Evidence map›Paper›PMID 26284031›Full record

ArticleFrontiers in microbiology2015

A reverse-phase protein microarray-based screen identifies host signaling dynamics upon Burkholderia spp. infection.

Chih-Yuan Chiang, Ijeoma Uzoma, Douglas J Lane, Vesna Memišević, Farhang Alem, Kuan Yao, Krishna P Kota, Sina Bavari, Anders Wallqvist, Ramin M Hakami and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Innate immune response to Burkholderia mallei.Current opinion in infectious diseases · 2017
    Review
  6. Review
  7. Article
  8. 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 3 institutions in 1 country.

Chih-Yuan ChiangMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases, Frederick MD, USA.
Ijeoma UzomaMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases, Frederick MD, USA.
Douglas J LaneMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases, Frederick MD, USA.
Vesna MemiševićDepartment of Defense Biotechnology High Performance Computing Software Applications Institute, Telemedicine and Advanced Technology Research Center, United States Army Medical Research and Materiel Command, Frederick MD, USA.
Farhang AlemNational Center for Biodefense and Infectious Diseases, and School of Systems Biology, George Mason University, Manassas VA, USA.
Kuan YaoNational Center for Biodefense and Infectious Diseases, and School of Systems Biology, George Mason University, Manassas VA, USA.
Krishna P KotaPerkinElmer, Inc., Waltham MA, USA.
Sina BavariMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases, Frederick MD, USA.
Anders WallqvistDepartment of Defense Biotechnology High Performance Computing Software Applications Institute, Telemedicine and Advanced Technology Research Center, United States Army Medical Research and Materiel Command, Frederick MD, USA.
Ramin M HakamiNational Center for Biodefense and Infectious Diseases, and School of Systems Biology, George Mason University, Manassas VA, USA.
Rekha G PanchalMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases, Frederick MD, USA.
PerkinElmer (United States) · USTelemedicine & Advanced Technology Research Center · USUnited States Army Medical Research and Development Command · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Burkholderia is a diverse genus of gram-negative bacteria that causes high mortality rate in humans, equines and cattle. The lack of effective therapeutic treatments poses serious public health threats. Developing insights toward host-Burkholderia spp. interaction is critical for understanding the pathogenesis of infection as well as identifying therapeutic targets for drug development. Reverse-phase protein microarray technology was previously proven to identify and characterize novel biomarkers and molecular signatures associated with infectious disease and cancer. In the present study, this technology was utilized to interrogate changes in host protein expression and phosphorylation events in macrophages infected with a collection of geographically diverse strains of Burkholderia spp. The expression or phosphorylation state of 25 proteins was altered during Burkholderia spp. infections of which eight proteins were selected for further characterization by immunoblotting. Increased phosphorylation of AMPK-α1, Src, and GSK3β suggested the importance of their roles in regulating Burkholderia spp. mediated innate immune response. Modulating the inflammatory response by perturbing their activities may provide therapeutic routes for future treatments.

Indexed as

Burkholderia malleiBurkholderia pseudomalleilipopolysaccharidereverse-phase protein microarrays

Identifiers

PMID26284031
PMCPMC4515560
OpenAlexW1930358088

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.