Departamento de Biología Funcional e IUOPA, Facultad de Medicina, Universidad de Oviedo, Oviedo, Spain.
Marta V Mendes1] i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal [2] IBMC-Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PTUniversidad de Oviedo · ESUniversidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Streptomyces are aerobic Gram-positive bacteria characterized by a complex life cycle that includes hyphae differentiation and spore formation. Morphological differentiation is triggered by stressful conditions and takes place in a pro-oxidant environment, which sets the basis for an involvement of the oxidative stress response in this cellular process. Characterization of the phenotypic traits of Streptomyces natalensis ΔkatA1 (mono-functional catalase) and ΔcatR (Fur-like repressor of katA1 expression) strains in solid medium revealed that both mutants had an impaired morphological development process. The sub-lethal oxidative stress caused by the absence of KatA1 resulted in the formation of a highly proliferative and undifferentiated vegetative mycelium, whereas de-repression of CatR regulon, from which KatA1 is the only known representative, resulted in the formation of scarce aerial mycelium. Both mutant strains had the transcription of genes associated with aerial mycelium formation and biosynthesis of the hyphae hydrophobic layer down-regulated. The first round of the programmed cell death (PCD) was inhibited in both strains which caused the prevalence of the transient primary mycelium (MI) over secondary mycelium (MII). Our data shows that the first round of PCD and morphological differentiation in S. natalensis is dependent on oxidative stress in the right amount at the right time.

Indexed as

ApoptosisOxidative StressBacterial ProteinsCatalaseDNA-Binding ProteinsDown-RegulationElectrophoresis, Gel, Two-DimensionalGenome, BacterialHigh-Throughput Nucleotide SequencingMicrobial ViabilityMicroscopy, ConfocalMyceliumPolymerase Chain ReactionProteomeSpores, BacterialStreptomycesBacterial ProteinsCatalaseCatR protein, bacteriaDNA-Binding ProteinsProteomeTranscription Factors

Identifiers

PMID26256439
PMCPMC4530454
OpenAlexW2461829184

What OpenQuestion holds

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LicenceCC BY
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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.