Evidence map›Paper›PMID 31882833›Full record

ArticleScientific reports2019

Differential immune response modulation in early Leishmania amazonensis infection of BALB/c and C57BL/6 macrophages based on transcriptome profiles.

Juliana Ide Aoki, Sandra Marcia Muxel, Ricardo Andrade Zampieri, Karl Erik Müller, Audun Helge Nerland, Lucile Maria Floeter-Winter

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 7% 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, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Experimental animal models of chronic inflammation.Current research in immunology · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Dissection of the macrophage response towards infection by theFrontiers in cellular and infection microbiology · 2022
    Article
  14. Article
  15. Article
  16. Metabolomic Reprogramming of C57BL/6-Macrophages during Early Infection withInternational journal of molecular sciences · 2021
    Article
  17. Advances in UnderstandingFrontiers in cell and developmental biology · 2021
    Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 3 countries.

Juliana Ide AokiDepartment of Physiology, Institute of Bioscience, University of São Paulo, São Paulo, Brazil. juaoki@usp.br.ORCID http://orcid.org/0000-0002-1745-0310
Sandra Marcia MuxelDepartment of Physiology, Institute of Bioscience, University of São Paulo, São Paulo, Brazil.
Ricardo Andrade ZampieriDepartment of Physiology, Institute of Bioscience, University of São Paulo, São Paulo, Brazil.
Karl Erik MüllerDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Audun Helge NerlandDepartment of Clinical Science, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0002-8272-0276
Lucile Maria Floeter-WinterDepartment of Physiology, Institute of Bioscience, University of São Paulo, São Paulo, Brazil. lucile@ib.usp.br.
Universidade de São Paulo · BRDrammen Hospital · NOUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fate of Leishmania infection can be strongly influenced by the host genetic background. In this work, we describe gene expression modulation of the immune system based on dual global transcriptome profiles of bone marrow-derived macrophages (BMDMs) from BALB/c and C57BL/6 mice infected with Leishmania amazonensis. A total of 12,641 host transcripts were identified according to the alignment to the Mus musculus genome. Differentially expressed genes (DEGs) profiling revealed a differential modulation of the basal genetic background between the two hosts independent of L. amazonensis infection. In addition, in response to early L. amazonensis infection, 10 genes were modulated in infected BALB/c vs. non-infected BALB/c macrophages; and 127 genes were modulated in infected C57BL/6 vs. non-infected C57BL/6 macrophages. These modulated genes appeared to be related to the main immune response processes, such as recognition, antigen presentation, costimulation and proliferation. The distinct gene expression was correlated with the susceptibility and resistance to infection of each host. Furthermore, upon comparing the DEGs in BMDMs vs. peritoneal macrophages, we observed no differences in the gene expression patterns of Jun, Fcgr1 and Il1b, suggesting a similar activation trends of transcription factor binding, recognition and phagocytosis, as well as the proinflammatory cytokine production in response to early L. amazonensis infection. Analysis of the DEG profile of the parasite revealed only one DEG among the 8,282 transcripts, indicating that parasite gene expression in early infection does not depend on the host genetic background.

Indexed as

TranscriptomeAnimalsGene Expression ProfilingHost-Parasite InteractionsLeishmaniaLeishmaniasisMacrophagesMacrophages, PeritonealMice, Inbred BALB CMice, Inbred C57BLReverse Transcriptase Polymerase Chain Reaction

Identifiers

PMID31882833
PMCPMC6934472
OpenAlexW2997806745

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.