Evidence map›Paper›PMID 16407112›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

The rat Toxo1 locus directs toxoplasmosis outcome and controls parasite proliferation and spreading by macrophage-dependent mechanisms.

Pierre Cavaillès, Véronique Sergent, Cordelia Bisanz, Olivier Papapietro, Céline Colacios, Magali Mas, Jean-François Subra, Dominique Lagrange, Maryline Calise, Sylvie Appolinaire and 7 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
2.1field-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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Unifying Virulence Evaluation inFrontiers in cellular and infection microbiology · 2022
    Review
  8. Forward Genetics in Apicomplexa Biology: The Host Side of the Story.Frontiers in cellular and infection microbiology · 2022
    Review
  9. Review
  10. Progesterone SuppressesFrontiers in microbiology · 2021
    Article
  11. Article
  12. The NLRP1 and CARD8 inflammasomes.Immunological reviews · 2020
    Review
  13. Influence of the Host and Parasite Strain on the Immune Response DuringFrontiers in cellular and infection microbiology · 2020
    Review
  14. Article
  15. Article
  16. ThreemBio · 2019
    Article
  17. Frontiers in cellular and infection microbiology · 2019
    Article
  18. Strategies Developed byFrontiers in microbiology · 2019
    Review
  19. 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

17 authors at 1 institution in 1 country.

Pierre CavaillèsInstitut National de la Santé et de la Recherche Médicale, Département de Génétique, Inserm U.563, Toulouse F-31300 France.
Véronique Sergent
Cordelia Bisanz
Olivier Papapietro
Céline Colacios
Magali Mas
Jean-François Subra
Dominique Lagrange
Maryline Calise
Sylvie Appolinaire
Thomas Faraut
Philippe Druet
Abdelhadi Saoudi
Marie-Hélène Bessieres
Bernard Pipy
Marie-France Cesbron-Delauw
Gilbert J Fournié
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toxoplasmosis is a healthcare problem in pregnant women and immunocompromised patients. Like humans, rats usually develop a subclinical chronic infection. LEW rats exhibit total resistance to Toxoplasma gondii infection, which is expressed in a dominant mode. A genome-wide search carried out in a cohort of F(2) progeny of susceptible BN and resistant LEW rats led to identify on chromosome 10 a major locus of control, which we called Toxo1. Using reciprocal BN and LEW lines congenic for chromosome 10 genomic regions from the other strain, Toxo1 was found to govern the issue of T. gondii infection whatever the remaining genome. Analyzes of rats characterized by genomic recombination within Toxo1, reduced the interval down to a 1.7-cM region syntenic to human 17p13. In vitro studies showed that the Toxo1-mediated refractoriness to T. gondii infection is associated with the ability of the macrophage to impede the proliferation of the parasite within the parasitophorous vacuole. In contrast, proliferation was observed in fibroblasts whatever the genomic origin of Toxo1. Furthermore, ex vivo studies indicate that macrophage controls parasitic infection spreading by a Toxo1-mediated mechanism. This forward genetics approach should ultimately unravel a major pathway of innate resistance to toxoplasmosis and possibly to other apicomplexan parasitic diseases.

Indexed as

Cell ProliferationGenetic Predisposition to DiseaseAnimalsAnimals, CongenicChromosome MappingFemaleFibroblastsGenetic LinkageGenetic MarkersInjections, IntraperitonealMacrophages, PeritonealMaleMicrosatellite RepeatsRatsRats, Inbred BNRats, Inbred LewGenetic Markers

Identifiers

PMID16407112
PMCPMC1334643
OpenAlexW2104144288

What OpenQuestion holds

Textmetadata
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.