Evidence map›Paper›PMID 20552280›Full record

ArticleMycopathologia2010

Pathogenesis of pulmonary Cryptococcus gattii infection: a rat model.

Mark B Krockenberger, Richard Malik, Popchai Ngamskulrungroj, Luciana Trilles, Patricia Escandon, Susan Dowd, Chris Allen, Uwe Himmelreich, Paul J Canfield, Tania C Sorrell and 1 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Mycopathologia, 2010. 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
1.3field-weighted citation impact, top 19% 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, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Models for Inducing Experimental Cryptococcosis in Mice.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  4. Cryptococcus spp. and Cryptococcosis: focusing on the infection in Brazil.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2022
    Review
  5. A Possible Link between the Environment andInternational journal of environmental research and public health · 2022
    Article
  6. Article
  7. Article
  8. Rearing and Maintenance ofJournal of fungi (Basel, Switzerland) · 2020
    Review
  9. Animal Models ofFrontiers in immunology · 2020
    Review
  10. Clonal Dispersal ofJournal of fungi (Basel, Switzerland) · 2019
    Article
  11. Article
  12. Genotypic and Phenotypic Diversity ofFrontiers in microbiology · 2018
    Article
  13. Review
  14. Article
  15. Cryptococcosis.Infectious disease clinics of North America · 2016
    Review
  16. Cryptococcus gattii infections.Clinical microbiology reviews · 2014
    Review
  17. Article
  18. A murine model of Cryptococcus gattii meningoencephalitis.The Journal of antimicrobial chemotherapy · 2012
    Article
  19. Review
  20. Experimental models of cryptococcosis.International journal of microbiology · 2012
    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

11 authors at 5 institutions in 4 countries.

Mark B KrockenbergerFaculty of Veterinary Science, Building B14, University of Sydney, Sydney, NSW, 2006, Australia.
Richard Malik
Popchai Ngamskulrungroj
Luciana Trilles
Patricia Escandon
Susan Dowd
Chris Allen
Uwe Himmelreich
Paul J Canfield
Tania C Sorrell
Wieland Meyer
University of Sydney · AUFundação Oswaldo Cruz · BRMahidol University · THMax Planck Society · DERoyal Children's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A model of pulmonary cryptococcosis in immunocompetent rats was developed to better understand the virulence of Cryptococcus gattii. Six isolates were studied, representing four molecular genotypes (VGI-MATα, VGIIa-MATα, VGIIa-MAT a, VGIIb-MATα), obtained from Australia, Vancouver (Canada) and Colombia. These originated from human patients, a cat and the environment and were administered intratracheally (i.t.) or transthoracically into Fischer 344 or Wistar-Furth rats in doses varying from 10(4) to 10(7) colony-forming units (CFU) in 0.1 ml of saline. With the exception of animals given the VGIIa-MAT a isolate, rats consistently became ill or died of progressive cryptococcal pneumonia following i.t. doses exceeding 10(7) CFU. Affected lungs increased in weight up to tenfold and contained numerous circumscribed, gelatinous lesions. These became larger and more extensive, progressing from limited hilar and/or tracheal lesions, to virtually confluent gelatinous masses. Disease was localized to the lungs for at least 3-4 weeks, with dissemination to the brain occurring in some animals after day 29. The dose-response relationship was steep for two VGI isolates studied (human WM179, environmental WM276); doses up to 10(6) CFU i.t. did not produce lesions, while 10(7) or more yeast cells produced progressive pneumonia. Intratracheal inoculation of rats with C. gattii provides an excellent model of human pulmonary cryptococcosis in healthy hosts, mimicking natural infections. Disease produced by C. gattii in rats is distinct from that caused by C. neoformans in that infections are progressive and ultimately fatal.

Indexed as

Disease Models, AnimalAnimalsAustraliaBrainCanadaCat DiseasesCatsColombiaCryptococcosisCryptococcus gattiiEnvironmental MicrobiologyFemaleHumansLungLung Diseases, FungalMale

Identifiers

PMID20552280
OpenAlexW2032547598

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.