Evidence map›Paper›PMID 28750194›Full record

ArticleVirulence2017

Ketoacidosis alone does not predispose to mucormycosis by Lichtheimia in a murine pulmonary infection model.

Bianca Schulze, Günter Rambach, Volker U Schwartze, Kerstin Voigt, Katja Schubert, Cornelia Speth, Ilse D Jacobsen

Open access · goldAbstract read
In one paragraph

Article in Virulence, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Molecular mechanisms that govern infection and antifungal resistance in Mucorales.Microbiology and molecular biology reviews : MMBR · 2024
    Review
  2. Review
  3. Hyphae ofJournal of fungi (Basel, Switzerland) · 2023
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. The impact of episporic modification ofComputational and structural biotechnology journal · 2021
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Animal Models to Study Mucormycosis.Journal of fungi (Basel, Switzerland) · 2019
    Review
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Bianca Schulzea Research Group Microbial Immunology, Leibniz Institute for Natural Product Research and Infection Biology, Hans-Knöll-Institute (HKI) , Jena , Germany.
Günter Rambachb Division of Hygiene and Medical Microbiology , Medical University of Innsbruck , Austria.
Volker U Schwartzed Jena Microbial Resource Collection, Leibniz Institute for Natural Product Research and Infection Biology, Hans-Knöll-Institute (HKI) , Jena , Germany.
Kerstin Voigtd Jena Microbial Resource Collection, Leibniz Institute for Natural Product Research and Infection Biology, Hans-Knöll-Institute (HKI) , Jena , Germany.
Katja Schuberta Research Group Microbial Immunology, Leibniz Institute for Natural Product Research and Infection Biology, Hans-Knöll-Institute (HKI) , Jena , Germany.
Cornelia Spethb Division of Hygiene and Medical Microbiology , Medical University of Innsbruck , Austria.
Ilse D Jacobsena Research Group Microbial Immunology, Leibniz Institute for Natural Product Research and Infection Biology, Hans-Knöll-Institute (HKI) , Jena , Germany.ORCID 0000-0002-6033-9984
Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) · DEInnsbruck Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucormycosis is a rare fungal infection; however, the number of cases increased during the last decades. The main risk factors are immunosuppression and uncontrolled diabetes mellitus. Although Lichtheimia species represent a common cause of mucormycosis in Europe, virulence and pathogenesis of this genus has not been investigated in detail yet. Using murine pulmonary infection models, we found that immunosuppression is essential for establishment of infection. The disease was characterized by necrosis, angioinvasion, thrombosis, and the lethal course of infection was associated with systemic activation of platelets. Furthermore, dissemination to internal organs was frequently observed. While the virulence potential of individual L. corymbifera and L. ramosa isolates differed, pathogenicity of both species was comparable. Although ketoacidosis promoted Rhizopus infection in mice, it did not predispose mice to infection with Lichtheimia in the absence of additional immunosuppression. This might partially explain the dominance of Rhizopus as cause of mucormycosis in countries with high prevalence of ketoacidotic patients.

Indexed as

AnimalsDisease Models, AnimalDisease SusceptibilityFemaleHumansImmunosuppression TherapyKetosisMiceMucoralesMucormycosisRhizopusVirulencediabetesimmunosuppressionLichtheimiaMucormycosispulmonary fungal infection

Identifiers

PMID28750194
PMCPMC5810507
OpenAlexW2741341690

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.