Evidence map›Paper›PMID 20548954›Full record

ArticlePLoS pathogens2010

The Trw type IV secretion system of Bartonella mediates host-specific adhesion to erythrocytes.

Muriel Vayssier-Taussat, Danielle Le Rhun, Hong Kuan Deng, Francis Biville, Sandra Cescau, Antoine Danchin, Geneviève Marignac, Evelyne Lenaour, Henri Jean Boulouis, Maria Mavris and 7 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PLoS pathogens, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
9.7field-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

71 citing papers in PubMed, 120 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. The type IV secretion system ofMicrobial genomics · 2025
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  5. Review
  6. Review
  7. Article
  8. A novelmSystems · 2024
    Article
  9. Article
  10. Viability and Desiccation Resistance ofPathogens (Basel, Switzerland) · 2023
    Article
  11. Article
  12. Identification of theProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Review
  14. Review
  15. Frontiers in microbiology · 2022
    Article
  16. Frontiers in microbiology · 2022
    Article
  17. Overexpression of a "Frontiers in microbiology · 2021
    Article
  18. Article
  19. New microbes and new infections · 2020
    Article
  20. Article

11 more citing papers are in PubMed but not listed here.

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

17 authors at 6 institutions in 3 countries.

Muriel Vayssier-TaussatUnité Sous Contrat Bartonella, INRA, Maisons-Alfort, France. mvayssier@vet-alfort.fr
Danielle Le Rhun
Hong Kuan Deng
Francis Biville
Sandra Cescau
Antoine Danchin
Geneviève Marignac
Evelyne Lenaour
Henri Jean Boulouis
Maria Mavris
Lionel Arnaud
Huanming Yang
Jing Wang
Maxime Quebatte
Philipp Engel
Henri Saenz
Christoph Dehio
University of Basel · CHÉcole Nationale Vétérinaire d'Alfort · FRBGI Group (China) · CNCentre National de la Recherche Scientifique · FRInstitute of Psychology, Chinese Academy of Sciences · CNInstitut National de la Transfusion Sanguine · FR

Funding

Howard Hughes Medical Institute 55005501
6 · The paper itself

Abstract

Bacterial pathogens typically infect only a limited range of hosts; however, the genetic mechanisms governing host-specificity are poorly understood. The alpha-proteobacterial genus Bartonella comprises 21 species that cause host-specific intraerythrocytic bacteremia as hallmark of infection in their respective mammalian reservoirs, including the human-specific pathogens Bartonella quintana and Bartonella bacilliformis that cause trench fever and Oroya fever, respectively. Here, we have identified bacterial factors that mediate host-specific erythrocyte colonization in the mammalian reservoirs. Using mouse-specific Bartonella birtlesii, human-specific Bartonella quintana, cat-specific Bartonella henselae and rat-specific Bartonella tribocorum, we established in vitro adhesion and invasion assays with isolated erythrocytes that fully reproduce the host-specificity of erythrocyte infection as observed in vivo. By signature-tagged mutagenesis of B. birtlesii and mutant selection in a mouse infection model we identified mutants impaired in establishing intraerythrocytic bacteremia. Among 45 abacteremic mutants, five failed to adhere to and invade mouse erythrocytes in vitro. The corresponding genes encode components of the type IV secretion system (T4SS) Trw, demonstrating that this virulence factor laterally acquired by the Bartonella lineage is directly involved in adherence to erythrocytes. Strikingly, ectopic expression of Trw of rat-specific B. tribocorum in cat-specific B. henselae or human-specific B. quintana expanded their host range for erythrocyte infection to rat, demonstrating that Trw mediates host-specific erythrocyte infection. A molecular evolutionary analysis of the trw locus further indicated that the variable, surface-located TrwL and TrwJ might represent the T4SS components that determine host-specificity of erythrocyte parasitism. In conclusion, we show that the laterally acquired Trw T4SS diversified in the Bartonella lineage to facilitate host-restricted adhesion to erythrocytes in a wide range of mammals.

Indexed as

Cell AdhesionAnimalsBacteremiaBacterial ProteinsBartonellaBartonella InfectionsCatsErythrocytesFemaleHumansMiceMice, Inbred BALB CRatsVirulence FactorsBacterial ProteinsVirulence Factors

Identifiers

PMID20548954
PMCPMC2883598
OpenAlexW2025265211

What OpenQuestion holds

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LicenceCC BY
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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.