Evidence map›Paper›PMID 26545875›Full record

ArticleBMC microbiology2015

Characterization of the murine macrophage response to infection with virulent and avirulent Burkholderia species.

Chih-Yuan Chiang, Ricky L Ulrich, Melanie P Ulrich, Brett Eaton, Jenifer F Ojeda, Douglas J Lane, Krishna P Kota, Tara A Kenny, Jason T Ladner, Samuel P Dickson and 7 more

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Mitogen-activated protein kinases (MAPKs) are modulated during in vitro and in vivo infection with the intracellular bacterium Burkholderia pseudomallei.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2017
    Article
  9. Article
  10. Innate immune response to Burkholderia mallei.Current opinion in infectious diseases · 2017
    Review
  11. Article
  12. Review
  13. 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 5 institutions in 1 country.

Chih-Yuan ChiangMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, USA. chih-yuan.chiang.ctr@mail.mil.
Ricky L UlrichInstitute for Therapeutic Innovation, Department of Medicine, University of Florida, Orlando, FL, USA. labrat29@yahoo.com.
Melanie P UlrichFlorida SouthWestern State College, Fort Myers, FL, USA. Melanie.Ulrich@fsw.edu.
Brett EatonMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, USA. brett.p.eaton.ctr@mail.mil.
Jenifer F OjedaMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, USA. ojedaj2011@gmail.com.
Douglas J LaneMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, USA. douglas.j.lane.ctr@mail.mil.
Krishna P KotaPerkin Elmer, Waltham, MA, USA. krishna.p.kota.ctr@mail.mil.
Tara A KennyMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, USA. tara.a.kenny.ctr@mail.mil.
Jason T LadnerCenter for Genome Sciences, USAMRIID, Fort Detrick, MD, USA. jason.t.ladner.ctr@mail.mil.
Samuel P DicksonOffice of Regulated Studies, USAMRIID, Fort Detrick, MD, USA. spdickson@gmail.com.
Kathleen KuehlPathology Division, USAMRIID, Fort Detrick, MD, USA. kathleen.a.kuehl.civ@mail.mil.
Rahul RaychaudhuriPathology Division, USAMRIID, Fort Detrick, MD, USA. rahul.raychaudhuri.mil@mail.mil.
Mei SunPathology Division, USAMRIID, Fort Detrick, MD, USA. mei.g.sun.ctr@mail.mil.
Sina BavariMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, USA. sina.bavari.civ@mail.mil.
Mark J WolcottDiagnostic Systems Division, USAMRIID, Fort Detrick, MD, USA. mark.j.wolcott.civ@mail.mil.
David CovellScreening Technologies Branch, Developmental Therapeutics Program, National Cancer Institute, Frederick, MD, USA. CovellD@mail.nih.gov.
Rekha G PanchalMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, MD, USA. rekha.g.panchal.civ@mail.mil.
United States Army Medical Research Institute of Infectious Diseases · USFlorida SouthWestern State College · USNational Cancer Institute · USPerkinElmer (United States) · USUniversity of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBurkholderia pseudomallei (Bp) and Burkholderia mallei (Bm) are Gram-negative facultative intracellular pathogens, which are the causative agents of melioidosis and glanders, respectively. Depending on the route of exposure, aerosol or transcutaneous, infection by Bp or Bm can result in an extensive range of disease - from acute to chronic, relapsing illness to fatal septicemia. Both diseases are associated with difficult diagnosis and high fatality rates. About ninety five percent of patients succumb to untreated septicemic infections and the fatality rate is 50 % even when standard antibiotic treatments are administered.

resultsThe goal of this study is to profile murine macrophage-mediated phenotypic and molecular responses that are characteristic to a collection of Bp, Bm, Burkholderia thailandensis (Bt) and Burkholderia oklahomensis (Bo) strains obtained from humans, animals, environment and geographically diverse locations. Burkholderia spp. (N = 21) were able to invade and replicate in macrophages, albeit to varying degrees. All Bp (N = 9) and four Bm strains were able to induce actin polymerization on the bacterial surface following infection. Several Bp and Bm strains showed reduced ability to induce multinucleated giant cell (MNGC) formation, while Bo and Bp 776 were unable to induce this phenotype. Measurement of host cytokine responses revealed a statistically significant Bm mediated IL-6 and IL-10 production compared to Bp strains. Hierarchical clustering of transcriptional data from 84 mouse cytokines, chemokines and their corresponding receptors identified 29 host genes as indicators of differential responses between the Burkholderia spp. Further validation confirmed Bm mediated Il-1b, Il-10, Tnfrsf1b and Il-36a mRNA expressions were significantly higher when compared to Bp and Bt.

conclusionsThese results characterize the phenotypic and immunological differences in the host innate response to pathogenic and avirulent Burkholderia strains and provide insight into the phenotypic alterations and molecular targets underlying host-Burkholderia interactions.

Indexed as

ActinsAnimalsBurkholderia malleiBurkholderia pseudomalleiChemokinesGene Expression RegulationGiant CellsImmunity, InnateMacrophagesMiceRAW 264.7 CellsActinsChemokines

Identifiers

PMID26545875
PMCPMC4636792
OpenAlexW2160046626

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LicenceCC BY
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Registered trials

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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.