Evidence map›Paper›PMID 35215152›Full record

ArticlePathogens (Basel, Switzerland)2022

Engineered Cell Line Imaging Assay Differentiates Pathogenic from Non-Pathogenic Bacteria.

Shelby M B Phillips, Carson Bergstrom, Brian Walker, George Wang, Trinidad Alfaro, Zachary R Stromberg, Becky M Hess

Open access · goldAbstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Shelby M B PhillipsChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA 99352, USA.ORCID 0000-0003-4036-9681
Carson BergstromChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA 99352, USA.
Brian WalkerChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA 99352, USA.
George WangChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA 99352, USA.
Trinidad AlfaroChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA 99352, USA.
Zachary R StrombergChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA 99352, USA.ORCID 0000-0002-1137-1128
Becky M HessChemical and Biological Signatures Group, Pacific Northwest National Laboratory, Richland, WA 99352, USA.ORCID 0000-0003-1093-5478
Pacific Northwest National Laboratory · US

Funding

Defense Advanced Research Projects Agency HR0011046601
6 · The paper itself

Abstract

Cell culture systems have greatly expanded our understanding of how bacterial pathogens target signaling pathways to manipulate the host and cause infection. Advances in genetic engineering have allowed for the creation of fluorescent protein readouts within signaling pathways, but these techniques have been underutilized in pathogen biology. Here, we genetically engineered a lung cell line with fluorescent reporters for extracellular signal-related kinase (ERK) and the downstream transcription factor FOS-related antigen 1 (Fra1) and evaluated signaling after inoculation with pathogenic and non-pathogenic bacteria. Cells were inoculated with 100 colony-forming units of

Indexed as

bio-agent agnostic signaturesdetectionfluorescent reportersmammalian cell engineeringpathogenicityprotein kinase

Identifiers

PMID35215152
PMCPMC8874627
OpenAlexW4210665691

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.