Evidence map›Paper›PMID 25827421›Full record

ArticlemBio2015

Genome sequence of the Drosophila melanogaster male-killing Spiroplasma strain MSRO endosymbiont.

Juan C Paredes, Jeremy K Herren, Fanny Schüpfer, Ray Marin, Stéphane Claverol, Chih-Horng Kuo, Bruno Lemaitre, Laure Béven

Open access · goldAbstract readComparative Study
In one paragraph

Article in mBio, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
11.7field-weighted citation impact, top 1% 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

57 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. The endosymbiontmBio · 2024
    Article
  8. Article
  9. The toxins of vertically transmittedFrontiers in microbiology · 2023
    Article
  10. Article
  11. Disproportionate investment in Spiralin B production limits in-host growth and favors the vertical transmission ofProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Article
  13. Article
  14. The genome and antigen proteome analysis ofFrontiers in microbiology · 2022
    Article
  15. Frontiers in microbiology · 2022
    Article
  16. Male-killing mechanisms vary betweenFrontiers in microbiology · 2022
    Article
  17. Article
  18. The wall-less bacteriumiScience · 2021
    Article
  19. Article
  20. Rapid molecular evolution ofMicrobial genomics · 2021
    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

8 authors at 5 institutions in 4 countries.

Juan C ParedesGlobal Health Institute, School of Life Science, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Jeremy K Herren
Fanny SchüpferGlobal Health Institute, School of Life Science, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Ray MarinCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
Stéphane ClaverolPôle Protéomique, Plateforme Génomique Fonctionnelle de Bordeaux, University of Bordeaux, Bordeaux, France.
Chih-Horng KuoInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-2857-0529
Bruno LemaitreGlobal Health Institute, School of Life Science, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland laure.beven@bordeaux.inra.fr bruno.lemaitre@epfl.ch.
Laure BévenINRA, University of Bordeaux, Unité Mixte de Recherche 1332, Villenave d'Ornon, France laure.beven@bordeaux.inra.fr bruno.lemaitre@epfl.ch.
École Polytechnique Fédérale de Lausanne · CHUniversité de Bordeaux · FRInstitute of Plant and Microbial Biology, Academia Sinica · TWInternational Centre of Insect Physiology and Ecology · KEUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledSpiroplasmas are helical and motile members of a cell wall-less eubacterial group called Mollicutes. Although all spiroplasmas are associated with arthropods, they exhibit great diversity with respect to both their modes of transmission and their effects on their hosts; ranging from horizontally transmitted pathogens and commensals to endosymbionts that are transmitted transovarially (i.e., from mother to offspring). Here we provide the first genome sequence, along with proteomic validation, of an endosymbiotic inherited Spiroplasma bacterium, the Spiroplasma poulsonii MSRO strain harbored by Drosophila melanogaster. Comparison of the genome content of S. poulsonii with that of horizontally transmitted spiroplasmas indicates that S. poulsonii has lost many metabolic pathways and transporters, demonstrating a high level of interdependence with its insect host. Consistent with genome analysis, experimental studies showed that S. poulsonii metabolizes glucose but not trehalose. Notably, trehalose is more abundant than glucose in Drosophila hemolymph, and the inability to metabolize trehalose may prevent S. poulsonii from overproliferating. Our study identifies putative virulence genes, notably, those for a chitinase, the H2O2-producing glycerol-3-phosphate oxidase, and enzymes involved in the synthesis of the eukaryote-toxic lipid cardiolipin. S. poulsonii also expresses on the cell membrane one functional adhesion-related protein and two divergent spiralin proteins that have been implicated in insect cell invasion in other spiroplasmas. These lipoproteins may be involved in the colonization of the Drosophila germ line, ensuring S. poulsonii vertical transmission. The S. poulsonii genome is a valuable resource to explore the mechanisms of male killing and symbiont-mediated protection, two cardinal features of many facultative endosymbionts. IMPORTANCE: Most insect species, including important disease vectors and crop pests, harbor vertically transmitted endosymbiotic bacteria. These endosymbionts play key roles in their hosts' fitness, including protecting them against natural enemies and manipulating their reproduction in ways that increase the frequency of symbiont infection. Little is known about the molecular mechanisms that underlie these processes. Here, we provide the first genome draft of a vertically transmitted male-killing Spiroplasma bacterium, the S. poulsonii MSRO strain harbored by D. melanogaster. Analysis of the S. poulsonii genome was complemented by proteomics and ex vivo metabolic experiments. Our results indicate that S. poulsonii has reduced metabolic capabilities and expresses divergent membrane lipoproteins and potential virulence factors that likely participate in Spiroplasma-host interactions. This work fills a gap in our knowledge of insect endosymbionts and provides tools with which to decipher the interaction between Spiroplasma bacteria and their well-characterized host D. melanogaster, which is emerging as a model of endosymbiosis.

Indexed as

Genome, BacterialSequence Analysis, DNAAnimalsDNA, BacterialDrosophila melanogasterMolecular Sequence DataSpiroplasmaSymbiosisDNA, Bacterial

Identifiers

PMID25827421
PMCPMC4453565
OpenAlexW2072176628

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.