Evidence map›Paper›PMID 26162030›Full record

ArticlePLoS genetics2015

Common Cell Shape Evolution of Two Nasopharyngeal Pathogens.

Frédéric J Veyrier, Nicolas Biais, Pablo Morales, Nouria Belkacem, Cyril Guilhen, Sylvia Ranjeva, Odile Sismeiro, Gérard Péhau-Arnaudet, Eduardo P Rocha, Catherine Werts and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. International journal of systematic and evolutionary microbiology · 2024
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  9. Review
  10. Genus-Wide Comparative Genomics Analysis ofInternational journal of genomics · 2019
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. UnravelingF1000Research · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. Isolation and characterization of Neisseria musculi sp. nov., from the wild house mouse.International journal of systematic and evolutionary microbiology · 2016
    Article
  20. Article
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

12 authors at 6 institutions in 3 countries.

Frédéric J VeyrierInstitut Pasteur, Infection Bactériennes Invasives, Département Infection et Epidémiologie, Paris, France; Institut Pasteur, Groupe Biologie et Génétique de la Paroi Bactérienne, Département de Microbiologie, Paris, France; INSERM, Groupe Avenir, Paris, France; INRS-Institut Armand-Frappier, Bacterial Symbionts Evolution, Laval, Quebec, Canada.
Nicolas BiaisBrooklyn College, Graduate Center City University of New York, Brooklyn, New York, New York, United States of America.
Pablo MoralesINRS-Institut Armand-Frappier, Bacterial Symbionts Evolution, Laval, Quebec, Canada.
Nouria BelkacemInstitut Pasteur, Infection Bactériennes Invasives, Département Infection et Epidémiologie, Paris, France.
Cyril GuilhenInstitut Pasteur, Infection Bactériennes Invasives, Département Infection et Epidémiologie, Paris, France.
Sylvia RanjevaInstitut Pasteur, Infection Bactériennes Invasives, Département Infection et Epidémiologie, Paris, France.
Odile SismeiroInstitut Pasteur, Plate-forme de Transcriptome et Epigénome, Département de Génome et Génétique, Paris, France.
Gérard Péhau-ArnaudetInstitut Pasteur, Plate-forme de Microscopie Ultrastructurale, Département de Biologie Cellulaire et Infection, Paris, France.
Eduardo P RochaInstitut Pasteur, Microbial Evolutionary Genomics, Département Génome et Génétique, and CNRS, UMR3525, Paris, France.
Catherine WertsInstitut Pasteur, Groupe Biologie et Génétique de la Paroi Bactérienne, Département de Microbiologie, Paris, France; INSERM, Groupe Avenir, Paris, France.
Muhamed-Kheir TahaInstitut Pasteur, Infection Bactériennes Invasives, Département Infection et Epidémiologie, Paris, France.
Ivo G BonecaInstitut Pasteur, Groupe Biologie et Génétique de la Paroi Bactérienne, Département de Microbiologie, Paris, France; INSERM, Groupe Avenir, Paris, France.
Institut Pasteur · FRInserm · FRCentre National de la Recherche Scientifique · FRCity University of New York · USFondation de l'Avenir · FRInstitut National de la Recherche Scientifique · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory infectious diseases are the third cause of worldwide death. The nasopharynx is the portal of entry and the ecological niche of many microorganisms, of which some are pathogenic to humans, such as Neisseria meningitidis and Moraxella catarrhalis. These microbes possess several surface structures that interact with the actors of the innate immune system. In our attempt to understand the past evolution of these bacteria and their adaption to the nasopharynx, we first studied differences in cell wall structure, one of the strongest immune-modulators. We were able to show that a modification of peptidoglycan (PG) composition (increased proportion of pentapeptides) and a cell shape change from rod to cocci had been selected for along the past evolution of N. meningitidis. Using genomic comparison across species, we correlated the emergence of the new cell shape (cocci) with the deletion, from the genome of N. meningitidis ancestor, of only one gene: yacF. Moreover, the reconstruction of this genetic deletion in a bacterium harboring the ancestral version of the locus together with the analysis of the PG structure, suggest that this gene is coordinating the transition from cell elongation to cell division. Accompanying the loss of yacF, the elongation machinery was also lost by several of the descendants leading to the change in the PG structure observed in N. meningitidis. Finally, the same evolution was observed for the ancestor of M. catarrhalis. This suggests a strong selection of these genetic events during the colonization of the nasopharynx. This selection may have been forced by the requirement of evolving permissive interaction with the immune system, the need to reduce the cellular surface exposed to immune attacks without reducing the intracellular storage capacity, or the necessity to better compete for adhesion to target cells.

Indexed as

Adaptation, PhysiologicalBiological EvolutionCell Cycle ProteinsCell Membrane StructuresHumansMoraxella catarrhalisNasopharynxNeisseria meningitidisPeptidoglycanRespiratory MucosaCell Cycle ProteinsPeptidoglycan

Identifiers

PMID26162030
PMCPMC4498754
OpenAlexW838157302

What OpenQuestion holds

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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.