Evidence map›Paper›PMID 34339477›Full record

ArticlePLoS pathogens2021

The pentose phosphate pathway constitutes a major metabolic hub in pathogenic Francisella.

Héloise Rytter, Anne Jamet, Jason Ziveri, Elodie Ramond, Mathieu Coureuil, Pauline Lagouge-Roussey, Daniel Euphrasie, Fabiola Tros, Nicolas Goudin, Cerina Chhuon and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

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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

15 authors at 2 institutions in 2 countries.

Héloise RytterUniversité de Paris, Paris, France.ORCID 0000-0001-5565-6726
Anne JametUniversité de Paris, Paris, France.ORCID 0000-0002-1902-6943
Jason ZiveriUniversité de Paris, Paris, France.
Elodie RamondUniversité de Paris, Paris, France.ORCID 0000-0003-4775-7070
Mathieu CoureuilUniversité de Paris, Paris, France.ORCID 0000-0001-7655-9685
Pauline Lagouge-RousseyUniversité de Paris, Paris, France.ORCID 0000-0002-5736-8493
Daniel EuphrasieUniversité de Paris, Paris, France.
Fabiola TrosUniversité de Paris, Paris, France.ORCID 0000-0001-5282-929X
Nicolas GoudinPole Bio-analyse d'images, Structure Fédérative de Recherche Necker INSERM US24- CNRS UMS 3633, Paris, France.ORCID 0000-0002-3967-4016
Cerina ChhuonUniversité de Paris, Paris, France.
Ivan NemazanyyUniversité de Paris, Paris, France.
Fabricio Edgar de MoraesLaboratório Max Feffer de Genética de Plantas, Departamento de Genética, Escola Superior de Agricultura Luiz de Queiroz, Universidade de São Paulo, Piracicaba, Brazil.ORCID 0000-0001-5495-8968
Carlos LabateLaboratório Max Feffer de Genética de Plantas, Departamento de Genética, Escola Superior de Agricultura Luiz de Queiroz, Universidade de São Paulo, Piracicaba, Brazil.
Ida Chiara GuerreraUniversité de Paris, Paris, France.ORCID 0000-0002-4832-6793
Alain CharbitUniversité de Paris, Paris, France.ORCID 0000-0001-5243-4861
Centre National de la Recherche Scientifique · FRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic pathways are now considered as intrinsic virulence attributes of pathogenic bacteria and thus represent potential targets for antibacterial strategies. Here we focused on the role of the pentose phosphate pathway (PPP) and its connections with other metabolic pathways in the pathophysiology of Francisella novicida. The involvement of the PPP in the intracellular life cycle of Francisella was first demonstrated by studying PPP inactivating mutants. Indeed, we observed that inactivation of the tktA, rpiA or rpe genes severely impaired intramacrophage multiplication during the first 24 hours. However, time-lapse video microscopy demonstrated that rpiA and rpe mutants were able to resume late intracellular multiplication. To better understand the links between PPP and other metabolic networks in the bacterium, we also performed an extensive proteo-metabolomic analysis of these mutants. We show that the PPP constitutes a major bacterial metabolic hub with multiple connections to glycolysis, the tricarboxylic acid cycle and other pathways, such as fatty acid degradation and sulfur metabolism. Altogether our study highlights how PPP plays a key role in the pathogenesis and growth of Francisella in its intracellular niche.

Indexed as

MetabolomePentose Phosphate PathwayProteomeAnimalsBacterial ProteinsDrosophila melanogasterFrancisellaGene Expression Regulation, BacterialGlycolysisGram-Negative Bacterial InfectionsMacrophagesMaleMiceMice, Inbred C57BLMutationBacterial ProteinsProteome

Identifiers

PMID34339477
PMCPMC8360588
OpenAlexW3191864713

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.