Evidence map›Paper›PMID 27973535›Full record

ArticlePLoS pathogens2016

The Influence of Programmed Cell Death in Myeloid Cells on Host Resilience to Infection with Legionella pneumophila or Streptococcus pyogenes.

Pia Gamradt, Yun Xu, Nina Gratz, Kellyanne Duncan, Lester Kobzik, Sandra Högler, Pavel Kovarik, Thomas Decker, Amanda M Jamieson

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2016. 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  8. Group AMicrobiology spectrum · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Pia GamradtMax F. Perutz Laboratories, University of Vienna, Vienna, Austria.
Yun XuDivision of Biology and Medicine, Department of Molecular Microbiology and Immunology, Brown University, Providence, Rhode Island, United States.
Nina GratzMax F. Perutz Laboratories, University of Vienna, Vienna, Austria.
Kellyanne DuncanDivision of Biology and Medicine, Department of Molecular Microbiology and Immunology, Brown University, Providence, Rhode Island, United States.
Lester KobzikDepartment of Environmental Health, Harvard School of Public Health, Boston, Massachusetts, United States.
Sandra HöglerInstitute of Pathology and Forensic Veterinary Medicine, Department of Pathobiology, University of Veterinary Medicine Vienna, Vienna, Austria.
Pavel KovarikMax F. Perutz Laboratories, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0003-2956-0944
Thomas DeckerMax F. Perutz Laboratories, University of Vienna, Vienna, Austria.
Amanda M JamiesonMax F. Perutz Laboratories, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-5781-9231
University of Vienna · ATBrown University · USUniversité Claude Bernard Lyon 1 · FRUniversity of Veterinary Medicine Vienna · AT

Funding

The role of Sirtuins in neurodegenerative diseaseP20GM109035 · NIGMS · BROWN UNIVERSITY · PI LIU, YAJUN · 2016 to 2025
$22.6M
Austrian Science Fund FWF P 25235NIGMS NIH HHS P20 GM109035
6 · The paper itself

Abstract

Pathogen clearance and host resilience/tolerance to infection are both important factors in surviving an infection. Cells of the myeloid lineage play important roles in both of these processes. Neutrophils, monocytes, macrophages, and dendritic cells all have important roles in initiation of the immune response and clearance of bacterial pathogens. If these cells are not properly regulated they can result in excessive inflammation and immunopathology leading to decreased host resilience. Programmed cell death (PCD) is one possible mechanism that myeloid cells may use to prevent excessive inflammation. Myeloid cell subsets play roles in tissue repair, immune response resolution, and maintenance of homeostasis, so excessive PCD may also influence host resilience in this way. In addition, myeloid cell death is one mechanism used to control pathogen replication and dissemination. Many of these functions for PCD have been well defined in vitro, but the role in vivo is less well understood. We created a mouse that constitutively expresses the pro-survival B-cell lymphoma (bcl)-2 protein in myeloid cells (CD68(bcl2tg), thus decreasing PCD specifically in myeloid cells. Using this mouse model we explored the impact that decreased cell death of these cells has on infection with two different bacterial pathogens, Legionella pneumophila and Streptococcus pyogenes. Both of these pathogens target multiple cell death pathways in myeloid cells, and the expression of bcl2 resulted in decreased PCD after infection. We examined both pathogen clearance and host resilience and found that myeloid cell death was crucial for host resilience. Surprisingly, the decreased myeloid PCD had minimal impact on pathogen clearance. These data indicate that the most important role of PCD during infection with these bacteria is to minimize inflammation and increase host resilience, not to aid in the clearance or prevent the spread of the pathogen.

Indexed as

AnimalsApoptosisFlow CytometryImmunity, InnateLegionella pneumophilaLegionnaires' DiseaseMiceMice, TransgenicMyeloid CellsStreptococcal InfectionsStreptococcus pyogenes

Identifiers

PMID27973535
PMCPMC5156374
OpenAlexW2564455569

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.